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Cell plasticity in epithelial homeostasis and tumorigenesis

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jcp.22264openalex-snapshot

TNFalpha up‐regulates SLUG via the NF‐kappaB/HIF1alpha axis, which imparts breast cancer cells with a stem cell‐like phenotype

inferredcites →https://doi.org/10.1002/stem.1296openalex-snapshot

Brief Report: Intravital Imaging of Cancer Stem Cell Plasticity in Mammary Tumors

inferredcites →https://doi.org/10.1007/s00428-010-1030-5openalex-snapshot

Frequent concomitant inactivation of miR-34a and miR-34b/c by CpG methylation in colorectal, pancreatic, mammary, ovarian, urothelial, and renal cell carcinomas and soft tissue sarcomas

inferredcites →https://doi.org/10.1016/j.ajpath.2013.01.009openalex-snapshot

Wounds That Will Not Heal

inferredcites →https://doi.org/10.1016/j.bpj.2013.07.011openalex-snapshot

Coupled Reversible and Irreversible Bistable Switches Underlying TGFβ-induced Epithelial to Mesenchymal Transition

inferredcites →https://doi.org/10.1016/j.ccell.2015.10.003openalex-snapshot

Mist1 Expressing Gastric Stem Cells Maintain the Normal and Neoplastic Gastric Epithelium and Are Supported by a Perivascular Stem Cell Niche

inferredcites →https://doi.org/10.1016/j.ccell.2015.11.001openalex-snapshot

HOXA5 Counteracts Stem Cell Traits by Inhibiting Wnt Signaling in Colorectal Cancer

inferredcites →https://doi.org/10.1016/j.ccell.2016.03.005openalex-snapshot

Tumoral Immune Cell Exploitation in Colorectal Cancer Metastases Can Be Targeted Effectively by Anti-CCR5 Therapy in Cancer Patients

inferredcites →https://doi.org/10.1016/j.ccr.2009.01.023openalex-snapshot

Cancer Metastasis Is Accelerated through Immunosuppression during Snail-Induced EMT of Cancer Cells

inferredcites →https://doi.org/10.1016/j.ccr.2009.03.016openalex-snapshot

Stabilization of Snail by NF-κB Is Required for Inflammation-Induced Cell Migration and Invasion

inferredcites →https://doi.org/10.1016/j.ccr.2011.09.009openalex-snapshot

Direct Signaling between Platelets and Cancer Cells Induces an Epithelial-Mesenchymal-Like Transition and Promotes Metastasis

inferredcites →https://doi.org/10.1016/j.ccr.2012.09.022openalex-snapshot

Spatiotemporal Regulation of Epithelial-Mesenchymal Transition Is Essential for Squamous Cell Carcinoma Metastasis

inferredcites →https://doi.org/10.1016/j.ccr.2012.10.012openalex-snapshot

Metastatic Colonization Requires the Repression of the Epithelial-Mesenchymal Transition Inducer Prrx1

inferredcites →https://doi.org/10.1016/j.ccr.2012.11.014openalex-snapshot

Loss of p53 in Enterocytes Generates an Inflammatory Microenvironment Enabling Invasion and Lymph Node Metastasis of Carcinogen-Induced Colorectal Tumors

inferredcites →https://doi.org/10.1016/j.ccr.2014.03.021openalex-snapshot

A Positive Feedback Loop between Mesenchymal-like Cancer Cells and Macrophages Is Essential to Breast Cancer Metastasis

inferredcites →https://doi.org/10.1016/j.cell.2010.01.025openalex-snapshot

Immunity, Inflammation, and Cancer

inferredcites →https://doi.org/10.1016/j.cell.2010.02.027openalex-snapshot

A Chromatin-Mediated Reversible Drug-Tolerant State in Cancer Cell Subpopulations

inferredcites →https://doi.org/10.1016/j.cell.2010.09.016openalex-snapshot

Intestinal Crypt Homeostasis Results from Neutral Competition between Symmetrically Dividing Lgr5 Stem Cells

inferredcites →https://doi.org/10.1016/j.cell.2011.07.026openalex-snapshot

Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells

inferredcites →https://doi.org/10.1016/j.cell.2011.11.025openalex-snapshot

EMT and Dissemination Precede Pancreatic Tumor Formation

inferredcites →https://doi.org/10.1016/j.cell.2012.12.012openalex-snapshot

Intestinal Tumorigenesis Initiated by Dedifferentiation and Acquisition of Stem-Cell-like Properties

inferredcites →https://doi.org/10.1016/j.cell.2013.02.021openalex-snapshot

Glioblastoma Stem Cells Generate Vascular Pericytes to Support Vessel Function and Tumor Growth

inferredcites →https://doi.org/10.1016/j.cell.2013.07.042openalex-snapshot

A Mechanical Checkpoint Controls Multicellular Growth through YAP/TAZ Regulation by Actin-Processing Factors

inferredcites →https://doi.org/10.1016/j.cell.2013.09.008openalex-snapshot

Differentiated Troy+ Chief Cells Act as Reserve Stem Cells to Generate All Lineages of the Stomach Epithelium

inferredcites →https://doi.org/10.1016/j.cell.2014.02.031openalex-snapshot

Genetic and Clonal Dissection of Murine Small Cell Lung Carcinoma Progression by Genome Sequencing

inferredcites →https://doi.org/10.1016/j.cell.2014.06.004openalex-snapshot

KRAS and YAP1 Converge to Regulate EMT and Tumor Survival

inferredcites →https://doi.org/10.1016/j.cell.2015.05.033openalex-snapshot

Apc Restoration Promotes Cellular Differentiation and Reestablishes Crypt Homeostasis in Colorectal Cancer

inferredcites →https://doi.org/10.1016/j.cell.2016.01.009openalex-snapshot

TGF-β Tumor Suppression through a Lethal EMT

inferredcites →https://doi.org/10.1016/j.cell.2016.05.052openalex-snapshot

Nfib Promotes Metastasis through a Widespread Increase in Chromatin Accessibility

inferredcites →https://doi.org/10.1016/j.cell.2016.06.028openalex-snapshot

EMT: 2016

inferredcites →https://doi.org/10.1016/j.celrep.2014.12.032openalex-snapshot

Stem-Cell-like Properties and Epithelial Plasticity Arise as Stable Traits after Transient Twist1 Activation

inferredcites →https://doi.org/10.1016/j.celrep.2015.11.025openalex-snapshot

Mesenchymal Cancer Cell-Stroma Crosstalk Promotes Niche Activation, Epithelial Reversion, and Metastatic Colonization

inferredcites →https://doi.org/10.1016/j.celrep.2016.02.034openalex-snapshot

Plasticity between Epithelial and Mesenchymal States Unlinks EMT from Metastasis-Enhancing Stem Cell Capacity

inferredcites →https://doi.org/10.1016/j.celrep.2016.03.088openalex-snapshot

Wnt Ligands Secreted by Subepithelial Mesenchymal Cells Are Essential for the Survival of Intestinal Stem Cells and Gut Homeostasis

inferredcites →https://doi.org/10.1016/j.chom.2014.05.003openalex-snapshot

The Cytosolic Bacterial Peptidoglycan Sensor Nod2 Affords Stem Cell Protection and Links Microbes to Gut Epithelial Regeneration

inferredcites →https://doi.org/10.1016/j.coph.2016.05.002openalex-snapshot

YAP/TAZ as therapeutic targets in cancer

inferredcites →https://doi.org/10.1016/j.devcel.2014.03.006openalex-snapshot

Mammary Morphogenesis and Regeneration Require the Inhibition of EMT at Terminal End Buds by Ovol2 Transcriptional Repressor

inferredcites →https://doi.org/10.1016/j.stem.2010.07.007openalex-snapshot

Oxygen in Stem Cell Biology: A Critical Component of the Stem Cell Niche

inferredcites →https://doi.org/10.1016/j.stem.2011.02.021openalex-snapshot

Nerve-Derived Sonic Hedgehog Defines a Niche for Hair Follicle Stem Cells Capable of Becoming Epidermal Stem Cells

inferredcites →https://doi.org/10.1016/j.stem.2013.03.002openalex-snapshot

A microRNA miR-34a-Regulated Bimodal Switch Targets Notch in Colon Cancer Stem Cells

inferredcites →https://doi.org/10.1016/j.stem.2013.07.010openalex-snapshot

The Epidermis Comprises Autonomous Compartments Maintained by Distinct Stem Cell Populations

inferredcites →https://doi.org/10.1016/j.stem.2014.02.006openalex-snapshot

Evolution of the Cancer Stem Cell Model

inferredcites →https://doi.org/10.1016/j.stem.2014.08.004openalex-snapshot

Liver Stem Cells, Where Art Thou?

inferredcites →https://doi.org/10.1016/j.stem.2015.02.015openalex-snapshot

The Cancer Stem Cell Niche: How Essential Is the Niche in Regulating Stemness of Tumor Cells?

inferredcites →https://doi.org/10.1016/j.stem.2015.04.014openalex-snapshot

Stem Cell Heterogeneity and Plasticity in Epithelia

inferredcites →https://doi.org/10.1016/j.stem.2016.01.001openalex-snapshot

Replacement of Lost Lgr5-Positive Stem Cells through Plasticity of Their Enterocyte-Lineage Daughters

inferredcites →https://doi.org/10.1016/j.stem.2016.01.006openalex-snapshot

A miR-34a-Numb Feedforward Loop Triggered by Inflammation Regulates Asymmetric Stem Cell Division in Intestine and Colon Cancer

inferredcites →https://doi.org/10.1016/j.stem.2016.03.016openalex-snapshot

Dclk1 Defines Quiescent Pancreatic Progenitors that Promote Injury-Induced Regeneration and Tumorigenesis

inferredcites →https://doi.org/10.1016/j.stem.2016.08.009openalex-snapshot

Induction of Expandable Tissue-Specific Stem/Progenitor Cells through Transient Expression of YAP/TAZ

inferredcites →https://doi.org/10.1016/j.stem.2016.10.018openalex-snapshot

Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition

inferredcites →https://doi.org/10.1016/j.stem.2016.11.003openalex-snapshot

Adaptive Chromatin Remodeling Drives Glioblastoma Stem Cell Plasticity and Drug Tolerance

inferredcites →https://doi.org/10.1016/j.tcb.2014.09.003openalex-snapshot

Plasticity within stem cell hierarchies in mammalian epithelia

inferredcites →https://doi.org/10.1016/j.tcb.2014.12.006openalex-snapshot

Integrins and cancer: regulators of cancer stemness, metastasis, and drug resistance

inferredcites →https://doi.org/10.1016/j.tcb.2015.07.012openalex-snapshot

Epithelial–Mesenchymal Plasticity: A Central Regulator of Cancer Progression

inferredcites →https://doi.org/10.1016/j.trecan.2015.07.006openalex-snapshot

En Route to Metastasis: Circulating Tumor Cell Clusters and Epithelial-to-Mesenchymal Transition

inferredcites →https://doi.org/10.1038/cddis.2013.442openalex-snapshot

An EMT spectrum defines an anoikis-resistant and spheroidogenic intermediate mesenchymal state that is sensitive to e-cadherin restoration by a src-kinase inhibitor, saracatinib (AZD0530)

inferredcites →https://doi.org/10.1038/nature05766openalex-snapshot

Wnt-dependent de novo hair follicle regeneration in adult mouse skin after wounding

inferredcites →https://doi.org/10.1038/nature06835openalex-snapshot

Cutaneous cancer stem cell maintenance is dependent on β-catenin signalling

inferredcites →https://doi.org/10.1038/nature07602openalex-snapshot

Crypt stem cells as the cells-of-origin of intestinal cancer

inferredcites →https://doi.org/10.1038/nature09624openalex-snapshot

Glioblastoma stem-like cells give rise to tumour endothelium

inferredcites →https://doi.org/10.1038/nature09637openalex-snapshot

Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts

inferredcites →https://doi.org/10.1038/nature10137openalex-snapshot

Role of YAP/TAZ in mechanotransduction

inferredcites →https://doi.org/10.1038/nature10408openalex-snapshot

A reserve stem cell population in small intestine renders Lgr5-positive cells dispensable

inferredcites →https://doi.org/10.1038/nature10694openalex-snapshot

Interactions between cancer stem cells and their niche govern metastatic colonization

inferredcites →https://doi.org/10.1038/nature11163openalex-snapshot

mTORC1 in the Paneth cell niche couples intestinal stem-cell function to calorie intake

inferredcites →https://doi.org/10.1038/nature11344openalex-snapshot

Defining the mode of tumour growth by clonal analysis

inferredcites →https://doi.org/10.1038/nature11965openalex-snapshot

Intestinal label-retaining cells are secretory precursors expressing Lgr5

inferredcites →https://doi.org/10.1038/nature12602openalex-snapshot

Spatial organization within a niche as a determinant of stem-cell fate

inferredcites →https://doi.org/10.1038/nature12777openalex-snapshot

Dedifferentiation of committed epithelial cells into stem cells in vivo

inferredcites →https://doi.org/10.1038/nature12783openalex-snapshot

Distinct fibroblast lineages determine dermal architecture in skin development and repair

inferredcites →https://doi.org/10.1038/nature12903openalex-snapshot

Broadly permissive intestinal chromatin underlies lateral inhibition and cell plasticity

inferredcites →https://doi.org/10.1038/nature14289openalex-snapshot

Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice

inferredcites →https://doi.org/10.1038/nature14347openalex-snapshot

The evolutionary history of lethal metastatic prostate cancer

inferredcites →https://doi.org/10.1038/nature14403openalex-snapshot

A model of breast cancer heterogeneity reveals vascular mimicry as a driver of metastasis

inferredcites →https://doi.org/10.1038/nature15260openalex-snapshot

Single-cell analysis reveals a stem-cell program in human metastatic breast cancer cells

inferredcites →https://doi.org/10.1038/nature15748openalex-snapshot

Epithelial-to-mesenchymal transition is not required for lung metastasis but contributes to chemoresistance

inferredcites →https://doi.org/10.1038/nature16064openalex-snapshot

Epithelial-to-mesenchymal transition is dispensable for metastasis but induces chemoresistance in pancreatic cancer

inferredcites →https://doi.org/10.1038/nature16460openalex-snapshot

Interleukin-22 promotes intestinal-stem-cell-mediated epithelial regeneration

inferredcites →https://doi.org/10.1038/nature17173openalex-snapshot

High-fat diet enhances stemness and tumorigenicity of intestinal progenitors

inferredcites →https://doi.org/10.1038/nature21713openalex-snapshot

A distinct role for Lgr5+ stem cells in primary and metastatic colon cancer

inferredcites →https://doi.org/10.1038/nature22816openalex-snapshot

Upholding a role for EMT in breast cancer metastasis

inferredcites →https://doi.org/10.1038/nature22817openalex-snapshot

Fischer et al. reply

inferredcites →https://doi.org/10.1038/nature22963openalex-snapshot

Upholding a role for EMT in pancreatic cancer metastasis

inferredcites →https://doi.org/10.1038/ncb2581openalex-snapshot

Dll1+ secretory progenitor cells revert to stem cells upon crypt damage

inferredcites →https://doi.org/10.1038/ncb2910openalex-snapshot

MicroRNA-146a directs the symmetric division of Snail-dominant colorectal cancer stem cells

inferredcites →https://doi.org/10.1038/ncb3157openalex-snapshot

Matrix stiffness drives epithelial–mesenchymal transition and tumour metastasis through a TWIST1–G3BP2 mechanotransduction pathway

inferredcites →https://doi.org/10.1038/ncb3309openalex-snapshot

Stem cells versus plasticity in liver and pancreas regeneration

inferredcites →https://doi.org/10.1038/ncb3340openalex-snapshot

Macrophage-secreted granulin supports pancreatic cancer metastasis by inducing liver fibrosis

inferredcites →https://doi.org/10.1038/ncb3513openalex-snapshot

The EMT-activator Zeb1 is a key factor for cell plasticity and promotes metastasis in pancreatic cancer

inferredcites →https://doi.org/10.1038/ncb3541openalex-snapshot

Lgr5-expressing chief cells drive epithelial regeneration and cancer in the oxyntic stomach

inferredcites →https://doi.org/10.1038/ncomms10916openalex-snapshot

Bcl-2 is a critical mediator of intestinal transformation

inferredcites →https://doi.org/10.1038/ncomms13096openalex-snapshot

Macrophage-derived extracellular vesicle-packaged WNTs rescue intestinal stem cells and enhance survival after radiation injury

inferredcites →https://doi.org/10.1038/ncomms6241openalex-snapshot

Metastasis is regulated via microRNA-200/ZEB1 axis control of tumour cell PD-L1 expression and intratumoral immunosuppression

inferredcites →https://doi.org/10.1038/ncomms6671openalex-snapshot

miR-205 acts as a tumour radiosensitizer by targeting ZEB1 and Ubc13

inferredcites →https://doi.org/10.1038/ncomms6728openalex-snapshot

Transformation of intestinal stem cells into gastric stem cells on loss of transcription factor Cdx2

inferredcites →https://doi.org/10.1038/ng.165openalex-snapshot

Bmi1 is expressed in vivo in intestinal stem cells

inferredcites →https://doi.org/10.1038/ng.2481openalex-snapshot

Dclk1 distinguishes between tumor and normal stem cells in the intestine

inferredcites →https://doi.org/10.1038/ng.3165openalex-snapshot

BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence

inferredcites →https://doi.org/10.1038/ng.3224openalex-snapshot

Stromal contribution to the colorectal cancer transcriptome

inferredcites →https://doi.org/10.1038/ng.3225openalex-snapshot

Stromal gene expression defines poor-prognosis subtypes in colorectal cancer

inferredcites →https://doi.org/10.1038/ng.3398openalex-snapshot

Virtual microdissection identifies distinct tumor- and stroma-specific subtypes of pancreatic ductal adenocarcinoma

inferredcites →https://doi.org/10.1038/ni.2408openalex-snapshot

Monocytes-macrophages that express α-smooth muscle actin preserve primitive hematopoietic cells in the bone marrow

inferredcites →https://doi.org/10.1038/ni.3492openalex-snapshot

Tumor-induced stromal reprogramming drives lymph node transformation

inferredcites →https://doi.org/10.1038/nm.2344openalex-snapshot

Subtypes of pancreatic ductal adenocarcinoma and their differing responses to therapy

inferredcites →https://doi.org/10.1038/nm.2401openalex-snapshot

Direct targeting of Sec23a by miR-200s influences cancer cell secretome and promotes metastatic colonization

inferredcites →https://doi.org/10.1038/nm.3174openalex-snapshot

Poor-prognosis colon cancer is defined by a molecularly distinct subtype and develops from serrated precursor lesions

inferredcites →https://doi.org/10.1038/nm.3175openalex-snapshot

A colorectal cancer classification system that associates cellular phenotype and responses to therapy

inferredcites →https://doi.org/10.1038/nm.3181openalex-snapshot

Fgf9 from dermal γδ T cells induces hair follicle neogenesis after wounding

inferredcites →https://doi.org/10.1038/nm.3418openalex-snapshot

Self-renewal as a therapeutic target in human colorectal cancer

inferredcites →https://doi.org/10.1038/nm.3750openalex-snapshot

Aberrant epithelial GREM1 expression initiates colonic tumorigenesis from cells outside the stem cell niche

inferredcites →https://doi.org/10.1038/nm.3967openalex-snapshot

The consensus molecular subtypes of colorectal cancer

inferredcites →https://doi.org/10.1038/nm1328openalex-snapshot

Stem cells in the hair follicle bulge contribute to wound repair but not to homeostasis of the epidermis

inferredcites →https://doi.org/10.1038/nrc3265openalex-snapshot

To differentiate or not — routes towards metastasis

inferredcites →https://doi.org/10.1038/nrclinonc.2017.44openalex-snapshot

EMT, CSCs, and drug resistance: the mechanistic link and clinical implications

inferredcites →https://doi.org/10.1038/nrm.2016.24openalex-snapshot

Adult cell plasticity in vivo: de-differentiation and transdifferentiation are back in style

inferredcites →https://doi.org/10.1038/nrm3620openalex-snapshot

Role of the extracellular matrix in regulating stem cell fate

inferredcites →https://doi.org/10.1038/onc.2009.180openalex-snapshot

Interleukin-6 induces an epithelial–mesenchymal transition phenotype in human breast cancer cells

inferredcites →https://doi.org/10.1038/sj.onc.1209808openalex-snapshot

NF-κB represses E-cadherin expression and enhances epithelial to mesenchymal transition of mammary epithelial cells: potential involvement of ZEB-1 and ZEB-2

inferredcites →https://doi.org/10.1053/j.gastro.2011.01.005openalex-snapshot

Dll1- and Dll4-Mediated Notch Signaling Are Required for Homeostasis of Intestinal Stem Cells

inferredcites →https://doi.org/10.1053/j.gastro.2012.03.044openalex-snapshot

Interleukin-22 Promotes Proliferation of Liver Stem/Progenitor Cells in Mice and Patients With Chronic Hepatitis B Virus Infection

inferredcites →https://doi.org/10.1053/j.gastro.2016.11.049openalex-snapshot

Mesenchymal Cells in Colon Cancer

inferredcites →https://doi.org/10.1073/pnas.1012720108openalex-snapshot

Identifying the cellular origin of squamous skin tumors

inferredcites →https://doi.org/10.1073/pnas.1206653109openalex-snapshot

Critical role for lysyl oxidase in mesenchymal stem cell-driven breast cancer malignancy

inferredcites →https://doi.org/10.1073/pnas.1318192110openalex-snapshot

MicroRNA-based regulation of epithelial–hybrid–mesenchymal fate determination

inferredcites →https://doi.org/10.1073/pnas.1411082111openalex-snapshot

Platelets guide the formation of early metastatic niches

inferredcites →https://doi.org/10.1074/jbc.m112.375881openalex-snapshot

Toll-like Receptor 4 Is Expressed on Intestinal Stem Cells and Regulates Their Proliferation and Apoptosis via the p53 Up-regulated Modulator of Apoptosis

inferredcites →https://doi.org/10.1083/jcb.201102147openalex-snapshot

The extracellular matrix: A dynamic niche in cancer progression

inferredcites →https://doi.org/10.1083/jcb.201301001openalex-snapshot

Macrophage-secreted cytokines drive pancreatic acinar-to-ductal metaplasia through NF-κB and MMPs

inferredcites →https://doi.org/10.1084/jem.20122308openalex-snapshot

Innate lymphoid cells sustain colon cancer through production of interleukin-22 in a mouse model

inferredcites →https://doi.org/10.1101/gad.207803.112openalex-snapshot

Robust cellular reprogramming occurs spontaneously during liver regeneration

inferredcites →https://doi.org/10.1101/gad.277681.116openalex-snapshot

Distinctive properties of metastasis-initiating cells

inferredcites →https://doi.org/10.1126/science.1065718openalex-snapshot

Requirement of Math1 for Secretory Cell Lineage Commitment in the Mouse Intestine

inferredcites →https://doi.org/10.1126/science.1196236openalex-snapshot

Intestinal Stem Cell Replacement Follows a Pattern of Neutral Drift

inferredcites →https://doi.org/10.1126/science.1224676openalex-snapshot

Lineage Tracing Reveals Lgr5 + Stem Cell Activity in Mouse Intestinal Adenomas

inferredcites →https://doi.org/10.1126/science.1228522openalex-snapshot

Circulating Breast Tumor Cells Exhibit Dynamic Changes in Epithelial and Mesenchymal Composition

inferredcites →https://doi.org/10.1126/science.1239730openalex-snapshot

Interfollicular Epidermal Stem Cells Self-Renew via Autocrine Wnt Signaling

inferredcites →https://doi.org/10.1126/science.1240104openalex-snapshot

Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation

inferredcites →https://doi.org/10.1126/science.1242281openalex-snapshot

Plasticity of epithelial stem cells in tissue regeneration

inferredcites →https://doi.org/10.1126/scisignal.aaa7540openalex-snapshot

Reserve stem cells: Differentiated cells reprogram to fuel repair, metaplasia, and neoplasia in the adult gastrointestinal tract

inferredcites →https://doi.org/10.1158/0008-5472.can-11-2905openalex-snapshot

Myeloid Progenitor Cells in the Premetastatic Lung Promote Metastases by Inducing Mesenchymal to Epithelial Transition

inferredcites →https://doi.org/10.1158/0008-5472.can-12-4085openalex-snapshot

Connective Tissue Growth Factor Activates Pluripotency Genes and Mesenchymal–Epithelial Transition in Head and Neck Cancer Cells

inferredcites →https://doi.org/10.1158/0008-5472.can-14-0923openalex-snapshot

Transient SNAIL1 Expression Is Necessary for Metastatic Competence in Breast Cancer

inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-6735openalex-snapshot

Snail Up-regulates Proinflammatory Mediators and Inhibits Differentiation in Oral Keratinocytes

inferredcites →https://doi.org/10.1158/1535-7163.mct-10-1120openalex-snapshot

Cancer Cells Cyclically Lose and Regain Drug-Resistant Highly Tumorigenic Features Characteristic of a Cancer Stem-like Phenotype

inferredcites →https://doi.org/10.1158/2159-8290.cd-15-0120openalex-snapshot

Pancreatic Cancer Metastases Harbor Evidence of Polyclonality

inferredcites →https://doi.org/10.1172/jci41004openalex-snapshot

The therapeutic promise of the cancer stem cell concept

inferredcites →https://doi.org/10.1172/jci43414openalex-snapshot

Human prostate cancer metastases target the hematopoietic stem cell niche to establish footholds in mouse bone marrow

inferredcites →https://doi.org/10.1172/jci59218openalex-snapshot

Epithelial-mesenchymal transition can suppress major attributes of human epithelial tumor-initiating cells

inferredcites →https://doi.org/10.1172/jci63212openalex-snapshot

Cholangiocarcinomas can originate from hepatocytes in mice

inferredcites →https://doi.org/10.1172/jci73434openalex-snapshot

Long-lived intestinal tuft cells serve as colon cancer–initiating cells

inferredcites →https://doi.org/10.1172/jci73531openalex-snapshot

IL-6R/STAT3/miR-34a feedback loop promotes EMT-mediated colorectal cancer invasion and metastasis

inferredcites →https://doi.org/10.1177/1535370213480714openalex-snapshot

CD44 integrates signaling in normal stem cell, cancer stem cell and (pre)metastatic niches

inferredcites →https://doi.org/10.1182/blood-2013-02-486142openalex-snapshot

Deletion of the NF-κB subunit p65/RelA in the hematopoietic compartment leads to defects in hematopoietic stem cell function

inferredcites →https://doi.org/10.1186/gb-2013-14-5-r50openalex-snapshot

DNA methylation dynamics during intestinal stem cell differentiation reveals enhancers driving gene expression in the villus

inferredcites →https://doi.org/10.1242/dev.133132openalex-snapshot

Regulation and plasticity of intestinal stem cells during homeostasis and regeneration

inferredcites →https://doi.org/10.15252/emmm.201404208openalex-snapshot

Epithelial‐mesenchymal transition spectrum quantification and its efficacy in deciphering survival and drug responses of cancer patients

inferredcites →https://doi.org/10.15252/emmm.201404396openalex-snapshot

ZEB1‐associated drug resistance in cancer cells is reversed by the class I HDAC inhibitor mocetinostat

inferredcites →https://doi.org/10.18632/oncotarget.4629openalex-snapshot

Coupling the modules of EMT and stemness: A tunable ‘stemness window’ model

inferredcites →https://doi.org/10.18632/oncotarget.8166openalex-snapshot

Stability of the hybrid epithelial/mesenchymal phenotype

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3992681openalex-extracted

Intercellular Regulation of Apical-Basal Polarity Coordinates Tissue Homeostasis and Growth

inferred← citeshttps://doi.org/10.1002/adtp.202000065openalex-snapshot

Id1 and Id3 Are Regulated Through Matrix‐Assisted Autocrine BMP Signaling and Represent Therapeutic Targets in Melanoma

inferred← citeshttps://doi.org/10.1002/advs.202002825openalex-snapshot

Engineered Tools to Study Intercellular Communication

inferred← citeshttps://doi.org/10.1002/glia.23643openalex-snapshot

Schwann cell plasticity‐roles in tissue homeostasis, regeneration, and disease

inferred← citeshttps://doi.org/10.1002/jcp.29880openalex-snapshot

Long noncoding RNA EPB41L4A‐AS1 functions as an oncogene by regulating the Rho/ROCK pathway in colorectal cancer

inferred← citeshttps://doi.org/10.1002/jcp.30393openalex-snapshot

Long noncoding RNAs in intestinal homeostasis, regeneration, and cancer

inferred← citeshttps://doi.org/10.1002/tox.24475openalex-snapshot

Intervention of a Communication Between PI3K /Akt and β‐Catenin by (−)‐Epigallocatechin‐3‐Gallate Suppresses TGF ‐β1‐Promoted Epithelial‐Mesenchymal Transition and Invasive Phenotype of NSCLC Cells

inferred← citeshttps://doi.org/10.1007/978-1-0716-1979-7_24openalex-snapshot

Reprogramming Mouse Oviduct Epithelial Cells Using In Vivo Electroporation and CRISPR/Cas9-Mediated Genetic Manipulation

inferred← citeshttps://doi.org/10.1007/978-3-030-32656-2_19openalex-snapshot

Neural Transcription Factors in Disease Progression

inferred← citeshttps://doi.org/10.1007/978-3-319-90695-9_12openalex-snapshot

Stem Cells and Cancer

inferred← citeshttps://doi.org/10.1007/978-3-662-65873-4_12openalex-snapshot

Onkologische Krankheiten

inferred← citeshttps://doi.org/10.1007/s00441-019-03153-0openalex-snapshot

Plakophilins and their roles in diseased states

inferred← citeshttps://doi.org/10.1007/s10142-025-01564-7openalex-snapshot

Single-cell RNA sequencing revealed changes in the tumor microenvironment induced by radiotherapy for cervical cancer and the molecular mechanism of mast cells in immunosuppression

inferred← citeshttps://doi.org/10.1007/s10555-021-09970-6openalex-snapshot

Chemokines orchestrate tumor cells and the microenvironment to achieve metastatic heterogeneity

inferred← citeshttps://doi.org/10.1007/s10555-021-10006-2openalex-snapshot

The role of metabolic ecosystem in cancer progression — metabolic plasticity and mTOR hyperactivity in tumor tissues

inferred← citeshttps://doi.org/10.1007/s10585-018-9930-xopenalex-snapshot

The role of hypoxic signalling in metastasis: towards translating knowledge of basic biology into novel anti-tumour strategies

inferred← citeshttps://doi.org/10.1007/s13167-021-00257-yopenalex-snapshot

Flavonoids against non-physiologic inflammation attributed to cancer initiation, development, and progression—3PM pathways

inferred← citeshttps://doi.org/10.1007/s13346-021-00931-8openalex-snapshot

Delivery of transcription factors as modulators of cell differentiation

inferred← citeshttps://doi.org/10.1007/s13402-021-00623-yopenalex-snapshot

The impact of mitochondria on cancer treatment resistance

inferred← citeshttps://doi.org/10.1007/s41745-020-00182-5openalex-snapshot

Interaction of cancer cells with mesenchymal stem cells: implications in metastatic progression

inferred← citeshttps://doi.org/10.1016/b978-0-12-823397-9.00003-xopenalex-snapshot

Inflammation and cancer

inferred← citeshttps://doi.org/10.1016/bs.acr.2023.02.008openalex-snapshot

Deciphering epithelial-to-mesenchymal transition in pancreatic cancer

inferred← citeshttps://doi.org/10.1016/bs.acr.2025.06.001openalex-snapshot

Plasticity in cell adhesion during tumor progression

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2018.12.011openalex-snapshot

Serum CEA levels in 49 different types of cancer and noncancer diseases

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2018.12.012openalex-snapshot

Serum CA125 levels are decreased in rectal cancer but increased in fibrosis-associated diseases and in most types of cancers

inferred← citeshttps://doi.org/10.1016/j.archoralbio.2026.106520openalex-snapshot

Comparative analysis of patient-derived organoids among oral squamous cell carcinoma and mucosa identifies the distinct features

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118784openalex-snapshot

Impact of intercellular connectivity on epithelial mesenchymal transition plasticity

inferred← citeshttps://doi.org/10.1016/j.bbcan.2018.07.001openalex-snapshot

Hybrid epithelial/mesenchymal phenotype(s): The ‘fittest’ for metastasis?

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.01.184openalex-snapshot

ILK-induced epithelial-mesenchymal transition promotes the invasive phenotype in adenomyosis

inferred← citeshttps://doi.org/10.1016/j.bcp.2021.114657openalex-snapshot

MALAT1: A Promising Therapeutic Target for the Treatment of Metastatic Colorectal Cancer

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.01.048openalex-snapshot

Nucleus-targeted nano delivery system eradicates cancer stem cells by combined thermotherapy and hypoxia-activated chemotherapy

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2022.121785openalex-snapshot

Substratum interactions modulate interplay between endothelial cell, epithelial cell, and fibroblast phenotype and immunomodulatory function

inferred← citeshttps://doi.org/10.1016/j.canlet.2018.06.005openalex-snapshot

Human colorectal cancer initiation is bidirectional, and cell growth, metabolic genes and transporter genes are early drivers of tumorigenesis

inferred← citeshttps://doi.org/10.1016/j.celrep.2019.11.019openalex-snapshot

Modeling Progressive Fibrosis with Pluripotent Stem Cells Identifies an Anti-fibrotic Small Molecule

inferred← citeshttps://doi.org/10.1016/j.colsurfa.2025.136744openalex-snapshot

Mechanobiological reprogramming in liver cancer: Conjugated linoleic acid disrupts EMT and cytoskeletal dynamics

inferred← citeshttps://doi.org/10.1016/j.cossms.2020.100872openalex-snapshot

Mechanical regulation of histone modifications and cell plasticity

inferred← citeshttps://doi.org/10.1016/j.cub.2021.03.094openalex-snapshot

EPHA2-dependent outcompetition of KRASG12D mutant cells by wild-type neighbors in the adult pancreas

inferred← citeshttps://doi.org/10.1016/j.cytogfr.2023.05.003openalex-snapshot

Acinar cells and the development of pancreatic fibrosis

inferred← citeshttps://doi.org/10.1016/j.devcel.2022.01.011openalex-snapshot

SRSF1 governs progenitor-specific alternative splicing to maintain adult epithelial tissue homeostasis and renewal

inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174058openalex-snapshot

Inhibition of the Notch signaling pathway attenuates progression of cell motility, metastasis, and epithelial-to-mesenchymal transition-like phenomena induced by low concentrations of cisplatin in osteosarcoma

inferred← citeshttps://doi.org/10.1016/j.immuni.2019.06.025openalex-snapshot

Inflammation and Cancer: Triggers, Mechanisms, and Consequences

inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110760openalex-snapshot

Natural killer cells contribute to ‘hot’ tumor regression in the allergic inflammatory environment

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112067openalex-snapshot

FOXF1 reverses lung fibroblasts transdifferentiation via inhibiting TGF-β/SMAD2/3 pathway in silica-induced pulmonary fibrosis

inferred← citeshttps://doi.org/10.1016/j.intimp.2026.116832openalex-snapshot

cGAS-STING Signalling in the tumour microenvironment: Implications for immune surveillance and therapeutic strategies

inferred← citeshttps://doi.org/10.1016/j.isci.2023.106490openalex-snapshot

Coordination of tissue homeostasis and growth by the Scribble-α-Catenin-Septate junction complex

inferred← citeshttps://doi.org/10.1016/j.jceh.2023.08.004openalex-snapshot

Preoperative Locoregional Therapy May Relate with Stemness and Distinct Transitions Between Epithelial and Mesenchymal States in Hepatocellular Carcinoma

inferred← citeshttps://doi.org/10.1016/j.jgg.2021.05.002openalex-snapshot

Single-cell transcriptomic profiling of non-hematopoietic circulating cells in mid-gestational mouse embryos

inferred← citeshttps://doi.org/10.1016/j.jnutbio.2019.108219openalex-snapshot

Sulforaphane inhibits epithelial–mesenchymal transition by activating extracellular signal-regulated kinase 5 in lung cancer cells

inferred← citeshttps://doi.org/10.1016/j.lfs.2019.05.076openalex-snapshot

Cancer stem cell (a)symmetry & plasticity: Tumorigenesis and therapy relevance

inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118589openalex-snapshot

Cellular plasticity and drug resistance in sarcoma

inferred← citeshttps://doi.org/10.1016/j.metop.2025.100347openalex-snapshot

Unveiling the link between chronic inflammation and cancer

inferred← citeshttps://doi.org/10.1016/j.molimm.2018.11.006openalex-snapshot

Grainyhead-like-2 confers NK-sensitivity through interactions with epigenetic modifiers

inferred← citeshttps://doi.org/10.1016/j.molmet.2020.02.005openalex-snapshot

A non-proliferative role of pyrimidine metabolism in cancer

inferred← citeshttps://doi.org/10.1016/j.nantod.2026.103039openalex-snapshot

Lipid nanoparticle used in mRNA vaccine promotes tumor metastasis in mouse model via mtDNA-induced neutrophil activation and NETosis

inferred← citeshttps://doi.org/10.1016/j.neo.2019.10.001openalex-snapshot

Prostaglandin F2α-induced Prostate Transmembrane Protein, Androgen Induced 1 mediates ovarian cancer progression increasing epithelial plasticity

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2025.04.001openalex-snapshot

Advances in the study of epithelial mesenchymal transition in cancer progression: Role of miRNAs

inferred← citeshttps://doi.org/10.1016/j.phymed.2022.154359openalex-snapshot

Xanthorrhizol, a potential anticancer agent, from Curcuma xanthorrhiza Roxb

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2022.101148openalex-snapshot

Cell identity changes in ocular surface Epithelia

inferred← citeshttps://doi.org/10.1016/j.stem.2018.11.011openalex-snapshot

Phenotypic Plasticity: Driver of Cancer Initiation, Progression, and Therapy Resistance

inferred← citeshttps://doi.org/10.1016/j.suronc.2020.04.017openalex-snapshot

Cell plasticity in cancer: A complex interplay of genetic, epigenetic mechanisms and tumor micro-environment

inferred← citeshttps://doi.org/10.1016/j.tcb.2018.01.010openalex-snapshot

Recent Advances in Lgr5 + Stem Cell Research

inferred← citeshttps://doi.org/10.1038/s41368-020-00090-5openalex-snapshot

Loss of oral mucosal stem cell markers in oral submucous fibrosis and their reactivation in malignant transformation

inferred← citeshttps://doi.org/10.1038/s41388-018-0551-2openalex-snapshot

Loss of Stat6 affects chromatin condensation in intestinal epithelial cells causing diverse outcome in murine models of inflammation-associated and sporadic colon carcinogenesis

inferred← citeshttps://doi.org/10.1038/s41388-021-01847-wopenalex-snapshot

Transglutaminase 2 promotes tumorigenicity of colon cancer cells by inactivation of the tumor suppressor p53

inferred← citeshttps://doi.org/10.1038/s41388-022-02429-0openalex-snapshot

A high-throughput drug screen reveals means to differentiate triple-negative breast cancer

inferred← citeshttps://doi.org/10.1038/s41392-020-00313-5openalex-snapshot

Emerging role of tumor cell plasticity in modifying therapeutic response

inferred← citeshttps://doi.org/10.1038/s41416-020-01127-6openalex-snapshot

Genomic control of metastasis

inferred← citeshttps://doi.org/10.1038/s41419-020-2257-yopenalex-snapshot

Lipid desaturation-associated endoplasmic reticulum stress regulates MYCN gene expression in hepatocellular carcinoma cells

inferred← citeshttps://doi.org/10.1038/s41419-020-2560-7openalex-snapshot

LGR5+ epithelial tumor stem-like cells generate a 3D-organoid model for ameloblastoma

inferred← citeshttps://doi.org/10.1038/s41419-021-03757-xopenalex-snapshot

DNAJB9 suppresses the metastasis of triple-negative breast cancer by promoting FBXO45-mediated degradation of ZEB1

inferred← citeshttps://doi.org/10.1038/s41419-023-05847-4openalex-snapshot

Targeting transglutaminase 2 mediated exostosin glycosyltransferase 1 signaling in liver cancer stem cells with acyclic retinoid

inferred← citeshttps://doi.org/10.1038/s41420-024-02275-xopenalex-snapshot

The plasticity of epithelial cells and its potential in the induced differentiation of gastric cancer

inferred← citeshttps://doi.org/10.1038/s41421-022-00474-3openalex-snapshot

Identification of a rare Gli1+ progenitor cell population contributing to liver regeneration during chronic injury

inferred← citeshttps://doi.org/10.1038/s41467-021-20906-0openalex-snapshot

Epithelial expression of Gata4 and Sox2 regulates specification of the squamous–columnar junction via MAPK/ERK signaling in mice

inferred← citeshttps://doi.org/10.1038/s41467-021-27322-4openalex-snapshot

Single-cell analysis of human primary prostate cancer reveals the heterogeneity of tumor-associated epithelial cell states

inferred← citeshttps://doi.org/10.1038/s41467-022-34863-9openalex-snapshot

Breast cancer plasticity is restricted by a LATS1-NCOR1 repressive axis

inferred← citeshttps://doi.org/10.1038/s41467-023-37161-0openalex-snapshot

YBX1 integration of oncogenic PI3K/mTOR signalling regulates the fitness of malignant epithelial cells

inferred← citeshttps://doi.org/10.1038/s41467-025-67078-9openalex-snapshot

Actin dysregulation induces neuroendocrine plasticity and immune evasion: a vulnerability of small cell lung cancer

inferred← citeshttps://doi.org/10.1038/s41556-018-0145-9openalex-snapshot

Metastatic niche functions and therapeutic opportunities

inferred← citeshttps://doi.org/10.1038/s41556-018-0195-zopenalex-snapshot

Mesenchymal–epithelial transition in development and reprogramming

inferred← citeshttps://doi.org/10.1038/s41556-018-0196-yopenalex-snapshot

Non-redundant functions of EMT transcription factors

inferred← citeshttps://doi.org/10.1038/s41556-021-00679-wopenalex-snapshot

A biomechanical switch regulates the transition towards homeostasis in oesophageal epithelium

inferred← citeshttps://doi.org/10.1038/s41575-024-00980-7openalex-snapshot

Dietary and metabolic effects on intestinal stem cells in health and disease

inferred← citeshttps://doi.org/10.1038/s41586-026-10890-0openalex-snapshot

ZFP36L2 orchestrates stress-adaptive plasticity in regeneration and cancer

inferred← citeshttps://doi.org/10.1038/s41598-021-03708-8openalex-snapshot

Generation of a lung squamous cell carcinoma three-dimensional culture model with keratinizing structures

inferred← citeshttps://doi.org/10.1038/s41598-021-97351-yopenalex-snapshot

Expression of LGR5 in mammary myoepithelial cells and in triple-negative breast cancers

inferred← citeshttps://doi.org/10.1038/s41598-024-75219-1openalex-snapshot

Chromosome 8q24 amplification associated with human hepatocellular carcinoma predicts MYC/ZEB1/MIZ1 transcriptional regulation

inferred← citeshttps://doi.org/10.1038/s42003-018-0215-3openalex-snapshot

Sox9 regulates cell state and activity of embryonic mouse mammary progenitor cells

inferred← citeshttps://doi.org/10.1038/s42003-022-03637-wopenalex-snapshot

PI3Kδ activity controls plasticity and discriminates between EMT and stemness based on distinct TGFβ signaling

inferred← citeshttps://doi.org/10.1038/s43018-019-0006-xopenalex-snapshot

L1CAM defines the regenerative origin of metastasis-initiating cells in colorectal cancer

inferred← citeshttps://doi.org/10.1073/pnas.1808740115openalex-snapshot

Reply to Yoshida: Liver cancer stem cells: Identification and lipid metabolic reprogramming

inferred← citeshttps://doi.org/10.1084/jem.20181739openalex-snapshot

Modulating inflammation for cancer therapy

inferred← citeshttps://doi.org/10.1084/jem.20191515openalex-snapshot

AKT-dependent NOTCH3 activation drives tumor progression in a model of mesenchymal colorectal cancer

inferred← citeshttps://doi.org/10.1084/jem.20201017openalex-snapshot

A third Notch in colorectal cancer progression and metastasis

inferred← citeshttps://doi.org/10.1088/1478-3975/ab0032openalex-snapshot

Investigating epithelial-to-mesenchymal transition with integrated computational and experimental approaches

inferred← citeshttps://doi.org/10.1091/mbc.e20-02-0092openalex-snapshot

Integrin-linked kinase tunes cell–cell and cell-matrix adhesions to regulate the switch between apoptosis and EMT downstream of TGFβ1

inferred← citeshttps://doi.org/10.1091/mbc.e24-09-0400openalex-snapshot

MAL2 and rab17 selectively redistribute invadopodia proteins to laterally-induced protrusions in hepatocellular carcinoma cells

inferred← citeshttps://doi.org/10.1091/mbc.e25-07-0349openalex-snapshot

Epithelial–mesenchymal cell state heterogeneity predetermines differential phospho-signaling responses to EGF stimulation

inferred← citeshttps://doi.org/10.1093/abbs/gmab065openalex-snapshot

Collagen prolyl 4-hydroxylases modify tumor progression

inferred← citeshttps://doi.org/10.1093/bib/bbaf165openalex-snapshot

A multi-step completion process model of cell plasticity

inferred← citeshttps://doi.org/10.1093/carcin/bgz119openalex-snapshot

Functional balance between Tcf21–Slug defines cellular plasticity and migratory modalities in high grade serous ovarian cancer cell lines

inferred← citeshttps://doi.org/10.1098/rsif.2022.0346openalex-snapshot

The role of evolutionary game theory in spatial and non-spatial models of the survival of cooperation in cancer: a review

inferred← citeshttps://doi.org/10.1101/2020.07.24.219238openalex-snapshot

Phenotypic plasticity underlies local invasion and distant metastasis in colon cancer

inferred← citeshttps://doi.org/10.1101/2021.10.11.463906openalex-snapshot

Intercellular alignment of apical-basal polarity coordinates tissue homeostasis and growth

inferred← citeshttps://doi.org/10.1101/267849openalex-snapshot

Cell atlas of human uterus

inferred← citeshttps://doi.org/10.1101/401059openalex-snapshot

Quantifying local malignant adaptation in tissue-specific evolutionary trajectories by harnessing cancer’s repeatability at the genetic level

inferred← citeshttps://doi.org/10.1101/cshperspect.a036905openalex-snapshot

Cancer Stem Cells and Epithelial-to-Mesenchymal Transition in Cancer Metastasis

inferred← citeshttps://doi.org/10.1103/physreve.103.032407openalex-snapshot

Roles of phenotypic heterogeneity and microenvironment feedback in early tumor development

inferred← citeshttps://doi.org/10.1111/eva.12781openalex-snapshot

Quantifying local malignant adaptation in tissue‐specific evolutionary trajectories by harnessing cancer’s repeatability at the genetic level

inferred← citeshttps://doi.org/10.1111/odi.13347openalex-snapshot

Proliferative ability and accumulation of cancer stem cells in oral submucous fibrosis epithelium

inferred← citeshttps://doi.org/10.1126/sciadv.aav3235openalex-snapshot

USP1 links platinum resistance to cancer cell dissemination by regulating Snail stability

inferred← citeshttps://doi.org/10.1126/sciadv.aax5611openalex-snapshot

Compression-induced dedifferentiation of adipocytes promotes tumor progression

inferred← citeshttps://doi.org/10.1155/2018/4598195openalex-snapshot

Tumorigenic Cell Reprogramming and Cancer Plasticity: Interplay between Signaling, Microenvironment, and Epigenetics

inferred← citeshttps://doi.org/10.1155/2022/8347125openalex-snapshot

Single-Cell RNA Sequencing Reveals the Role of Epithelial Cell Marker Genes in Predicting the Prognosis of Colorectal Cancer Patients

inferred← citeshttps://doi.org/10.1155/2024/6616979openalex-snapshot

Retinoid Treatment for Oral Leukoplakia: Current Evidence and Future Development

inferred← citeshttps://doi.org/10.1158/0008-5472.can-18-2070openalex-snapshot

Collagen Prolyl Hydroxylation–Dependent Metabolic Perturbation Governs Epigenetic Remodeling and Mesenchymal Transition in Pluripotent and Cancer Cells

inferred← citeshttps://doi.org/10.1172/jci137967openalex-snapshot

ERG orchestrates chromatin interactions to drive prostate cell fate reprogramming

inferred← citeshttps://doi.org/10.1177/15330338221085348openalex-snapshot

LncRNA NEAT1 Promotes the Malignant Progression of Colorectal Cancer by Targeting ZEB1 via miR-448

inferred← citeshttps://doi.org/10.1186/s12885-020-06773-wopenalex-snapshot

The A818–6 system as an in-vitro model for studying the role of the transportome in pancreatic cancer

inferred← citeshttps://doi.org/10.1186/s12920-023-01634-4openalex-snapshot

Obesity and head and neck cancer risk: a mendelian randomization study

inferred← citeshttps://doi.org/10.1186/s12943-019-1014-2openalex-snapshot

m6A-induced lncRNA RP11 triggers the dissemination of colorectal cancer cells via upregulation of Zeb1

inferred← citeshttps://doi.org/10.1186/s12943-025-02365-zopenalex-snapshot

Targeting metastasis in paediatric bone sarcomas

inferred← citeshttps://doi.org/10.1186/s12967-023-04633-2openalex-snapshot

Integrated machine learning identifies epithelial cell marker genes for improving outcomes and immunotherapy in prostate cancer

inferred← citeshttps://doi.org/10.1186/s12967-024-05369-3openalex-snapshot

Spatiotemporal heterogeneity of LMOD1 expression summarizes two modes of cell communication in colorectal cancer

inferred← citeshttps://doi.org/10.1186/s13045-022-01347-8openalex-snapshot

The molecular mechanisms and therapeutic strategies of EMT in tumor progression and metastasis

inferred← citeshttps://doi.org/10.1186/s13059-018-1416-2openalex-snapshot

Single-cell RNA-seq analysis unveils a prevalent epithelial/mesenchymal hybrid state during mouse organogenesis

inferred← citeshttps://doi.org/10.1186/s13578-022-00827-1openalex-snapshot

H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.1186/s40170-019-0197-8openalex-snapshot

Epithelial to mesenchymal transition (EMT) is associated with attenuation of succinate dehydrogenase (SDH) in breast cancer through reduced expression of SDHC

inferred← citeshttps://doi.org/10.1242/dev.170316openalex-snapshot

The regulation of the homeostasis and regeneration of peripheral nerve is distinct from the CNS and independent of a stem cell population

inferred← citeshttps://doi.org/10.1242/dmm.033373openalex-snapshot

Plasticity of differentiated cells in wound repair and tumorigenesis, part I: stomach and pancreas

inferred← citeshttps://doi.org/10.1242/dmm.044404openalex-snapshot

Quantitative single-cell interactomes in normal and virus-infected mouse lungs

inferred← citeshttps://doi.org/10.12659/msm.909452openalex-snapshot

Cervical Cancer Cell Growth, Drug Resistance, and Epithelial-Mesenchymal Transition Are Suppressed by g-Secretase Inhibitor RO4929097

inferred← citeshttps://doi.org/10.1371/journal.pone.0218279openalex-snapshot

ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing

inferred← citeshttps://doi.org/10.1371/journal.pone.0296017openalex-snapshot

A Mendelian randomization study on the causal association of circulating cytokines with colorectal cancer

inferred← citeshttps://doi.org/10.1515/tjb-2022-0218openalex-snapshot

Epithelial-mesenchymal transition as a potential route for DAPT resistance in breast cancer cells

inferred← citeshttps://doi.org/10.15252/embj.2019103148openalex-snapshot

Nomenclature for cellular plasticity: are the terms as plastic as the cells themselves?

inferred← citeshttps://doi.org/10.18632/oncotarget.25692openalex-snapshot

A mechanism-based computational model to capture the interconnections among epithelial-mesenchymal transition, cancer stem cells and Notch-Jagged signaling

inferred← citeshttps://doi.org/10.20517/2394-4722.2019.26openalex-snapshot

Cellular plasticity and metastasis in breast cancer: a pre- and post-malignant problem

inferred← citeshttps://doi.org/10.21248/gups.68107openalex-snapshot

Inflammatory cancer associated fibroblasts decisive role in therapy resistance among rectal cancer patients

inferred← citeshttps://doi.org/10.2147/ott.s214133openalex-snapshot

The Exosome And Breast Cancer Cell Plasticity

inferred← citeshttps://doi.org/10.22201/fesz.23958723e.2020.0.225openalex-snapshot

La plasticidad del hepatocito y su relevancia en la fisiología y la patología hepática

inferred← citeshttps://doi.org/10.2967/jnumed.118.214361openalex-snapshot

Fibroblast-Activating Protein: Targeting the Roots of the Tumor Microenvironment

inferred← citeshttps://doi.org/10.3389/fcell.2022.938685openalex-snapshot

Asymmetric Cell Division and Tumor Heterogeneity

inferred← citeshttps://doi.org/10.3389/fmolb.2020.00130openalex-snapshot

Dynamics of Cellular Plasticity in Prostate Cancer Progression

inferred← citeshttps://doi.org/10.3389/fonc.2018.00357openalex-snapshot

Transforming Growth Factor-β-Induced Cell Plasticity in Liver Fibrosis and Hepatocarcinogenesis

inferred← citeshttps://doi.org/10.3389/fonc.2018.00475openalex-snapshot

Soft Tissue Sarcoma Cancer Stem Cells: An Overview

inferred← citeshttps://doi.org/10.3389/fonc.2018.00505openalex-snapshot

Cellular Phenotype Plasticity in Cancer Dormancy and Metastasis

inferred← citeshttps://doi.org/10.3389/fonc.2020.618515openalex-snapshot

Non-Genomic Control of Dynamic MYCN Gene Expression in Liver Cancer

inferred← citeshttps://doi.org/10.3389/fonc.2021.617597openalex-snapshot

Communication Between Epithelial–Mesenchymal Plasticity and Cancer Stem Cells: New Insights Into Cancer Progression

inferred← citeshttps://doi.org/10.3389/fonc.2022.952228openalex-snapshot

Osteosarcoma immune prognostic index can indicate the nature of indeterminate pulmonary nodules and predict the metachronous metastasis in osteosarcoma patients

inferred← citeshttps://doi.org/10.3389/fphar.2021.688625openalex-snapshot

The Role of Tumor Inflammatory Microenvironment in Lung Cancer

inferred← citeshttps://doi.org/10.3389/fphar.2022.899208openalex-snapshot

Therapeutic Effects of Natural Products on Cervical Cancer: Based on Inflammatory Pathways

inferred← citeshttps://doi.org/10.3390/biom11020310openalex-snapshot

Organ Fibrosis and Autoimmunity: The Role of Inflammation in TGFβ-Dependent EMT

inferred← citeshttps://doi.org/10.3390/biomedicines6020050openalex-snapshot

Mammary Stem Cells and Breast Cancer Stem Cells: Molecular Connections and Clinical Implications

inferred← citeshttps://doi.org/10.3390/cancers11091368openalex-snapshot

Cell Heterogeneity and Phenotypic Plasticity in Metastasis Formation: The Case of Colon Cancer

inferred← citeshttps://doi.org/10.3390/cancers12051340openalex-snapshot

Hakin-1, a New Specific Small-Molecule Inhibitor for the E3 Ubiquitin-Ligase Hakai, Inhibits Carcinoma Growth and Progression

inferred← citeshttps://doi.org/10.3390/cancers12123674openalex-snapshot

The Intimate Relationship among EMT, MET and TME: A T(ransdifferentiation) E(nhancing) M(ix) to Be Exploited for Therapeutic Purposes

inferred← citeshttps://doi.org/10.3390/cancers12123716openalex-snapshot

Impact of the Tumor Microenvironment on Tumor Heterogeneity and Consequences for Cancer Cell Plasticity and Stemness

inferred← citeshttps://doi.org/10.3390/cancers13051097openalex-snapshot

Functional States in Tumor-Initiating Cell Differentiation in Human Colorectal Cancer

inferred← citeshttps://doi.org/10.3390/cancers13061316openalex-snapshot

Shifting the Gears of Metabolic Plasticity to Drive Cell State Transitions in Cancer

inferred← citeshttps://doi.org/10.3390/cancers13143602openalex-snapshot

Lineage Plasticity in Cancer: The Tale of a Skin-Walker

inferred← citeshttps://doi.org/10.3390/cancers13205123openalex-snapshot

The Balance between Differentiation and Terminal Differentiation Maintains Oral Epithelial Homeostasis

inferred← citeshttps://doi.org/10.3390/cancers13236062openalex-snapshot

Therapeutic Influence on Important Targets Associated with Chronic Inflammation and Oxidative Stress in Cancer Treatment

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The Cytokine Network in Colorectal Cancer: Implications for New Treatment Strategies

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Dedifferentiated Leiomyosarcoma of the Uterine Corpus with Heterologous Component: Clinicopathological Analysis of Five Consecutive Cases from a Single Institution and Comprehensive Literature Review

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Inhibition of Stearoyl-CoA Desaturase-1 Activity Suppressed SREBP Signaling in Colon Cancer Cells and Their Spheroid Growth

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Influence of Ce3+ Substitution on Antimicrobial and Antibiofilm Properties of ZnCexFe2−xO4 Nanoparticles (X = 0.0, 0.02, 0.04, 0.06, and 0.08) Conjugated with Ebselen and Its Role Subsidised with γ-Radiation in Mitigating Human TNBC and Colorectal Adenocarcinoma Proliferation In Vitro

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Tumour Stem Cells in Breast Cancer

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Concentration of Selected Adipokines and Factors Regulating Carbohydrate Metabolism in Patients with Head and Neck Cancer in Respect to Their Body Mass Index

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Oat Beta-Glucan as a Metabolic Regulator in Early Stage of Colorectal Cancer—A Model Study on Azoxymethane-Treated Rats

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Omics-Mediated Treatment for Advanced Prostate Cancer: Moving Towards Precision Oncology

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Quantifying Cancer Epithelial-Mesenchymal Plasticity and its Association with Stemness and Immune Response

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Dynamics of Phenotypic Heterogeneity Associated with EMT and Stemness during Cancer Progression

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Pentadecanoic Acid, an Odd-Chain Fatty Acid, Suppresses the Stemness of MCF-7/SC Human Breast Cancer Stem-Like Cells through JAK2/STAT3 Signaling

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In Vitro Antitumor and Anti-Inflammatory Activities of Allium-Derived Compounds Propyl Propane Thiosulfonate (PTSO) and Propyl Propane Thiosulfinate (PTS)

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Targeting SMAD-Dependent Signaling: Considerations in Epithelial and Mesenchymal Solid Tumors

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Cytokines Involved in the Progression of Liver Fibrosis by Influencing DNA Synthesis

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Advances in landscape and related therapeutic targets of the prostate tumor microenvironment

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Copy number alterations and epithelial‑mesenchymal transition genes in diffuse and intestinal gastric cancers in Mexican patients

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Molecular features and gene expression signature of metastatic colorectal cancer (Review)

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Widespread activation and critical role of EMT and stemness in the neuroendocrine differentiation of prostate cancer (Review)

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C-Reactive Protein Signaling Pathways in Tumor Progression

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Colorectal carcinogenesis: Insights into the cell death and signal transduction pathways: A review

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Cell reprogramming in cancer: Interplay of genetic, epigenetic mechanisms, and the tumor microenvironment in carcinogenesis and metastasis

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Additional file 10 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088144openalex-snapshot

Additional file 11 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088147openalex-snapshot

Additional file 12 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088150openalex-snapshot

Additional file 13 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088153openalex-snapshot

Additional file 14 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088156openalex-snapshot

Additional file 1 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088159openalex-snapshot

Additional file 2 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088162openalex-snapshot

Additional file 3 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088165openalex-snapshot

Additional file 4 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088171openalex-snapshot

Additional file 5 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088174openalex-snapshot

Additional file 6 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088177openalex-snapshot

Additional file 7 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088180openalex-snapshot

Additional file 8 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.20088183openalex-snapshot

Additional file 9 of H3K27ac mediated SS18/BAFs relocation regulates JUN induced pluripotent-somatic transition

inferred← citeshttps://doi.org/10.6084/m9.figshare.24500862openalex-snapshot

Additional file 1 of Integrated machine learning identifies epithelial cell marker genes for improving outcomes and immunotherapy in prostate cancer

inferred← citeshttps://doi.org/10.6084/m9.figshare.24500889openalex-snapshot

Additional file 2 of Integrated machine learning identifies epithelial cell marker genes for improving outcomes and immunotherapy in prostate cancer

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