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Cancer stem cells: The challenges ahead
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.2010.1862openalex-snapshot
Association of a Leukemic Stem Cell Gene Expression Signature With Clinical Outcomes in Acute Myeloid Leukemia
inferredcites →https://doi.org/10.1002/ijc.24408openalex-snapshot
Tumor microvasculature supports proliferation and expansion of glioma‐propagating cells
inferredcites →https://doi.org/10.1007/s11060-010-0488-yopenalex-snapshot
CD133+ niches and single cells in glioblastoma have different phenotypes
inferredcites →https://doi.org/10.1007/s12015-010-9208-4openalex-snapshot
The Role of Human Aldehyde Dehydrogenase in Normal and Cancer Stem Cells
inferredcites →https://doi.org/10.1016/j.ccr.2006.11.020openalex-snapshot
A Perivascular Niche for Brain Tumor Stem Cells
inferredcites →https://doi.org/10.1016/j.ccr.2012.03.003openalex-snapshot
Cancer Stem Cells: Impact, Heterogeneity, and Uncertainty
inferredcites →https://doi.org/10.1016/j.ceb.2007.02.007openalex-snapshot
Wnt/β-catenin signaling in cancer stemness and malignant behavior
inferredcites →https://doi.org/10.1016/j.cell.2008.03.027openalex-snapshot
The Epithelial-Mesenchymal Transition Generates Cells with Properties of Stem Cells
inferredcites →https://doi.org/10.1016/j.cell.2009.12.007openalex-snapshot
Biological and Molecular Heterogeneity of Breast Cancers Correlates with Their Cancer Stem Cell Content
inferredcites →https://doi.org/10.1016/j.cell.2011.04.029openalex-snapshot
Paracrine and Autocrine Signals Induce and Maintain Mesenchymal and Stem Cell States in the Breast
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.devcel.2008.05.009openalex-snapshot
Epithelial-Mesenchymal Transition: At the Crossroads of Development and Tumor Metastasis
inferredcites →https://doi.org/10.1016/j.stem.2007.06.002openalex-snapshot
Distinct Populations of Cancer Stem Cells Determine Tumor Growth and Metastatic Activity in Human Pancreatic Cancer
inferredcites →https://doi.org/10.1016/j.stem.2007.08.014openalex-snapshot
ALDH1 Is a Marker of Normal and Malignant Human Mammary Stem Cells and a Predictor of Poor Clinical Outcome
inferredcites →https://doi.org/10.1016/j.stem.2010.04.001openalex-snapshot
A Subpopulation of CD26+ Cancer Stem Cells with Metastatic Capacity in Human Colorectal Cancer
inferredcites →https://doi.org/10.1016/j.stem.2011.02.020openalex-snapshot
The Intestinal Stem Cell Signature Identifies Colorectal Cancer Stem Cells and Predicts Disease Relapse
inferredcites →https://doi.org/10.1016/j.stem.2011.08.010openalex-snapshot
Distinct Types of Tumor-Initiating Cells Form Human Colon Cancer Tumors and Metastases
inferredcites →https://doi.org/10.1016/j.stem.2011.10.001openalex-snapshot
Nodal/Activin Signaling Drives Self-Renewal and Tumorigenicity of Pancreatic Cancer Stem Cells and Provides a Target for Combined Drug Therapy
inferredcites →https://doi.org/10.1016/j.stem.2011.10.008openalex-snapshot
Methylation of Cancer-Stem-Cell-Associated Wnt Target Genes Predicts Poor Prognosis in Colorectal Cancer Patients
inferredcites →https://doi.org/10.1016/s0074-7696(08)62230-5openalex-snapshot
The Cellular Basis of Tumor Progression
inferredcites →https://doi.org/10.1016/s1470-2045(11)70257-1openalex-snapshot
The developing cancer stem-cell model: clinical challenges and opportunities
inferredcites →https://doi.org/10.1038/367645a0openalex-snapshot
A cell initiating human acute myeloid leukaemia after transplantation into SCID mice
inferredcites →https://doi.org/10.1038/cdd.2008.20openalex-snapshot
Cancer stem cells – old concepts, new insights
inferredcites →https://doi.org/10.1038/embor.2008.74openalex-snapshot
A reciprocal repression between ZEB1 and members of the miR‐200 family promotes EMT and invasion in cancer cells
inferredcites →https://doi.org/10.1038/labinvest.2009.54openalex-snapshot
Identification of CD44v6+/CD24− breast carcinoma cells in primary human tumors by quantum dot-conjugated antibodies
inferredcites →https://doi.org/10.1038/nature05349openalex-snapshot
Bone morphogenetic proteins inhibit the tumorigenic potential of human brain tumour-initiating cells
inferredcites →https://doi.org/10.1038/nature05372openalex-snapshot
A human colon cancer cell capable of initiating tumour growth in immunodeficient mice
inferredcites →https://doi.org/10.1038/nature05384openalex-snapshot
Identification and expansion of human colon-cancer-initiating cells
inferredcites →https://doi.org/10.1038/nature06489openalex-snapshot
Identification of cells initiating human melanomas
inferredcites →https://doi.org/10.1038/nature07567openalex-snapshot
Efficient tumour formation by single human melanoma cells
inferredcites →https://doi.org/10.1038/nature09229openalex-snapshot
Nuclear reprogramming to a pluripotent state by three approaches
inferredcites →https://doi.org/10.1038/nature09557openalex-snapshot
Tumour vascularization via endothelial differentiation of glioblastoma stem-like cells
inferredcites →https://doi.org/10.1038/nature09624openalex-snapshot
Glioblastoma stem-like cells give rise to tumour endothelium
inferredcites →https://doi.org/10.1038/nature10212openalex-snapshot
Microenvironmental regulation of stem cells in intestinal homeostasis and cancer
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/nature11287openalex-snapshot
A restricted cell population propagates glioblastoma growth after chemotherapy
inferredcites →https://doi.org/10.1038/nature11344openalex-snapshot
Defining the mode of tumour growth by clonal analysis
inferredcites →https://doi.org/10.1038/ncb2048openalex-snapshot
Wnt activity defines colon cancer stem cells and is regulated by the microenvironment
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/ncomms2039openalex-snapshot
TGFβ induces the formation of tumour-initiating cells in claudinlow breast cancer
inferredcites →https://doi.org/10.1038/nrc1694openalex-snapshot
Migrating cancer stem cells — an integrated concept of malignant tumour progression
inferredcites →https://doi.org/10.1038/nrc3265openalex-snapshot
To differentiate or not — routes towards metastasis
inferredcites →https://doi.org/10.1038/nrc3368openalex-snapshot
Cancer stem cell definitions and terminology: the devil is in the details
inferredcites →https://doi.org/10.1038/onc.2011.400openalex-snapshot
The BMP2/7 heterodimer inhibits the human breast cancer stem cell subpopulation and bone metastases formation
inferredcites →https://doi.org/10.1038/pcan.2008.22openalex-snapshot
Prostate cancer stem cell therapy: hype or hope?
inferredcites →https://doi.org/10.1038/sj.onc.1210356openalex-snapshot
Sonic Hedgehog promotes multiple drug resistance by regulation of drug transport
inferredcites →https://doi.org/10.1053/j.gastro.2006.08.039openalex-snapshot
The Intestinal Wnt/TCF Signature
inferredcites →https://doi.org/10.1053/j.gastro.2009.12.063openalex-snapshot
Colon Cancer Stem Cells: Promise of Targeted Therapy
inferredcites →https://doi.org/10.1053/j.gastro.2010.10.005openalex-snapshot
Bone Morphogenetic Protein 4 Induces Differentiation of Colorectal Cancer Stem Cells and Increases Their Response to Chemotherapy in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2011.05.045openalex-snapshot
Mesenchymal Stem Cells Promote Formation of Colorectal Tumors in Mice
inferredcites →https://doi.org/10.1073/pnas.0530291100openalex-snapshot
Prospective identification of tumorigenic breast cancer cells
inferredcites →https://doi.org/10.1073/pnas.0703478104openalex-snapshot
Phenotypic characterization of human colorectal cancer stem cells
inferredcites →https://doi.org/10.1074/jbc.m111.261545openalex-snapshot
CD133 Protein N-Glycosylation Processing Contributes to Cell Surface Recognition of the Primitive Cell Marker AC133 Epitope
inferredcites →https://doi.org/10.1089/scd.2008.0055openalex-snapshot
ALDH1 as a Functional Marker of Cancer Stem and Progenitor Cells
inferredcites →https://doi.org/10.1101/gad.1640608openalex-snapshot
The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2
inferredcites →https://doi.org/10.1111/j.1349-7006.2009.01318.xopenalex-snapshot
Maintenance of HCT116 colon cancer cell line conforms to a stochastic model but not a cancer stem cell model
inferredcites →https://doi.org/10.1126/science.1142596openalex-snapshot
Tumor Growth Need Not Be Driven by Rare Cancer Stem Cells
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.1226929openalex-snapshot
Dedifferentiation of Neurons and Astrocytes by Oncogenes Can Induce Gliomas in Mice
inferredcites →https://doi.org/10.1158/0008-5472.can-05-3153openalex-snapshot
Cancer Stem Cells: An Old Idea—A Paradigm Shift
inferredcites →https://doi.org/10.1158/0008-5472.can-05-3450openalex-snapshot
Identifying Cancer Stem Cells in Solid Tumors: Case Not Proven
inferredcites →https://doi.org/10.1158/0008-5472.can-06-0054openalex-snapshot
Hedgehog Signaling and Bmi-1 Regulate Self-renewal of Normal and Malignant Human Mammary Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-06-3126openalex-snapshot
Cancer Stem Cells—Perspectives on Current Status and Future Directions: AACR Workshop on Cancer Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-07-6208openalex-snapshot
Abnormal DNA Methylation of CD133 in Colorectal and Glioblastoma Tumors
inferredcites →https://doi.org/10.1158/0008-5472.can-09-1820openalex-snapshot
The AC133 Epitope, but not the CD133 Protein, Is Lost upon Cancer Stem Cell Differentiation
inferredcites →https://doi.org/10.1158/0008-5472.can-09-3663openalex-snapshot
Cancer Stem Cell Tumor Model Reveals Invasive Morphology and Increased Phenotypical Heterogeneity
inferredcites →https://doi.org/10.1158/0008-5472.can-10-0538openalex-snapshot
Breast Cancer Stem Cells Are Regulated by Mesenchymal Stem Cells through Cytokine Networks
inferredcites →https://doi.org/10.1158/0008-5472.can-10-3220openalex-snapshot
Cancer Stem Cell Niche: The Place to Be
inferredcites →https://doi.org/10.1158/0008-5472.can-11-0221openalex-snapshot
ABCB5 Identifies a Therapy-Refractory Tumor Cell Population in Colorectal Cancer Patients
inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-0169openalex-snapshot
Most Early Disseminated Cancer Cells Detected in Bone Marrow of Breast Cancer Patients Have a Putative Breast Cancer Stem Cell Phenotype
inferredcites →https://doi.org/10.1371/journal.pone.0002888openalex-snapshot
Generation of Breast Cancer Stem Cells through Epithelial-Mesenchymal Transition
inferredcites →https://doi.org/10.1371/journal.pone.0010277openalex-snapshot
Distinct Expression Levels and Patterns of Stem Cell Marker, Aldehyde Dehydrogenase Isoform 1 (ALDH1), in Human Epithelial Cancers
inferredcites →https://doi.org/10.1371/journal.pone.0024217openalex-snapshot
CD44v6 Regulates Growth of Brain Tumor Stem Cells Partially through the AKT-Mediated Pathway
inferredcites →https://doi.org/10.1373/clinchem.2006.079509openalex-snapshot
Detection and Characterization of Putative Metastatic Precursor Cells in Cancer Patients
inferredcites →https://doi.org/10.18632/oncotarget.173openalex-snapshot
Molecular identification and targeting of colorectal cancer stem cells
inferredcites →https://doi.org/10.3892/ijmm.19.6.967openalex-snapshot
Comparative genomics on PROM1 gene encoding stem cell marker CD133
inferredcites →https://doi.org/10.4161/cc.19679openalex-snapshot
Pancreatic stellate cells form a niche for cancer stem cells and promote their self-renewal and invasiveness
inferredcites →https://doi.org/10.4161/cc.8.20.9761openalex-snapshot
Retinoid signaling regulates breast cancer stem cell differentiation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1878-0261.12771openalex-snapshot
Downregulation of STK4 promotes colon cancer invasion/migration through blocking β‐catenin degradation
inferred← citeshttps://doi.org/10.1002/1878-0261.12979openalex-snapshot
Playing cancer at its own game: activating mitogenic signaling as a paradoxical intervention
inferred← citeshttps://doi.org/10.1002/2211-5463.13550openalex-snapshot
A curcumin analogue GO‐Y030 depletes cancer stem cells by inhibiting the interaction between the HSP70 / HSP40 complex and its substrates
inferred← citeshttps://doi.org/10.1002/9781118512074.ch31openalex-snapshot
Neoplasia of the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1002/adbi.201800200openalex-snapshot
Integrated Microfluidic Chip for Efficient Isolation and Deformability Analysis of Circulating Tumor Cells
inferred← citeshttps://doi.org/10.1002/adfm.201907572openalex-snapshot
Detecting the Origin of Cancer‐Mobile Quantum Probe for Single Cancer Stem Cell Detection
inferred← citeshttps://doi.org/10.1002/adhm.201600644openalex-snapshot
Engineered Breast Cancer Cell Spheroids Reproduce Biologic Properties of Solid Tumors
inferred← citeshttps://doi.org/10.1002/adhm.201700535openalex-snapshot
Synthetic Biomaterials to Rival Nature's Complexity—a Path Forward with Combinatorics, High‐Throughput Discovery, and High‐Content Analysis
inferred← citeshttps://doi.org/10.1002/adhm.202304648openalex-snapshot
Graphene Quantum Dots Eradicate Resistant and Metastatic Cancer Cells by Enhanced Interfacial Inhibition
inferred← citeshttps://doi.org/10.1002/adma.201800106openalex-snapshot
Molecular Cancer Imaging in the Second Near‐Infrared Window Using a Renal‐Excreted NIR‐II Fluorophore‐Peptide Probe
inferred← citeshttps://doi.org/10.1002/adma.202302916openalex-snapshot
Cancer Stem‐Like Cells‐Oriented Surface Self‐Assembly to Conquer Radioresistance
inferred← citeshttps://doi.org/10.1002/advs.201801012openalex-snapshot
Deep Tumor‐Penetrated Nanocages Improve Accessibility to Cancer Stem Cells for Photothermal‐Chemotherapy of Breast Cancer Metastasis
inferred← citeshttps://doi.org/10.1002/ar.24206openalex-snapshot
Aspartyl Aminopeptidase Suppresses Proliferation, Invasion, and Stemness of Breast Cancer Cells via Targeting CD44
inferred← citeshttps://doi.org/10.1002/bmm2.70099openalex-snapshot
Tackling cancer stemness with nanotechnology in the era of precision medicine
inferred← citeshttps://doi.org/10.1002/cam4.629openalex-snapshot
Cancer stem cells: a metastasizing menace!
inferred← citeshttps://doi.org/10.1002/cbf.3649openalex-snapshot
A three‐dimensional microenvironment alters CD73 expression in cervical cancer
inferred← citeshttps://doi.org/10.1002/cjp2.300openalex-snapshot
Olfactomedin 4 associates with expression of differentiation markers but not with properties of cancer stemness, EMT nor metastatic spread in colorectal cancer
inferred← citeshttps://doi.org/10.1002/exp.20240259openalex-snapshot
One‐Stone‐Two‐Birds Carrier‐Free Nano‐Cocktail Enables Synergistic Eradication of Cancer Cells/Stem Cells in Breast Cancer Treatment
inferred← citeshttps://doi.org/10.1002/ijc.28804openalex-snapshot
Tumor heterogeneity and cancer stem cell paradigm: Updates in concept, controversies and clinical relevance
inferred← citeshttps://doi.org/10.1002/ijc.29642openalex-snapshot
A self‐enforcing CD 44s/ ZEB 1 feedback loop maintains EMT and stemness properties in cancer cells
inferred← citeshttps://doi.org/10.1002/ijc.30006openalex-snapshot
Single‐cell profiling approaches to probing tumor heterogeneity
inferred← citeshttps://doi.org/10.1002/ijc.30787openalex-snapshot
Associations between RNA splicing regulatory variants of stemness‐related genes and racial disparities in susceptibility to prostate cancer
inferred← citeshttps://doi.org/10.1002/ijc.30898openalex-snapshot
Breast cancer stem cells as last soldiers eluding therapeutic burn: A hard nut to crack
inferred← citeshttps://doi.org/10.1002/iub.2461openalex-snapshot
T‐cell immunoglobulin and ITIM domain, as a potential immune checkpoint target for immunotherapy of colorectal cancer
inferred← citeshttps://doi.org/10.1002/jcb.25656openalex-snapshot
CD114: A New Member of the Neural Crest-Derived Cancer Stem Cell Marker Family
inferred← citeshttps://doi.org/10.1002/jcb.28015openalex-snapshot
Investigating the role of CRIPTO‐1 (TDGF‐1) in glioblastoma multiforme U87 cell line
inferred← citeshttps://doi.org/10.1002/jcp.28824openalex-snapshot
New emerging roles of CD133 in cancer stem cell: Signaling pathway and miRNA regulation
inferred← citeshttps://doi.org/10.1002/jcp.30063openalex-snapshot
The oncogenic potential of NANOG: An important cancer induction mediator
inferred← citeshttps://doi.org/10.1002/jcp.31344openalex-snapshot
Cancer‐associated fibroblasts‐secreted exosomal miR‐92a‐3p promotes tumor growth and stemness in hepatocellular carcinoma through activation of Wnt/β‐catenin signaling pathway by suppressing AXIN1
inferred← citeshttps://doi.org/10.1002/mc.22344openalex-snapshot
Areca nut contributes to oral malignancy through facilitating the conversion of cancer stem cells
inferred← citeshttps://doi.org/10.1002/mog2.70009openalex-snapshot
Unraveling the underlying mechanisms of cancer stem cells in therapeutic resistance for optimizing treatment strategies
inferred← citeshttps://doi.org/10.1002/smll.202410410openalex-snapshot
Precise PEGylation Modulates the in Vivo Fate of Peptide Radiopharmaceuticals
inferred← citeshttps://doi.org/10.1002/stem.1795openalex-snapshot
MiR-7, Inhibited Indirectly by LincRNA HOTAIR, Directly Inhibits SETDB1 and Reverses the EMT of Breast Cancer Stem Cells by Downregulating the STAT3 Pathway
inferred← citeshttps://doi.org/10.1002/stem.1837openalex-snapshot
Lipid Droplets: A New Player in Colorectal Cancer Stem Cells Unveiled by Spectroscopic Imaging
inferred← citeshttps://doi.org/10.1002/stem.2851openalex-snapshot
Conclusive Evidence for OCT4 Transcription in Human Cancer Cell Lines: Possible Role of a Small OCT4-Positive Cancer Cell Population
inferred← citeshttps://doi.org/10.1002/stem.3157openalex-snapshot
cPLA2α reversibly regulates different subsets of cancer stem cells transformation in cervical cancer
inferred← citeshttps://doi.org/10.1007/5584_2022_758openalex-snapshot
Cancer Stem Cells and Their Therapeutic Usage
inferred← citeshttps://doi.org/10.1007/7651_2018_179openalex-snapshot
Isolation, Propagation, and Clonogenicity of Intestinal Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-0716-0810-4_2openalex-snapshot
Leukemia Stem Cells: Concept and Implications
inferred← citeshttps://doi.org/10.1007/978-1-0716-3730-2_1openalex-snapshot
Cancer Stem Cells: Current Challenges and Future Perspectives
inferred← citeshttps://doi.org/10.1007/978-1-4939-1381-7_4openalex-snapshot
Understanding Cancer at the Genomic Level
inferred← citeshttps://doi.org/10.1007/978-1-4939-3363-1_9openalex-snapshot
CTC Analysis: FISH, ISH, Array-CGH, and Other Molecular Assays
inferred← citeshttps://doi.org/10.1007/978-3-030-14366-4_3openalex-snapshot
Heterogeneity of Small Cell Lung Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-030-23629-8_10openalex-snapshot
Cancer Stem Cells and Stem Cell Tumors in Drosophila
inferred← citeshttps://doi.org/10.1007/978-3-030-46306-9_22openalex-snapshot
Discrete and Continuum Models for the Evolutionary and Spatial Dynamics of Cancer: A Very Short Introduction Through Two Case Studies
inferred← citeshttps://doi.org/10.1007/978-3-030-55359-3_5openalex-snapshot
Cancer Stem Cells and the Development of Cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-64668-4_4openalex-snapshot
Recent Therapeutic Strategies for the Treatment of Colon Cancer
inferred← citeshttps://doi.org/10.1007/978-3-031-04379-6_8openalex-snapshot
Local Quantitative and Qualitative Sensitivity Analysis of CSC Dynamical Simulation
inferred← citeshttps://doi.org/10.1007/978-3-031-19089-6_16openalex-snapshot
Fluorescent Imaging In Vivo
inferred← citeshttps://doi.org/10.1007/978-3-319-21030-8_16openalex-snapshot
Targeting Cancer Stem Cells and the Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-3-319-21030-8_3openalex-snapshot
Cytokine Networks and Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-3-319-21030-8_4openalex-snapshot
Implications of CXCR4/CXCL12 Interaction for Cancer Stem Cell Maintenance and Cancer Progression
inferred← citeshttps://doi.org/10.1007/978-3-319-21702-4_10openalex-snapshot
Insight into Cancer Stem Cell Niche; Lessons from Cancer Stem Cell Models Generated In Vitro
inferred← citeshttps://doi.org/10.1007/978-3-319-26666-4_11openalex-snapshot
Isolation of Glioma-Initiating Cells for Biological Study
inferred← citeshttps://doi.org/10.1007/978-3-319-29073-7_7openalex-snapshot
Regulation of Stem Cell Self-Renewal and Oncogenesis by RNA-Binding Proteins
inferred← citeshttps://doi.org/10.1007/978-3-319-49343-5_8openalex-snapshot
The Emerging Role of Sphingolipids in Cancer Stem Cell Biology
inferred← citeshttps://doi.org/10.1007/978-3-319-55947-6_6openalex-snapshot
Enrichment and Detection of Circulating Tumor Cells and Other Rare Cell Populations by Microfluidic Filtration
inferred← citeshttps://doi.org/10.1007/978-3-319-98065-2_4openalex-snapshot
Cancer Stem Cells (CSCs) and Their Application in Cancer Immunotherapy
inferred← citeshttps://doi.org/10.1007/978-3-662-44946-2_8openalex-snapshot
Cancer Stem Cells: Biology and Potential Therapeutic Applications
inferred← citeshttps://doi.org/10.1007/978-3-662-44946-2_9openalex-snapshot
Immunologic Approaches to Targeting Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-4-431-55327-4_6openalex-snapshot
Anchorage-Dependent Multicellular Aggregate Formation Induces CD44 High Cancer Stem Cell-Like Phenotypes in Adult T Cell Leukemia/Lymphoma Cells
inferred← citeshttps://doi.org/10.1007/978-94-017-9639-2_2openalex-snapshot
Biodynamic Phenotypic and Epigenetics Changes of Circulating Tumor Cells: Their Application in Cancer Prognosis and Treatment
inferred← citeshttps://doi.org/10.1007/978-981-10-3647-7_4openalex-snapshot
Nano-therapeutic Approaches for Targeting Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-10-6469-2_3openalex-snapshot
Clinical Application of Stem Cell Biology in Esophageal Cancer
inferred← citeshttps://doi.org/10.1007/978-981-10-7941-2_6openalex-snapshot
Emerging Role of CD44 Variant 6 in Driving the Metastatic Journey of Ovarian Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-16-1247-3_101-1openalex-snapshot
Oxidative Stress-Related Mechanisms That Mediate Chemoresistance in Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-16-1638-9_4openalex-snapshot
Glycosylation of Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-16-5422-0_101openalex-snapshot
Oxidative Stress-Related Mechanisms That Mediate Chemoresistance in Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-96-7336-0_5openalex-snapshot
Signaling Pathways in Cancer Drug Resistance: Potential Targets for Therapeutic Intervention
inferred← citeshttps://doi.org/10.1007/978-981-97-1666-1_3openalex-snapshot
Role of Cancer Stem Cells in Drug Resistance
inferred← citeshttps://doi.org/10.1007/978-981-99-3185-9_6openalex-snapshot
Plasticity of Cancer Stem Cell
inferred← citeshttps://doi.org/10.1007/s00018-015-1989-9openalex-snapshot
p53 regulates cytoskeleton remodeling to suppress tumor progression
inferred← citeshttps://doi.org/10.1007/s00018-024-05138-xopenalex-snapshot
FBP1 inhibits NSCLC stemness by promoting ubiquitination of Notch1 intracellular domain and accelerating degradation
inferred← citeshttps://doi.org/10.1007/s00210-020-01808-2openalex-snapshot
RETRACTED ARTICLE: LncRNA XIST inhibits ovarian cancer cell growth and metastasis via regulating miR-150-5p/PDCD4 signaling pathway
inferred← citeshttps://doi.org/10.1007/s00280-023-04600-0openalex-snapshot
Pharmacodynamic effects of the PARP inhibitor talazoparib (MDV3800, BMN 673) in patients with BRCA-mutated advanced solid tumors
inferred← citeshttps://doi.org/10.1007/s00405-020-06389-7openalex-snapshot
Cancer stem cell markers in adenocarcinoma of the salivary glands - reliable prognostic markers?
inferred← citeshttps://doi.org/10.1007/s00441-018-2928-5openalex-snapshot
Nanomedicine in cancer stem cell therapy: from fringe to forefront
inferred← citeshttps://doi.org/10.1007/s10238-023-01066-5openalex-snapshot
Extirpating the cancer stem cell hydra: Differentiation therapy and Hyperthermia therapy for targeting the cancer stem cell hierarchy
inferred← citeshttps://doi.org/10.1007/s10549-015-3645-3openalex-snapshot
Simvastatin prevents triple-negative breast cancer metastasis in pre-clinical models through regulation of FOXO3a
inferred← citeshttps://doi.org/10.1007/s10555-025-10270-6openalex-snapshot
The invadosome of stem-like cancer cells: metastasis machinery and targetable vulnerability
inferred← citeshttps://doi.org/10.1007/s10637-019-00847-8openalex-snapshot
Effects of salinomycin and niclosamide on small cell lung cancer and small cell lung cancer circulating tumor cell lines
inferred← citeshttps://doi.org/10.1007/s11033-020-05761-4openalex-snapshot
Inhibition of semaphorin 4D enhances chemosensitivity by increasing 5-fluorouracile-induced apoptosis in colorectal cancer cells
inferred← citeshttps://doi.org/10.1007/s11102-013-0543-8openalex-snapshot
Adamantinomatous craniopharyngiomas express tumor stem cell markers in cells with activated Wnt signaling: further evidence for the existence of a tumor stem cell niche?
inferred← citeshttps://doi.org/10.1007/s11427-017-9188-xopenalex-snapshot
Prognostic significance of combining high mobility group Box-1 and OV-6 expression in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s11523-017-0507-4openalex-snapshot
Targeting the Wnt Pathway in Cancer: A Review of Novel Therapeutics
inferred← citeshttps://doi.org/10.1007/s11538-017-0359-1openalex-snapshot
Modeling the Dynamics of Heterogeneity of Solid Tumors in Response to Chemotherapy
inferred← citeshttps://doi.org/10.1007/s11596-017-1820-yopenalex-snapshot
Look into hepatic progenitor cell associated trait: Histological heterogeneity of hepatitis B-related combined hepatocellular-cholangiocarcinoma
inferred← citeshttps://doi.org/10.1007/s11748-016-0682-8openalex-snapshot
Biology of lung cancer: genetic mutation, epithelial-mesenchymal transition, and cancer stem cells
inferred← citeshttps://doi.org/10.1007/s11888-013-0194-1openalex-snapshot
Stem Cell Signaling Pathways in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/s11888-017-0353-xopenalex-snapshot
Innovative Therapeutic Strategies Targeting Colorectal Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/s12010-023-04609-4openalex-snapshot
Production of a Ribosome-Displayed Mouse scFv Antibody Against CD133, Analysis of Its Molecular Docking, and Molecular Dynamic Simulations of Their Interactions
inferred← citeshttps://doi.org/10.1007/s12015-017-9743-3openalex-snapshot
Do Cancer Cell Lines Have Fixed or Fluctuating Stem Cell Phenotypes? – Studies with the NTera2 Cell Line
inferred← citeshttps://doi.org/10.1007/s12038-016-9624-yopenalex-snapshot
Therapeutic resistance and cancer recurrence mechanisms: Unfolding the story of tumour coming back
inferred← citeshttps://doi.org/10.1007/s12672-024-01121-xopenalex-snapshot
Identification of placenta-specific protein 1 (PLAC-1) expression on human PC-3 cell line-derived prostate cancer stem cells compared to the tumor parental cells
inferred← citeshttps://doi.org/10.1007/s13105-020-00780-yopenalex-snapshot
Gastrin-17 induces gastric cancer cell epithelial-mesenchymal transition via the Wnt/β-catenin signaling pathway
inferred← citeshttps://doi.org/10.1007/s13238-020-00819-2openalex-snapshot
3D chromatin architecture and epigenetic regulation in cancer stem cells
inferred← citeshttps://doi.org/10.1007/s13277-015-3731-5openalex-snapshot
High expression of OCT4 is frequent and may cause undesirable treatment outcomes in patients with acute myeloid leukemia
inferred← citeshttps://doi.org/10.1007/s13402-023-00803-yopenalex-snapshot
Induction of promyelocytic leukemia zinc finger protein by miR-200c-3p restores sensitivity to anti-androgen therapy in androgen-refractory prostate cancer and inhibits the cancer progression via down-regulation of integrin α3β4
inferred← citeshttps://doi.org/10.1007/s40336-021-00444-xopenalex-snapshot
Toward radiotheranostics in cancer stem cells: a promising initial step for tumour eradication
inferred← citeshttps://doi.org/10.1007/s40778-019-00156-zopenalex-snapshot
Mathematical Models of Stem Cell Differentiation and Dedifferentiation
inferred← citeshttps://doi.org/10.1007/s43152-024-00053-6openalex-snapshot
Comprehensive Review on the Effect of Stem Cells in Cancer Progression
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11239-5openalex-snapshot
Tumor Dormancy in The Bone
inferred← citeshttps://doi.org/10.1016/b978-0-12-803395-1.00001-0openalex-snapshot
A Brief Introduction to Chromatin Regulation and Dynamics
inferred← citeshttps://doi.org/10.1016/b978-0-12-803892-5.00003-6openalex-snapshot
Enrichment and Interrogation of Cancer Stem Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-811161-1.00003-7openalex-snapshot
Pathogenesis and biology
inferred← citeshttps://doi.org/10.1016/b978-0-12-811783-5.00009-4openalex-snapshot
Animal Models of Brain Tumor Surgery
inferred← citeshttps://doi.org/10.1016/b978-0-12-816909-4.00015-4openalex-snapshot
In vitro and in vivo technologies: an up to date overview in tissue engineering
inferred← citeshttps://doi.org/10.1016/b978-0-12-819840-7.00009-1openalex-snapshot
Ovarian cancer stem cell biology and chemoresistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-821310-0.00002-4openalex-snapshot
Preventing phenotypic plasticity in cancer to mitigate therapy resistance
inferred← citeshttps://doi.org/10.1016/b978-0-443-13209-4.00018-0openalex-snapshot
Cancer stem cells—Challenges for cancer therapies
inferred← citeshttps://doi.org/10.1016/b978-0-443-13212-4.00020-9openalex-snapshot
Role of cancer stem cells in developing chemoresistance of solid tumor
inferred← citeshttps://doi.org/10.1016/b978-0-443-21834-7.00004-9openalex-snapshot
Theoretical developments, instrumentation, and biological applications of surface-enhanced Raman spectroscopy
inferred← citeshttps://doi.org/10.1016/b978-0-443-40471-9.00008-2openalex-snapshot
Stem cells and pyroptosis in cancer
inferred← citeshttps://doi.org/10.1016/j.addr.2013.09.016openalex-snapshot
Can nanomedicines kill cancer stem cells?
inferred← citeshttps://doi.org/10.1016/j.apm.2018.07.025openalex-snapshot
Modeling continuous levels of resistance to multidrug therapy in cancer
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.01.004openalex-snapshot
Integrins as attractive targets for cancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.bbabio.2017.01.012openalex-snapshot
Mitochondria and cancer chemoresistance
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2014.07.003openalex-snapshot
Tumoral reprogramming: Plasticity takes a walk on the wild side
inferred← citeshttps://doi.org/10.1016/j.bbcan.2015.05.005openalex-snapshot
Snail1-driven plasticity of epithelial and mesenchymal cells sustains cancer malignancy
inferred← citeshttps://doi.org/10.1016/j.bbcan.2016.10.003openalex-snapshot
Heterogeneity of Cancer Stem Cells: Rationale for Targeting the Stem Cell Niche
inferred← citeshttps://doi.org/10.1016/j.bbcan.2024.189236openalex-snapshot
Circulating tumor cells in solid malignancies: From advanced isolation technologies to biological understanding and clinical relevance in early diagnosis and prognosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.12.016openalex-snapshot
Inversed relationship between CD44 variant and c-Myc due to oxidative stress-induced canonical Wnt activation
inferred← citeshttps://doi.org/10.1016/j.bcp.2019.01.020openalex-snapshot
Understanding the cancer stem cell phenotype: A step forward in the therapeutic management of cancer
inferred← citeshttps://doi.org/10.1016/j.bcp.2026.118386openalex-snapshot
eIF4A1 enhances p70S6K mRNA translation and promotes nuclear β-catenin levels to augment stemness and metastasis in gastric cancer cells
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2015.09.037openalex-snapshot
Nanomedicine-mediated cancer stem cell therapy
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121180openalex-snapshot
A novel prodrug and its nanoformulation suppress cancer stem cells by inducing immunogenic cell death and inhibiting indoleamine 2, 3-dioxygenase
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121305openalex-snapshot
Cascade-responsive nano-assembly for efficient photothermal-chemo synergistic inhibition of tumor metastasis by targeting cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109396openalex-snapshot
Long non-coding RNAs and endometrial cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111875openalex-snapshot
Recent advances in regenerative medicine strategies for cancer treatment
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112339openalex-snapshot
Musarin, a novel protein with tyrosine kinase inhibitory activity from Trametes versicolor, inhibits colorectal cancer stem cell growth
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116172openalex-snapshot
Astragalus polysaccharide ameliorates CD8+ T cell dysfunction through STAT3/Gal-3/LAG3 pathway in inflammation‐induced colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.bios.2017.11.049openalex-snapshot
Selective isolation and noninvasive analysis of circulating cancer stem cells through Raman imaging
inferred← citeshttps://doi.org/10.1016/j.btre.2017.11.004openalex-snapshot
Cancer cell lines involving cancer stem cell populations respond to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.canlet.2013.07.031openalex-snapshot
Inflammation and cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2013.11.012openalex-snapshot
Cancer stem cells: A contentious hypothesis now moving forward
inferred← citeshttps://doi.org/10.1016/j.canlet.2014.12.004openalex-snapshot
Pancreatic cancer stem cells: New insight into a stubborn disease
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.10.013openalex-snapshot
Panaxynol, a natural Hsp90 inhibitor, effectively targets both lung cancer stem and non-stem cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2020.01.008openalex-snapshot
DNA damage response and resistance of cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2022.215855openalex-snapshot
ITGA2 overexpression inhibits DNA repair and confers sensitivity to radiotherapies in pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2024.217108openalex-snapshot
Targeting of human cancer stem cells predicts efficacy and toxicity of FDA-approved oncology drugs
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111790openalex-snapshot
HCT116 cell line heterogeneity: A useful tool for preclinical research
inferred← citeshttps://doi.org/10.1016/j.ccell.2022.08.010openalex-snapshot
Acquired semi-squamatization during chemotherapy suggests differentiation as a therapeutic strategy for bladder cancer
inferred← citeshttps://doi.org/10.1016/j.cej.2020.127874openalex-snapshot
Deep tumor‐penetrated nanosystem eliminates cancer stem cell for highly efficient liver cancer therapy
inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109845openalex-snapshot
CircTP53 promotes colorectal cancer by acting as a miR-876-3p sponge to increase cyclin-dependent kinase-like 3 expression
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.04.034openalex-snapshot
Direct Upregulation of STAT3 by MicroRNA-551b-3p Deregulates Growth and Metastasis of Ovarian Cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.02.037openalex-snapshot
CD95/Fas Increases Stemness in Cancer Cells by Inducing a STAT1-Dependent Type I Interferon Response
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109757openalex-snapshot
HIF-1 recruits NANOG as a coactivator for TERT gene transcription in hypoxic breast cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115359openalex-snapshot
Adhesion strength of tumor cells predicts metastatic disease in vivo
inferred← citeshttps://doi.org/10.1016/j.clbc.2017.01.007openalex-snapshot
Expression Profiling of Clinical Specimens Supports the Existence of Neural Progenitor-Like Stem Cells in Basal Breast Cancers
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2013.08.023openalex-snapshot
Water bath hyperthermia reduces stemness of colon cancer cells
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2015.04.007openalex-snapshot
Cancer stem cells in oesophageal squamous cell carcinoma: Identification, prognostic and treatment perspectives
inferred← citeshttps://doi.org/10.1016/j.csbj.2024.12.020openalex-snapshot
Tumour heterogeneity and personalized treatment screening based on single-cell transcriptomics
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.03.004openalex-snapshot
Cancer stem cells, cancer-initiating cells and methods for their detection
inferred← citeshttps://doi.org/10.1016/j.ejcb.2016.06.007openalex-snapshot
Causes and consequences of nuclear envelope alterations in tumour progression
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.034openalex-snapshot
A comprehensive review of salinomycin derivatives as potent anticancer and anti-CSCs agents
inferred← citeshttps://doi.org/10.1016/j.fct.2016.03.011openalex-snapshot
In vivo relevant mixed urolithins and ellagic acid inhibit phenotypic and molecular colon cancer stem cell features: A new potentiality for ellagitannin metabolites against cancer
inferred← citeshttps://doi.org/10.1016/j.gde.2014.09.009openalex-snapshot
Reprogramming by lineage specifiers: blurring the lines between pluripotency and differentiation
inferred← citeshttps://doi.org/10.1016/j.gendis.2016.01.001openalex-snapshot
Cancer stem cells may contribute to the difficulty in treating cancer
inferred← citeshttps://doi.org/10.1016/j.gendis.2018.12.003openalex-snapshot
Regulation and functions of integrin α2 in cell adhesion and disease
inferred← citeshttps://doi.org/10.1016/j.gmg.2025.100067openalex-snapshot
Characterization of stem cell landscape and identification of stemness-related gene ENY2 in colorectal cancer by intergrated transcriptomic analysis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e33030openalex-snapshot
Identification of TNFAIP6 as a reliable prognostic indicator of low-grade glioma
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.11.180openalex-snapshot
The effects of chitosan-based materials on glioma: Recent advances in its applications for diagnosis and treatment
inferred← citeshttps://doi.org/10.1016/j.intimp.2018.10.003openalex-snapshot
Restoration of stemness-high tumor cell-mediated suppression of murine dendritic cell activity and inhibition of tumor growth by low molecular weight oyster polysaccharide
inferred← citeshttps://doi.org/10.1016/j.intimp.2026.116738openalex-snapshot
Stem cells at the tumor frontier: Mechanistic insights, therapeutic challenges, and emerging horizons
inferred← citeshttps://doi.org/10.1016/j.isci.2018.08.015openalex-snapshot
Single-Cell Tracking of Breast Cancer Cells Enables Prediction of Sphere Formation from Early Cell Divisions
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104317openalex-snapshot
Emergence of hybrid states of stem-like cancer cells correlates with poor prognosis in oral cancer
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2021.12.015openalex-snapshot
A High-Fat Diet Activates the BAs-FXR Axis and Triggers Cancer-Associated Fibroblast Properties in the Colon
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2024.05.006openalex-snapshot
Sorted-Cell Sequencing on HCC Specimens Reveals EPS8L3 as a Key Player in CD24/CD13/EpCAM-Triple Positive, Stemness-Related HCC Cells
inferred← citeshttps://doi.org/10.1016/j.jconrel.2013.09.005openalex-snapshot
HPMA copolymer-based combination therapy toxic to both prostate cancer stem/progenitor cells and differentiated cells induces durable anti-tumor effects
inferred← citeshttps://doi.org/10.1016/j.jconrel.2014.04.013openalex-snapshot
Macromolecular therapeutics
inferred← citeshttps://doi.org/10.1016/j.jconrel.2025.113784openalex-snapshot
Design Strategies for Hyaluronic Acid-based Drug Delivery Systems in Cancer Immunotherapy
inferred← citeshttps://doi.org/10.1016/j.jds.2024.09.018openalex-snapshot
Oleanolic acid inhibits aldo-keto reductase family 1 member B10-induced cancer stemness and avoids cisplatin-based chemotherapy resistance via the Snail signaling pathway in oral squamous cell carcinoma cell lines
inferred← citeshttps://doi.org/10.1016/j.jff.2016.06.007openalex-snapshot
Indian gooseberry (Emblica officinalis Gaertn.) suppresses cell proliferation and induces apoptosis in human colon cancer stem cells independent of p53 status via suppression of c-Myc and cyclin D1
inferred← citeshttps://doi.org/10.1016/j.jtbi.2017.11.025openalex-snapshot
Activation of the HGF/c-Met axis in the tumor microenvironment: A multispecies model
inferred← citeshttps://doi.org/10.1016/j.mam.2013.06.002openalex-snapshot
Ovarian cancer stem cells: Molecular concepts and relevance as therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.mam.2013.08.003openalex-snapshot
Lung cancer stem cells: Molecular features and therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.matt.2022.02.015openalex-snapshot
Nanomaterial-mediated ablation therapy for cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.molonc.2015.01.007openalex-snapshot
The Hippo transducer TAZ promotes epithelial to mesenchymal transition and cancer stem cell maintenance in oral cancer
inferred← citeshttps://doi.org/10.1016/j.nano.2017.11.015openalex-snapshot
Delivery of NF-κB shRNA using carbamate-mannose modified PEI for eliminating cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.nano.2019.102124openalex-snapshot
Eradication of cancer stem cells in triple negative breast cancer using doxorubicin/pluronic polymeric micelles
inferred← citeshttps://doi.org/10.1016/j.neo.2018.06.001openalex-snapshot
Glycosylation of Cancer Stem Cells: Function in Stemness, Tumorigenesis, and Metastasis
inferred← citeshttps://doi.org/10.1016/j.neulet.2017.07.057openalex-snapshot
FERMT3 contributes to glioblastoma cell proliferation and chemoresistance to temozolomide through integrin mediated Wnt signaling
inferred← citeshttps://doi.org/10.1016/j.nut.2014.02.016openalex-snapshot
Colon carcinogenesis: Influence of Western diet-induced obesity and targeting stem cells using dietary bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.omtn.2022.01.022openalex-snapshot
Membrane tethering of CreER decreases uninduced cell labeling and cytotoxicity while maintaining recombination efficiency
inferred← citeshttps://doi.org/10.1016/j.omto.2021.06.015openalex-snapshot
miR-519d-3p suppresses tumorigenicity and metastasis by inhibiting Bcl-w and HIF-1α in NSCLC
inferred← citeshttps://doi.org/10.1016/j.oraloncology.2016.05.013openalex-snapshot
Evaluation of the immunogenicity of ALDHhigh human head and neck squamous cell carcinoma cancer stem cells in vitro
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.pdpdt.2023.103648openalex-snapshot
Effect of photothermal and photodynamic therapy with cobalt ferrite superparamagnetic nanoparticles loaded with ICG and PpIX on cancer stem cells in MDA-MB-231 and A375 cell lines
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2015.12.001openalex-snapshot
Cancer stem cells in drug resistant lung cancer: Targeting cell surface markers and signaling pathways
inferred← citeshttps://doi.org/10.1016/j.phrs.2021.105609openalex-snapshot
Microvesicles – promising tiny players’ of cancer stem cells targeted liver cancer treatments: The interesting interactions and therapeutic aspects
inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106222openalex-snapshot
Sinomenine hydrochloride suppresses the stemness of breast cancer stem cells by inhibiting Wnt signaling pathway through down-regulation of WNT10B
inferred← citeshttps://doi.org/10.1016/j.prp.2014.06.005openalex-snapshot
Stem cell markers OCT4 and nestin in laryngeal squamous cell carcinoma and their relation to survivin expression
inferred← citeshttps://doi.org/10.1016/j.prp.2019.152437openalex-snapshot
LETM1 is a potential cancer stem-like cell marker and predicts poor prognosis in colorectal adenocarcinoma
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