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The molecular mechanisms of chemoresistance in cancers
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3 of the 116 references listed on this page are in the Retraction Watch database as retracted (export 2026-10-28): 10.1186/s12943-017-0586-y (notice 2022-12-28), 10.18632/oncotarget.12718 (notice 2019-06-25), 10.18632/oncotarget.5352 (notice 2026-05-20).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ijc.23049openalex-snapshot
Phosphoinositide 3‐kinase/Akt pathway plays an important role in chemoresistance of gastric cancer cells against etoposide and doxorubicin induced cell death
inferredcites →https://doi.org/10.1002/jcb.26107openalex-snapshot
Long Noncoding RNA lncARSR Promotes Doxorubicin Resistance in Hepatocellular Carcinoma via Modulating PTEN‐PI3K/Akt Pathway
inferredcites →https://doi.org/10.1002/mc.22526openalex-snapshot
Cancer stem cell mediated acquired chemoresistance in head and neck cancer can be abrogated by aldehyde dehydrogenase 1 A1 inhibition
inferredcites →https://doi.org/10.1007/s00428-005-1264-9openalex-snapshot
NF-kB in development and progression of human cancer
inferredcites →https://doi.org/10.1007/s00432-016-2302-5openalex-snapshot
53BP1 loss induces chemoresistance of colorectal cancer cells to 5-fluorouracil by inhibiting the ATM–CHK2–P53 pathway
inferredcites →https://doi.org/10.1007/s10495-016-1339-xopenalex-snapshot
Adipocyte microenvironment promotes Bclxl expression and confers chemoresistance in ovarian cancer cells
inferredcites →https://doi.org/10.1007/s13277-014-2242-0openalex-snapshot
Exosomes from docetaxel-resistant breast cancer cells alter chemosensitivity by delivering microRNAs
inferredcites →https://doi.org/10.1007/s13277-015-4755-6openalex-snapshot
Upregulation of CD44v6 contributes to acquired chemoresistance via the modulation of autophagy in colon cancer SW480 cells
inferredcites →https://doi.org/10.1007/s13277-016-4848-xopenalex-snapshot
NANOG regulates epithelial-mesenchymal transition and chemoresistance through activation of the STAT3 pathway in epithelial ovarian cancer
inferredcites →https://doi.org/10.1007/s13277-016-5209-5openalex-snapshot
ABCG2 is required for self-renewal and chemoresistance of CD133-positive human colorectal cancer cells
inferredcites →https://doi.org/10.1007/s13277-016-5254-0openalex-snapshot
Decreased expression of LncRNA SLC25A25-AS1 promotes proliferation, chemoresistance, and EMT in colorectal cancer cells
inferredcites →https://doi.org/10.1016/j.bbabio.2017.01.012openalex-snapshot
Mitochondria and cancer chemoresistance
inferredcites →https://doi.org/10.1016/j.bbcan.2010.01.002openalex-snapshot
Targeting transcription factor NF-κB to overcome chemoresistance and radioresistance in cancer therapy
inferredcites →https://doi.org/10.1016/j.bbrc.2015.05.031openalex-snapshot
Chemoresistance of CD133 + colon cancer may be related with increased survivin expression
inferredcites →https://doi.org/10.1016/j.biocel.2008.04.011openalex-snapshot
The strand separation and nuclease activities associated with YB-1 are dispensable for cisplatin resistance but overexpression of YB-1 in MCF7 and MDA-MB-231 breast tumor cells generates several chemoresistance signatures
inferredcites →https://doi.org/10.1016/j.biopha.2013.08.001openalex-snapshot
Lgr5 promotes cancer stemness and confers chemoresistance through ABCB1 in colorectal cancer
inferredcites →https://doi.org/10.1016/j.bmcl.2014.11.076openalex-snapshot
Role of the ERK1/2 pathway in tumor chemoresistance and tumor therapy
inferredcites →https://doi.org/10.1016/j.canlet.2007.12.004openalex-snapshot
Gambogic acid, a potent inhibitor of survivin, reverses docetaxel resistance in gastric cancer cells
inferredcites →https://doi.org/10.1016/j.canlet.2012.01.030openalex-snapshot
Hsp70 promotes chemoresistance by blocking Bax mitochondrial translocation in ovarian cancer cells
inferredcites →https://doi.org/10.1016/j.canlet.2016.12.023openalex-snapshot
CD133 confers cancer stem-like cell properties by stabilizing EGFR-AKT signaling in hepatocellular carcinoma
inferredcites →https://doi.org/10.1016/j.cell.2013.08.015openalex-snapshot
EGFR-Mediated Beclin 1 Phosphorylation in Autophagy Suppression, Tumor Progression, and Tumor Chemoresistance
inferredcites →https://doi.org/10.1016/j.febslet.2005.12.036openalex-snapshot
Substrate recognition and transport by multidrug resistance protein 1 (ABCC1)
inferredcites →https://doi.org/10.1016/j.febslet.2014.04.024openalex-snapshot
MiR‐489 regulates chemoresistance in breast cancer via epithelial mesenchymal transition pathway
inferredcites →https://doi.org/10.1016/j.jhep.2015.11.011openalex-snapshot
Laminin-332 sustains chemoresistance and quiescence as part of the human hepatic cancer stem cell niche
inferredcites →https://doi.org/10.1016/j.lungcan.2009.03.015openalex-snapshot
Inhibition of heme oxygenase-1 with an epidermal growth factor receptor inhibitor and cisplatin decreases proliferation of lung cancer A549 cells
inferredcites →https://doi.org/10.1016/s0360-3016(03)00511-xopenalex-snapshot
The epidermal growth factor receptor mediates radioresistance
inferredcites →https://doi.org/10.1038/cddis.2011.33openalex-snapshot
Disruption of the MDM2–p53 interaction strongly potentiates p53-dependent apoptosis in cisplatin-resistant human testicular carcinoma cells via the Fas/FasL pathway
inferredcites →https://doi.org/10.1038/cddis.2013.526openalex-snapshot
Galectin-1 overexpression promotes progression and chemoresistance to cisplatin in epithelial ovarian cancer
inferredcites →https://doi.org/10.1038/cddis.2016.370openalex-snapshot
ERK/Drp1-dependent mitochondrial fission is involved in the MSC-induced drug resistance of T-cell acute lymphoblastic leukemia cells
inferredcites →https://doi.org/10.1038/cddiscovery.2016.87openalex-snapshot
Aquaporin 3 facilitates chemoresistance in gastric cancer cells to cisplatin via autophagy
inferredcites →https://doi.org/10.1038/ncomms9904openalex-snapshot
Wnt/β-catenin pathway regulates MGMT gene expression in cancer and inhibition of Wnt signalling prevents chemoresistance
inferredcites →https://doi.org/10.1038/onc.2011.149openalex-snapshot
HAb18G/CD147 promotes epithelial–mesenchymal transition through TGF-β signaling and is transcriptionally regulated by Slug
inferredcites →https://doi.org/10.1038/onc.2011.426openalex-snapshot
Cisplatin regulates the MAPK kinase pathway to induce increased expression of DNA repair gene ERCC1 and increase melanoma chemoresistance
inferredcites →https://doi.org/10.1038/onc.2012.259openalex-snapshot
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutations
inferredcites →https://doi.org/10.1038/onc.2013.106openalex-snapshot
Gain-of-function mutant p53 downregulates miR-223 contributing to chemoresistance of cultured tumor cells
inferredcites →https://doi.org/10.1038/onc.2016.353openalex-snapshot
Cancer-associated fibroblast exosomes regulate survival and proliferation of pancreatic cancer cells
inferredcites →https://doi.org/10.1038/onc.2017.152openalex-snapshot
Proteomic identification of ERP29 as a key chemoresistant factor activated by the aggregating p53 mutant Arg282Trp
inferredcites →https://doi.org/10.1038/oncsis.2017.25openalex-snapshot
miRNA-34c-5p inhibits amphiregulin-induced ovarian cancer stemness and drug resistance via downregulation of the AREG-EGFR-ERK pathway
inferredcites →https://doi.org/10.1038/srep41942openalex-snapshot
MicroRNA-130b targets PTEN to mediate drug resistance and proliferation of breast cancer cells via the PI3K/Akt signaling pathway
inferredcites →https://doi.org/10.1042/bsr20160247openalex-snapshot
NANOG regulates epithelial–mesenchymal transition and chemoresistance in ovarian cancer
inferredcites →https://doi.org/10.1073/pnas.0510834103openalex-snapshot
MAGE-A tumor antigens target p53 transactivation function through histone deacetylase recruitment and confer resistance to chemotherapeutic agents
inferredcites →https://doi.org/10.1073/pnas.95.26.15665openalex-snapshot
A multidrug resistance transporter from human MCF-7 breast cancer cells
inferredcites →https://doi.org/10.1074/jbc.m115.700021openalex-snapshot
Up-regulation of Histone Methyltransferase, DOT1L, by Matrix Hyaluronan Promotes MicroRNA-10 Expression Leading to Tumor Cell Invasion and Chemoresistance in Cancer Stem Cells from Head and Neck Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1080/09674845.2011.11730326openalex-snapshot
Multidrug resistance-associated biomarkers PGP, GST-π, Topo-II and LRP as prognostic factors in primary ovarian carcinoma
inferredcites →https://doi.org/10.1080/15384101.2015.1005530openalex-snapshot
Exosomes derived from human mesenchymal stem cells confer drug resistance in gastric cancer
inferredcites →https://doi.org/10.1080/15548627.2016.1239676openalex-snapshot
GFRA1 promotes cisplatin-induced chemoresistance in osteosarcoma by inducing autophagy
inferredcites →https://doi.org/10.1080/15548627.2016.1245263openalex-snapshot
Targeting autophagy to overcome chemoresistance in acute myleogenous leukemia
inferredcites →https://doi.org/10.1089/biores.2014.0035openalex-snapshot
Autophagy in Cancer Stem Cells: A Potential Link Between Chemoresistance, Recurrence, and Metastasis
inferredcites →https://doi.org/10.1093/nar/gks818openalex-snapshot
DNA repair endonuclease ERCC1-XPF as a novel therapeutic target to overcome chemoresistance in cancer therapy
inferredcites →https://doi.org/10.1111/cas.12712openalex-snapshot
Src/ STAT 3‐dependent heme oxygenase‐1 induction mediates chemoresistance of breast cancer cells to doxorubicin by promoting autophagy
inferredcites →https://doi.org/10.1111/cas.13150openalex-snapshot
Increasing circulating exosomes‐carrying TRPC 5 predicts chemoresistance in metastatic breast cancer patients
inferredcites →https://doi.org/10.1111/cas.13275openalex-snapshot
β2‐AR activation induces chemoresistance by modulating p53 acetylation through upregulating Sirt1 in cervical cancer cells
inferredcites →https://doi.org/10.1111/nyas.12883openalex-snapshot
Mitochondrial dynamics regulating chemoresistance in gynecological cancers
inferredcites →https://doi.org/10.1126/science.1360704openalex-snapshot
Overexpression of a Transporter Gene in a Multidrug-Resistant Human Lung Cancer Cell Line
inferredcites →https://doi.org/10.1158/0008-5472.can-08-3722openalex-snapshot
Mitochondrial Uncoupling and the Warburg Effect: Molecular Basis for the Reprogramming of Cancer Cell Metabolism
inferredcites →https://doi.org/10.1158/0008-5472.can-11-1674openalex-snapshot
Intracellular ATP Levels Are a Pivotal Determinant of Chemoresistance in Colon Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-15-0037openalex-snapshot
Heparanase Enhances Tumor Growth and Chemoresistance by Promoting Autophagy
inferredcites →https://doi.org/10.1158/0008-5472.can-15-1360openalex-snapshot
Aspirin Suppresses the Acquisition of Chemoresistance in Breast Cancer by Disrupting an NFκB–IL6 Signaling Axis Responsible for the Generation of Cancer Stem Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-16-0980openalex-snapshot
Ovarian Cancer Chemoresistance Relies on the Stem Cell Reprogramming Factor PBX1
inferredcites →https://doi.org/10.1158/0008-5472.can-16-1151openalex-snapshot
DNA Repair Capacity in Multiple Pathways Predicts Chemoresistance in Glioblastoma Multiforme
inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-0149openalex-snapshot
Targeting Inflammatory Pathways for Prevention and Therapy of Cancer: Short-Term Friend, Long-Term Foe
inferredcites →https://doi.org/10.1158/1078-0432.ccr-14-0610openalex-snapshot
Low Expression of the E3 Ubiquitin Ligase CBL Confers Chemoresistance in Human Pancreatic Cancer and Is Targeted by Epidermal Growth Factor Receptor Inhibition
inferredcites →https://doi.org/10.1158/1078-0432.ccr-14-2191openalex-snapshot
The Hippo Coactivator YAP1 Mediates EGFR Overexpression and Confers Chemoresistance in Esophageal Cancer
inferredcites →https://doi.org/10.1158/1078-0432.ccr-16-2530openalex-snapshot
MUC16 Regulates TSPYL5 for Lung Cancer Cell Growth and Chemoresistance by Suppressing p53
inferredcites →https://doi.org/10.1158/1535-7163.mct-12-0448openalex-snapshot
Deficient DNA Damage Signaling Leads to Chemoresistance to Cisplatin in Oral Cancer
inferredcites →https://doi.org/10.1159/000430191openalex-snapshot
β-Elemene Reverses Chemoresistance of Breast Cancer Cells by Reducing Resistance Transmission via Exosomes
inferredcites →https://doi.org/10.1182/blood-2005-09-3926openalex-snapshot
Oncogenic RAS mutations in myeloma cells selectively induce cox-2 expression, which participates in enhanced adhesion to fibronectin and chemoresistance
inferredcites →https://doi.org/10.1186/s12885-015-1239-4openalex-snapshot
Chemoresistance is associated with increased cytoprotective autophagy and diminished apoptosis in bladder cancer cells treated with the BH3 mimetic (−)-Gossypol (AT-101)
inferredcites →https://doi.org/10.1186/s12943-017-0586-yopenalex-snapshot
RETRACTED ARTICLE: Decreased expression of miR-939 contributes to chemoresistance and metastasis of gastric cancer via dysregulation of SLC34A2 and Raf/MEK/ERK pathway
inferredcites →https://doi.org/10.1186/s12967-016-1056-9openalex-snapshot
Exosomes in tumor microenvironment: novel transporters and biomarkers
inferredcites →https://doi.org/10.1186/s13046-016-0387-yopenalex-snapshot
Nestin overexpression in hepatocellular carcinoma associates with epithelial-mesenchymal transition and chemoresistance
inferredcites →https://doi.org/10.1371/journal.pone.0024665openalex-snapshot
Acquisition of Chemoresistance in Gliomas Is Associated with Increased Mitochondrial Coupling and Decreased ROS Production
inferredcites →https://doi.org/10.1371/journal.pone.0088193openalex-snapshot
Exosome Release and Low pH Belong to a Framework of Resistance of Human Melanoma Cells to Cisplatin
inferredcites →https://doi.org/10.1371/journal.pone.0107109openalex-snapshot
Expression of Mitochondrial Regulators PGC1α and TFAM as Putative Markers of Subtype and Chemoresistance in Epithelial Ovarian Carcinoma
inferredcites →https://doi.org/10.1371/journal.pone.0125625openalex-snapshot
Fibroblast-Derived Exosomes Contribute to Chemoresistance through Priming Cancer Stem Cells in Colorectal Cancer
inferredcites →https://doi.org/10.1515/bmc-2016-0015openalex-snapshot
Bcl-2 family proteins: master regulators of cell survival
inferredcites →https://doi.org/10.15252/embj.201695669openalex-snapshot
USP49 negatively regulates tumorigenesis and chemoresistance through FKBP51‐AKT signaling
inferredcites →https://doi.org/10.18632/oncotarget.10252openalex-snapshot
CD147 knockdown improves the antitumor efficacy of trastuzumab in HER2-positive breast cancer cells
inferredcites →https://doi.org/10.18632/oncotarget.10326openalex-snapshot
Capsaicin triggers autophagic cell survival which drives epithelial mesenchymal transition and chemoresistance in bladder cancer cells in an Hedgehog-dependent manner
inferredcites →https://doi.org/10.18632/oncotarget.10736openalex-snapshot
MiR-770-5p inhibits cisplatin chemoresistance in human ovarian cancer by targeting ERCC2
inferredcites →https://doi.org/10.18632/oncotarget.12718openalex-snapshot
Activation of endoplasmic reticulum stress promotes autophagy and apoptosis and reverses chemoresistance of human small cell lung cancer cells by inhibiting the PI3K/AKT/mTOR signaling pathway
inferredcites →https://doi.org/10.18632/oncotarget.14021openalex-snapshot
Chemoresistance and targeted therapies in ovarian and endometrial cancers
inferredcites →https://doi.org/10.18632/oncotarget.1471openalex-snapshot
Chemoresistance to gemcitabine in hepatoma cells induces epithelial-mesenchymal transition and involves activation of PDGF-D pathway
inferredcites →https://doi.org/10.18632/oncotarget.15001openalex-snapshot
Derlin-1 overexpression confers poor prognosis in muscle invasive bladder cancer and contributes to chemoresistance and invasion through PI3K/AKT and ERK/MMP signaling
inferredcites →https://doi.org/10.18632/oncotarget.16931openalex-snapshot
WP1130 attenuates cisplatin resistance by decreasing P53 expression in non-small cell lung carcinomas
inferredcites →https://doi.org/10.18632/oncotarget.16950openalex-snapshot
Trefoil factor 3 mediation of oncogenicity and chemoresistance in hepatocellular carcinoma is AKT-BCL-2 dependent
inferredcites →https://doi.org/10.18632/oncotarget.2894openalex-snapshot
Morphine promotes cancer stem cell properties, contributing to chemoresistance in breast cancer
inferredcites →https://doi.org/10.18632/oncotarget.3563openalex-snapshot
MiR-203 downregulation is responsible for chemoresistance in human glioblastoma by promoting epithelial-mesenchymal transition via SNAI2
inferredcites →https://doi.org/10.18632/oncotarget.5352openalex-snapshot
MiR-200b regulates autophagy associated with chemoresistance in human lung adenocarcinoma
inferredcites →https://doi.org/10.18632/oncotarget.8049openalex-snapshot
Increased chemoresistance via Snail-Raf kinase inhibitor protein signaling in colorectal cancer in response to a nicotine derivative
inferredcites →https://doi.org/10.2174/156800910791190175openalex-snapshot
Epithelial Mesenchymal Transition and Cancer Stem Cell-Like Phenotypes Facilitate Chemoresistance in Recurrent Ovarian Cancer
inferredcites →https://doi.org/10.2174/156800961407140926104458openalex-snapshot
Targeting Oncogenes and Tumor Suppressors genes to Mitigate Chemoresistance
inferredcites →https://doi.org/10.2174/1568011043482160openalex-snapshot
Structure of Multidrug-Resistance Proteins of the ATP-Binding Cassette (ABC) Superfamily
inferredcites →https://doi.org/10.21873/anticanres.11094openalex-snapshot
High Expression of MRE11–RAD50–NBS1 Is Associated with Poor Prognosis and Chemoresistance in Gastric Cancer
inferredcites →https://doi.org/10.3109/10428194.2011.616962openalex-snapshot
Up-regulated autophagy by endogenous high mobility group box-1 promotes chemoresistance in leukemia cells
inferredcites →https://doi.org/10.3390/cancers8120111openalex-snapshot
The Enrichment of Survivin in Exosomes from Breast Cancer Cells Treated with Paclitaxel Promotes Cell Survival and Chemoresistance
inferredcites →https://doi.org/10.3390/ijms15033432openalex-snapshot
Genistein-Inhibited Cancer Stem Cell-Like Properties and Reduced Chemoresistance of Gastric Cancer
inferredcites →https://doi.org/10.3390/ijms18010163openalex-snapshot
Estrogen Enhances the Expression of the Multidrug Transporter Gene ABCG2—Increasing Drug Resistance of Breast Cancer Cells through Estrogen Receptors
inferredcites →https://doi.org/10.3727/096504010x12828372551759openalex-snapshot
AP-1-Dependent miR-21 Expression Contributes to Chemoresistance in Cancer Stem Cell-Like SP Cells
inferredcites →https://doi.org/10.3727/096504015x14424348426071openalex-snapshot
Inhibition of NF-κB Activity Enhances Sensitivity to Anticancer Drugs in Cholangiocarcinoma Cells
inferredcites →https://doi.org/10.3892/ijo.2015.2898openalex-snapshot
Continuous exposure of non-small cell lung cancer cells with wild-type EGFR to an inhibitor of EGFR tyrosine kinase induces chemoresistance by activating STAT3
inferredcites →https://doi.org/10.3892/ijo.2015.3256openalex-snapshot
NF-κB signaling plays irreplaceable roles in cisplatin-induced bladder cancer chemoresistance and tumor progression
inferredcites →https://doi.org/10.3892/ijo.2016.3560openalex-snapshot
Exosome-derived microRNAs contribute to prostate cancer chemoresistance
inferredcites →https://doi.org/10.3892/mmr.2015.3356openalex-snapshot
Chemoresistance to doxorubicin induces epithelial-mesenchymal transition via upregulation of transforming growth factor β signaling in HCT116 colon cancer cells
inferredcites →https://doi.org/10.3892/mmr.2015.4217openalex-snapshot
DAL-1/4.1B contributes to epithelial-mesenchymal transition via regulation of transforming growth factor-β in lung cancer cell lines
inferredcites →https://doi.org/10.3892/or.12.6.1365openalex-snapshot
Effect of lung resistance-related protein on the resistance to cisplatin in human ovarian cancer cell lines
inferredcites →https://doi.org/10.3892/or.2015.4278openalex-snapshot
High mobility group box 1-mediated autophagy promotes neuroblastoma cell chemoresistance
inferredcites →https://doi.org/10.3892/or.2015.4497openalex-snapshot
MicroRNA-30a downregulation contributes to chemoresistance of osteosarcoma cells through activating Beclin-1-mediated autophagy
inferredcites →https://doi.org/10.3892/or.2016.4549openalex-snapshot
REV3L, the catalytic subunit of DNA polymerase ζ, is involved in the progression and chemoresistance of esophageal squamous cell carcinoma
inferredcites →https://doi.org/10.3892/or.2016.4991openalex-snapshot
Downregulation of DNA-PKcs suppresses P-gp expression via inhibition of the Akt/NF-κB pathway in CD133-positive osteosarcoma MG-63 cells
inferredcites →https://doi.org/10.3892/or.2016.5154openalex-snapshot
Proton pump inhibitor pantoprazole inhibits the proliferation, self-renewal and chemoresistance of gastric cancer stem cells via the EMT/β-catenin pathways
inferredcites →https://doi.org/10.3892/or.2016.5259openalex-snapshot
miR-20b reduces 5-FU resistance by suppressing the ADAM9/EGFR signaling pathway in colon cancer
inferredcites →https://doi.org/10.4161/auto.5.8.9996openalex-snapshot
Hypoxia-induced autophagy contributes to the chemoresistance of hepatocellular carcinoma cells
inferredcites →https://doi.org/10.7314/apjcp.2015.16.15.6663openalex-snapshot
High Expression of Lung Resistance Protein mRNA at Diagnosis Predicts Poor Early Response to Induction Chemotherapy in Childhood Acute Lymphoblastic Leukemia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Oncogenic Roles of John Cunningham Polyomavirus T Antigen in Cervical Cancer
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Loss of scinderin decreased expression of epidermal growth factor receptor and promoted apoptosis of castration‐resistant prostate cancer cells
inferred← citeshttps://doi.org/10.1002/9781119042280.ch8openalex-snapshot
Maternal Antibodies to Fetal Brain Neurons and Autism
inferred← citeshttps://doi.org/10.1002/adhm.202002227openalex-snapshot
The Influence of Ligand Density and Degradability on Hydrogel Induced Breast Cancer Dormancy and Reactivation
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Photoacid Generators for Biomedical Applications
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Prognostic and predictive values of tumour budding in stage IV colorectal cancer
inferred← citeshttps://doi.org/10.1002/btm2.10741openalex-snapshot
Establishment of a chemoresistant laryngeal cancer cell model to study chemoresistance and chemosensitization responses via transcriptomic analysis and a tumor‐on‐a‐chip platform
inferred← citeshttps://doi.org/10.1002/cam4.1993openalex-snapshot
Resveratrol promotes sensitization to Doxorubicin by inhibiting epithelial‐mesenchymal transition and modulating SIRT1/β‐catenin signaling pathway in breast cancer
inferred← citeshttps://doi.org/10.1002/cbin.11368openalex-snapshot
In vitro and in vivo studies of cancer cell behavior under nutrient deprivation
inferred← citeshttps://doi.org/10.1002/chem.202004278openalex-snapshot
Regulating Mitochondrial pH with Light and Implications for Chemoresistance
inferred← citeshttps://doi.org/10.1002/cnr2.1942openalex-snapshot
Mitochondrion: Main organelle in orchestrating cancer escape from chemotherapy
inferred← citeshttps://doi.org/10.1002/cnr2.70448openalex-snapshot
Transmembrane Protein TMEM59L Modulates 5‐ FU Resistance via PTPRN ‐Mediated DNA Damage Repair in Colorectal Cancer
inferred← citeshttps://doi.org/10.1002/ddr.21834openalex-snapshot
CircMYBL2 regulates the resistance of cervical cancer cells to paclitaxel via miR ‐665‐dependent regulation of EGFR
inferred← citeshttps://doi.org/10.1002/ddr.21994openalex-snapshot
α‐Pinene inhibits the growth of cervical cancer cells through its proapoptotic activity by regulating the miR‐34a‐5p/Bcl‐2 signaling axis
inferred← citeshttps://doi.org/10.1002/ddr.22105openalex-snapshot
FAM64A aggravates proliferation, invasion, lipid droplet formation, and chemoresistance in gastric cancer: A biomarker for aggressiveness and a gene therapy target
inferred← citeshttps://doi.org/10.1002/fsn3.72027openalex-snapshot
Dietary Polyphenols as Natural Modulators of NF ‐ κB Signaling in Inflammation‐Driven Non‐Communicable Diseases: Focus on Cancer
inferred← citeshttps://doi.org/10.1002/ijc.31881openalex-snapshot
KDM5 demethylases and their role in cancer cell chemoresistance
inferred← citeshttps://doi.org/10.1002/ijc.32730openalex-snapshot
HIV‐1, HAART and cancer: A complex relationship
inferred← citeshttps://doi.org/10.1002/ijc.34668openalex-snapshot
The effect of diet and nutrition on T cell function in cancer
inferred← citeshttps://doi.org/10.1002/iub.2773openalex-snapshot
Therapeutic targeting of nuclear export and import receptors in cancer and their potential in combination chemotherapy
inferred← citeshttps://doi.org/10.1002/jbt.23587openalex-snapshot
Lysine demethylase 5B (KDM5B): A key regulator of cancer drug resistance
inferred← citeshttps://doi.org/10.1002/jbt.23732openalex-snapshot
Using nanotechnology to progress the utilization of marine natural products in combating multidrug resistance in cancer: A prospective strategy
inferred← citeshttps://doi.org/10.1002/jbt.71028openalex-snapshot
Apigenin, Selenium, and Combinations Are Effective in Preventing 5‐Fluorouracil Induced Cardiovascular Damage
inferred← citeshttps://doi.org/10.1002/jcb.27063openalex-snapshot
Scutellaria baicalensis targets the hypoxia‐inducible factor‐1α and enhances cisplatin efficacy in ovarian cancer
inferred← citeshttps://doi.org/10.1002/jcb.28262openalex-snapshot
Plumbagin induces autophagy and apoptosis of SMMC‐7721 cells in vitro and in vivo
inferred← citeshttps://doi.org/10.1002/jcb.29318openalex-snapshot
Effects of dexmedetomidine on glioma cells in the presence or absence of cisplatin
inferred← citeshttps://doi.org/10.1002/jcp.31048openalex-snapshot
Shielding and nurturing: Fibronectin as a modulator of cancer drug resistance
inferred← citeshttps://doi.org/10.1002/jmr.3109openalex-snapshot
Role of Circular RNA MMP9 in Glioblastoma Progression: From Interaction With hnRNPC and hnRNPA1 to Affecting the Expression of BIRC5 by Sequestering miR ‐149
inferred← citeshttps://doi.org/10.1002/mc.23878openalex-snapshot
HGF/c‐Met Promotes Breast Cancer Tamoxifen Resistance Through the EZH2/HOTAIR‐miR‐141/200a Feedback Signaling Pathway
inferred← citeshttps://doi.org/10.1002/mco2.70162openalex-snapshot
Pancreatic Cancer: Pathogenesis and Clinical Studies
inferred← citeshttps://doi.org/10.1002/pbc.28764openalex-snapshot
A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome
inferred← citeshttps://doi.org/10.1002/ptr.7291openalex-snapshot
Piperine for treating breast cancer: A review of molecular mechanisms, combination with anticancer drugs, and nanosystems
inferred← citeshttps://doi.org/10.1002/ptr.7808openalex-snapshot
Oxymatrine suppresses colorectal cancer progression by inhibiting NLRP3 inflammasome activation through mitophagy induction in vitro and in vivo
inferred← citeshttps://doi.org/10.1002/tox.22942openalex-snapshot
Hyperforin induces apoptosis through extrinsic/intrinsic pathways and inhibits EGFR / ERK / NF‐κB ‐mediated anti‐apoptotic potential in glioblastoma
inferred← citeshttps://doi.org/10.1002/tox.23484openalex-snapshot
Involvement of the NF‐κB and PI3K /Akt/ mTOR pathways in cell death triggered by stypoldione, an o‐quinone isolated from the brown algae Stypopodium zonale
inferred← citeshttps://doi.org/10.1002/wnan.1876openalex-snapshot
Innovative nanotheranostics: Smart nanoparticles based approach to overcome breast cancer stem cells mediated chemo‐ and radioresistances
inferred← citeshttps://doi.org/10.1002/wnan.1909openalex-snapshot
Implantable smart hyperthermia nanofibers for cancer therapy: Challenges and opportunities
inferred← citeshttps://doi.org/10.1007/978-1-0716-3056-3_3openalex-snapshot
Three-Dimensional Spheroids for Cancer Research
inferred← citeshttps://doi.org/10.1007/978-1-4939-8973-7_4openalex-snapshot
Cell-Free DNA in the Liquid Biopsy Context: Role and Differences Between ctDNA and CTC Marker in Cancer Management
inferred← citeshttps://doi.org/10.1007/978-3-030-63369-1_10openalex-snapshot
Short-Chain Fatty Acids as Therapeutic Agents in Colon Malignancies
inferred← citeshttps://doi.org/10.1007/978-3-030-72702-4_7openalex-snapshot
Chemoresistance in Colorectal Malignancies: Molecular Mechanisms and Strategies to Overcome.
inferred← citeshttps://doi.org/10.1007/978-981-15-4501-6_16-1openalex-snapshot
Impact of Caenorhabditis elegans in Cancer Drug Resistance Development
inferred← citeshttps://doi.org/10.1007/978-981-15-9411-3_16openalex-snapshot
Impact of Caenorhabditis elegans in Cancer Drug Resistance Development
inferred← citeshttps://doi.org/10.1007/978-981-19-7188-4_33openalex-snapshot
Porous Carbon Materials Enhanced the Therapeutic Efficacy of Anticancer Drugs
inferred← citeshttps://doi.org/10.1007/978-981-95-7012-6_9openalex-snapshot
The Role of Ion Channels in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-981-97-1666-1_11openalex-snapshot
Novel Strategies for Overcoming Drug Resistance
inferred← citeshttps://doi.org/10.1007/s00210-025-03879-5openalex-snapshot
Metformin reverses 5-FU chemoresistance by downregulating DKK1, WNT5A, and ABCB1 expressions in gastric cancer: An experimental and bioinformatic study
inferred← citeshttps://doi.org/10.1007/s00280-025-04770-zopenalex-snapshot
Napabucasin targets resistant triple negative breast cancer through suppressing STAT3 and mitochondrial function
inferred← citeshttps://doi.org/10.1007/s00432-019-02892-5openalex-snapshot
Controlling metastatic cancer: the role of phytochemicals in cell signaling
inferred← citeshttps://doi.org/10.1007/s00441-022-03699-6openalex-snapshot
Crosstalk between exosomes and autophagy in spinal cord injury: fresh positive target for therapeutic application
inferred← citeshttps://doi.org/10.1007/s10238-022-00951-9openalex-snapshot
Bim downregulation by activation of NF-κB p65, Akt, and ERK1/2 is associated with adriamycin and dexamethasone resistance in multiple myeloma cells
inferred← citeshttps://doi.org/10.1007/s10238-025-01757-1openalex-snapshot
β-catenin as a key regulator of the cisplatin response in tumor cells
inferred← citeshttps://doi.org/10.1007/s10495-024-01981-2openalex-snapshot
Integrated analysis reveals a novel 5-fluorouracil resistance-based prognostic signature with promising implications for predicting the efficacy of chemotherapy and immunotherapy in patients with colorectal cancer
inferred← citeshttps://doi.org/10.1007/s10555-024-10169-8openalex-snapshot
Tumor-associated fibrosis: a unique mechanism promoting ovarian cancer metastasis and peritoneal dissemination
inferred← citeshttps://doi.org/10.1007/s10565-020-09553-1openalex-snapshot
Autophagy-mediating microRNAs in cancer chemoresistance
inferred← citeshttps://doi.org/10.1007/s10585-023-10243-5openalex-snapshot
The role of host response to chemotherapy: resistance, metastasis and clinical implications
inferred← citeshttps://doi.org/10.1007/s10637-021-01196-1openalex-snapshot
FX1, a BCL6 inhibitor, reactivates BCL6 target genes and suppresses HTLV-1-infected T cells
inferred← citeshttps://doi.org/10.1007/s11010-022-04456-7openalex-snapshot
Serine-Arginine Protein Kinase 1 (SRPK1): a systematic review of its multimodal role in oncogenesis
inferred← citeshttps://doi.org/10.1007/s11033-020-05261-5openalex-snapshot
Implication and role of neutrophil gelatinase-associated lipocalin in cancer: lipocalin-2 as a potential novel emerging comprehensive therapeutic target for a variety of cancer types
inferred← citeshttps://doi.org/10.1007/s11033-020-05609-xopenalex-snapshot
Emerging role of long non-coding RNAs in cancer chemoresistance: unravelling the multifaceted role and prospective therapeutic targeting
inferred← citeshttps://doi.org/10.1007/s11033-021-06141-2openalex-snapshot
Cytotoxic effect of 6-Shogaol in Imatinib sensitive and resistant K562 cells
inferred← citeshttps://doi.org/10.1007/s11033-022-07399-wopenalex-snapshot
STAT signaling as a target for intervention: from cancer inflammation and angiogenesis to non-coding RNAs modulation
inferred← citeshttps://doi.org/10.1007/s12015-020-10031-8openalex-snapshot
Regulatory Role of Quiescence in the Biological Function of Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/s12032-021-01563-1openalex-snapshot
Molecular analysis of cell survival and death pathways in the proteasome inhibitor bortezomib-resistant PC3 prostate cancer cell line
inferred← citeshttps://doi.org/10.1007/s12032-023-02042-5openalex-snapshot
Heat shock factor 1 is a promising therapeutic target against adult T-cell leukemia
inferred← citeshttps://doi.org/10.1007/s12032-025-02791-5openalex-snapshot
Unveiling the power of exosomal non-coding RNAs: key drivers of lung cancer progression in the tumor microenvironment
inferred← citeshttps://doi.org/10.1007/s12032-025-03072-xopenalex-snapshot
Cancer Metastasis: Therapeutic Challenges and Opportunities
inferred← citeshttps://doi.org/10.1007/s12033-023-00921-wopenalex-snapshot
Crosstalk Between m6A RNA Methylation and miRNA Biogenesis in Cancer: An Unholy Nexus
inferred← citeshttps://doi.org/10.1007/s12275-022-1533-1openalex-snapshot
Lactobacillus plantarum-derived metabolites sensitize the tumor-suppressive effects of butyrate by regulating the functional expression of SMCT1 in 5-FU-resistant colorectal cancer cells
inferred← citeshttps://doi.org/10.1007/s12307-018-0211-7openalex-snapshot
Exosomes: Definition, Role in Tumor Development and Clinical Implications
inferred← citeshttps://doi.org/10.1007/s12672-024-01003-2openalex-snapshot
circPDK1 competitively binds miR-4731-5p to mediate GIGYF1 expression and increase paclitaxel sensitivity in non-small cell lung cancer
inferred← citeshttps://doi.org/10.1007/s12672-024-01270-zopenalex-snapshot
MicroRNA-98 as a novel diagnostic marker and therapeutic target in cancer patients
inferred← citeshttps://doi.org/10.1007/s12672-025-02198-8openalex-snapshot
Advancements and limitations in traditional anti-cancer therapies: a comprehensive review of surgery, chemotherapy, radiation therapy, and hormonal therapy
inferred← citeshttps://doi.org/10.1007/s12672-026-04660-7openalex-snapshot
Integrative single-cell transcriptomic and multi-dimensional bioinformatic analysis reveals proliferation-associated gene expression signatures and cellular heterogeneity in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s13205-021-02971-wopenalex-snapshot
Research updates on the clinical implication of long noncoding RNA in digestive system cancers and chemoresistance
inferred← citeshttps://doi.org/10.1007/s43441-022-00375-3openalex-snapshot
Anti-lung Cancer Marine Compounds: A Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-817890-4.00007-xopenalex-snapshot
Adjunct therapeutic potential of phytochemicals against cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-819547-5.00022-5openalex-snapshot
Oxidative stress and cancer: Role of n-3 PUFAs
inferred← citeshttps://doi.org/10.1016/b978-0-12-819840-7.00008-xopenalex-snapshot
Novel agents to target treatment resistance in ovarian cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-820050-6.00024-2openalex-snapshot
The role of the free β-subunit of human chorionic gonadotropin in human malignancy
inferred← citeshttps://doi.org/10.1016/b978-0-12-824299-5.00007-1openalex-snapshot
Drug resistance in gynecologic cancers: Findings and underlying mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-323-85881-6.00002-6openalex-snapshot
Mechanisms of multidrug resistance in cancer
inferred← citeshttps://doi.org/10.1016/b978-0-323-91287-7.00006-5openalex-snapshot
Akt inhibitors in cancer therapy
inferred← citeshttps://doi.org/10.1016/b978-0-323-99988-5.00001-2openalex-snapshot
Targeting cancer-inducing inflammation: Current advancements and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-443-22354-9.00006-1openalex-snapshot
The role of nitric oxide in gemcitabine resistance of pancreatic cancer cells
inferred← citeshttps://doi.org/10.1016/b978-0-443-26635-5.00001-8openalex-snapshot
Natural compounds as potential cancer therapeutics: a focus on curcumin and resveratrol
inferred← citeshttps://doi.org/10.1016/b978-0-443-33206-7.00003-0openalex-snapshot
Microbiome-based strategies to overcome chemoresistance: Probiotics and prebiotics in cancer therapy
inferred← citeshttps://doi.org/10.1016/b978-0-443-33206-7.00004-2openalex-snapshot
Microbiome-based diagnostics and biomarkers: The search for mechanistic connections
inferred← citeshttps://doi.org/10.1016/b978-0-443-33343-9.00010-7openalex-snapshot
Nanotechnology for overcoming acquired drug resistance in GIT cancers
inferred← citeshttps://doi.org/10.1016/b978-0-443-41551-7.00020-5openalex-snapshot
Role of chemokines and chemokine receptors in cancer immunology
inferred← citeshttps://doi.org/10.1016/b978-0-443-45717-3.00001-5openalex-snapshot
Advanced drug delivery strategies: Nanoparticles, liposomes, dendrimers, and smart biomaterials
inferred← citeshttps://doi.org/10.1016/b978-0-443-45717-3.00003-9openalex-snapshot
CRISPR/Cas9 and gene editing approaches as a solution for chemoresistance
inferred← citeshttps://doi.org/10.1016/b978-0-443-45717-3.00011-8openalex-snapshot
Exosome and extracellular vesicle-based therapeutics to overcome cancer chemoresistance
inferred← citeshttps://doi.org/10.1016/b978-0-443-45717-3.00012-xopenalex-snapshot
Revolutionizing precision oncology: Combating chemoresistance with nanorobotics
inferred← citeshttps://doi.org/10.1016/b978-0-443-45717-3.00016-7openalex-snapshot
Impact of hypoxia, angiogenesis, and immunosuppression in chemoresistance
inferred← citeshttps://doi.org/10.1016/bs.acr.2022.12.001openalex-snapshot
Epigenetically programmed resistance to chemo- and immuno-therapies
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2022.05.011openalex-snapshot
Translation initiation and its relationship with metabolic mechanisms in cancer development, progression and chemoresistance
inferred← citeshttps://doi.org/10.1016/j.adcanc.2022.100050openalex-snapshot
Cellular landscaping of exosomal miRNAs in cancer metastasis: From chemoresistance to prognostic markers
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2018.03.001openalex-snapshot
Decrease in paracellular permeability and chemosensitivity to doxorubicin by claudin-1 in spheroid culture models of human lung adenocarcinoma A549 cells
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119252openalex-snapshot
Calcium/calmodulin-dependent protein kinase kinase 2 mediates pleiotropic effects of epidermal growth factor in cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.189015openalex-snapshot
Small-molecule inhibitors targeting FOXM1: Current challenges and future perspectives in cancer treatments
inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189261openalex-snapshot
Combating chemoresistance: Current approaches & nanocarrier mediated targeted delivery
inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189420openalex-snapshot
STIM1-mediated calcium signalling in cancer: Its relation to tumour aggressiveness and therapeutic horizons
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.11.181openalex-snapshot
ASPP2 enhances chemotherapeutic sensitivity through the down-regulation of XIAP expression in a p53 independent manner in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.116openalex-snapshot
Dysregulation of the miR-325–3p/DPAGT1 axis supports HBV-positive HCC chemoresistance
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.154512openalex-snapshot
Cancer stemness-modulating (CSM) proteins in pan-cancer chemoresistance: regulatory roles and mechanisms
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115741openalex-snapshot
Nucleoside-based anticancer drugs: Mechanism of action and drug resistance
inferred← citeshttps://doi.org/10.1016/j.bioadv.2023.213354openalex-snapshot
State-of-the-art: MXene structures in nano-oncology
inferred← citeshttps://doi.org/10.1016/j.biocel.2020.105874openalex-snapshot
Competing endogenous RNAs and cancer: How coding and non-coding molecules cross-talk can impinge on disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109105openalex-snapshot
Chalcones and their derivatives as inhibitors of key ABC transporters (ABCB1, ABCG2) to overcome tumor multidrug resistance
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.109961openalex-snapshot
Silence of FAM83H-AS1 promotes chemosensitivity of gastric cancer through Wnt/β-catenin signaling pathway
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110484openalex-snapshot
Marine compounds targeting the PI3K/Akt signaling pathway in cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110570openalex-snapshot
Competitive endogenous network of lncRNA, miRNA, and mRNA in the chemoresistance of gastrointestinal tract adenocarcinomas
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111285openalex-snapshot
5-Fluorouracil (5-FU) resistance and the new strategy to enhance the sensitivity against cancer: Implication of DNA repair inhibition
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114615openalex-snapshot
The potential application of encapsulated exosomes: A new approach to increase exosomes therapeutic efficacy
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115539openalex-snapshot
Clofazimine: A journey of a drug
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115973openalex-snapshot
Promising applications of nanotechnology in inhibiting chemo-resistance in solid tumors by targeting epithelial-mesenchymal transition (EMT)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127424openalex-snapshot
Mdm2 inhibitors as a platform for the design of P-glycoprotein inhibitors
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.01.025openalex-snapshot
Potential Hydrodynamic Cytoplasmic Transfer between Mammalian Cells: Cell-Projection Pumping
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.12.013openalex-snapshot
Docetaxel-mediated autophagy promotes chemoresistance in castration-resistant prostate cancer cells by inhibiting STAT3
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.03.044openalex-snapshot
Survivin-targeted drug screening platform identifies a matrine derivative WM-127 as a potential therapeutics against hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.canlet.2020.01.018openalex-snapshot
Rho GTPases: Promising candidates for overcoming chemotherapeutic resistance
inferred← citeshttps://doi.org/10.1016/j.canlet.2020.08.022openalex-snapshot
Therapy-induced chemoexosomes: Sinister small extracellular vesicles that support tumor survival and progression
inferred← citeshttps://doi.org/10.1016/j.canlet.2021.08.003openalex-snapshot
Dysfunctional activity of classical DNA end-joining renders acquired resistance to carboplatin in human ovarian cancer cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216328openalex-snapshot
Natural killer cell therapy targeting cancer stem cells: Old wine in a new bottle
inferred← citeshttps://doi.org/10.1016/j.canlet.2024.216856openalex-snapshot
Autophagy in cancer immunotherapy: Perspective on immune evasion and cell death interactions
inferred← citeshttps://doi.org/10.1016/j.cbi.2022.110056openalex-snapshot
A novel glycosylated indolocarbazole derivative LCS1269 effectively inhibits growth of human cancer cells in vitro and in vivo through driving of both apoptosis and senescence by inducing of DNA damage and modulating of AKT/mTOR/S6K and ERK pathways
inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110569openalex-snapshot
Piperine analog PGP-41 treatment overcomes paclitaxel resistance in NCI/ADR-RES ovarian cells by inhibition of MDR1
inferred← citeshttps://doi.org/10.1016/j.ceca.2022.102673openalex-snapshot
Calcium signaling: A therapeutic target to overcome resistance to therapies in cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2023.04.026openalex-snapshot
Systematic identification of anticancer drug targets reveals a nucleus-to-mitochondria ROS-sensing pathway
inferred← citeshttps://doi.org/10.1016/j.cellsig.2023.110881openalex-snapshot
miRNA/epithelial-mesenchymal axis (EMT) axis as a key player in cancer progression and metastasis: A focus on gastric and bladder cancers
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116774openalex-snapshot
Lactylation-stabilized NOL6 promotes colorectal cancer progression via STAMBP-mediated YY1 deubiquitination and c-Myc transcription upregulation
inferred← citeshttps://doi.org/10.1016/j.clinre.2022.101976openalex-snapshot
Curcumae longae Rhizoma (Jianghuang) extract reverses the 5-Fluoruracil resistance in colorectal cancer cells via TLR4/PI3K/Akt/mTOR pathway
inferred← citeshttps://doi.org/10.1016/j.crimmu.2023.100068openalex-snapshot
Role of chemotherapeutic drugs in immunomodulation of cancer
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2019.102818openalex-snapshot
Clinical significance of aberrant microRNAs expression in predicting disease relapse/refractoriness to treatment in diffuse large B-cell lymphoma: A meta-analysis
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2022.103799openalex-snapshot
Exosomics in oral cancer diagnosis, prognosis, and therapeutics – An emergent and imperative non-invasive natural nanoparticle-based approach
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2025.104908openalex-snapshot
Chemotherapy modulates PD-L1 expression and its combination with immune checkpoint blockade requires precision
inferred← citeshttps://doi.org/10.1016/j.ctarc.2022.100584openalex-snapshot
Evaluation of targeting autophagy for the treatment of malignant rhabdoid tumours
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2019.11.002openalex-snapshot
Senescence in polyploid giant cancer cells: A road that leads to chemoresistance
inferred← citeshttps://doi.org/10.1016/j.drudis.2019.06.010openalex-snapshot
Exosomal miRNA in chemoresistance, immune evasion, metastasis and progression of cancer
inferred← citeshttps://doi.org/10.1016/j.drudis.2021.03.017openalex-snapshot
Long noncoding RNAs have pivotal roles in chemoresistance of acute myeloid leukemia
inferred← citeshttps://doi.org/10.1016/j.drudis.2025.104339openalex-snapshot
Emerging role of deubiquitinases in modulating cancer chemoresistance
inferred← citeshttps://doi.org/10.1016/j.drup.2019.100645openalex-snapshot
The multi-factorial nature of clinical multidrug resistance in cancer
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112627openalex-snapshot
Anticancer property of ginsenoside Rh2 from ginseng
inferred← citeshttps://doi.org/10.1016/j.ejphar.2019.172705openalex-snapshot
Anti-tumor activity of neratinib, a pan-HER inhibitor, in gastric adenocarcinoma cells
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.172953openalex-snapshot
Evaluation of artesunate for the treatment of adult T-cell leukemia/lymphoma
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174373openalex-snapshot
The antipsychotic drug pimozide is effective against human T-cell leukemia virus type 1-infected T cells
inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.177210openalex-snapshot
NRF-mediated autophagy and UPR: Exploring new avenues to overcome cancer chemo-resistance
inferred← citeshttps://doi.org/10.1016/j.ejphar.2026.178923openalex-snapshot
Downregulation of claudin-2 expression and chemoresistance by saquinavir in human lung adenocarcinoma cells
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.123565openalex-snapshot
Endoplasmic reticulum stress responses and epigenetic alterations in arsenic carcinogenesis
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104173openalex-snapshot
Chemosensitizing activity of Cuban propolis and nemorosone in doxorubicin resistant human colon carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.humgen.2023.201151openalex-snapshot
Pan-cancer chemoresistance-associated genes, affected pathways and potential therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.07.253openalex-snapshot
Find new channel for overcoming chemoresistance in cancers: Role of stem cells-derived exosomal microRNAs
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.09.203openalex-snapshot
Non-coding RNAs targeting notch signaling pathway in cancer: From proliferation to cancer therapy resistance
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2025.125936openalex-snapshot
Innovations in cancer treatment: evaluating drug resistance with lab-on-a-chip technologies
inferred← citeshttps://doi.org/10.1016/j.ijpx.2022.100126openalex-snapshot
Nanoparticles design considerations to co-deliver nucleic acids and anti-cancer drugs for chemoresistance reversal
inferred← citeshttps://doi.org/10.1016/j.ijpx.2024.100276openalex-snapshot
M1 macrophage-membrane-cloaked paclitaxel/β-elemene nanoparticles targeting cervical cancer for enhanced therapy
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.106991openalex-snapshot
Curcumin may be a potential adjuvant treatment drug for colon cancer by targeting CD44
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114200openalex-snapshot
Dkk3 inhibits the aggressiveness and mitigates chemoresistance through low lipid droplet formation in gastric cancer: A biomarker and gene therapy target
inferred← citeshttps://doi.org/10.1016/j.jare.2025.10.067openalex-snapshot
Flavonoid-modulated JAK-STAT signaling mitigates malignant transformation and drug resistance in breast tumors: A clinically relevant 3PM-guided innovation
inferred← citeshttps://doi.org/10.1016/j.jbior.2018.09.007openalex-snapshot
Gle1 mediates stress granule-dependent survival during chemotoxic stress
inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.06.021openalex-snapshot
Metal-coordinated nanomedicine for combined tumor therapy by inducing paraptosis and apoptosis
inferred← citeshttps://doi.org/10.1016/j.jddst.2023.105326openalex-snapshot
Nanocarriers for delivering nucleic acids and chemotherapeutic agents as combinational approach: Challenges, clinical progress, and unmet needs
inferred← citeshttps://doi.org/10.1016/j.jddst.2024.105942openalex-snapshot
Innovative phytoceutical-based drug delivery in the management of pulmonary fibrosis: A roadmap towards inhaled therapeutics
inferred← citeshttps://doi.org/10.1016/j.jddst.2026.108220openalex-snapshot
Multifunctional Pluronic nanomedicine: Bridging the gap between chemoresistance and effective cancer therapy
inferred← citeshttps://doi.org/10.1016/j.jgeb.2025.100594openalex-snapshot
Expression and interaction of RNA binding protein HuR with multidrug transporters (P-GP, MRP1, and ABCG2) in chemoresistant breast and colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2018.02.002openalex-snapshot
Silica nanoparticles with Tb(III)-centered luminescence decorated by Ag0 as efficient cellular contrast agent with anticancer effect
inferred← citeshttps://doi.org/10.1016/j.leukres.2021.106523openalex-snapshot
Assessment of azithromycin as an anticancer agent for treatment of imatinib sensitive and resistant CML cells
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.116586openalex-snapshot
CRISPR/Cas9-mediated knockout of Lcn2 effectively enhanced CDDP-induced apoptosis and reduced cell migration capacity of PC3 cells
inferred← citeshttps://doi.org/10.1016/j.lfs.2019.116680openalex-snapshot
The impact of tumor and gut microbiotas on cancer therapy: Beneficial or detrimental?
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.117639openalex-snapshot
Thymoquinone synergizes with arsenic and interferon alpha to target human T-cell leukemia/lymphoma
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118362openalex-snapshot
The functional role of long non-coding RNAs and their underlying mechanisms in drug resistance of non-small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.118523openalex-snapshot
Paracrine HGF promotes EMT and mediates the effects of PSC on chemoresistance by activating c-Met/PI3K/Akt signaling in pancreatic cancer in vitro
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.120072openalex-snapshot
FOXM1 inhibitor, Siomycin A, synergizes and restores 5-FU cytotoxicity in human cholangiocarcinoma cell lines via targeting thymidylate synthase
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.121499openalex-snapshot
Emerging roles and mechanisms of semaphorins activity in cancer
inferred← citeshttps://doi.org/10.1016/j.mce.2020.111090openalex-snapshot
PCB153 reduces apoptosis in primary cultures of murine pituitary cells through the activation of NF-κB mediated by PI3K/Akt
inferred← citeshttps://doi.org/10.1016/j.mgene.2020.100699openalex-snapshot
HMG2D: A tool to identify miRNAs/drugs/genes associated with diseases like cancers
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131216openalex-snapshot
New 1,2,3-triazole linked flavonoid conjugates: Microwave-assisted synthesis, cytotoxic activity and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.mtbio.2025.102240openalex-snapshot
Cancer-metastasis-on-a-chip reveals efficacy of bevacizumab and siRNA in overcoming carboplatin resistance in SKOV3 ovarian cancer within a fibrotic metastatic microenvironment
inferred← citeshttps://doi.org/10.1016/j.ncrna.2024.05.001openalex-snapshot
Exploring the impact of circRNAs on cancer glycolysis: Insights into tumor progression and therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.neo.2019.09.002openalex-snapshot
APC loss affects DNA damage repair causing doxorubicin resistance in breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.neo.2023.100903openalex-snapshot
Mitochondrial rewiring drives metabolic adaptation to NAD(H) shortage in triple negative breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.neo.2025.101254openalex-snapshot
Dynasore as a dual modulator of lipid rafts and cell death in pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.nexres.2025.100403openalex-snapshot
Natural products-based cancer vaccination strategy
inferred← citeshttps://doi.org/10.1016/j.nexres.2025.100508openalex-snapshot
CircRNA-miRNA-mRNA interactome analysis to explore potential pathogenesis of ovarian cancer
inferred← citeshttps://doi.org/10.1016/j.omto.2019.04.005openalex-snapshot
Restoring E-cadherin Expression by Natural Compounds for Anticancer Therapies in Genital and Urinary Cancers
inferred← citeshttps://doi.org/10.1016/j.oraloncology.2019.04.019openalex-snapshot
Prognostic significance of CD68+ and CD163+ tumor associated macrophages in head and neck squamous cell carcinoma: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2019.107447openalex-snapshot
5-fluorouracil and other fluoropyrimidines in colorectal cancer: Past, present and future
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2020.107717openalex-snapshot
A decade of cell death studies: Breathing new life into necroptosis
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2022.108300openalex-snapshot
Nucleoside transporters and immunosuppressive adenosine signaling in the tumor microenvironment: Potential therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105387openalex-snapshot
Baicalin mediated regulation of key signaling pathways in cancer
inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106441openalex-snapshot
Nucleic acid therapy in pediatric cancer
inferred← citeshttps://doi.org/10.1016/j.prp.2023.154702openalex-snapshot
The impact of microRNAs on the resistance of breast cancer subtypes to chemotherapy
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155190openalex-snapshot
Deciphering the oncogenic landscape: Unveiling the molecular machinery and clinical significance of LncRNA TMPO-AS1 in human cancers
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155457openalex-snapshot
The function and mechanism of circRNAs in 5-fluorouracil resistance in tumors: Biological mechanisms and future potential
inferred← citeshttps://doi.org/10.1016/j.prp.2025.156347openalex-snapshot
Unveiling the role of PGCCs in tumor recurrence and therapeutic resistance: Hidden architects of cancer’s comeback
inferred← citeshttps://doi.org/10.1016/j.radonc.2021.03.012openalex-snapshot
Deciphering the epigenetic network in cancer radioresistance
inferred← citeshttps://doi.org/10.1016/j.redox.2021.102194openalex-snapshot
Redox regulation of DUBs and its therapeutic implications in cancer
inferred← citeshttps://doi.org/10.1016/j.rmed.2021.106535openalex-snapshot
Exploration of potential risk factors for COVID-19 severity in patients participating in oncology clinical trials
inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.09.004openalex-snapshot
Emerging roles of ECM remodeling processes in cancer
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