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Hypoxia induces the breast cancer stem cell phenotype by HIF-dependent and ALKBH5-mediated m 6 A-demethylation of NANOG mRNA

https://doi.org/10.1073/pnas.1602883113
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2 of the 48 references listed on this page are in the Retraction Watch database as retracted (export 2026-10-21): 10.1038/onc.2011.365 (notice 2023-05-23), 10.1073/pnas.1421438111 (notice 2022-09-02).

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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.28690openalex-snapshot
Emerging role of nanog in tumorigenesis and cancer stem cells
inferredcites →https://doi.org/10.1007/s12282-012-0357-yopenalex-snapshot
Prognostic significance of NANOG and KLF4 for breast cancer
inferredcites →https://doi.org/10.1016/j.bbamcr.2015.05.036openalex-snapshot
The hypoxic tumor microenvironment: A driving force for breast cancer progression
inferredcites →https://doi.org/10.1016/j.ccr.2006.10.008openalex-snapshot
A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes
inferredcites →https://doi.org/10.1016/j.cell.2005.08.020openalex-snapshot
Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells
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.2012.01.021openalex-snapshot
Hypoxia-Inducible Factors in Physiology and Medicine
inferredcites →https://doi.org/10.1016/j.cell.2014.08.005openalex-snapshot
Emerging Roles of RNA Modification: m6A and U-Tail
inferredcites →https://doi.org/10.1016/j.celrep.2014.04.040openalex-snapshot
TET1-Mediated Hydroxymethylation Facilitates Hypoxic Gene Induction in Neuroblastoma
inferredcites →https://doi.org/10.1016/j.molcel.2012.10.015openalex-snapshot
ALKBH5 Is a Mammalian RNA Demethylase that Impacts RNA Metabolism and Mouse Fertility
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.2014.02.002openalex-snapshot
Metastatic Stem Cells: Sources, Niches, and Vital Pathways
inferredcites →https://doi.org/10.1016/j.stem.2014.09.019openalex-snapshot
m6A RNA Modification Controls Cell Fate Transition in Mammalian Embryonic Stem Cells
inferredcites →https://doi.org/10.1038/nature11112openalex-snapshot
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
inferredcites →https://doi.org/10.1038/nature12730openalex-snapshot
N6-methyladenosine-dependent regulation of messenger RNA stability
inferredcites →https://doi.org/10.1038/nature14281openalex-snapshot
N6-methyladenosine marks primary microRNAs for processing
inferredcites →https://doi.org/10.1038/ng.127openalex-snapshot
An embryonic stem cell–like gene expression signature in poorly differentiated aggressive human tumors
inferredcites →https://doi.org/10.1038/nprot.2012.148openalex-snapshot
Transcriptome-wide mapping of N6-methyladenosine by m6A-seq based on immunocapturing and massively parallel sequencing
inferredcites →https://doi.org/10.1038/nrg3724openalex-snapshot
Gene expression regulation mediated through reversible m6A RNA methylation
inferredcites →https://doi.org/10.1038/nrm3785openalex-snapshot
The dynamic epitranscriptome: N6-methyladenosine and gene expression control
inferredcites →https://doi.org/10.1038/onc.2010.591openalex-snapshot
Kruppel-like factor 4 (KLF4) is required for maintenance of breast cancer stem cells and for cell migration and invasion
inferredcites →https://doi.org/10.1038/onc.2011.338openalex-snapshot
Sox2 expression in breast tumours and activation in breast cancer stem cells
inferredcites →https://doi.org/10.1038/onc.2011.365openalex-snapshot
RETRACTED ARTICLE: HIF-1-dependent expression of angiopoietin-like 4 and L1CAM mediates vascular metastasis of hypoxic breast cancer cells to the lungs
inferredcites →https://doi.org/10.1042/bj20081238openalex-snapshot
Regulation of Jumonji-domain-containing histone demethylases by hypoxia-inducible factor (HIF)-1α
inferredcites →https://doi.org/10.1073/pnas.0530291100openalex-snapshot
Prospective identification of tumorigenic breast cancer cells
inferredcites →https://doi.org/10.1073/pnas.1018866109openalex-snapshot
Antiangiogenic agents increase breast cancer stem cells via the generation of tumor hypoxia
inferredcites →https://doi.org/10.1073/pnas.1217394109openalex-snapshot
Histone demethylase JMJD2C is a coactivator for hypoxia-inducible factor 1 that is required for breast cancer progression
inferredcites →https://doi.org/10.1073/pnas.1421438111openalex-snapshot
RETRACTED: Hypoxia-inducible factors are required for chemotherapy resistance of breast cancer stem cells
inferredcites →https://doi.org/10.1073/pnas.1513433112openalex-snapshot
Chemotherapy triggers HIF-1–dependent glutathione synthesis and copper chelation that induces the breast cancer stem cell phenotype
inferredcites →https://doi.org/10.1073/pnas.1520032112openalex-snapshot
HIF-1 regulates CD47 expression in breast cancer cells to promote evasion of phagocytosis and maintenance of cancer stem cells
inferredcites →https://doi.org/10.1089/ars.2007.1628openalex-snapshot
Detection and Characterization of Tumor Hypoxia Using pO 2 Histography
inferredcites →https://doi.org/10.1101/gad.1061803openalex-snapshot
In vitro propagation and transcriptional profiling of human mammary stem/progenitor cells
inferredcites →https://doi.org/10.1126/science.1261417openalex-snapshot
m 6 A mRNA methylation facilitates resolution of naïve pluripotency toward differentiation
inferredcites →https://doi.org/10.1126/scisignal.2002072openalex-snapshot
HIF-1α Mediates Tumor Hypoxia to Confer a Perpetual Mesenchymal Phenotype for Malignant ProgressionA presentation from the Keystone Symposium on Epithelial Plasticity and Epithelial-to-Mesenchymal Transition, Vancouver, British Columbia, Canada, 21 to 26 January 2011.
inferredcites →https://doi.org/10.1158/0008-5472.can-07-6642openalex-snapshot
Octamer 4 Small Interfering RNA Results in Cancer Stem Cell–Like Cell Apoptosis
inferredcites →https://doi.org/10.1158/0008-5472.can-08-2741openalex-snapshot
Breast Cancer Cell Lines Contain Functional Cancer Stem Cells with Metastatic Capacity and a Distinct Molecular Signature
inferredcites →https://doi.org/10.1158/0008-5472.can-10-3320openalex-snapshot
HIF Induces Human Embryonic Stem Cell Markers in Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-13-0523openalex-snapshot
Breast Tumor Kinase (Brk/PTK6) Is a Mediator of Hypoxia-Associated Breast Cancer Progression
inferredcites →https://doi.org/10.1158/0008-5472.can-14-3208openalex-snapshot
Hypoxia Drives Breast Tumor Malignancy through a TET–TNFα–p38–MAPK Signaling Axis
inferredcites →https://doi.org/10.1158/1055-9965.epi-15-0535openalex-snapshot
International Variation in Female Breast Cancer Incidence and Mortality Rates
inferredcites →https://doi.org/10.1158/1538-7445.am2011-4640openalex-snapshot
Abstract 4640: Quantification of gamma-H2AX expression in whole blood culture as a risk predictor for renal cell carcinoma
inferredcites →https://doi.org/10.1186/bcr3087openalex-snapshot
Hypoxia-inducible factor 1α promotes primary tumor growth and tumor-initiating cell activity in breast cancer
inferredcites →https://doi.org/10.1371/journal.pone.0016210openalex-snapshot
Human AlkB Homologue 5 Is a Nuclear 2-Oxoglutarate Dependent Oxygenase and a Direct Target of Hypoxia-Inducible Factor 1α (HIF-1α)
inferredcites →https://doi.org/10.1530/rep-09-0300openalex-snapshot
Hypoxia inducible factors regulate pluripotency and proliferation in human embryonic stem cells cultured at reduced oxygen tensions
inferredcites →https://doi.org/10.1634/theoncologist.10-90003-20openalex-snapshot
Extending Survival with Chemotherapy in Metastatic Breast Cancer
inferredcites →https://doi.org/10.18632/oncotarget.2997openalex-snapshot
Hypoxia-inducible factor 1 mediates TAZ expression and nuclear localization to induce the breast cancer stem cell phenotype
inferredcites →https://doi.org/10.18632/oncotarget.5564openalex-snapshot
Distinct breast cancer stem/progenitor cell populations require either HIF1α or loss of PHD3 to expand under hypoxic conditions
inferredcites →https://doi.org/10.3322/caac.20134openalex-snapshot
Breast cancer statistics, 2011

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3745154openalex-extracted
inferred← citeshttps://doi.org/10.2139/ssrn.3858812openalex-extracted
inferred← citeshttps://doi.org/10.2139/ssrn.3864033openalex-extracted
GDF11 Mitigates Diabetic Cardiomyopathy Injury Via Regulation of the ALKBH5-FOXO3-CDR1as/Hippo Pathway
inferred← citeshttps://doi.org/10.2139/ssrn.3904910openalex-extracted
A Prognostic Model of M6a-Related Lipid Metabolism-Associated Genes in Pancreatic Adenocarcinoma
inferred← citeshttps://doi.org/10.2139/ssrn.4057520openalex-extracted
ALKBH5 Contributes to the Malignant Progression of Gastric Cancer by Resisting Cisplatin-Induced Oxidative Stress Through CHAC1
inferred← citeshttps://doi.org/10.1002/1873-3468.13092openalex-snapshot
FTO , m6Am, and the hypothesis of reversible epitranscriptomic mRNA modifications
inferred← citeshttps://doi.org/10.1002/1873-3468.14145openalex-snapshot
The RNA demethylase ALKBH5 promotes osteoblast differentiation by modulating Runx2 mRNA stability
inferred← citeshttps://doi.org/10.1002/1878-0261.12488openalex-snapshot
Targeting AMP ‐activated kinase impacts hepatocellular cancer stem cells induced by long‐term treatment with sorafenib
inferred← citeshttps://doi.org/10.1002/1878-0261.12593openalex-snapshot
Loss of RDM1 enhances hepatocellular carcinoma progression via p53 and Ras/Raf/ERK pathways
inferred← citeshttps://doi.org/10.1002/1878-0261.13326openalex-snapshot
RNA m 6 A methylation in cancer
inferred← citeshttps://doi.org/10.1002/1878-0261.70321openalex-snapshot
Unraveling the epigenetic code in cancer cell–tumor microenvironment crosstalk
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.202202609openalex-snapshot
3D Biomimetic Models to Reconstitute Tumor Microenvironment In Vitro: Spheroids, Organoids, and Tumor‐on‐a‐Chip
inferred← citeshttps://doi.org/10.1002/advs.202307639openalex-snapshot
HnRNPA2B1 ISGylation Regulates m6A‐Tagged mRNA Selective Export via ALYREF/NXF1 Complex to Foster Breast Cancer Development
inferred← citeshttps://doi.org/10.1002/advs.202508376openalex-snapshot
Tendon Organoids Enable Functional Tendon Rejuvenation Through ALKBH5‐Dependent RNA Demethylation
inferred← citeshttps://doi.org/10.1002/ame2.12208openalex-snapshot
Circular RNAs in pulmonary hypertension: Emerging biological concepts and potential mechanism
inferred← citeshttps://doi.org/10.1002/bies.201700093openalex-snapshot
mRNA Traffic Control Reviewed: N6‐Methyladenosine (m6A) Takes the Driver's Seat
inferred← citeshttps://doi.org/10.1002/cac2.12161openalex-snapshot
N 6 ‐methyladenosine Steers RNA Metabolism and Regulation in Cancer
inferred← citeshttps://doi.org/10.1002/cai2.103openalex-snapshot
ALKBH5 gene polymorphisms and risk of neuroblastoma in Chinese children from Jiangsu Province
inferred← citeshttps://doi.org/10.1002/cam4.2360openalex-snapshot
Reduced m6A modification predicts malignant phenotypes and augmented Wnt/PI3K‐Akt signaling in gastric cancer
inferred← citeshttps://doi.org/10.1002/cbin.11773openalex-snapshot
Emerging role of m6A modification in cardiovascular diseases
inferred← citeshttps://doi.org/10.1002/ctm2.1198openalex-snapshot
ALKBH5‐mediated m 6 A demethylation of TIRAP mRNA promotes radiation‐induced liver fibrosis and decreases radiosensitivity of hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/ctm2.1279openalex-snapshot
RNA demethylase ALKBH5 promotes colorectal cancer progression by posttranscriptional activation of RAB5A in an m6A‐YTHDF2‐dependent manner
inferred← citeshttps://doi.org/10.1002/ctm2.1564openalex-snapshot
The involvement of RNA N6‐methyladenosine and histone methylation modification in decidualization and endometriosis‐associated infertility
inferred← citeshttps://doi.org/10.1002/ctm2.1777openalex-snapshot
LncRNA CARMN m6A demethylation by ALKBH5 inhibits mutant p53‐driven tumour progression through miR‐5683/FGF2
inferred← citeshttps://doi.org/10.1002/ctm2.352openalex-snapshot
AMD1 upregulates hepatocellular carcinoma cells stemness by FTO mediated mRNA demethylation
inferred← citeshttps://doi.org/10.1002/ctm2.525openalex-snapshot
RNA N6‐methyladenosine modification in the lethal teamwork of cancer stem cells and the tumor immune microenvironment: Current landscape and therapeutic potential
inferred← citeshttps://doi.org/10.1002/ctm2.70458openalex-snapshot
Persistent lineage plasticity driving lung cancer development and progression
inferred← citeshttps://doi.org/10.1002/ctm2.765openalex-snapshot
m6A hypomethylation of DNMT3B regulated by ALKBH5 promotes intervertebral disc degeneration via E4F1 deficiency
inferred← citeshttps://doi.org/10.1002/ctm2.906openalex-snapshot
ZNF677 suppresses renal cell carcinoma progression through N6‐methyladenosine and transcriptional repression of CDKN3
inferred← citeshttps://doi.org/10.1002/ctm2.940openalex-snapshot
N6‐methyladenosine demethylase ALKBH5 suppresses colorectal cancer progression potentially by decreasing PHF20 mRNA methylation
inferred← citeshttps://doi.org/10.1002/hep.28885openalex-snapshot
METTL14 suppresses the metastatic potential of hepatocellular carcinoma by modulating N 6‐methyladenosine‐dependent primary MicroRNA processing
inferred← citeshttps://doi.org/10.1002/hep.29683openalex-snapshot
RNA N6‐methyladenosine methyltransferase‐like 3 promotes liver cancer progression through YTHDF2‐dependent posttranscriptional silencing of SOCS2
inferred← citeshttps://doi.org/10.1002/hep.31222openalex-snapshot
SIRT1 Regulates N6‐Methyladenosine RNA Modification in Hepatocarcinogenesis by Inducing RANBP2‐Dependent FTO SUMOylation
inferred← citeshttps://doi.org/10.1002/hep.31846openalex-snapshot
Loss‐of‐Function Genetic Screening Identifies Aldolase A as an Essential Driver for Liver Cancer Cell Growth Under Hypoxia
inferred← citeshttps://doi.org/10.1002/ibra.70000openalex-snapshot
Epigenetic regulation in cognitive impairment: Focus on N6‐methyladenosine modification and its potential role in perioperative neurocognitive disorders
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.2276openalex-snapshot
Human and Arabidopsis alpha‐ketoglutarate‐dependent dioxygenase homolog proteins—New players in important regulatory processes
inferred← citeshttps://doi.org/10.1002/jcla.23251openalex-snapshot
ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five‐center case‐control study
inferred← citeshttps://doi.org/10.1002/jcla.23655openalex-snapshot
The m6A methyltransferase METTL14 inhibits the proliferation, migration, and invasion of gastric cancer by regulating the PI3K/AKT/mTOR signaling pathway
inferred← citeshttps://doi.org/10.1002/jcla.23779openalex-snapshot
A ten N6‐methyladenosine‐related long non‐coding RNAs signature predicts prognosis of triple‐negative breast cancer
inferred← citeshttps://doi.org/10.1002/jcla.24118openalex-snapshot
Expression and prognostic significance of m6A‐related genes in TP53‐mutant non‐small‐cell lung cancer
inferred← citeshttps://doi.org/10.1002/jcla.24514openalex-snapshot
RNA demethylase ALKBH5 regulates hypopharyngeal squamous cell carcinoma ferroptosis by posttranscriptionally activating NFE2L2 / NRF2 in an m6A‐IGF2BP2 ‐dependent manner
inferred← citeshttps://doi.org/10.1002/jcp.28014openalex-snapshot
A dynamic reversible RNA N6‐methyladenosine modification: current status and perspectives
inferred← citeshttps://doi.org/10.1002/jcp.29531openalex-snapshot
Contributions and prognostic values of m6A RNA methylation regulators in non‐small‐cell lung cancer
inferred← citeshttps://doi.org/10.1002/jcp.29608openalex-snapshot
RNA m6A methylation regulates uveal melanoma cell proliferation, migration, and invasion by targeting c‐Met
inferred← citeshttps://doi.org/10.1002/jcp.29645openalex-snapshot
KIAA1429 regulates cell proliferation by targeting c‐Jun messenger RNA directly in gastric cancer
inferred← citeshttps://doi.org/10.1002/jcp.30136openalex-snapshot
The momentous role of N6‐methyladenosine in lung cancer
inferred← citeshttps://doi.org/10.1002/jcsm.12929openalex-snapshot
m 6 A demethylase ALKBH5 drives denervation‐induced muscle atrophy by targeting HDAC4 to activate FoxO3 signalling
inferred← citeshttps://doi.org/10.1002/mc.22782openalex-snapshot
FTO regulates the chemo‐radiotherapy resistance of cervical squamous cell carcinoma (CSCC) by targeting β‐catenin through mRNA demethylation
inferred← citeshttps://doi.org/10.1002/mc.23330openalex-snapshot
ALKBH5‐mediated m6A‐demethylation of USP1 regulated T‐cell acute lymphoblastic leukemia cell glucocorticoid resistance by Aurora B
inferred← citeshttps://doi.org/10.1002/mco2.427openalex-snapshot
Oncofetal reprogramming in tumor development and progression: novel insights into cancer therapy
inferred← citeshttps://doi.org/10.1002/mco2.640openalex-snapshot
Liquid–liquid phase separation in diseases
inferred← citeshttps://doi.org/10.1002/mco2.70108openalex-snapshot
TDP‐43/ALKBH5‐mediated m6A modification of CDC25A mRNA promotes glioblastoma growth by facilitating G1/S cell cycle transition
inferred← citeshttps://doi.org/10.1002/mco2.70341openalex-snapshot
RNA Modifications in Health and Disease
inferred← citeshttps://doi.org/10.1002/mco2.70816openalex-snapshot
RNA Modifications in Tumor Microenvironment: A New Dimension for Cancer Treatment
inferred← citeshttps://doi.org/10.1002/mog2.70000openalex-snapshot
Epigenetic remodeling under oxidative stress: Mechanisms driving tumor metastasis
inferred← citeshttps://doi.org/10.1002/pld3.508openalex-snapshot
N6‐methyladenosine modification changes during the recovery processes for Paulownia witches' broom disease under the methyl methanesulfonate treatment
inferred← citeshttps://doi.org/10.1002/pmic.202200208openalex-snapshot
Exploring the role of m6A modification in cancer
inferred← citeshttps://doi.org/10.1002/prm2.12093openalex-snapshot
ALKBH5 involves in osteosarcoma tumor progression by mediating Notch signaling
inferred← citeshttps://doi.org/10.1002/rmv.1983openalex-snapshot
RNA epitranscriptomics: Regulation of infection of RNA and DNA viruses by N 6 ‐methyladenosine (m 6 A)
inferred← citeshttps://doi.org/10.1002/smll.202005086openalex-snapshot
Regulating Tumor N6‐Methyladenosine Methylation Landscape using Hypoxia‐Modulating OsSx Nanoparticles
inferred← citeshttps://doi.org/10.1002/stem.2621openalex-snapshot
Hypoxia-Mediated Epigenetic Regulation of Stemness in Brain Tumor Cells
inferred← citeshttps://doi.org/10.1002/tox.23454openalex-snapshot
Inhibition of ALKBH5 ‐mediated m 6 A modification of PPARG mRNA alleviates H/R‐induced oxidative stress and apoptosis in placenta trophoblast
inferred← citeshttps://doi.org/10.1002/tox.24114openalex-snapshot
Identification of a novel signature based on M6a modification regulators related LncRNA for stratification of the prognosis of prostate cancer
inferred← citeshttps://doi.org/10.1002/tox.24139openalex-snapshot
N6‐Methyladenosine reader HNRNPC ‐mediated downregulation of circITCH prevents miR ‐224‐3p sequestering and contributes to tumorigenesis in nasopharyngeal carcinoma
inferred← citeshttps://doi.org/10.1002/wrna.1507openalex-snapshot
Dynamic and reversible RNA N6‐methyladenosine methylation
inferred← citeshttps://doi.org/10.1002/wrna.1586openalex-snapshot
A molecular‐level perspective on the frequency, distribution, and consequences of messenger RNA modifications
inferred← citeshttps://doi.org/10.1002/wrna.1691openalex-snapshot
RNA nucleotide methylation: 2021 update
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Molecular regulation of hypoxia through the lenses of noncoding RNAs and epitranscriptome
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RNA epigenetic modifications in ovarian cancer: The changes, chances, and challenges
inferred← citeshttps://doi.org/10.1002/wrna.1829openalex-snapshot
RNA m6A modifications regulate crosstalk between tumor metabolism and immunity
inferred← citeshttps://doi.org/10.1007/5584_2024_820openalex-snapshot
Influence of RNA Methylation on Cancerous Cells: A Prospective Approach for Alteration of In Vivo Cellular Composition
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In Vitro Assays of Breast Cancer Stem Cells
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Hypoxia-Induced Phenotypes that Mediate Tumor Heterogeneity
inferred← citeshttps://doi.org/10.1007/978-3-030-17086-8_2openalex-snapshot
Chemical Modifications and Their Role in Long Non-coding RNAs
inferred← citeshttps://doi.org/10.1007/978-3-030-71612-7_13openalex-snapshot
RNA m6A Modification: The Mediator Between Cellular Stresses and Biological Effects
inferred← citeshttps://doi.org/10.1007/978-3-030-71612-7_4openalex-snapshot
Epitranscriptomics and Diseases
inferred← citeshttps://doi.org/10.1007/978-3-031-07634-3_11openalex-snapshot
Epigenetic Regulation During Hypoxia and Its Implications in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-031-07634-3_17openalex-snapshot
Modulation of DNA/RNA Methylation by Small-Molecule Modulators and Their Implications in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-031-45654-1_2openalex-snapshot
RNA Modifications in Cancer Stem Cell Biology
inferred← citeshttps://doi.org/10.1007/978-3-031-45654-1_3openalex-snapshot
Recent Advances of RNA m6A Modifications in Cancer Immunoediting and Immunotherapy
inferred← citeshttps://doi.org/10.1007/978-3-031-74842-4_10openalex-snapshot
Understanding the Role of Cancer Stem Cells in Brain Tumor Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-032-12166-0_11openalex-snapshot
Influence of RNA Modifications on Cancer Metabolism: Interplay with Hypoxia and Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/978-3-662-65902-1_15openalex-snapshot
Recent Development of Computational Methods in the Field of Epitranscriptomics
inferred← citeshttps://doi.org/10.1007/978-981-10-8684-7_7openalex-snapshot
Dysregulated Epigenetic Modifications in the Pathogenesis of NAFLD-HCC
inferred← citeshttps://doi.org/10.1007/978-981-99-1183-7_17openalex-snapshot
Cancer Stem Cells (CSCs) in Tumor Ecosystem
inferred← citeshttps://doi.org/10.1007/s00018-016-2334-7openalex-snapshot
Breast cancer stem cell: the roles and therapeutic implications
inferred← citeshttps://doi.org/10.1007/s00018-020-03581-0openalex-snapshot
Metabolic crosstalk in the tumor microenvironment regulates antitumor immunosuppression and immunotherapy resisitance
inferred← citeshttps://doi.org/10.1007/s00018-020-03594-9openalex-snapshot
Multi-substrate selectivity based on key loops and non-homologous domains: new insight into ALKBH family
inferred← citeshttps://doi.org/10.1007/s00018-023-04799-4openalex-snapshot
Overexpression of VIRMA confers vulnerability to breast cancers via the m6A-dependent regulation of unfolded protein response
inferred← citeshttps://doi.org/10.1007/s00277-023-05302-6openalex-snapshot
N6-methyladenosine RNA modifications: a potential therapeutic target for AML
inferred← citeshttps://doi.org/10.1007/s00432-022-04158-zopenalex-snapshot
RNA N6-methyladenosine modification in regulating cancer stem cells and tumor immune microenvironment and its implication for cancer therapy
inferred← citeshttps://doi.org/10.1007/s00432-022-04345-yopenalex-snapshot
Prognostic value of comprehensive typing based on m6A and gene cluster in TNBC
inferred← citeshttps://doi.org/10.1007/s00432-023-05309-6openalex-snapshot
The ALKBH5/SOX4 axis promotes liver cancer stem cell properties via activating the SHH signaling pathway
inferred← citeshttps://doi.org/10.1007/s00432-024-05785-4openalex-snapshot
The emerging role and mechanism of HMGA2 in breast cancer
inferred← citeshttps://doi.org/10.1007/s00432-026-06525-6openalex-snapshot
The relevance of m6A RNA modifications in cancer stem cells
inferred← citeshttps://doi.org/10.1007/s10142-026-02016-6openalex-snapshot
RNA modifications as determinants of cancer cell death: from epitranscriptomic mechanisms to therapeutic targeting
inferred← citeshttps://doi.org/10.1007/s10238-023-01026-zopenalex-snapshot
Predictive significance of HIF-1α, Snail, and PD-L1 expression in breast cancer
inferred← citeshttps://doi.org/10.1007/s10238-025-01872-zopenalex-snapshot
FTO promotes the progression of triple-negative breast cancer by regulating the m6A methylation of NFKBIE
inferred← citeshttps://doi.org/10.1007/s10495-020-01591-8openalex-snapshot
DDX3 modulates cisplatin resistance in OSCC through ALKBH5-mediated m6A-demethylation of FOXM1 and NANOG
inferred← citeshttps://doi.org/10.1007/s10495-025-02102-3openalex-snapshot
Targeting cell signaling pathway ALKBH5/Beclin1/ULK1 in lung cancer by 5-flurouracil- loaded P (AAm/SA) nanogel in rats
inferred← citeshttps://doi.org/10.1007/s10555-020-09884-9openalex-snapshot
RNA-biology ruling cancer progression? Focus on 3′UTRs and splicing
inferred← citeshttps://doi.org/10.1007/s10555-023-10120-3openalex-snapshot
Cancer metastasis under the magnifying glass of epigenetics and epitranscriptomics
inferred← citeshttps://doi.org/10.1007/s10555-024-10177-8openalex-snapshot
Deciphering cellular and molecular mechanism of MUC13 mucin involved in cancer cell plasticity and drug resistance
inferred← citeshttps://doi.org/10.1007/s10557-020-07019-4openalex-snapshot
Epigenetic Regulation of Endothelial Cell Function by Nucleic Acid Methylation in Cardiac Homeostasis and Disease
inferred← citeshttps://doi.org/10.1007/s10565-021-09627-8openalex-snapshot
RNA methylation in mammalian development and cancer
inferred← citeshttps://doi.org/10.1007/s10565-026-10141-yopenalex-snapshot
RNA m6A modification is a driver and therapeutic target in gastric cancer
inferred← citeshttps://doi.org/10.1007/s10585-018-9930-xopenalex-snapshot
The role of hypoxic signalling in metastasis: towards translating knowledge of basic biology into novel anti-tumour strategies
inferred← citeshttps://doi.org/10.1007/s10620-018-5452-2openalex-snapshot
Expression of Demethylase Genes, FTO and ALKBH1, Is Associated with Prognosis of Gastric Cancer
inferred← citeshttps://doi.org/10.1007/s10735-026-10825-zopenalex-snapshot
Icariin suppresses glycolysis in prostate cancer by upregulating ALKBH5 to mediate EARS2 m6A demethylation
inferred← citeshttps://doi.org/10.1007/s10863-025-10054-1openalex-snapshot
METTL3 mediates CPB1 expression by regulating transcription factor BACH2 to promote apoptosis and oxidative stress of lens epithelial cells
inferred← citeshttps://doi.org/10.1007/s10911-019-09435-1openalex-snapshot
The Milk Protein Alpha-Casein Suppresses Triple Negative Breast Cancer Stem Cell Activity Via STAT and HIF-1alpha Signalling Pathways in Breast Cancer Cells and Fibroblasts
inferred← citeshttps://doi.org/10.1007/s11010-022-04408-1openalex-snapshot
NAD+ centric mechanisms and molecular determinants of skeletal muscle disease and aging
inferred← citeshttps://doi.org/10.1007/s11033-018-4471-6openalex-snapshot
Functions of RNA N6-methyladenosine modification in cancer progression
inferred← citeshttps://doi.org/10.1007/s11033-019-04655-4openalex-snapshot
Functions of RNA N6-methyladenosine modification in cancer progression
inferred← citeshttps://doi.org/10.1007/s11033-022-07126-5openalex-snapshot
Advances in the functional roles of N6-methyladenosine modification in cancer progression: mechanisms and clinical implications
inferred← citeshttps://doi.org/10.1007/s11033-022-07802-6openalex-snapshot
Acute vs. chronic vs. intermittent hypoxia in breast Cancer: a review on its application in in vitro research
inferred← citeshttps://doi.org/10.1007/s11033-024-10138-yopenalex-snapshot
RNA methylation and breast cancer: insights into m6A, m7G and m5C
inferred← citeshttps://doi.org/10.1007/s11033-025-10419-0openalex-snapshot
Modifications of RNA in cancer: a comprehensive review
inferred← citeshttps://doi.org/10.1007/s11033-026-12620-1openalex-snapshot
Postoperative wound microenvironment regulates breast cancer stem cell fate and clinical implications
inferred← citeshttps://doi.org/10.1007/s11064-021-03408-9openalex-snapshot
ALKBH5 Promotes the Proliferation of Glioma Cells via Enhancing the mRNA Stability of G6PD
inferred← citeshttps://doi.org/10.1007/s11306-020-1635-xopenalex-snapshot
Extracellular volatilomic alterations induced by hypoxia in breast cancer cells
inferred← citeshttps://doi.org/10.1007/s11426-017-9186-yopenalex-snapshot
Modificaomics: deciphering the functions of biomolecule modifications
inferred← citeshttps://doi.org/10.1007/s11427-019-9826-7openalex-snapshot
TNF-α suppresses sweat gland differentiation of MSCs by reducing FTO-mediated m6A-demethylation of Nanog mRNA
inferred← citeshttps://doi.org/10.1007/s11684-023-1028-4openalex-snapshot
Arginine methylation of ALKBH5 by PRMT6 promotes breast tumorigenesis via LDHA-mediated glycolysis
inferred← citeshttps://doi.org/10.1007/s11684-024-1107-1openalex-snapshot
Canonical and noncanonical NOTCH signaling in the nongenetic resistance of cancer: distinct and concerted control
inferred← citeshttps://doi.org/10.1007/s12032-019-1260-6openalex-snapshot
Importance of m N6-methyladenosine (m6A) RNA modification in cancer
inferred← citeshttps://doi.org/10.1007/s12032-024-02347-zopenalex-snapshot
Recent developments in targeting breast cancer stem cells (BCSCs): a descriptive review of therapeutic strategies and emerging therapies
inferred← citeshttps://doi.org/10.1007/s12033-020-00269-5openalex-snapshot
m6A RNA Methylation: Ramifications for Gene Expression and Human Health
inferred← citeshttps://doi.org/10.1007/s12035-018-1138-1openalex-snapshot
m6A RNA Methylation Controls Neural Development and Is Involved in Human Diseases
inferred← citeshttps://doi.org/10.1007/s12035-024-04316-zopenalex-snapshot
Role of Non-coding RNAs in the Response of Glioblastoma to Temozolomide
inferred← citeshttps://doi.org/10.1007/s12192-018-00965-xopenalex-snapshot
The role of N6-methyladenosine RNA methylation in the heat stress response of sheep (Ovis aries)
inferred← citeshttps://doi.org/10.1007/s12253-019-00737-7openalex-snapshot
ALKBH5 Holds Prognostic Values and Inhibits the Metastasis of Colon Cancer
inferred← citeshttps://doi.org/10.1007/s12672-024-01205-8openalex-snapshot
The role of the ALKBH5 RNA demethylase in invasive breast cancer
inferred← citeshttps://doi.org/10.1007/s12672-025-04085-8openalex-snapshot
Epigenetic reprogramming as the nexus of cancer stemness and therapy resistance: implications for biomarker discovery
inferred← citeshttps://doi.org/10.1007/s13258-016-0507-2openalex-snapshot
Epitranscriptome: m6A and its function in stem cell biology
inferred← citeshttps://doi.org/10.1007/s13258-024-01601-yopenalex-snapshot
The diverse landscape of RNA modifications in cancer development and progression
inferred← citeshttps://doi.org/10.1007/s13346-024-01704-9openalex-snapshot
Research trends on nanomaterials in triple negative breast cancer (TNBC): a bibliometric analysis from 2010 to 2024
inferred← citeshttps://doi.org/10.1007/s13402-022-00666-9openalex-snapshot
Bioactive peptide inhibits acute myeloid leukemia cell proliferation by downregulating ALKBH5-mediated m6A demethylation of EIF4EBP1 and MLST8 mRNA
inferred← citeshttps://doi.org/10.1007/s13402-024-01004-xopenalex-snapshot
ALKBH4 functions as a hypoxia-responsive tumor suppressor and inhibits metastasis and tumorigenesis
inferred← citeshttps://doi.org/10.1007/s40778-017-0102-8openalex-snapshot
Radiotherapy and Glioma Stem Cells: Searching for Chinks in Cellular Armor
inferred← citeshttps://doi.org/10.1007/s42994-025-00240-5openalex-snapshot
Regulatory roles of RNA modifications in plant development and fruit ripening
inferred← citeshttps://doi.org/10.1007/s43657-021-00043-wopenalex-snapshot
Emerging Regulatory Mechanisms of N6-Methyladenosine Modification in Cancer Metastasis
inferred← citeshttps://doi.org/10.1016/b978-0-12-817193-6.00011-xopenalex-snapshot
RNA in cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-824476-0.00006-1openalex-snapshot
Nanomedicine for targeting breast cancer stem cells
inferred← citeshttps://doi.org/10.1016/b978-0-323-99873-4.00001-3openalex-snapshot
Cancer stem cells in glioblastoma – an update
inferred← citeshttps://doi.org/10.1016/b978-0-443-13209-4.00019-2openalex-snapshot
Involvement of epigenetic modifications in cancer stem cells and chemoresistance
inferred← citeshttps://doi.org/10.1016/b978-0-443-13937-6.00007-xopenalex-snapshot
Photothermal-chemotherapy: the emerging supramolecular photothermal molecules and the recent advances
inferred← citeshttps://doi.org/10.1016/bs.acr.2018.11.001openalex-snapshot
Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy
inferred← citeshttps://doi.org/10.1016/j.ab.2019.05.005openalex-snapshot
Role of identified RNA N6-methyladenosine methylation in liver
inferred← citeshttps://doi.org/10.1016/j.abb.2021.109023openalex-snapshot
m6A-seq analysis of microRNAs reveals that the N6-methyladenosine modification of miR-21–5p affects its target expression
inferred← citeshttps://doi.org/10.1016/j.apsb.2018.06.001openalex-snapshot
N6-Methyladenosine modification: a novel pharmacological target for anti-cancer drug development
inferred← citeshttps://doi.org/10.1016/j.apsb.2022.01.003openalex-snapshot
Detailed resume of RNA m6A demethylases
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2016.11.010openalex-snapshot
Apigenin inhibited hypoxia induced stem cell marker expression in a head and neck squamous cell carcinoma cell line
inferred← citeshttps://doi.org/10.1016/j.bbadis.2024.167307openalex-snapshot
FTO alleviated ferroptosis in septic cardiomyopathy via mediating the m6A modification of BACH1
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.09.008openalex-snapshot
The m6A‑methylase complex and mRNA export
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.09.010openalex-snapshot
It's complicated… m6A-dependent regulation of gene expression in cancer
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2018.12.001openalex-snapshot
The role of RNA adenosine demethylases in the control of gene expression
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2019.07.003openalex-snapshot
Small changes, big implications: The impact of m6A RNA methylation on gene expression in pluripotency and development
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.118526openalex-snapshot
Upregulation of PD-L1 expression in breast cancer cells through the formation of 3D multicellular cancer aggregates under different chemical and mechanical conditions
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118644openalex-snapshot
Roles for Ca2+ and K+ channels in cancer cells exposed to the hypoxic tumour microenvironment
inferred← citeshttps://doi.org/10.1016/j.bbcan.2021.188522openalex-snapshot
The role of N6-methyladenosine mRNA in the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.10.145openalex-snapshot
ALKBH5-m6A-FOXM1 signaling axis promotes proliferation and invasion of lung adenocarcinoma cells under intermittent hypoxia
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.12.063openalex-snapshot
Hypoxia-inducible factor-1α mediates the expression of mature β cell-disallowed genes in hypoxia-induced β cell dedifferentiation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.12.017openalex-snapshot
Oxidative demethylase ALKBH5 repairs DNA alkylation damage and protects against alkylation-induced toxicity
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115441openalex-snapshot
Cancer stem cells: Recent insights and therapies
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115565openalex-snapshot
Insights into the potential of Sanguinarine as a promising therapeutic option for breast cancer
inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115750openalex-snapshot
RNA methylations in depression, from pathological mechanism to therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.biocel.2018.12.017openalex-snapshot
Self-renewal signaling pathways in breast cancer stem cells
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120330openalex-snapshot
Hypoxia-stimulated tumor therapy associated with the inhibition of cancer cell stemness
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.108613openalex-snapshot
The role of m6A RNA methylation in cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109694openalex-snapshot
New sights in cancer: Component and function of N6-methyladenosine modification
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110098openalex-snapshot
The emerging molecular mechanism of m6A modulators in tumorigenesis and cancer progression
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110731openalex-snapshot
Principles of RNA methylation and their implications for biology and medicine
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114846openalex-snapshot
N6-methyladenosine (m6A) in cancer stem cell: From molecular mechanisms to therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115409openalex-snapshot
RNA methylation, homologous recombination repair and therapeutic resistance
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116365openalex-snapshot
N6-methyladenosine (m6A) modification in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116559openalex-snapshot
Epigenetic deregulation in breast cancer microenvironment: Implications for tumor progression and therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.bios.2018.07.035openalex-snapshot
Integrated phosphorescence-based photonic biosensor (iPOB) for monitoring oxygen levels in 3D cell culture systems
inferred← citeshttps://doi.org/10.1016/j.bios.2024.116788openalex-snapshot
Rapid and direct detection of m6A methylation by DNAzyme-based and smartphone-assisted electrochemical biosensor
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2020.107656openalex-snapshot
Advances in the profiling of N6-methyladenosine (m6A) modifications
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.115300openalex-snapshot
3D proteome-wide scale screening and activity evaluation of a new ALKBH5 inhibitor in U87 glioblastoma cell line
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.04.046openalex-snapshot
Influence of Cholesterol on the Oxygen Permeability of Membranes: Insight from Atomistic Simulations
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.08.030openalex-snapshot
Roles of RNA methylation by means of N6-methyladenosine (m6A) in human cancers
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.11.006openalex-snapshot
YTHDF2 suppresses cell proliferation and growth via destabilizing the EGFR mRNA in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.canlet.2020.01.021openalex-snapshot
Writers, readers and erasers of RNA modifications in cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2020.07.004openalex-snapshot
Hypoxia-driven intratumor heterogeneity and immune evasion
inferred← citeshttps://doi.org/10.1016/j.canlet.2021.03.009openalex-snapshot
Tumor microenvironment in head and neck squamous cell carcinoma: Functions and regulatory mechanisms
inferred← citeshttps://doi.org/10.1016/j.canlet.2021.08.027openalex-snapshot
VIRMA contributes to non-small cell lung cancer progression via N6-methyladenosine-dependent DAPK3 post-transcriptional modification
inferred← citeshttps://doi.org/10.1016/j.canlet.2024.216823openalex-snapshot
Hypoxia-associated autophagy flux dysregulation in human cancers
inferred← citeshttps://doi.org/10.1016/j.canlet.2026.218559openalex-snapshot
Mechanistic study of pharmacodynamic regulation in tumorigenesis: Epigenetic targeting of key enzymes by active ginsenoside components
inferred← citeshttps://doi.org/10.1016/j.cbpa.2017.10.008openalex-snapshot
Epitranscriptomics: regulation of mRNA metabolism through modifications
inferred← citeshttps://doi.org/10.1016/j.ccell.2016.11.017openalex-snapshot
FTO Plays an Oncogenic Role in Acute Myeloid Leukemia as a N 6 -Methyladenosine RNA Demethylase
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.02.013openalex-snapshot
m 6 A Demethylase ALKBH5 Maintains Tumorigenicity of Glioblastoma Stem-like Cells by Sustaining FOXM1 Expression and Cell Proliferation Program
inferred← citeshttps://doi.org/10.1016/j.ccell.2017.03.010openalex-snapshot
Messenger RNA Methylation Regulates Glioblastoma Tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.ccell.2020.02.004openalex-snapshot
m6A Modification in Coding and Non-coding RNAs: Roles and Therapeutic Implications in Cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2016.09.022openalex-snapshot
Beyond the Triplet Code: Context Cues Transform Translation
inferred← citeshttps://doi.org/10.1016/j.cell.2017.05.045openalex-snapshot
Dynamic RNA Modifications in Gene Expression Regulation
inferred← citeshttps://doi.org/10.1016/j.cellsig.2026.112563openalex-snapshot
NSUN5–CBX8 m5C axis promotes gastric tumorigenesis by activating JAK–STAT3 signaling
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