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The Importance of Cancer Cell Lines as in vitro Models in Cancer Methylome Analysis and Anticancer Drugs Testing

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1 of the 77 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1038/nature02889 (notice 2006-06-29).

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What this work says

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

inferredcites →https://doi.org/10.1001/archotol.128.2.167openalex-snapshot
Analysis of Cell-Cycle Checkpoint Pathways in Head and Neck Cancer Cell Lines
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19991112)83:4<555::aid-ijc19>3.0.co;2-2openalex-snapshot
Widespread intraspecies cross-contamination of human tumor cell lines arising at source
inferredcites →https://doi.org/10.1002/ijc.11176openalex-snapshot
Role of hMLH1 promoter hypermethylation in drug resistance to 5‐fluorouracil in colorectal cancer cell lines
inferredcites →https://doi.org/10.1002/ijc.23607openalex-snapshot
Modes of action of the DNA methyltransferase inhibitors azacytidine and decitabine
inferredcites →https://doi.org/10.1002/path.1024openalex-snapshot
Cancer as an epigenetic disease: DNA methylation and chromatin alterations in human tumours
inferredcites →https://doi.org/10.1007/bf01807363openalex-snapshot
Biological differences among MCF-7 human breast cancer cell lines from different laboratories
inferredcites →https://doi.org/10.1007/s10585-008-9169-zopenalex-snapshot
Characterisation of breast cancer cell lines and establishment of a novel isogenic subclone to study migration, invasion and tumourigenicity
inferredcites →https://doi.org/10.1016/0277-5379(84)90169-xopenalex-snapshot
The use of human cancer cell lines as a primary screening system for antineoplastic compounds
inferredcites →https://doi.org/10.1016/j.bbcan.2008.12.004openalex-snapshot
Human cancer cell lines: Experimental models for cancer cells in situ? For cancer stem cells?
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.critrevonc.2006.07.010openalex-snapshot
Decitabine—Bedside to bench
inferredcites →https://doi.org/10.1016/j.ejmech.2011.09.029openalex-snapshot
Anti-hepatocellular carcinoma activity using human HepG2 cells and hepatotoxicity of 6-substituted methyl 3-aminothieno[3,2-b]pyridine-2-carboxylate derivatives: In vitro evaluation, cell cycle analysis and QSAR studies
inferredcites →https://doi.org/10.1016/j.oraloncology.2010.10.003openalex-snapshot
Establishment and characterization of a rabbit oral squamous cell carcinoma cell line as a model for in vivo studies
inferredcites →https://doi.org/10.1016/s1521-6616(03)00207-9openalex-snapshot
Inhibitors of DNA methylation in the treatment of hematological malignancies and MDS
inferredcites →https://doi.org/10.1021/bi0350147openalex-snapshot
Direct Analysis of Tubulin Expression in Cancer Cell Lines by Electrospray Ionization Mass Spectrometry
inferredcites →https://doi.org/10.1023/a:1006151427889openalex-snapshot
Breast Cancer Research and Treatment
inferredcites →https://doi.org/10.1023/a:1018770417964openalex-snapshot
Cell Cycle Checkpoints as Therapeutic Targets
inferredcites →https://doi.org/10.1023/b:brea.0000014042.54925.ccopenalex-snapshot
Relevance of Breast Cancer Cell Lines as Models for Breast Tumours: An Update
inferredcites →https://doi.org/10.1038/35078107openalex-snapshot
Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells
inferredcites →https://doi.org/10.1038/cgt.2012.22openalex-snapshot
Nanovector delivery of siRNA for cancer therapy
inferredcites →https://doi.org/10.1038/nature02889openalex-snapshot
Induction of DNA methylation and gene silencing by short interfering RNAs in human cells
inferredcites →https://doi.org/10.1038/nature08956openalex-snapshot
Evidence of RNAi in humans from systemically administered siRNA via targeted nanoparticles
inferredcites →https://doi.org/10.1038/nature11003openalex-snapshot
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
inferredcites →https://doi.org/10.1038/nature11005openalex-snapshot
Systematic identification of genomic markers of drug sensitivity in cancer cells
inferredcites →https://doi.org/10.1038/nrc1317openalex-snapshot
Microtubules as a target for anticancer drugs
inferredcites →https://doi.org/10.1038/nrc1841openalex-snapshot
Targeting polo-like kinase 1 for cancer therapy
inferredcites →https://doi.org/10.1038/nrc1951openalex-snapshot
The NCI60 human tumour cell line anticancer drug screen
inferredcites →https://doi.org/10.1038/nrc2193openalex-snapshot
Modelling breast cancer: one size does not fit all
inferredcites →https://doi.org/10.1038/sj.bjc.6602972openalex-snapshot
Promoter methylation of P16, RARβ, E-cadherin, cyclin A1 and cytoglobin in oral cancer: quantitative evaluation using pyrosequencing
inferredcites →https://doi.org/10.1038/sj.bjc.6690041openalex-snapshot
DNA methylation in the promoter region of the p16 (CDKN2/MTS-1/INK4A) gene in human breast tumours
inferredcites →https://doi.org/10.1038/sj.onc.1202415openalex-snapshot
Detailed methylation analysis of the glutathione S-transferase π (GSTP1) gene in prostate cancer
inferredcites →https://doi.org/10.1038/sj.onc.1205651openalex-snapshot
DNA methylation in cancer: too much, but also too little
inferredcites →https://doi.org/10.1038/sj.onc.1209763openalex-snapshot
5-Aza-2′-deoxycytidine-mediated reductions in G9A histone methyltransferase and histone H3 K9 di-methylation levels are linked to tumor suppressor gene reactivation
inferredcites →https://doi.org/10.1073/pnas.0511340103openalex-snapshot
High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays
inferredcites →https://doi.org/10.1093/annonc/mdf314openalex-snapshot
DNA methyltransferase inhibitors—state of the art
inferredcites →https://doi.org/10.1093/bfgp/elp013openalex-snapshot
Advantages of next-generation sequencing versus the microarray in epigenetic research
inferredcites →https://doi.org/10.1093/bfgp/elq035openalex-snapshot
Next generation sequencing based approaches to epigenomics
inferredcites →https://doi.org/10.1093/bioinformatics/btq040openalex-snapshot
SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors
inferredcites →https://doi.org/10.1093/clinchem/45.8.1148openalex-snapshot
Real-Time Reverse Transcription-PCR Assay for Future Management of ERBB2-based Clinical Applications
inferredcites →https://doi.org/10.1093/hmg/10.7.687openalex-snapshot
Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer
inferredcites →https://doi.org/10.1093/jnci/92.7.564openalex-snapshot
Promoter Hypermethylation and BRCA1 Inactivation in Sporadic Breast and Ovarian Tumors
inferredcites →https://doi.org/10.1093/jnci/93.9.691openalex-snapshot
Epigenetic Inactivation of RASSF1A in Lung and Breast Cancers and Malignant Phenotype Suppression
inferredcites →https://doi.org/10.1093/jnci/djq279openalex-snapshot
Lung Cancer Cell Lines as Tools for Biomedical Discovery and Research
inferredcites →https://doi.org/10.1111/j.1349-7006.2003.tb01345.xopenalex-snapshot
Molecular targeting therapy of cancer: drug resistance, apoptosis and survival signal
inferredcites →https://doi.org/10.1111/j.1755-3768.2009.2234.xopenalex-snapshot
Chromosomal number aberrations and transformation in adult mouse retinal stem cells in vitro
inferredcites →https://doi.org/10.1128/mcb.01799-07openalex-snapshot
DNA Methylation Inhibitor 5-Aza-2′-Deoxycytidine Induces Reversible Genome-Wide DNA Damage That Is Distinctly Influenced by DNA Methyltransferases 1 and 3B
inferredcites →https://doi.org/10.1136/jmedgenet-2011-100242openalex-snapshot
Studying the epigenome using next generation sequencing
inferredcites →https://doi.org/10.1158/0008-5472.can-05-2853openalex-snapshot
BRCA1 Mutation Analysis of 41 Human Breast Cancer Cell Lines Reveals Three New Deleterious Mutants
inferredcites →https://doi.org/10.1158/0008-5472.can-06-0343openalex-snapshot
Down-regulation of Polo-like Kinase 1 Elevates Drug Sensitivity of Breast Cancer CellsIn vitroandIn vivo
inferredcites →https://doi.org/10.1158/0008-5472.can-06-0594openalex-snapshot
Establishment of Human Colon Cancer Cell Lines from Fresh Tumors versus Xenografts: Comparison of Success Rate and Cell Line Features
inferredcites →https://doi.org/10.1158/0008-5472.can-07-1502openalex-snapshot
Drug Sensitivity Prediction by CpG Island Methylation Profile in the NCI-60 Cancer Cell Line Panel
inferredcites →https://doi.org/10.1158/0008-5472.can-07-2703openalex-snapshot
Genetic Alterations in the Tyrosine Kinase Transcriptome of Human Cancer Cell Lines
inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-2218openalex-snapshot
Potent siRNA Inhibitors of Ribonucleotide Reductase Subunit RRM2 Reduce Cell Proliferation In vitro and In vivo
inferredcites →https://doi.org/10.1158/1535-7163.mct-04-0234openalex-snapshot
Chemosensitivity profile of cancer cell lines and identification of genes determining chemosensitivity by an integrated bioinformatical approach using cDNA arrays
inferredcites →https://doi.org/10.1158/1535-7163.mct-05-0536openalex-snapshot
Efficacy of a nitric oxide–releasing nonsteroidal anti-inflammatory drug and cytotoxic drugs in human colon cancer cell linesin vitroand xenografts
inferredcites →https://doi.org/10.1158/1535-7163.mct-06-0433openalex-snapshot
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set
inferredcites →https://doi.org/10.1167/iovs.08-3091openalex-snapshot
Chromosomal Number Aberrations and Transformation in Adult Mouse Retinal Stem Cells In Vitro
inferredcites →https://doi.org/10.1186/1471-2164-11-137openalex-snapshot
Genome-wide analysis of aberrant methylation in human breast cancer cells using methyl-DNA immunoprecipitation combined with high-throughput sequencing
inferredcites →https://doi.org/10.1186/bcr2231openalex-snapshot
Prediction of paclitaxel sensitivity by CDK1 and CDK2 activity in human breast cancer cells
inferredcites →https://doi.org/10.1186/bcr2925openalex-snapshot
Epigenetics in breast cancer: what's new?
inferredcites →https://doi.org/10.1186/bcr577openalex-snapshot
Breast cancer cell lines: friend or foe?
inferredcites →https://doi.org/10.1200/jco.2004.07.151openalex-snapshot
DNA Methylation and Cancer
inferredcites →https://doi.org/10.1309/ajcpr1svt1vhugxwopenalex-snapshot
Whole Cancer Genome Sequencing by Next-Generation Methods
inferredcites →https://doi.org/10.1309/e9b5-5jyh-d84l-8y17openalex-snapshot
The Use of Cell Line Standards to Reduce HER-2/neu Assay Variation in Multiple European Cancer Centers and the Potential of Automated Image Analysis to Provide for More Accurate Cut Points for Predicting Clinical Response to Trastuzumab
inferredcites →https://doi.org/10.1309/e9b55jyhd84l8y17openalex-snapshot
The Use of Cell Line Standards to Reduce HER-2/neu Assay Variation in Multiple European Cancer Centers and the Potential of Automated Image Analysis to Provide for More Accurate Cut Points for Predicting Clinical Response to Trastuzumab
inferredcites →https://doi.org/10.1371/journal.pmed.0030486openalex-snapshot
A Genome-Wide Screen for Promoter Methylation in Lung Cancer Identifies Novel Methylation Markers for Multiple Malignancies
inferredcites →https://doi.org/10.1371/journal.pone.0006146openalex-snapshot
Molecular Profiling of Breast Cancer Cell Lines Defines Relevant Tumor Models and Provides a Resource for Cancer Gene Discovery
inferredcites →https://doi.org/10.1371/journal.pone.0009201openalex-snapshot
Delineating Genetic Alterations for Tumor Progression in the MCF10A Series of Breast Cancer Cell Lines
inferredcites →https://doi.org/10.1371/journal.pone.0011379openalex-snapshot
Methylation of the Tumor Suppressor Protein, BRCA1, Influences Its Transcriptional Cofactor Function
inferredcites →https://doi.org/10.1371/journal.pone.0029923openalex-snapshot
Defining the Sister Rat Mammary Tumor Cell Lines HH-16 cl.2/1 and HH-16.cl.4 as an In Vitro Cell Model for Erbb2
inferredcites →https://doi.org/10.1387/ijdb.041822aaopenalex-snapshot
The "chemoinvasion assay": a tool to study tumor and endothelial cell invasion of basement membranes
inferredcites →https://doi.org/10.1677/erc.0.0100409openalex-snapshot
Validation of real-time RT-PCR for analysis of human breast cancer cell lines resistant or sensitive to treatment with antiestrogens.
inferredcites →https://doi.org/10.2174/138920212800793294openalex-snapshot
Epigenome-Wide Association Studies (EWAS) in Cancer
inferredcites →https://doi.org/10.4161/epi.1.1.2375openalex-snapshot
Reactivation of Epigenetically Silenced Genes by DNA Methyltransferase Inhibitors: Basic Concepts and Clinical Applications
inferredcites →https://doi.org/10.53390/ijbsopenalex-snapshot
International Journal on Biological Sciences
inferredcites →https://doi.org/10.5772/1745openalex-snapshot
Oncogenomics and Cancer Proteomics - Novel Approaches in Biomarkers Discovery and Therapeutic Targets in Cancer
inferredcites →https://doi.org/10.7150/ijbs.6.784openalex-snapshot
S-Adenosylmethionine Inhibits the Growth of Cancer Cells by Reversing the Hypomethylation Status of c-myc and H-ras in Human Gastric Cancer and Colon Cancer

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

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Initial assessment of suitability of MCF-7 and HepG2 cancer cell lines for AQP3 research in cancer biology
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КЛЕТОЧНЫЕ ТЕХНОЛОГИИ В ФАРМАКОЛОГИЧЕСКИХ ИССЛЕДОВАНИЯХ. НАСТОЯЩЕЕ И БУДУЩЕЕ, "Цитология"
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.