The history of cancer epigenetics (Q29617273)

Europe PubMed Central

title

The history of cancer epigenetics (English)

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30 April 2017

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Feinberg AP

1

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30 April 2017

Tycko B

series ordinal

2

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14732866

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14732866

30 April 2017

language of work or name

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30 April 2017

publication date

February 2004

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30 April 2017

published in

Nature Reviews Cancer

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volume

4

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issue

2

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page(s)

143-53

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14732866

Hypomethylation distinguishes genes of some human cancers from their normal counterparts

30 April 2017

cites work

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The 5-methylcytosine content of DNA from human tumors

31 March 2020

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Hypomethylation of DNA from benign and malignant human colon neoplasms

31 March 2020

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A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes

31 March 2020

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Hypomethylation of ras oncogenes in primary human cancers

31 March 2020

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The activation of human gene MAGE-1 in tumor cells is correlated with genome-wide demethylation.

31 March 2020

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Promoter hypomethylation of a novel cancer/testis antigen gene CAGE is correlated with its aberrant expression and is seen in premalignant stage of gastric carcinoma

31 March 2020

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Tumour class prediction and discovery by microarray-based DNA methylation analysis

31 March 2020

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Exploration of global gene expression patterns in pancreatic adenocarcinoma using cDNA microarrays

31 March 2020

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Cell-Type-Specific Repression of the Maspin Gene Is Disrupted Frequently by Demethylation at the Promoter Region in Gastric Intestinal Metaplasia and Cancer Cells

31 March 2020

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Hypomethylation of the MN/CA9 promoter and upregulated MN/CA9 expression in human renal cell carcinoma

31 March 2020

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Hypomethylation of the metastasis-associated S100A4 gene correlates with gene activation in human colon adenocarcinoma cell lines

31 March 2020

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CpG methylation of human papillomavirus type 16 DNA in cervical cancer cell lines and in clinical specimens: genomic hypomethylation correlates with carcinogenic progression

31 March 2020

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Race- and age-dependent alterations in global methylation of DNA in squamous cell carcinoma of the lung (United States)

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DNA methylation and genetic instability in colorectal cancer cells

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DNA methylator and mismatch repair phenotypes are not mutually exclusive in colorectal cancer cell lines

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Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

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Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16

31 March 2020

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Chromosome arm 16q in Wilms tumors: unbalanced chromosomal translocations, loss of heterozygosity, and assessment of the CTCF gene

31 March 2020

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The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

31 March 2020

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

31 March 2020

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DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

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Chromosomal Instability and Tumors Promoted by DNA Hypomethylation

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Hypomethylation of L1 retrotransposons in colorectal cancer and adjacent normal tissue

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Effects of cadmium on DNA-(Cytosine-5) methyltransferase activity and DNA methylation status during cadmium-induced cellular transformation

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Sodium arsenite administration via drinking water increases genome-wide and Ha-ras DNA hypomethylation in methyl-deficient C57BL/6J mice

31 March 2020

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Host cell-dependent expression of latent Epstein-Barr virus genomes: regulation by DNA methylation

31 March 2020

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Folate status, genomic DNA hypomethylation, and risk of colorectal adenoma and cancer: a case control study

31 March 2020

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Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

31 March 2020

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Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

31 March 2020

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Overexpression of a splice variant of DNA methyltransferase 3b, DNMT3b4, associated with DNA hypomethylation on pericentromeric satellite regions during human hepatocarcinogenesis

31 March 2020

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Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

31 March 2020

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Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma

31 March 2020

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Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

31 March 2020

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5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

31 March 2020

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Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

31 March 2020

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CpG island methylator phenotype in colorectal cancer

31 March 2020

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Inactivation of a tumor suppressor function in immortal Syrian hamster cells by N-methyl-N'-nitro-N-nitrosoguanidine and by 5-aza-2'-deoxycytidine

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DNMT1 and DNMT3b cooperate to silence genes in human cancer cells

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DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells

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Unanswered Questions about the Role of Promoter Methylation in Carcinogenesis

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Extinction of E-cadherin expression in breast cancer via a dominant repression pathway acting on proximal promoter elements

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Histone modifications and silencing prior to DNA methylation of a tumor suppressor gene.

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DNA methylation and gene silencing in cancer: which is the guilty party?

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Hypomethylation and hypermethylation of DNA in Wilms tumors.

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Hypomethylation and increased gene expression of p16INK4a in primary and metastatic breast carcinoma as compared to normal breast tissue

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Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

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Androgenetic origin of hydatidiform mole

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Parthenogenic Origin of Benign Ovarian Teratomas

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A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

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Maternal allele loss in Wilms' tumour

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Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

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Monoallelic expression of the human H19 gene

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Parental genomic imprinting of the human IGF2 gene

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IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

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Relaxation of imprinted genes in human cancer.

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

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Parental imprinting of the mouse H19 gene

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Parental imprinting of the mouse insulin-like growth factor II gene.

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Functional imprinting and epigenetic modification of the human SNRPN gene

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Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

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Role for DNA methylation in genomic imprinting

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Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

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The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

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IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes

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Epigenetic lesions at the H19 locus in Wilms' tumour patients

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Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

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Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

31 March 2020

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Tumour-suppressor activity of H19 RNA

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Deregulation of both imprinted and expressed alleles of the insulin–like growth factor 2 gene during β–cell tumorigenesis

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A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis

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Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor

31 March 2020

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Preferential loss of paternal 19q, but not 1p, alleles in oligodendrogliomas.

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Epigenetic silencing of PEG3 gene expression in human glioma cell lines

31 March 2020

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Pilot evaluation of 1p and 19q deletions in anaplastic oligodendrogliomas collected by a national cooperative cancer treatment group

31 March 2020

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Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

31 March 2020

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Tumour suppressor activity of human imprinted gene PEG3 in a glioma cell line

31 March 2020

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Chromosome bands 1p35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted

31 March 2020

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Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia

31 March 2020

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Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

31 March 2020

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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

31 March 2020

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Chromatin structure is required to block transcription of the methylated herpes simplex virus thymidine kinase gene

31 March 2020

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DNA methylation affects the formation of active chromatin

31 March 2020

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Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

31 March 2020

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Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

31 March 2020

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

31 March 2020

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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

31 March 2020

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DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci

31 March 2020

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Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation

31 March 2020

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Transcriptional repression by Drosophila methyl-CpG-binding proteins.

31 March 2020

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Regulation of chromatin structure by site-specific histone H3 methyltransferases

31 March 2020

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Methylation of histone H3 at lysine 4 is highly conserved and correlates with transcriptionally active nuclei in Tetrahymena

31 March 2020

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Cytosine methylation and the ecology of intragenomic parasites

31 March 2020

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Histone H3 variants specify modes of chromatin assembly

31 March 2020

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Histone methylation: dynamic or static?

31 March 2020

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Sequence-specific DNA-binding proteins which interact with (G + C)-rich sequences flanking the chicken c-myc gene.

31 March 2020

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CpG methylation regulates the Igf2/H19 insulator

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CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

31 March 2020

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The protein CTCF is required for the enhancer blocking activity of vertebrate insulators

31 March 2020

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BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

31 March 2020

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The polycomb group protein EZH2 is involved in progression of prostate cancer

31 March 2020

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Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

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Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

31 March 2020

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An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

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Genomic imprinting and cancer

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Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

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Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

31 March 2020

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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

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Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

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Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

31 March 2020

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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

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Aberrant methylation of p16(INK4a) is an early event in lung cancer and a potential biomarker for early diagnosis

31 March 2020

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Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions

31 March 2020

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Suppression of intestinal neoplasia by DNA hypomethylation.

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Induction of Tumors in Mice by Genomic Hypomethylation

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Heterozygous disruption of Hic1 predisposes mice to a gender-dependent spectrum of malignant tumors

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Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias

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Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias

31 March 2020

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The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 gene

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ALL-1 is a histone methyltransferase that assembles a supercomplex of proteins involved in transcriptional regulation

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High expression of the DNA methyltransferase gene characterizes human neoplastic cells and progression stages of colon cancer

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Limited up-regulation of DNA methyltransferase in human colon cancer reflecting increased cell proliferation.

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Methyltransferase recruitment and DNA hypermethylation of target promoters by an oncogenic transcription factor

31 March 2020

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Cancer epigenetics and methylation

31 March 2020

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The retinoblastoma protein and BRG1 form a complex and cooperate to induce cell cycle arrest

31 March 2020

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Rb interacts with histone deacetylase to repress transcription

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Retinoblastoma protein represses transcription by recruiting a histone deacetylase

31 March 2020

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Linking the Rb and polycomb pathways

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The retinoblastoma gene product interacts with maintenance human DNA (cytosine-5) methyltransferase and modulates its activity

31 March 2020

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DNMT1 forms a complex with Rb, E2F1 and HDAC1 and represses transcription from E2F-responsive promoters

31 March 2020

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Tumor formation and inactivation of RIZ1, an Rb-binding member of a nuclear protein-methyltransferase superfamily

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Effects of 5-azacytidine on the progressive nature of cell transformation

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Multiple new phenotypes induced in and 3T3 cells treated with 5-azacytidine

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Demethylation of a hypermethylated P15/INK4B gene in patients with myelodysplastic syndrome by 5-Aza-2'-deoxycytidine (decitabine) treatment

31 March 2020

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Toxicity of 5-aza-2'-deoxycytidine to mammalian cells is mediated primarily by covalent trapping of DNA methyltransferase rather than DNA demethylation

31 March 2020

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Inhibition of DNA methylation and reactivation of silenced genes by zebularine

31 March 2020

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Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer

31 March 2020

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Preclinical evaluation of antineoplastic activity of inhibitors of DNA methylation (5-aza-2'-deoxycytidine) and histone deacetylation (trichostatin A, depsipeptide) in combination against myeloid leukemic cells

31 March 2020

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Comment on "Chromosomal instability and tumors promoted by DNA hypomethylation" and "Induction of tumors in nice by genomic hypomethylation".

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Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation

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Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

31 March 2020

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Specific protection of methylated CpGs in mammalian nuclei

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5-Azacytidine-induced reactivation of the human X chromosome-linked PGK1 gene is associated with a large region of cytosine demethylation in the 5' CpG island

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The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression

31 March 2020

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31 March 2020

Identifiers

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30 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1009116910

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Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14732866

PubMed publication ID

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017