We have investigated differences in C * pG methylation between F9 embryonal carcinoma cells in vitro and as tumor cells grown in vivo using Msp I and Hpa II restriction isoschizomers. Southerns were hybridized with two low copy number probes, mouse major β-globin (f7) and a class I, histocompatibility-2 cDNA clone (pH-2 d -4). In each case, the tumor-DNA was hypomethylated while the DNA from F9 cells grown in vitro was moderately methylated. We conclude that growth conditions or cell-cell interactions can greatly affect methylation of C * pG sites.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43248/1/11033_2004_Article_BF00776983.pd
Oesophageal adenocarcinoma (OAC) is increasing in incidence and has a poor prognosis. Tumour derived...
Culture expansion of primary cells evokes highly reproducible DNA methylation (DNAm) changes. We hav...
CpG island methylation within single gene promoters can silence expression of associated genes. We f...
AbstractWe show here that the genome of F9 teratocarcinoma cells growing in culture is heavily methy...
Genetic and epigenetic alterations are essential for the initiation and progression of human cancer....
For the past 25 years, it has been known that alterations in DNA methylation (DNAm) occur in cancer,...
The proto-oncogene, c-mos, which is expressed only in the germ cells of both testis and ovary, plays...
Background: Cutaneous squamous cell carcinomas (cSCC) are among the most common and highly mutated h...
Alterations of DNA methylation in carcinogenesis have attracted much attention because such changes ...
AbstractThe ubiquitous transcription factor Sp1 has been implicated in the mechanism which maintains...
Aberrant DNA methylation is an important cancer hallmark, yet the dynamics of DNA methylation change...
Alterations in DNA methylation in cancer include global hypomethylation and gene-specific hypermethy...
Mouse embryonic stem cells (mESCs) are an excellent model to study epigenetics and chromatin struct...
Alterations in DNA methylation in cancer include global hypomethylation and gene-specific hypermethy...
In vitro and in vivo models are widely used in cancer research. Characterizing the similarities and ...
Oesophageal adenocarcinoma (OAC) is increasing in incidence and has a poor prognosis. Tumour derived...
Culture expansion of primary cells evokes highly reproducible DNA methylation (DNAm) changes. We hav...
CpG island methylation within single gene promoters can silence expression of associated genes. We f...
AbstractWe show here that the genome of F9 teratocarcinoma cells growing in culture is heavily methy...
Genetic and epigenetic alterations are essential for the initiation and progression of human cancer....
For the past 25 years, it has been known that alterations in DNA methylation (DNAm) occur in cancer,...
The proto-oncogene, c-mos, which is expressed only in the germ cells of both testis and ovary, plays...
Background: Cutaneous squamous cell carcinomas (cSCC) are among the most common and highly mutated h...
Alterations of DNA methylation in carcinogenesis have attracted much attention because such changes ...
AbstractThe ubiquitous transcription factor Sp1 has been implicated in the mechanism which maintains...
Aberrant DNA methylation is an important cancer hallmark, yet the dynamics of DNA methylation change...
Alterations in DNA methylation in cancer include global hypomethylation and gene-specific hypermethy...
Mouse embryonic stem cells (mESCs) are an excellent model to study epigenetics and chromatin struct...
Alterations in DNA methylation in cancer include global hypomethylation and gene-specific hypermethy...
In vitro and in vivo models are widely used in cancer research. Characterizing the similarities and ...
Oesophageal adenocarcinoma (OAC) is increasing in incidence and has a poor prognosis. Tumour derived...
Culture expansion of primary cells evokes highly reproducible DNA methylation (DNAm) changes. We hav...
CpG island methylation within single gene promoters can silence expression of associated genes. We f...