Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0006141,
umls-concept:C0007589,
umls-concept:C0007600,
umls-concept:C0007634,
umls-concept:C0017262,
umls-concept:C0023043,
umls-concept:C0038975,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0205217,
umls-concept:C0332281,
umls-concept:C0521026,
umls-concept:C0929301,
umls-concept:C1510411,
umls-concept:C1511938,
umls-concept:C1707937,
umls-concept:C2911684
|
pubmed:issue |
3
|
pubmed:dateCreated |
1990-4-24
|
pubmed:abstractText |
Cloned simian virus 40 (SV40)-transformed human breast epithelial cell lines can differentiate to myoepithelial-like cells, and these can be isolated as clonal cell lines. Immunofluorescent and immunocytochemical analysis of such cell lines growing on plastic surfaces, collagen gels, and as tumor-nodules in nude mice indicate that all the cell lines produce SV40 large T antigen, but that the production of this antigen is qualitatively increased in the myoepithelial-like cells and cell lines. The myoepithelial-like cell lines produce 4-6 times more immunoprecipitable large T antigen than the parental epithelial cells. The amount of mRNA for large T antigen is also increased by 3.5-5-fold in the myoepithelial-like cell lines when analysed by dot-blot or by Northern hybridisations. Thus, differentiation along the myoepithelial-like cell pathway is associated in these SV40-transformed cells with increased expression of the viral large T antigen. It is suggested that immortalization of primary breast epithelial cell cultures may be, in part, due to the expression of large T antigen preventing processes of terminal keratinization.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0021-9541
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
142
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
657-65
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2155912-Antigens, Polyomavirus Transforming,
pubmed-meshheading:2155912-Breast,
pubmed-meshheading:2155912-Cell Differentiation,
pubmed-meshheading:2155912-Cell Transformation, Viral,
pubmed-meshheading:2155912-Epithelial Cells,
pubmed-meshheading:2155912-Fluorescent Antibody Technique,
pubmed-meshheading:2155912-Gene Expression,
pubmed-meshheading:2155912-Humans,
pubmed-meshheading:2155912-Precipitin Tests,
pubmed-meshheading:2155912-RNA, Messenger,
pubmed-meshheading:2155912-RNA, Viral,
pubmed-meshheading:2155912-Simian virus 40
|
pubmed:year |
1990
|
pubmed:articleTitle |
Differentiation of simian virus 40 transformed human mammary epithelial stem cell lines to myoepithelial-like cells is associated with increased expression of viral large T antigen.
|
pubmed:affiliation |
Biochemistry Department, University of Liverpool, England.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|