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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1993-10-19
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pubmed:abstractText |
Investigations of mechanisms of human prostate carcinogenesis are limited by the unavailability of a suitable in vitro model system. We have demonstrated that an immortal, but nontumorigenic, human epithelial cell line (267B1) established from fetal prostate tissue can be malignantly transformed by a biological carcinogen, and can serve as a useful model for investigations of the progression steps of carcinogenesis. Activated Ki-ras was introduced into 267B1 cells by infection with the Kirsten murine sarcoma virus. Morphological alterations and anchorage-independent growth were observed; when cells were injected into nude mice, poorly differentiated adenocarcinomas developed. These findings represent the first evidence of malignant transformation of human prostate epithelial cells in culture, and support a role for Ki-ras activation in a multistep process for prostate neoplastic transformation.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0270-4137
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
91-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8378190-Cell Line,
pubmed-meshheading:8378190-Cell Transformation, Neoplastic,
pubmed-meshheading:8378190-Epithelial Cells,
pubmed-meshheading:8378190-Genes, ras,
pubmed-meshheading:8378190-Humans,
pubmed-meshheading:8378190-Male,
pubmed-meshheading:8378190-Oncogene Protein p21(ras),
pubmed-meshheading:8378190-Prostate,
pubmed-meshheading:8378190-Prostatic Neoplasms
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pubmed:year |
1993
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pubmed:articleTitle |
Neoplastic transformation of a human prostate epithelial cell line by the v-Ki-ras oncogene.
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pubmed:affiliation |
Department of Radiation Medicine, Vincent T. Lombardi Cancer Research Center, Georgetown University School of Medicine, Washington, D.C. 20007.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|