Establishment and characterization of a human primary prostate carcinoma cell line, HH870
BACKGROUND Development of new therapeutic modalities for human prostate carcinoma has been impeded by a lack of adequate in vitro and in vivo models. Most in vitro studies have been carried out using a limited number of human prostate cancer cell lines that are mostly derived from metastatic tumors...
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Published in | The Prostate Vol. 63; no. 1; pp. 91 - 103 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.04.2005
Wiley-Liss |
Subjects | |
Online Access | Get full text |
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Summary: | BACKGROUND
Development of new therapeutic modalities for human prostate carcinoma has been impeded by a lack of adequate in vitro and in vivo models. Most in vitro studies have been carried out using a limited number of human prostate cancer cell lines that are mostly derived from metastatic tumors sites or are immortalized.
METHODS
Characterization of the prostate cancer cell line, HH870, included description of morphology, determination of doubling time, response to androgens, immunocytochemistry, and immunoblotting of proteins known to be associated with prostate carcinoma, karyotyping, fluorescence in situ hybridization (FISH), DNA profiling, and growth as xenograft in athymic rodents.
RESULTS
HH870 expresses various epithelial marker antigens that correlate with known basic immunostaining profiles of prostate adenocarcinoma, although the cell line does not express PSA, PSMA, or PAP. HH870 exhibits complex chromosomal abnormalities and harbors no immortalizing HPV, BKV, JCV, and SV40 DNA.
CONCLUSIONS
We report the successful establishment and characterization of a new long‐term primary human prostate tumor cell line HH870. © 2004 Wiley‐Liss, Inc. |
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Bibliography: | ark:/67375/WNG-F1R75HD7-W istex:3B087FA95E7BC88BC6E8549196E018474F826BFC Hoag Hospital Foundation, Newport Beach, CA ArticleID:PROS20162 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0270-4137 1097-0045 |
DOI: | 10.1002/pros.20162 |