Source:http://linkedlifedata.com/resource/pubmed/id/16728343
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2006-5-26
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pubmed:abstractText |
The differential expression of genes and related proteins of multidrug resistance in chemoresistant prostate cancer cell lines were elucidated in this study. RNA extracted from doxorubicin-resistant rat prostate cancer (PCa) cells (AT3/ADR1000) and native PCa cells was hybridized to expression arrays containing cDNAs from 588 known genes. Differential expression of selected genes was confirmed by quantitative reverse-transcription polymerase chain reaction (RT-PCR) analysis. Protein contents were measured by fluorescent flow cytometry and immunoblotting. Localization of selected proteins in cells was observed by immunocytochemical staining. Up-regulation of eleven genes and down-regulation of one single gene were displayed in the chemoresistant prostate cancer cells. Overexpression of mRNAs in macrophage migration inhibitory factor (MIF), DNA binding protein inhibitor 1 (ID1), and glutathione S-transferase-pi (GST-pi) were confirmed by gene-specific RT-PCR. Protein over-expression of GST-pi, MIF, and ID1 in resistant cells were 3.3-, 1.5-, and 1.5-fold to native cells, respectively. Immunocytochemistry revealed that GST-pi, MIF, and ID1 were present primarily in the cytoplasm of tumor cells, but ID1 also could be found in the nucleus. AT3/ADR1000 drug-resistant PCa cells displayed significantly increased expression of GST-pi, MIF, and ID1 proteins when compared with native PCa cells. It indicates these genes may play a role in drug resistance of prostate cancer.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione S-Transferase pi,
http://linkedlifedata.com/resource/pubmed/chemical/ID1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Inhibitor of Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Migration-Inhibitory...
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pubmed:status |
MEDLINE
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pubmed:issn |
0148-5016
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
275-81
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16728343-Animals,
pubmed-meshheading:16728343-Base Sequence,
pubmed-meshheading:16728343-Cell Line, Tumor,
pubmed-meshheading:16728343-DNA, Complementary,
pubmed-meshheading:16728343-DNA Primers,
pubmed-meshheading:16728343-Drug Resistance, Neoplasm,
pubmed-meshheading:16728343-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:16728343-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:16728343-Glutathione S-Transferase pi,
pubmed-meshheading:16728343-Inhibitor of Differentiation Protein 1,
pubmed-meshheading:16728343-Macrophage Migration-Inhibitory Factors,
pubmed-meshheading:16728343-Male,
pubmed-meshheading:16728343-Prostatic Neoplasms,
pubmed-meshheading:16728343-Rats,
pubmed-meshheading:16728343-Reverse Transcriptase Polymerase Chain Reaction
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pubmed:articleTitle |
Increasing expression of GST-pi MIF, and ID1 genes in chemoresistant prostate cancer cells.
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pubmed:affiliation |
Uro-Oncology Laboratory, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China. yuds@ms21.hinet.net
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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