Source:http://linkedlifedata.com/resource/pubmed/id/11255259
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007585,
umls-concept:C0014597,
umls-concept:C0017262,
umls-concept:C0025723,
umls-concept:C0038317,
umls-concept:C0185117,
umls-concept:C0205282,
umls-concept:C0205307,
umls-concept:C0812260,
umls-concept:C0851285,
umls-concept:C1335075,
umls-concept:C1522384,
umls-concept:C1522721,
umls-concept:C1548328,
umls-concept:C1553412,
umls-concept:C2911684
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pubmed:issue |
1
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pubmed:dateCreated |
2001-3-20
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pubmed:abstractText |
RET fused gene (RFG)/ELE1alpha/androgen receptor-associated protein 70(ARA70) was first found to be involved in the activation of the RET proto-oncogene in thyroid neoplasm and has recently been shown to be a ligand-dependent transcriptional coregulator for androgen receptor (AR). The functionality of RFG/ELE1alpha/ARA70 remains controversial, and little is known about factors regulating its expression in the prostate. Of significant interest is whether this molecule is involved in prostate carcinogenesis. Using reverse transcriptase-polymerase chain reaction semiquantitation, we compared RFG/ELE1alpha/ARA70 mRNA levels in four prostate cancer cell lines (LNCaP, TSU-Pr1, DU-145, and PC-3) with those found in primary cultures of normal prostatic epithelial cells (PrECs). In addition, we examined the effects of androgen and antiandrogen, estrogen and antiestrogen, and a demethylating agent on RFG/ELE1alpha/ARA70 mRNA expression levels in AR- and AR+ PC-3 cells. Reduced levels of RFG/ELE1alpha/ARA70 message were observed in all four prostate cancer cell lines when compared with normal PrECs in primary cultures. RFG/ELE1alpha/ARA70 mRNA levels in PC-3 cells, which express both estrogen receptor subtypes, were upregulated by 17beta-estradiol and inhibited by the antiestrogen ICI-182780. In PC-3(AR+) cells, which were genetically engineered to express AR, exposure to androgen upregulated RFG/ELE1alpha/ARA70 mRNA expression, whereas treatment with 4-hydroxyflutamide lowered expression of this transcript. Furthermore, treatment of DU-145 cells, which did not express RFG/ELE1alpha/ARA70 transcripts, with a demethylating agent reactivated transcription of this gene. Polymerase chain reaction analyses of monochromosomal human-rodent hybrid panels localized a putative RFG/ELE1alpha/ARA70 isoform on human chromosome 5q31.1-31.2. In summary, we identified sex hormones and DNA hypermethylation as regulators of RFG/ELE1alpha/ARA70 expression in prostate cancer cells. In addition, we found reduced levels of RFG/ELE1alpha/ARA70 expression in prostate cancer cell lines when compared with expression levels in normal PrECs in culture. These findings suggest that RFG/ELE1alpha/ARA70 may be involved prostate carcinogenesis and that it may serve as a key mediator of estrogen-androgen synergism.
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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:month |
Jan
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pubmed:issn |
0899-1987
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-13
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11255259-Androgens,
pubmed-meshheading:11255259-Base Sequence,
pubmed-meshheading:11255259-Chromosome Mapping,
pubmed-meshheading:11255259-Chromosomes, Human, Pair 5,
pubmed-meshheading:11255259-DNA Methylation,
pubmed-meshheading:11255259-DNA Primers,
pubmed-meshheading:11255259-Epithelial Cells,
pubmed-meshheading:11255259-Estrogens,
pubmed-meshheading:11255259-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:11255259-Humans,
pubmed-meshheading:11255259-Male,
pubmed-meshheading:11255259-Prostate,
pubmed-meshheading:11255259-Prostatic Neoplasms,
pubmed-meshheading:11255259-Recombinant Fusion Proteins,
pubmed-meshheading:11255259-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:11255259-Tumor Cells, Cultured
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pubmed:year |
2001
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pubmed:articleTitle |
Expression of RFG/ELE1alpha/ARA70 in normal and malignant prostatic epithelial cell cultures and lines: regulation by methylation and sex steroids.
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pubmed:affiliation |
Division of Urology, Department of Surgery, University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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