Abstract |
In the present study, we demonstrate that ectopic expression of 56-kDa human selenium binding protein-1 ( hSP56) in PC-3 cells that do not normally express hSP56 results in a marked inhibition of cell growth in vitro and in vivo. Down-regulation of hSP56 in LNCaP cells that normally express hSP56 results in enhanced anchorage-independent growth. PC-3 cells expressing hSP56 exhibit a significant reduction of hypoxia inducible protein (HIF)-1α protein levels under hypoxic conditions without altering HIF-1α mRNA (HIF1A) levels. Taken together, our findings strongly suggest that hSP56 plays a critical role in prostate cells by mechanisms including negative regulation of HIF-1α, thus identifying hSP56 as a candidate anti-oncogene product.
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Authors | Jee-Yeong Jeong, Jin-Rong Zhou, Chong Gao, Laurie Feldman, Arthur J Sytkowski |
Journal | BMB reports
(BMB Rep)
Vol. 47
Issue 7
Pg. 411-6
(Jul 2014)
ISSN: 1976-670X [Electronic] Korea (South) |
PMID | 24874852
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Hypoxia-Inducible Factor 1, alpha Subunit
- RNA, Messenger
- SELENBP1 protein, human
- Selenium-Binding Proteins
- USP20 protein, human
- USP33 protein, human
- Ubiquitin Thiolesterase
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Topics |
- Animals
- COS Cells
- Cell Line, Tumor
- Cell Transformation, Neoplastic
- Chlorocebus aethiops
- Down-Regulation
- Humans
- Hypoxia-Inducible Factor 1, alpha Subunit
(antagonists & inhibitors, genetics, metabolism)
- Male
- Mice
- Mice, Inbred ICR
- Mice, SCID
- Prostatic Neoplasms
(metabolism, pathology)
- Protein Binding
- RNA Interference
- RNA, Messenger
(metabolism)
- Selenium-Binding Proteins
(metabolism)
- Transplantation, Heterologous
- Ubiquitin Thiolesterase
(metabolism)
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