pubmed-article:16469805 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C0033578 | lld:lifeskim |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C0037657 | lld:lifeskim |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C0598934 | lld:lifeskim |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C1167622 | lld:lifeskim |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C0599946 | lld:lifeskim |
pubmed-article:16469805 | lifeskim:mentions | umls-concept:C0441712 | lld:lifeskim |
pubmed-article:16469805 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:16469805 | pubmed:dateCreated | 2006-4-17 | lld:pubmed |
pubmed-article:16469805 | pubmed:abstractText | IGF binding protein (IGFBP)-3 inhibits cell growth and promotes apoptosis by sequestering free IGFs. In addition IGFBP-3 has IGF-independent, proapoptotic, antiproliferative effects on prostate cancer cells in vitro. Expression of the large T-antigen (Tag) under the long probasin promoter (LPB) in LPB-Tag mice results in prostate tumorigenesis. To investigate the IGF-dependent and IGF-independent effects of IGFBP-3 on prostate tumor growth, we crossed LPB-Tag mice with cytomegalovirus (CMVBP-3) and phosphoglycerate kinase (PGKBP-3) mice that overexpress IGFBP-3 under the cytomegalovirus promoter and the phosphoglycerate kinase promoter, respectively, and also I56G/L80G/L81G-mutant IGFBP-3 (PGKmBP-3) mice that express I56G/L80G/L81G-IGFBP-3, a mutant, that does not bind IGF-I but retains IGF-independent proapoptotic effects in vitro. Prostate tumor size and the steady-state level of p53 were attenuated in LPB-Tag/CMVBP-3 and LPB-Tag/PGKBP-3 mice, compared with LPB-Tag/wild-type (Wt) mice. A more marked effect was observed in LPB-Tag/CMVBP-3, compared with LPB-Tag/PGKBP-3, reflecting increased levels of transgene expression in CMVBP-3 prostate tissue. No attenuation of tumor growth was observed in LPB-Tag/PGKmBP-3 mice during the early tumor development, indicating that the inhibitory effects of IGFBP-3 were most likely IGF dependent during the initiation of tumorigenesis. At 15 wk of age, epidermal growth factor receptor expression was increased in LPB-Tag/Wt and LPB-Tag/PGKmBP-3 tissue, compared with LPB-Tag/PGKBP-3. IGF receptor was increased in all transgenic mice, but pAkt expression, a marker of downstream IGF-I action, was increased only in LPB-Tag/Wt and LPB-Tag/PGKmBP-3. After 15 wk of age, a marked reduction in tumor growth was apparent in LPB-Tag/PGKmBP-3 mice, indicating that the IGF-independent effects of IGFBP-3 may be important in inhibiting tumor progression. | lld:pubmed |
pubmed-article:16469805 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:language | eng | lld:pubmed |
pubmed-article:16469805 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16469805 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16469805 | pubmed:month | May | lld:pubmed |
pubmed-article:16469805 | pubmed:issn | 0013-7227 | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:GuiYaotingY | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:MurphyLiam... | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:SilhaJosef... | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:DoddJanice... | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:MishraSureshS | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:SheppardPatri... | lld:pubmed |
pubmed-article:16469805 | pubmed:author | pubmed-author:SchwartzJacqu... | lld:pubmed |
pubmed-article:16469805 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16469805 | pubmed:volume | 147 | lld:pubmed |
pubmed-article:16469805 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16469805 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16469805 | pubmed:pagination | 2112-21 | lld:pubmed |
pubmed-article:16469805 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:16469805 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16469805 | pubmed:articleTitle | Insulin-like growth factor (IGF) binding protein-3 attenuates prostate tumor growth by IGF-dependent and IGF-independent mechanisms. | lld:pubmed |
pubmed-article:16469805 | pubmed:affiliation | Department of Physiology, University of Manitoba, Winnipeg, Canada. | lld:pubmed |
pubmed-article:16469805 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16469805 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:16469805 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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