Source:http://linkedlifedata.com/resource/pubmed/id/19020727
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2008-11-21
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pubmed:abstractText |
Several lines of evidence support an important role of TGF-beta in the development of colorectal cancer, although the molecular consequences are largely unknown. Soluble transforming growth factor-beta receptor type II (sTbetaRII) is a target of transforming growth factors-beta (TGF-beta) that plays an important role in regulation tumorigenesis, angiogenesis and metastasis of cancer. To elucidate whether overexpression of sTbetaRII could antagonize TGF-beta in colon cancer cells, we constructed a plasmid that contains a cDNA encoding human extracellular region of TbetaRII and transfected this construction into LoVo cells. Surprisingly, in the absence of TGF-beta1, the overexpression of sTbetaRII antagonized TGF-beta-induced cell proliferation, invasion, motility and angiogenesis, and decreased expression of VEGF and MMP-9. Also, sTbetaRII inhibited TGF-beta-induced apoptosis and improved the induction of antitumor immunity. Our data indicated that sTbetaRII attenuated the biological activities of TGF-beta, suggesting that sTbetaRII may have a therapeutic benefit in colorectal 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/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Transforming Growth...,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1,
http://linkedlifedata.com/resource/pubmed/chemical/transforming growth factor-beta...
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1021-335X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1449-56
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pubmed:meshHeading |
pubmed-meshheading:19020727-Antineoplastic Agents,
pubmed-meshheading:19020727-Apoptosis,
pubmed-meshheading:19020727-Cell Line, Tumor,
pubmed-meshheading:19020727-Cell Movement,
pubmed-meshheading:19020727-Cell Proliferation,
pubmed-meshheading:19020727-Colorectal Neoplasms,
pubmed-meshheading:19020727-DNA, Complementary,
pubmed-meshheading:19020727-Genetic Vectors,
pubmed-meshheading:19020727-Humans,
pubmed-meshheading:19020727-Leukocytes, Mononuclear,
pubmed-meshheading:19020727-Models, Biological,
pubmed-meshheading:19020727-Neoplasm Invasiveness,
pubmed-meshheading:19020727-Neovascularization, Pathologic,
pubmed-meshheading:19020727-Protein-Serine-Threonine Kinases,
pubmed-meshheading:19020727-Receptors, Transforming Growth Factor beta,
pubmed-meshheading:19020727-Transforming Growth Factor beta1
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pubmed:year |
2008
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pubmed:articleTitle |
Soluble transforming growth factor beta type II receptor attenuates TGF-beta1 activity in human colorectal cancer LoVo cells.
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pubmed:affiliation |
Department of Oncology, Zhongnan Hospital, Hubei Key Laboratory of Tumor Biological Behaviors, Hubei Cancer Clinical Study Center, Wuhan 430071, P.R. China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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