Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/17104
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dc.contributor.authorWang, Wei-
dc.contributor.authorLi, Tan-
dc.contributor.authorHan, Guang-
dc.contributor.authorLi, Ying-
dc.contributor.authorShi, Li-hua-
dc.contributor.authorLi, Hui-
dc.date.accessioned2013-04-18T07:36:26Z-
dc.date.available2013-04-18T07:36:26Z-
dc.date.issued2013-04-
dc.identifier.issn0975-0959 (Online); 0301-1208 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/17104-
dc.description87-92en_US
dc.description.abstractTo investigate the biological function of microRNA-34a (miR-34a) in bladder cancer, the expression of miR-34a was determined using quantitative real-time polymerase chain (qRT-PCR) reaction in 42 cases of bladder cancer. The relationship between the expression of miR-34a and development of bladder cancer was also studied. The mature mimics of miR-34a were chemically synthesized and transiently transfected into human bladder cancer T24 cells. The effects of miR-34a on apoptosis, cell cycle and proliferation in T24 cells were evaluated by flow cytometry and MTT, respectively. The results showed that the low expression rate of miR-34a was correlated with the malignancy and tumor size of bladder cancer. The up-regulation of miR-34a in T24 cells contributed to cell growth and cell cycle arrest, but not caspase-3 pathway. These findings suggest that the relative low expression of miRNA-34a might be involved in the tumorigenesis of bladder cancer. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBB Vol.50(2) [April 2013]en_US
dc.subjectMicroRNA-34aen_US
dc.subjectBladder canceren_US
dc.subjectPathological variablesen_US
dc.subjectProliferationen_US
dc.subjectApoptosisen_US
dc.titleExpression and role of miR-34a in bladder canceren_US
dc.typeArticleen_US
Appears in Collections:IJBB Vol.50(2) [April 2013]

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