Show simple item record

dc.contributor.authorBao, Le Tri
dc.date.accessioned2014-12-05T06:50:16Z
dc.date.accessioned2018-05-30T02:42:25Z
dc.date.available2014-12-05T06:50:16Z
dc.date.available2018-05-30T02:42:25Z
dc.date.issued2014
dc.identifier.urihttp://10.8.20.7:8080/xmlui/handle/123456789/1221
dc.description.abstractHepatocellular carcinoma (HCC), one of the most common cancers worldwide, is a highly vascularized tumor that requires formation of numerous blood vessels to receive sufficient blood for developing. Consequently, angiogenesis-the process through which new blood vessels are formed-plays a very important role in tumor progression. The purpose of this study is to suppress the vascular endothelial growth factor (VEGF), a key stimulating factor in angiogenesis, using specific small-interfering RNA (siRNA), and investigate its effect on HCC cell proliferation in vitro. The Hep3B cells were cultured and transfected with siRNA targeting VEGF (VEGF-siRNA) using Lipofectamine RNAiMAX kit. Then, VEGF mRNA and protein levels, as well as cell proliferation were analyzed. The results showed that the VEGF mRNA and protein levels of Hep3B cells were significantly decreased after treatment with VEGF-siRNA, leading to the reduction of cell proliferation rate. Hence, downregulation of VEGF using specific siRNA yields promising results for inhibition of cell proliferation in human HCC cells. Keywords: Cancer Hepatocellular carcinoma (HCC) Vascular endothelial growth factor (VEGF) Small interfering RNA (siRNA)en_US
dc.description.sponsorshipDr. Do Minh Sien_US
dc.language.isoen_USen_US
dc.publisherInternational University HCMC, Vietnamen_US
dc.relation.ispartofseries;22001728
dc.subjectCell proliferationen_US
dc.titleDownregulation of VEGF inhibits cell proliferation in human hepatocellular carcinoma (Hep3B) cellsen_US
dc.typeThesisen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record