نمایش مختصر رکورد

dc.date.accessioned1399-07-08T18:03:19Zfa_IR
dc.date.accessioned2020-09-29T18:03:19Z
dc.date.available1399-07-08T18:03:19Zfa_IR
dc.date.available2020-09-29T18:03:19Z
dc.date.issued2011-10-01en_US
dc.date.issued1390-07-09fa_IR
dc.identifier.citation(2011). The Antitumor Activity of Exogenous and Endogenous Canstatin on Colorectal Cancer Cells. Asian Pacific Journal of Cancer Prevention, 12(10), 2713-2716.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_25967.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/35211
dc.description.abstractColorectal cancer is the third most common malignancy and the third-leading cause of cancer-related deaths worldwide. In the last several years, recombinant DNA technology has made cancer gene therapy feasible in the clinic. In our studies, we used both exogenous and endogenous canstatin, a type IV collagen genetically distinct product. We detected the effects of canstatin on colorectal cancer cells HCT-15 and HCT-116. DAPI staining, FCM and migration analyse were used to detect the apoptotic cells, cell cycle and mobility. As shown in the results, the apoptotic cell numbers (p<0.05) and G1 arrest cell numbers (p<0.05) were higher than in the non-treatment case. The mobility of the cells was also decreased obviously (p<0.05). Simultaneously, combination effects of exogenous and endogenous canstatin were identified.en_US
dc.format.extent1439
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherWest Asia Organization for Cancer Prevention (WAOCP)en_US
dc.relation.ispartofAsian Pacific Journal of Cancer Preventionen_US
dc.subjectcolorectal canceren_US
dc.subjectcanstatinen_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.subjectMobilityen_US
dc.titleThe Antitumor Activity of Exogenous and Endogenous Canstatin on Colorectal Cancer Cellsen_US
dc.typeTexten_US
dc.citation.volume12
dc.citation.issue10
dc.citation.spage2713
dc.citation.epage2716


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