نمایش مختصر رکورد

dc.date.accessioned1399-07-08T17:51:26Zfa_IR
dc.date.accessioned2020-09-29T17:51:26Z
dc.date.available1399-07-08T17:51:26Zfa_IR
dc.date.available2020-09-29T17:51:26Z
dc.date.issued2006-02-01en_US
dc.date.issued1384-11-12fa_IR
dc.identifier.citation(2006). Evaluation of Apoptosis-Induction by Newly Synthesized Phthalazine Derivatives in Breast Cancer Cell Lines. Asian Pacific Journal of Cancer Prevention, 7(2), 249-252.en_US
dc.identifier.issn1513-7368
dc.identifier.issn2476-762X
dc.identifier.urihttp://journal.waocp.org/article_24462.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/30725
dc.description.abstractNewly synthesized phthalazine derivatives including copper and platinum complexes were evaluated forcytotoxicity in human breast cancer cell lines. The cells were incubated with the compounds (100 μM) for 72 h andcytotoxicity, apoptosis and DNA content were measured by flow cytometery. Our results suggest that the parent (H1-2), copper (C1-2)- and platinum (P1-2)-derivatized compounds were relatively more active in inducing apoptosisand cell killing in both human breast cancer cell lines, MDA-MB-231 cells being the more sensitive. Other compoundsshowed weak or no response towards these parameters except H-5 causing 40% apoptosis in MDA-MB-231 cells.Addition of copper or platinum in the structures generally reduced the apoptotic potential. Possible roles for structure activity relationships are discussed.en_US
dc.format.extent73
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.subjectPhthalazineen_US
dc.subjectplatinum compoundsen_US
dc.subjecthuman breast carcinoma cellsen_US
dc.subjectMCF-7en_US
dc.subjectMDA-MB-231en_US
dc.titleEvaluation of Apoptosis-Induction by Newly Synthesized Phthalazine Derivatives in Breast Cancer Cell Linesen_US
dc.typeTexten_US
dc.citation.volume7
dc.citation.issue2
dc.citation.spage249
dc.citation.epage252


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