مورد إلكتروني

Chelidonine and Homochelidonine Induce Cell Death through Cell Cycle Checkpoints and MAP Kinase Pathways

التفاصيل البيبلوغرافية
العنوان: Chelidonine and Homochelidonine Induce Cell Death through Cell Cycle Checkpoints and MAP Kinase Pathways
عناروين إضافية: Chelidonin a Homochelidonin indukují buněčnou smrt prostřednictvím drah checkpoint a MAP kináz
المؤلفون: Havelek, Radim, Seifrtova, Martina, Královec, Karel, Habartova, Klara, Cahlikova, Lucie, Rezacova, Martina
بيانات النشر: 2018-02-27T03:39:10Z 2018-02-27T03:39:10Z 2017
نوع الوثيقة: Electronic Resource
مستخلص: This study focuses on the comparative in vitro cytotoxicity of chelidonine and homochelidonine on human cancer and non-cancer cells. Both alkaloids produced a decrease in cellular growth in a dose-dependent manner exhibiting greater potency in cancer cells. The growth inhibitory effect was evidenced in both ovarian carcinoma A2780 and lung fibroblast MRC-5 cells by inducing G2 and mitotic phase cell cycle arrest. Results indicated that the extent of apoptosis induced by chelidonine and homochelidonine was correlated to sensitivity to the antiproliferative activity of the evaluated compounds. Western blotting suggested that the cellular toxicological mechanism of chelidonine is related to the differential upregulation of phospho-Chk2, p21(Cip1/Waf1), phospho-ERK1/2 and phospho-p38 in various cell types, leading to alternations in the suppression of proliferation and either induction or prevention of apoptosis. Chelidonine showed the more potent effects and also affected the cell cycle checkpoints and MAPK signaling pathways within cells.
Tato práce je zaměřena na srovnávací cytotoxicitu chelidoninu a homochelidoninu na lidských nádorových a nenádorových buňkách.
مصطلحات الفهرس: Chelidonine, Homochelidonine, In vitro, Antiproliferative activity, Mitogen-activated protein kinases, Chelidonin, Homochelidonin, Antiproliferační aktivita, Mitogenem aktivovaná proteinkináza, article
URL: https://hdl.handle.net/10195/70273
Natural Product Communications, volume 12, issue: 9
الإتاحة: Open access content. Open access content
Práce není přístupná
ملاحظة: p. 1419-1430
application/pdf
English
أرقام أخرى: CZPAR oai:dk.upce.cz:10195/70273
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2-s2.0-85030688926
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1100076031
المصدر المساهم: UNIV LIBR OF THE UNIV OF PARDUBICE
From OAIster®, provided by the OCLC Cooperative.
رقم الأكسشن: edsoai.on1100076031
قاعدة البيانات: OAIster