مورد إلكتروني
Comparative cytotoxicity of chelidonine and homochelidonine, the dimethoxy analogues isolated from Chelidonium majus L. (Papaveraceae), against human leukemic and lung carcinoma cells
| العنوان: | Comparative cytotoxicity of chelidonine and homochelidonine, the dimethoxy analogues isolated from Chelidonium majus L. (Papaveraceae), against human leukemic and lung carcinoma cells |
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| عناروين إضافية: | Porovnání cytotoxicity chelidoninu a homochelidoninu, dimethoxy analoga izolovaného z Chelidonium majus L. (Papaveraceae), vůči lidským leukemickým a plicním nádorovým buňkám |
| بيانات النشر: | Elsevier GmbH 2017-05-11T11:07:43Z 2017-05-11T11:07:43Z 2016 |
| تفاصيل مُضافة: | Havelek, Radim Seifrtova, Martina Královec, Karel Kročová, Eliška Tejkalová, Veronika Novotny, Ivan Cahlikova, Lucie Safratova, Marcela Opletal, Lubomir Bílková, Zuzana Vavrova, Jirina Rezacova, Martina |
| نوع الوثيقة: | Electronic Resource |
| مستخلص: | In this study the effects of naturally occurring homochelidonine in comparison to chelidonine on cell cycle progression and cell death in leukemic T-cells with different p53 status are described. We found that homochelidonine and chelidonine displayed significant cytotoxicity in examined blood cancer cells with the exception of HEL 92.1.7 and U-937 exposed to homochelidonine. Unexpectedly, homochelidonine and chelidonine-induced cytotoxicity was more pronounced in Jurkat cells contrary to MOLT-4 cells. Homochelidonine showed an antiproliferative effect on A549 cells but it was less effective compared to chelidonine. Biphasic dose-depended G1 and G2/M cell cycle arrest along with the population of sub-G1 was found after treatment with homochelidonine in MOLT-4 cells. In variance thereto, an increase in G2/M cells was detected after treatment with homochelidonine in Jurkat cells. Treatment with chelidonine induced cell cycle arrest in the G2/M cell cycle in both MOLT-4 and Jurkat cells. MOLT-4 and Jurkat cells treated with homochelidonine and chelidonine showed features of apoptosis such as phosphatidylserine exposure, a loss of mitochondrial membrane potential and an increase in the caspases -3/7, -8 and -9. Western blots indicate that homochelidonine and chelidonine exposure activates Chk1 and Chk2. Studies conducted with fluorescence microscopy demonstrated that chelidonine and homochelidonine inhibit tubulin polymerization in A549 cells. Collectively, the data indicate that chelidonine and homochelidonine are potent inducers of cell death in cancer cell lines, highlighting their potential relevance in leukemic cells. Tato práce porovnává cytotoxicitu chelidoninu a homochelidoninu vůči lidským leukemickým a plicním nádorovým buňkám. Výsledky studie naznačují, že chelidonin a homochelidonin jsou účinnými aktivátory apoptózy u nádorových buněčných linií. |
| مصطلحات الفهرس: | Homochelidonine, Apoptosis, Biphasic cell cycle arrest, Mitotic block, Homochelidonin, Apoptóza, Bifázická zástava buněčného cyklu, Mitotický blok, article |
| URL: | Phytomedicine, volume 23, issue: 3 |
| الإتاحة: | Open access content. Open access content práce není přístupná |
| ملاحظة: | p. 253-266 application/pdf English |
| أرقام أخرى: | CZPAR oai:dk.upce.cz:10195/67557 0944-7113 10.1016/j.phymed.2016.01.001 000371781500003 2-s2.0-84977621316 39877075 1100077474 |
| المصدر المساهم: | UNIV LIBR OF THE UNIV OF PARDUBICE From OAIster®, provided by the OCLC Cooperative. |
| رقم الأكسشن: | edsoai.on1100077474 |
| قاعدة البيانات: | OAIster |
| الوصف غير متاح. |