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Mechanisms of hela cell apoptosis induced by abnormal Savda Munziq total phenolics combined with chemotherapeutic agents.
Zhang, Yun-Xia; Abliz, Guzalnur; Ye, Wei-Jun; Mutalipu, Zuohelaguli; Li, Xiao-Wen; Wang, Hai-Qin; Buranjiang, Gulimire; Upur, Halmurat.
Afiliación
  • Zhang YX; The 6th Department of Gynecology, the Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi, China E-mail : guzalnurabliz@163.com.
Asian Pac J Cancer Prev ; 15(2): 743-7, 2014.
Article en En | MEDLINE | ID: mdl-24568489
ABSTRACT

OBJECTIVE:

To investigate the effects of abnormal Savda Munziq (ASMq) total phenolics combined with cisplatin and docetaxel on the Hela cell growth.

METHODS:

In vivo cultured Hela cells were treated with cisplatin, docetaxel, total phenolics, cisplatin+total phenolics or docetaxel+total phenolics. MTT was performed to assess inhibition of cell proliferation, flow cytometry to detect apoptosis, and semi-quantitative RT-PCR to test for survivin and Bcl-2 expression.

RESULTS:

The total phenolics, cisplatin and docetaxel had significant inhibitory and apoptosis-promoting effects on Hela cells (P<0.05), with the early apoptotic rates of 12.8±0.70%, 18.9±3.79% and 15.8±3.8)%; the total phenolics, cisplatin and docetaxel significantly decreased the expression of Bcl-2 and survivin (all P<0.01), especially when used in combination.

CONCLUSION:

ASMq total phenolics, combined with cisplatin and docetaxel, could promote the apoptosis of Hela cells possibly through reducing the expression of Bcl-2 and survivin.
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Bases de datos: MEDLINE Asunto principal: Fenoles / Plantas Medicinales / Protocolos de Quimioterapia Combinada Antineoplásica / Apoptosis / Proliferación Celular Límite: Humans Idioma: En Revista: Asian Pac J Cancer Prev Asunto de la revista: NEOPLASIAS Año: 2014 Tipo del documento: Article
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Bases de datos: MEDLINE Asunto principal: Fenoles / Plantas Medicinales / Protocolos de Quimioterapia Combinada Antineoplásica / Apoptosis / Proliferación Celular Límite: Humans Idioma: En Revista: Asian Pac J Cancer Prev Asunto de la revista: NEOPLASIAS Año: 2014 Tipo del documento: Article