دورية أكاديمية

Huang Qi Huai Granules Induce Apoptosis in Acute Lymphoblastic Leukemia Cells through the Akt/FoxO1 Pathway

التفاصيل البيبلوغرافية
العنوان: Huang Qi Huai Granules Induce Apoptosis in Acute Lymphoblastic Leukemia Cells through the Akt/FoxO1 Pathway
المؤلفون: Juan Han, Ming Lin, Dongfeng Zhou, Zhiquan Zhang, Runming Jin, Fen Zhou
المصدر: Cellular Physiology and Biochemistry, Vol 38, Iss 5, Pp 1803-1814 (2016)
بيانات النشر: Cell Physiol Biochem Press GmbH & Co KG, 2016.
سنة النشر: 2016
المجموعة: LCC:Physiology
LCC:Biochemistry
مصطلحات موضوعية: Huang Qi Huai granules, Leukemia, Apoptosis, Akt/FoxO1, Physiology, QP1-981, Biochemistry, QD415-436
الوصف: Background/Aims: In recent years, a traditional Chinese medicine named Huang Qi Huai (HQH) has been frequently used in China for solid tumor therapy. However, the role of HQH on leukemia cells and its underlying mechanisms have not been elucidated. In this study, we investigated the effect of HQH on the proliferation and apoptosis of acute lymphoblastic leukemia (ALL) cell lines. Methods: Sup-B15 and Nalm-6 cells were treated with gradient doses of HQH for 24, 48 or 72 h. Cell viability was measured using a CCK8 assay and cell cycle distribution and apoptosis levels were analyzed using flow cytometry. Western blotting was used to assess the levels of proteins associated with the apoptotic pathway. Results: The results revealed that cell survival decreased significantly with increasing concentrations of HQH. HQH induced G2 cell-cycle arrest and cell apoptosis in a dose-dependent manner. HQH inhibited phosphorylated-Akt, phosphorylated- FoxO1 and Bcl2 expression and upregulated Bim, cleaved-caspase-3 and Bax expression in a dose-dependent manner, which suggests that HQH induces the apoptosis of ALL cells via the Akt/FoxO1 pathway. Conclusion: HQH is a potential complementary agent for the treatment of acute lymphoblastic leukemia.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1015-8987
1421-9778
Relation: http://www.karger.com/Article/FullText/443119; https://doaj.org/toc/1015-8987; https://doaj.org/toc/1421-9778
DOI: 10.1159/000443119
URL الوصول: https://doaj.org/article/4451b887b3434184a4470a959229a2a6
رقم الأكسشن: edsdoj.4451b887b3434184a4470a959229a2a6
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10158987
14219778
DOI:10.1159/000443119