Schisandrin B induces apoptosis and cell cycle arrest of gallbladder cancer cells.

Schisandrin B induces apoptosis and cell cycle arrest of gallbladder cancer cells.
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DOI:
10.3390/molecules190913235
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发表时间:
2014-08-27
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
通讯作者:
Liu YB
Liu YB
中科院分区:
其他
文献类型:
--
作者:
Xiang SS;Wang XA;Li HF;Shu YJ;Bao RF;Zhang F;Cao Y;Ye YY;Weng H;Wu WG;Mu JS;Wu XS;Li ML;Hu YP;Jiang L;Tan ZJ;Lu W;Liu F;Liu YB

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Gallbladder cancer, with high aggressivity and extremely poor prognosis, is the most common malignancy of the bile duct. The main objective of the paper was to investigate the effects of schisandrin B (Sch B) on gallbladder cancer cells and identify the mechanisms underlying its potential anticancer effects. We showed that Sch B inhibited the viability and proliferation of human gallbladder cancer cells in a dose-, time -dependent manner through MTT and colony formation assays, and decrease mitochondrial membrane potential (ΔΨm) at a dose-dependent manner through flow cytometry. Flow cytometry assays also revealed G0/G1 phase arrest and apoptosis in GBC-SD and NOZ cells. Western blot analysis of Sch B-treated cells revealed the upregulation of Bax, cleaved caspase-9, cleaved caspase-3, cleaved PARP and downregulation of Bcl-2, NF-κB, cyclin D1 and CDK-4. Moreover, this drug also inhibited the tumor growth in nude mice carrying subcutaneous NOZ tumor xenografts. These data demonstrated that Sch B induced apoptosis in gallbladder cancer cells by regulating apoptosis-related protein expression, and suggests that Sch B may be a promising drug for the treatment of gallbladder cancer.
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