Activation of P27kip1-cyclin D1/E-CDK2 pathway by polysaccharide from Phellinus linteus leads to S-phase arrest in HT-29 cells
文献类型: 外文期刊
作者: Zhong, Shi 1 ; Ji, Dong-Feng 1 ; Li, You-Gui 1 ; Lin, Tian-Bao 1 ; Lv, Zhi-Qiang 1 ; Chen, Hua-Ping 2 ;
作者机构: 1.Zhejiang Acad Agr Sci, Sericultural Res Inst, Hangzhou 310021, Zhejiang, Peoples R China
2.Hangzhou Qing Zheng Biol Sci Technol Co, Hangzhou 311700, Zhejiang, Peoples R China
关键词: Cyclins/CDK complexes;P27kip1;Polysaccharide;S-phase arrest
期刊名称:CHEMICO-BIOLOGICAL INTERACTIONS ( 影响因子:5.192; 五年影响因子:4.61 )
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收录情况: SCI
摘要: Our previous study showed that polysaccharide (P1) from Phellinus linteus exhibits a significant inhibitive activity on human colorectal carcinoma cells (HT-29). However its novel molecular mechanism remains unknown. To obtain insights into P1's mechanism of action, we examined its effects on cell proliferation in vitro and in vivo, cell cycle distribution, apoptosis, autophagy, and expression of several cell cycle interrelated proteins in HT-29 cells. Interestingly, we found that volume and weight of the solid tumor significantly decreased in P1 (200 mg/kg)-treated mice compared with the control. However, slightly increased the body weight of the P1 treated tumor-bearing mice, with no significant increased ALT, AST levels in serum and LPO concentration in liver and kidney indicated that P1 has no toxicity to mammals at a dose of 200 mg/kg. Furthermore, P1 caused a significantly dose-dependent increase in the S-phase cell cycle, but no apoptosis and autophagy in HT-29 cells. RT-PCR and Western blot results showed significantly down-regulated expressions of cyclin D1, cyclin E, and CDK2, as well as increased expressions of P27kip1 in P1 (100 μg/mL)-treated HT-29 cells. These results suggested that the activation of P27kip1-cyclin D1/E-CDK2 pathway is involved in P1-induced S-phase cell cycle arrest in HT-29 cells.
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