| Literature DB >> 26732119 |
Yulin Zhang1, Jiaolin Bao1, Kai Wang1, Xuejing Jia1, Chao Zhang1, Borong Huang1, Meiwan Chen1, Jian-Bo Wan1, Huanxing Su1, Yitao Wang1, Chengwei He1.
Abstract
Pulsatilla saponin D (SB365), a saponin isolated from rhizoma of Pulsatilla chinensis (Bunge) Regel, exhibited anticancer activities in various cancer types. In the present study, we identified that SB365 was a potent inhibitor of autophagic flux in several cancer cell lines. SB365 induced a robust accumulation of autophagosomes as evidenced by monodansylaervarine (MDC) staining and increased protein levels of LC3-II. However, SB365 caused the accumulation of p62, a substrate that should be degraded through the autophagy-lysosomal pathway. These results indicated that SB365 was an inducer of autophagosome formation, but an inhibitor of autophagic flux. Interestingly, we found that SB365 synergistically enhanced the anticancer activity of chemotherapeutic agents against cervical cancer HeLa cells. Furthermore, our study demonstrated that SB365 increased the phosphorylation of ERK and inhibited the phosphorylation of mTOR and p70S6K, suggesting that their roles in the effects of SB365 on autophagy. These results suggest that SB365 could be a promising adjuvant anticancer agent.Entities:
Keywords: Anticancer; Autophagic Flux; HeLa Cells; Pulsatilla Saponin D
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Year: 2015 PMID: 26732119 DOI: 10.1142/S0192415X15500949
Source DB: PubMed Journal: Am J Chin Med ISSN: 0192-415X Impact factor: 4.667