| Literature DB >> 27079642 |
Hongyang Li1, Li Sun2, Evandro Lopes de Carvalho1, Xinxin Li3, Xiaodan Lv1, Ghulam Jilany Khan2, Herve Semukunzi1, Shengtao Yuan4, Sensen Lin5.
Abstract
Metabolic stress induces autophagy as a protective mechanism in tumorigenesis and development. Conversely, excessive autophagy in nutrient-deprived cancer cells would be beneficial for cancer therapy. DT-13, the saponin monomer 13 of the Dwarf lilyturf tuber, inhibited tumor metastasis and angiogenesis in previous studies. However, there is scarcity of data regarding the effect of DT-13 on autophagy process. Here, we demonstrated that DT-13 induced autophagy in human cancer cell lines and caused significant cell apoptosis under nutrient starvation. We firstly showed that DT-13 increased the accumulation of GFP-LC3 puncta and induced the expression of LC3-II in a dose- and time-dependent manner. DT-13 also upregulated the expression of Beclin-1, Atg-3 and Atg-7, and induced autophagic flux in human gastric cancer BGC-823 cells. We next found that low-toxic concentrations of DT-13 significantly induced apoptosis under nutrient deprivation. We finally demonstrated that the PI3K/Akt/mTOR signal pathway was involved in the cytotoxic effect of DT-13. Our data indicated that DT-13 was a novel autophagy inducer and might be considered in future treatment of cancer.Entities:
Keywords: Apoptosis; Autophagy; Bafilomycin A1 (PubChem CID: 6436223); Chloroquine (PubChem CID: 2719); DT-13; DT-13 (PubChem CID: 101514160); Nutrient deprivation; mTOR
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Year: 2016 PMID: 27079642 DOI: 10.1016/j.ejphar.2016.04.016
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432