4.7 Article

Exopolysaccharide from Trichoderma pseudokoningii induces the apoptosis of MCF-7 cells through an intrinsic mitochondrial pathway

期刊

CARBOHYDRATE POLYMERS
卷 136, 期 -, 页码 1065-1073

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2015.09.108

关键词

Trichoderma pseudokonngii; Exopolysaccharide; Human breast cancer; Apoptosis; Cell cycle arrest

资金

  1. National Basic Research Program of China [2012CB822102]
  2. National Natural Science Foundation of China [81370983, 81400864, 81500692]
  3. Foundation of National Key Scientific Instrument and Equipment Development Projects [2011YQ0301241403]
  4. Hunan Province Natural Science Key Fund Project [2014SK2003]
  5. Anhui Provincial Natural Science Foundation [1408085MH197, 1508085MH191]
  6. Key Program for the Excellent Young Talents in College of Anhui Province [2013SQRL054ZD]
  7. Natural Science Foundation of Education Department of Anhui Province [KJ2015A199]
  8. Scientific Research Project of Wannan Medical College [WK201517]

向作者/读者索取更多资源

In this study, we reported the anticancer efficacy of exopolysaccharide (EPS) derived from Trichoderma pseudokoningii, on human breast cancer MCF-7 cells. Our results showed that EPS inhibited the proliferation of MCF-7 cells and induced lactic dehydrogenase release by inducing apoptosis and cell arrest at S phase. Further study revealed that EPS-induced apoptosis of MCF-7 cells was associated with alteration of nuclear morphology, disruption of mitochondrial membrane potential and accumulation of intracellular reactive oxygen species. Sequentially, EPS increased the activation of caspase-9 and caspase-3 in a dose-dependent manner; however, caspase-8 remained intact. Western blot analysis revealed that EPS increased the ratio of Bax/Bcl-2 and promoted the release of cytochrome c into the cytoplasm. Taken together, these findings provided evidence that EPS induced the apoptosis of MCF-7 cells through an intrinsic mitochondrial apoptotic pathway and that EPS may therefore be considered as an effective adjuvant agent against human breast cancer. (C) 2015 Elsevier Ltd. All rights reserved.

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