Frontiers in Pharmacology (Apr 2017)

An Ethanolic Extract of Ampelopsis Radix Exerts Anti-colorectal Cancer Effects and Potently Inhibits STAT3 Signaling In Vitro

  • Zhi-Ling Yu,
  • Zhi-Ling Yu,
  • Zhi-Ling Yu,
  • Tao Su,
  • Tao Su,
  • Tao Su,
  • Jing-Xuan Bai,
  • Ying-Jie Chen,
  • Xin-Ning Wang,
  • Xiu-Qiong Fu,
  • Xiu-Qiong Fu,
  • Xiu-Qiong Fu,
  • Ting Li,
  • Ting Li,
  • Ting Li,
  • Hui Guo,
  • Hui Guo,
  • Hui Guo,
  • Pei-Li Zhu,
  • Pei-Li Zhu,
  • Pei-Li Zhu,
  • Yue Wang

DOI
https://doi.org/10.3389/fphar.2017.00227
Journal volume & issue
Vol. 8

Abstract

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Colorectal cancer (CRC) is a leading cause of cancer-related morbidity and mortality worldwide. Signal transducer and activator of transcription 3 (STAT3) signaling is constantly activated in CRC, and has been proposed as a pathogenic factor and a therapeutic target of CRC. Ampelopsis Radix (AR), a traditional Chinese medicinal herb, possesses low toxicity and has long been used clinically for the treatment of cancers including CRC. Some constituents of AR have been reported to exert anti-cancer properties by targeting STAT3. However, the anti-CRC mode and mechanism of action of AR have not been fully elucidated. Here, we investigated the involvement of STAT3 signaling in the anti-CRC effects of AR. Results showed that AR reduced cell viability, induced cell apoptosis, and suppressed cell migration and invasion in human HCT-116 and SW480 CRC cells. Mechanistic studies showed that AR potently suppressed STAT3 and Src phosphorylation, and inhibited STAT3 nuclear localization in cultured CRC cells. AR also downregulated the expression of STAT3 target genes Mcl-1, Bcl-xL, and MMP-2 that are involved in cell survival and mobility. Moreover, the cytotoxic effect of AR was diminished by overexpressing STAT3C, a persistent active variant of STAT3. In conclusion, AR exerted anti-CRC effects in vitro and these effects are at least in part attributed to the inhibition of STAT3 signaling. Our findings provide a molecular justification for the traditional use of AR in treating CRC, and a pharmacological basis for developing AR-derived modern anti-CRC agent(s).

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