4.2 Article

Anti-Tumor Effects of Paeoniflorin on Epithelial-To-Mesenchymal Transition in Human Colorectal Cancer Cells

期刊

MEDICAL SCIENCE MONITOR
卷 24, 期 -, 页码 6405-6413

出版社

INT SCIENTIFIC LITERATURE, INC
DOI: 10.12659/MSM.912227

关键词

Colorectal Neoplasms; Epithelial-Mesenchymal Transition; Medicine, Chinese Traditional; Neoplasm Metastasis

资金

  1. Three-Year Action Plan for the Development of Traditional Chinese Medicine (TCM) in Shanghai [ZY3-CCCX-3-3036]
  2. TCM Superiority Disease Species Breeding Program [Zybz-2017027]
  3. Shanghai Science and Technology Commission Project [2014JP009A]
  4. National Science Foundation of China [81472675]

向作者/读者索取更多资源

Background: Colorectal cancer is one of the leading causes of death in China, and the development of effective drugs is urgently needed. Here, we report on Paeoniflorin (PF), a product isolated from the roots of the peony plant, as a possible candidate because of its anti-tumor effects on epithelial-to-mesenchymal transition (EMT) of PF in human colorectal cancer (CRC). Material/Methods: Cell proliferation, wound healing, and Transwell assays were used to analyze the effects of PF on in vitro cell migration and invasion of HCT116 and SW480, 2 colorectal cancer cell lines. The tumor xenograft model was used to verify the anti-metastasis effects of PF in vivo. The RNA and protein levels of epithelia-cadherin (E-cadherin), Vimentin, and histone deacetylase2 (HDAC2) were measured by qPCR and Western blot analysis to explore the mechanism involved. Results: Our results showed that PF inhibited colorectal cancer cell migration and invasion and suppressed the metastatic potential of the cancer cells in vivo. Moreover, PF significantly decreased the expression of HDAC2 and Vimentin, while increasing the expression of E-cadherin. Conclusions: These results suggest that PF inhibits colorectal cancer cell migration and invasion ability and reverses the EMT process, through inhibiting the expression of HDAC2, and then affects the expression level of E-cadherin and Vimentin at the cell level. Our results were also verified in the tumor xenograft model. This indicates that PF may be a candidate for colorectal cancer treatment.

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