4.4 Article

Antimetastatic Effects of Celastrus orbiculatus on Human Gastric Adenocarcinoma by Inhibiting Epithelial-Mesenchymal Transition and NF-κB/Snail Signaling Pathway

Journal

INTEGRATIVE CANCER THERAPIES
Volume 14, Issue 3, Pages 271-281

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/1534735415572880

Keywords

Celastrus orbiculatus; gastric cancer; epithelial-mesenchymal transition; antimetastasis; nuclear factor B

Funding

  1. National Natural Science Foundation of China [81450051, 81274141]
  2. Jiangsu Provincial Social Development Project [BE2011738]
  3. Natural Science Foundation of Jiangsu Province [BK20141280, BK2012686]
  4. Administration of Traditional Chinese Medicine of Jiangsu Province [LZ11210]
  5. Plans of Colleges and Universities in Jiangsu Province to Postgraduate Research and Innovation [CXLX13-927]

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Aim of the Study. Celastrus orbiculatus has been used as a folk medicine in China for the treatment of many diseases. In the laboratory, the ethyl acetate extract of Celastrus orbiculatus (COE) displays a wide range of anticancer functions. However, the inhibition of the metastasis mechanism of COE in gastric cancer cells has not been investigated so far. The present study was undertaken to determine if the antimetastatic effects of COE were involved in inhibition of the epithelial-mesenchymal transition (EMT) of human gastric adenocarcinoma SGC-7901 cells. Methods. The adhesion, invasion, and migration of SGC-7901 cells were determined by COE treatment in vitro, using Matrigel-coated plate, transwell membrane chamber, and wound healing models, respectively. In vivo, the growth-inhibiting and antimetastatic effects of COE on the nude mice model of gastric cancer were tested and the mechanisms were explored. The expression of EMT markers and nuclear factor B (NF-B)/Snail signaling pathway were evaluated by using western blotting and immunohistochemistry. Results. Treatment with COE dose-dependently inhibited the proliferation, adhesion, invasion, and migration of SGC-7901 cells in vitro, which was realized by enhancing the expression of E-cadherin and reducing N-cadherin and vimentin expression. Moreover, COE suppressed the activation of NF-B/Snail signaling pathway induced by tumor necrosis factor-. In addition, COE effectively suppressed tumor growth and metastasis in the nude mice model due to reduced expression of N-cadherin, vimentin, NF-B p65, and Snail and increased expression of E-cadherin in the tumor tissues. Conclusion. Our findings provided new evidence that COE is an effective inhibitor of metastatic potential of SGC-7901 cells through suppression of EMT and NF-B/Snail signal pathway. Based on these findings, COE may be considered a novel anticancer agent for the treatment of metastasis in gastric cancer.

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