1. Academic Validation
  2. Brusatol Inhibits Proliferation and Metastasis of Colorectal Cancer by Targeting and Reversing the RhoA/ROCK1 Pathway

Brusatol Inhibits Proliferation and Metastasis of Colorectal Cancer by Targeting and Reversing the RhoA/ROCK1 Pathway

  • Biomed Res Int. 2022 May 18;2022:7132159. doi: 10.1155/2022/7132159.
Rui-Jin Lu 1 Guo-Zhi Zhao 2 Rong Jiang 1 Shuang He 1 Hang Xu 3 Jia-Ming He 1 Yue Sun 1 Meng-Na Wu 3 Jian-Hua Ran 3 Di-Long Chen 4 Jing Li 1
Affiliations

Affiliations

  • 1 Lab of Stem Cell and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing, China.
  • 2 Department of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • 3 Neuroscience Research Center, College of Basic Medicine, Chongqing Medical University, Chongqing, China.
  • 4 Chongqing Key Laboratory of Development and Utilization of Genuine Medicinal Materials in Three Gorges Reservoir Area, Chongqing, China.
Abstract

Brusatol (BRU) is an important compound extracted from Brucea javanica oil, whose pharmacological effects are able to induce a series of biological effects, including inhibition of tumor cell growth, anti-inflammatory, Antiviral, and antitumor. Currently, there are so few studies about the brusatol effects on colorectal Cancer that its Anticancer mechanism has not been clearly defined. In this study, we made an in-depth investigation into the brusatol effect towards the proliferation and metastasis of colon Cancer and the possible mechanism. The inhibitory effect of BRU on the proliferation of colorectal Cancer cells was unveiled via CCK-8 method and colony formation assay, while the inhibitory effect of BRU on migration and invasion of colorectal Cancer cells was revealed by scratch assay and transwell assay. In addition, Western blot results also revealed that BRU inhibited not only the expressions of RhoA and ROCK1 but also the protein expressions of EMT-related markers e-cadherin, N-Cadherin, Vimentin, MMP2, and MMP9 in colon Cancer cells. Through the xenotransplantation model, our in vivo experiment further verified the antitumor effect of BRU on colon Cancer cells in vitro, and the results were consistent with the protein expression trend. In conclusion, BRU may inhibit the proliferation and metastasis of colorectal Cancer by influencing EMT through RhoA/ROCK1 pathway.

Figures
Products