BMP9 mediates the anticancer activity of evodiamine through HIF‑1α/p53 in human colon cancer cells.

Colon cancer is one of the most common malignancies. Although there has been great development in treatment regimens over the last few decades, its prognosis remains poor. There is still a clinical need to find new drugs for colon cancer. Evodiamine (Evo) is a quinolone alkaloid extracted from the traditional herbal medicine plant Evodia rutaecarpa. In the present study, CCK8, flow cytometry, reverse transcription quantitative polymerase chain reaction, western blot analysis and a xenograft tumor model were used to evaluate the anticancer activity of Evo in human colon cancer cells and determine the possible mechanism underlying this process. It was revealed that Evo exhibited prominent antiproliferation and apoptosisinducing effects in HCT116 cells. Bone morphogenetic protein 9 (BMP9) was notably upregulated by Evo in HCT116 cells. Exogenous BMP9 potentiated the anticancer activity of Evo, and BMP9 silencing reduced this effect. In addition, HIF1alpha was also upregulated by Evo. The anticancer activity of Evo was enhanced by HIF1alpha, but was reduced by HIF1alpha silencing. BMP9 potentiated the effect of Evo on the upregulation of HIF1alpha, and enhanced the antitumor effect of Evo in colon cancer, which was clearly reduced by HIF1alpha silencing. In HCT116 cells, Evo increased the phosphorylation of p53, which was enhanced by BMP9 but reduced by BMP9 silencing. Furthermore, the effect of Evo on p53 was potentiated by HIF1alpha and reduced by HIF1alpha silencing. The present findings therefore strongly indicated that the anticancer activity of Evo may be partly mediated by BMP9 upregulation, which can activate p53 through upregulation of HIF1alpha, at least in human colon cancer.