Stigmasterol exhibits potent antitumor effects in human gastric cancer cells mediated via inhibition of cell migration, cell cycle arrest, mitochondrial mediated apoptosis and inhibition of JAK/STAT signalling pathway.

Abstract

The results showed that stigmasterol inhibited the growth of gastric cancer cells as observed by MTT and colony formation assay. The antiproliferative effects were due to induction of mitochondrial-mediated apoptosis as indicated by DAPI and annexin V/PI staining. This was further confirmed by Bax and Bcl-2 expression. Stigmasterol also inhibited cancer cell migration and induced G2/M cell cycle arrest in a dose-dependent manner. Furthermore, stigmasterol could also inhibit the JAK/STAT signalling pathway. Coclusion: The results of this study indicate that stigmasterol could prove beneficial in the treatment of gastric cancer and therefore further in vivo studies are required to confirm its efficacy within biosystems.