Extract from Butea monosperma inhibits β-catenin/Tcf signaling in SW480 human colon cancer cells.

The colorectal cancer (CRC) is the fourth leading cause of cancer death in worldwide. It has been found
that> 90% of CRC is caused by aberrant activation of canonical Wnt/β-catenin signaling pathway. Continuous
activation of this pathway believes to be an initiating event in colorectal carcinogenesis. There are growing
evidences suggest that traditional herbal plant medicines are being raised as a complementary alternative
treatment for cancer. In this series, Butea (B) monosperma has been illustrated as a valuable traditional medicinal
plant with> 45 medicinal traits. Therefore, by targets this pathway using n-butanol fraction of B. monosperma
flower extract (NBF-BMFE) could be a better therapeutic strategy for treating CRC. In this present study, we
evaluate the inhibitory effect of NBF-BMFE against over activated Wnt signaling mediated colon cancer cells
(SW480). Interestingly, the in vitro finding described that the NBF-BMFE had good antiproliferative effect against
SW480 human colon cancer cells. Moreover, it showed significant level of down regulated expression in Wnt
signaling proteins such as β-catenin, adenomatous polyposis coli (APC), glycogen synthase kinase 3β (GSK-3β),
cyclin D1 and c-myc in time-dependent manner. Further, the in silico results of NBF-BMFE derived compounds
have shown good binding interaction with target sites of β-catenin, APC and GSK-3β protein. In conclusion, NBFBMFE
may be used as an effective inhibitor for Wnt signaling targeted combined chemotherapeutic agents
against CRC.