Author/Authors :
Saito، نويسنده , , Teruyoshi and Sato، نويسنده , , Hiromi and Virgona، نويسنده , , Nantiga and Hagiwara، نويسنده , , Hiromi and Kashiwagi، نويسنده , , Korehito and Suzuki، نويسنده , , Kazuyuki and Asano، نويسنده , , Ryuji and Yano، نويسنده , , Tomohiro، نويسنده ,
Abstract :
Bowman–Birk protease inhibitor (BBI) from soybean acts as a potential chemopreventive agent in several types of tumors. However, the mechanism is still unclear. The present study was undertaken to estimate a mechanism of BBI-dependent negative growth control of human osteosarcoma cell (U2OS cell). BBI had negative growth control of the cells via induction of connexin (Cx) 43, a tumor suppressor gene in U2OS cells. This negative growth control by BBI was abrogated under down-regulation of Cx43 induced by a Cx43 antisense nucleotide treatment. It was also found that the BBI-dependent induction of Cx43 was due to elevation of Cx43 mRNA and stabilization of Cx43 protein. Especially, BBI-dependent inhibition of chymotrypsin-like activity in proteasome contributed to stabilization of Cx43 protein. These results suggest that a major negative growth effect of BBI is based on the restoration of Cx43 expression in U2OS cells.
Keywords :
Bowman–Birk protease inhibitor , Osteosarcoma cell , Proteasome inhibition , Connexin 43 , Cancer prevention