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KMID : 1161420160190121155
Journal of Medicinal Food
2016 Volume.19 No. 12 p.1155 ~ p.1165
Cytotoxicity and Proteasome Inhibition by Alkaloid Extract from Murraya koenigii Leaves in Breast Cancer Cells-Molecular Docking Studies
Ismail Ayesha

Noolu Bindu
Gogulothu Ramesh
Perugu Shyam
Rajanna Ajumeera
Babu Suresh K.
Abstract
Murraya koenigii (curry tree) leaves are rich in bioactive compounds such as flavonoids, alkaloids, and coumarins. Alkaloids from M. koenigii leaves have antianalgesic, antiulcerogenic, antiobesity, and antitumor activities. In this study, we tested the cytotoxic and proteasome-inhibitory potential of a total alkaloid extract (TAE) from M. koenigii leaves in the breast cancer cell line MDA-MB-231. The TAE decreased cell viability with an IC50 of 14.4?¥ìg/mL and altered growth kinetics of breast cancer cells. TAE (32?¥ìg/mL) arrested cells (35%) in the ¡°S¡± phase of the cell cycle and induced apoptosis. The 26S proteasome, a multicatalytic protease complex, promotes tumor cell proliferation and protects tumor cells from apoptosis. The TAE and mahanine, a carbazole alkaloid present in M. koenigii leaves, preferentially inhibited the trypsin-like, but not the chymotrypsin-like proteolytic activity of the proteasome with an IC50 of 162?¥ìg/mL and 287?¥ìM, respectively. In silico analysis of 26 compounds from M. koenigii leaves revealed significant docking scores for mahanine and two other carbazole alkaloids with the ¥â2 and ¥â5 subunits of the catalytic 20S proteasome. Taken together, this study demonstrates that inhibition of the proteasome is an important biological activity of M. koenigii alkaloids, which may lead to cancer cell death.
KEYWORD
alkaloids, breast cancer, Murraya koenigii, proteasome, Rutaceae
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