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补骨脂酚通过直接靶向Hck、Blk和p38丝裂原活化蛋白激酶来抑制皮肤癌细胞的增殖。

Bakuchiol suppresses proliferation of skin cancer cells by directly targeting Hck, Blk, and p38 MAP kinase.

作者信息

Kim Jong-Eun, Kim Jae Hwan, Lee Younghyun, Yang Hee, Heo Yong-Seok, Bode Ann M, Lee Ki Won, Dong Zigang

机构信息

Department of Agricultural Biotechnology and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul 151-742, Republic of Korea.

The Hormel Institute, University of Minnesota, MN 55912, USA.

出版信息

Oncotarget. 2016 Mar 22;7(12):14616-27. doi: 10.18632/oncotarget.7524.

Abstract

Bakuchiol is a meroterpene present in the medicinal plant Psoralea corylifolia, which has been traditionally used in China, India, Japan and Korea for the treatment of premature ejaculation, knee pain, alopecia spermatorrhea, enuresis, backache, pollakiuria, vitiligo, callus, and psoriasis. Here, we report the chemopreventive properties of bakuchiol, which acts by inhibiting epidermal growth factor (EGF)-induced neoplastic cell transformation. Bakuchiol also decreased viability and inhibited anchorage-independent growth of A431 human epithelial carcinoma cells. Bakuchiol reduced A431 xenograft tumor growth in an in vivo mouse model. Using kinase profiling, we identified Hck, Blk and p38 mitogen activated protein kinase (MAPK) as targets of bakuchiol, which directly bound to each kinase in an ATP-competitive manner. Bakuchiol also inhibited EGF-induced signaling pathways downstream of Hck, Blk and p38 MAPK, including the MEK/ERKs, p38 MAPK/MSK1 and AKT/p70S6K pathways. This report is the first mechanistic study identifying molecular targets for the anticancer activity of bakuchiol and our findings indicate that bakuchiol exhibits potent anticancer activity by targeting Hck, Blk and p38 MAPK.

摘要

补骨脂酚是一种存在于药用植物补骨脂中的半萜类化合物,在中国、印度、日本和韩国,传统上一直使用补骨脂来治疗早泄、膝盖疼痛、遗精、遗尿、背痛、尿频、白癜风、胼胝和牛皮癣。在此,我们报告了补骨脂酚的化学预防特性,它通过抑制表皮生长因子(EGF)诱导的肿瘤细胞转化发挥作用。补骨脂酚还降低了A431人上皮癌细胞的活力并抑制了其非贴壁依赖性生长。在体内小鼠模型中,补骨脂酚减少了A431异种移植肿瘤的生长。通过激酶谱分析,我们确定Hck、Blk和p38丝裂原活化蛋白激酶(MAPK)为补骨脂酚的靶点,补骨脂酚以ATP竞争性方式直接与每种激酶结合。补骨脂酚还抑制了Hck、Blk和p38 MAPK下游的EGF诱导信号通路,包括MEK/ERK、p38 MAPK/MSK1和AKT/p70S6K通路。本报告是首次确定补骨脂酚抗癌活性分子靶点的机制研究,我们的研究结果表明,补骨脂酚通过靶向Hck、Blk和p38 MAPK表现出强大的抗癌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f0c/4924739/aacb9d49e586/oncotarget-07-14616-g001.jpg

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