Denbinobin, a phenanthrene from dendrobium nobile, impairs prostate cancer migration by inhibiting Rac1 activity

Te Ling Lu, Chien Kuo Han, Yuan Shiun Chang, Te Jung Lu, Hui Chi Huang, Bo Ying Bao, Hsing Yu Wu, Chieh Hung Huang, Chia Yen Li, Tian Shung Wu

研究成果: Article

13 引文 斯高帕斯(Scopus)

摘要

Prostate cancer is the most prevalent type of cancer in the United States. The most common site of prostate cancer metastasis is bone. CXCL12 is preferentially expressed in bone and is targeted by prostate cancer cells, which over-express the receptor for CXCL12, CXCR4. In response to CXCL12 stimulation, Rac1, a GTPase, along with its effectors, regulates actin polymerization to form lamellipodia, which is a critical event for cell migration. Cortactin, an actin-binding protein, is recruited to the lamellipodia and is phosphorylated at tyrosine residues. The phosphorylated cortactin is also involved in cell migration. The inhibition of Rac1 activity using a dominant negative Rac1 impairs lamellipodial protrusion as well as cortactin translocation and cortactin phosphorylation. Denbinobin, a substance extracted from Dendrobium nobile, has anticancer effects in many cancer cell lines. Whether denbinobin can inhibit prostate cancer cell migration is not clear. Here, we report that denbinobin inhibited Rac1 activity. The inhibition of Rac1 activity prevented lamellipodial formation. Cortactin phosphorylation and translocation to the lamellipodia were also impaired, and PC3 cells were unable to migrate. These results indicate that denbinobin prevents CXCL12-induced PC3 cell migration by inhibiting Rac1 activity.

原文English
頁(從 - 到)1539-1554
頁數16
期刊American Journal of Chinese Medicine
42
發行號6
DOIs
出版狀態Published - 2014 五月 16

All Science Journal Classification (ASJC) codes

  • Complementary and alternative medicine

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    Lu, T. L., Han, C. K., Chang, Y. S., Lu, T. J., Huang, H. C., Bao, B. Y., Wu, H. Y., Huang, C. H., Li, C. Y., & Wu, T. S. (2014). Denbinobin, a phenanthrene from dendrobium nobile, impairs prostate cancer migration by inhibiting Rac1 activity. American Journal of Chinese Medicine, 42(6), 1539-1554. https://doi.org/10.1142/S0192415X14500967