TY - JOUR
T1 - Denbinobin, a phenanthrene from dendrobium nobile, impairs prostate cancer migration by inhibiting Rac1 activity
AU - Lu, Te Ling
AU - Han, Chien Kuo
AU - Chang, Yuan Shiun
AU - Lu, Te Jung
AU - Huang, Hui Chi
AU - Bao, Bo Ying
AU - Wu, Hsing Yu
AU - Huang, Chieh Hung
AU - Li, Chia Yen
AU - Wu, Tian Shung
N1 - Funding Information:
This study was supported by a research grant CMU99-ASIA-16 from the China Medical University, Taiwan and by a grant NSC 100-2320-B-039-025 from the National Science Council, Taiwan.
Publisher Copyright:
© 2014 World Scientific Publishing Company & Institute for Advanced Research in Asian Science and Medicine.
PY - 2014/5/16
Y1 - 2014/5/16
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/84928394763
UR - https://www.scopus.com/pages/publications/84928394763#tab=citedBy
U2 - 10.1142/S0192415X14500967
DO - 10.1142/S0192415X14500967
M3 - Article
C2 - 25427623
AN - SCOPUS:84928394763
SN - 0192-415X
VL - 42
SP - 1539
EP - 1554
JO - American Journal of Chinese Medicine
JF - American Journal of Chinese Medicine
IS - 6
ER -