Osthole inhibits the migration and invasion of highly metastatic breast cancer cells by suppressing ITGα3/ITGβ5 signaling

被引:0
|
作者
Yue-qiang Chen
Hai-yan Song
Zhong-yan Zhou
Jiao Ma
Zhan-yang Luo
Ying Zhou
Jian-yi Wang
Sheng Liu
Xiang-hui Han
机构
[1] Institute of Chinese Traditional Surgery,Department of Liver Disease
[2] Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine,undefined
[3] Institute of Digestive Diseases,undefined
[4] Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine,undefined
[5] Shanghai TCM-integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine,undefined
[6] Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine,undefined
来源
关键词
osthole; Wenshen Zhuanggu Formula; breast cancer; metastasis; ITGα3; ITGβ5; FAK/Src/Rac1 pathway;
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中图分类号
学科分类号
摘要
Metastasis is the leading cause of death in breast cancer patients. Osthole, as an active compound detected in the traditional Chinese medicine Wenshen Zhuanggu Formula, has shown a promising anti-metastatic activity in human breast cancer cells, but the underlying mechanisms remain ambiguous. In this study we elucidated the anti-metastatic mechanisms of osthole in highly metastatic breast cancer cells and a zebrafish xenograft model. We showed that the expression of integrin α3 (ITGα3) and integrin β5 (ITGβ5) was upregulated in highly metastatic MDA-MB-231, MDA-MB-231BO breast cancer cell lines but was downregulated in poorly metastatic MCF-7 breast cancer cell line, which might be the key targets of osthole’s anti-metastatic action. Furthermore, we showed that knockdown of ITGα3 and ITGβ5 attenuated breast cancer cell migration and invasion possibly via suppression of FAK/Src/Rac1 pathway, whereas overexpression of ITGα3 and ITGβ5 caused the opposite effects. Consistently, osthole significantly inhibited breast cancer metastasis by downregulating ITGα3/ITGβ5 signaling in vitro and in vivo. These results provide new evidence that osthole may be developed as a candidate therapeutic drug for metastatic breast cancer.
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页码:1544 / 1555
页数:11
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