Cofilin promotes vasculogenic mimicry by regulating the actin cytoskeleton in human breast cancer cells

被引:2
作者
Nakajima, Minami [1 ]
Kawahara, Ryota [1 ]
Simizu, Siro [1 ,2 ]
机构
[1] Keio Univ, Fac Sci & Technol, Dept Appl Chem, Yokohama, Japan
[2] Keio Univ, Fac Sci & Technol, Dept Appl Chem, 3-14-1 Hiyoshi,Kohoku ku, Yokohama 2238522, Japan
关键词
actin cytoskeleton; breast cancer; cofilin; cytochalasin; jasplakinolide; vasculogenic mimicry; DEPOLYMERIZING FACTOR; KINASE; PHOSPHORYLATION; MECHANISMS; MOTILITY; ROLES;
D O I
10.1002/1873-3468.14594
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vasculogenic mimicry (VM) is the formation of microvascular channels by cancer cells. VM requires cellular processes that are regulated by changes in cellular migration and morphology. Cofilin (CFL), a key regulator of actin depolymerization, has been reported to affect malignant phenotypes of cancer. We show that treatment with inhibitors of actin dynamics suppresses VM in MDA-MB-231 human breast cancer cells. We established CFL-knockout (KO) MDA-MB-231 cells and found that VM was attenuated in CFL-KO cells. Although the re-expression of wild-type CFL restored VM in CFL-KO cells, inactive phosphomimetic CFL failed to do so. Collectively, our results demonstrate that CFL is a critical regulator of VM and implicate CFL as a novel therapeutic target for breast cancer.
引用
收藏
页码:1114 / 1124
页数:11
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