Nischarin regulates focal adhesion and Invadopodia formation in breast cancer cells

被引:28
|
作者
Maziveyi, Mazvita [1 ]
Dong, Shengli [1 ]
Baranwal, Somesh [2 ]
Alahari, Suresh K. [1 ]
机构
[1] LSUHSC Sch Med, Dept Biochem & Mol Biol, New Orleans, LA 70112 USA
[2] Cent Univ Punjab, Dept Biochem & Microbial Sci, Bathinda 151001, India
来源
MOLECULAR CANCER | 2018年 / 17卷
关键词
Nischarin; Invasion; Invadopodia; Migration; Focal adhesion; Breast cancer; Integrins; EPITHELIAL-MESENCHYMAL TRANSITION; MIGRATION; INTEGRIN; PROTEIN; INVASION; EXPRESSION; KINASE; CORTACTIN; INTERACTS; STIFFNESS;
D O I
10.1186/s12943-018-0764-6
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
Background: During metastasis, tumor cells move through the tracks of extracellular matrix (ECM). Focal adhesions (FAs) are the protein complexes that link the cell cytoskeleton to the ECM and their presence is necessary for cell attachment. The tumor suppressor Nischarin interacts with a number of signaling proteins such as Integrin a5, PAK1, LIMK1, LKB1, and Rac1 to prevent cancer cell migration. Although previous findings have shown that Nischarin exerts this migratory inhibition by interacting with other proteins, the effects of these interactions on the entire FA machinery are unknown. Methods: RT-PCR, Western Blotting, invadopodia assays, and immunofluorescence were used to examine FA gene expression and determine whether Nischarin affects cell attachment, as well as the proteins that regulate it. Results: Our data show that Nischarin prevents cell migration and invasion by altering the expression of key focal adhesion proteins. Furthermore, we have found that Nischarin-expressing cells have reduced ability to attach the ECM, which in turn leads to a decrease in invadopodia-mediated matrix degradation. Conclusions: These experiments demonstrate an important role of Nischarin in regulating cell attachment, which adds to our understanding of the early events of the metastatic process in breast cancer.
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页数:11
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