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Mutational Drivers of Cancer Cell Migration and Invasion

Overview
Journal Br J Cancer
Specialty Oncology
Date 2020 Nov 18
PMID 33204027
Citations 89
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Abstract

Genomic instability and mutations underlie the hallmarks of cancer-genetic alterations determine cancer cell fate by affecting cell proliferation, apoptosis and immune response, and increasing data show that mutations are involved in metastasis, a crucial event in cancer progression and a life-threatening problem in cancer patients. Invasion is the first step in the metastatic cascade, when tumour cells acquire the ability to move, penetrate into the surrounding tissue and enter lymphatic and blood vessels in order to disseminate. A role for genetic alterations in invasion is not universally accepted, with sceptics arguing that cellular motility is related only to external factors such as hypoxia, chemoattractants and the rigidity of the extracellular matrix. However, increasing evidence shows that mutations might trigger and accelerate the migration and invasion of different types of cancer cells. In this review, we summarise data from published literature on the effect of chromosomal instability and genetic mutations on cancer cell migration and invasion.

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References
1.
Ryan M, Sohl C, Luo B, Anderson K . The FGFR1 V561M Gatekeeper Mutation Drives AZD4547 Resistance through STAT3 Activation and EMT. Mol Cancer Res. 2018; 17(2):532-543. PMC: 6647014. DOI: 10.1158/1541-7786.MCR-18-0429. View

2.
Blandino G, Di Agostino S . New therapeutic strategies to treat human cancers expressing mutant p53 proteins. J Exp Clin Cancer Res. 2018; 37(1):30. PMC: 5815234. DOI: 10.1186/s13046-018-0705-7. View

3.
Di Fiore R, DAnneo A, Tesoriere G, Vento R . RB1 in cancer: different mechanisms of RB1 inactivation and alterations of pRb pathway in tumorigenesis. J Cell Physiol. 2013; 228(8):1676-87. DOI: 10.1002/jcp.24329. View

4.
Li C, Egloff A, Sen M, Grandis J, Johnson D . Caspase-8 mutations in head and neck cancer confer resistance to death receptor-mediated apoptosis and enhance migration, invasion, and tumor growth. Mol Oncol. 2014; 8(7):1220-30. PMC: 4198498. DOI: 10.1016/j.molonc.2014.03.018. View

5.
Wang K, Ji W, Yu Y, Li Z, Niu X, Xia W . FGFR1-ERK1/2-SOX2 axis promotes cell proliferation, epithelial-mesenchymal transition, and metastasis in FGFR1-amplified lung cancer. Oncogene. 2018; 37(39):5340-5354. DOI: 10.1038/s41388-018-0311-3. View