RHO GTPases in cancer: known facts, open questions, and therapeutic challenges

被引:56
|
作者
Bustelo, Xose R. [1 ,2 ]
机构
[1] Univ Salamanca, Ctr Invest Canc, Inst Biol Mol & Celular Canc, Salamanca 37007, Spain
[2] Univ Salamanca, CSIC, Ctr Invest Biomed Red Canc CIBERONC, Salamanca 37007, Spain
关键词
NUCLEOTIDE EXCHANGE FACTOR; COMPREHENSIVE MOLECULAR CHARACTERIZATION; RAC ACTIVATOR TIAM1; SKIN TUMOR-FORMATION; NF-KAPPA-B; WHOLE-GENOME; MUTATIONAL LANDSCAPE; SOMATIC MUTATIONS; DRIVER MUTATIONS; STEM-CELLS;
D O I
10.1042/BST20170531
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
RHO GTPases have been traditionally associated with protumorigenic functions. While this paradigm is still valid in many cases, recent data have unexpectedly revealed that RHO proteins can also play tumor suppressor roles. RHO signaling elements can also promote both pro- and antitumorigenic effects using GTPase-independent mechanisms, thus giving an extra layer of complexity to the role of these proteins in cancer. Consistent with these variegated roles, both gain- and loss-of-function mutations in RHO pathway genes have been found in cancer patients. Collectively, these observations challenge long-held functional archetypes for RHO proteins in both normal and cancer cells. In this review, I will summarize these data and discuss new questions arising from them such as the functional and clinical relevance of the mutations found in patients, the mechanistic orchestration of those antagonistic functions in tumors, and the pros and cons that these results represent for the development of RHO-based anticancer drugs.
引用
收藏
页码:741 / 760
页数:20
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