4.6 Review

Signaling via PINCH: Functions, binding partners and implications in human diseases

Journal

GENE
Volume 594, Issue 1, Pages 10-15

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.gene.2016.08.039

Keywords

PINCH; IPP complex; ILK; Nck2; Adhesion; Focal adhesion; Protein-protein interaction; Tumor

Funding

  1. National Institutes of Health [AR068950, AR064874]
  2. National Natural Science Foundation of China [81630066, 81472049, 81500160]
  3. Shenzhen Municipal Science and Technology Innovation Council Grant [JCYJ20150331101823686]

Ask authors/readers for more resources

Particularly interesting new cysteine-histidine-rich protein (PINCH) is a LIM-domain-only adaptor that plays important roles in cytoskeletal organization and extracellular matrix adhesion, migration, proliferation and survival. Mammalian cells have two functional PINCH proteins, PINCH1 and PINCH2. PINCH not only binds to Nck2 and engages in the signaling of growth factor receptors, but also forms a ternary complex with ILK and parvin (IPP complex). Normally, the IPP complex locates to focal adhesions participating in the signaling of integrins and mediating the interaction of cytoskeleton and extracellular matrix (ECM). Accumulative evidence indicates that abnormalities in PINCH signaling are involved in the pathogenesis of important diseases, such as cancers, renal diseases, cardiomyopathy, and HIV. Therefore, clarifying the functions of PINCH and its interactions with key factors is important for better understanding of signaling events both in health and disease. (C) 2016 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available