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Inhibitor of Growth 4 Suppresses Cell Spreading and Cell Migration by Interacting with a Novel Binding Partner, Liprin α1

Authors :
Motoko Unoki
Jiang Cheng Shen
Damien Ythier
Kensuke Kumamoto
Alain Duperray
Rémy Pedeux
Lyuba Varticovski
Curtis C. Harris
Duperray, Alain
Laboratory of Human Carcinogenesis
National Institutes of Health [Bethesda] (NIH)
Groupe de Recherche Sur Le Cancer du Poumon : Bases Moléculaires de la Progression Tumorale, Dépistage et Thérapie Génique
Institut Albert Bonniot-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
Cancer Research, Cancer Research, American Association for Cancer Research, 2007, 67 (6), pp.2552-8. ⟨10.1158/0008-5472.CAN-06-3870⟩
Publication Year :
2007
Publisher :
American Association for Cancer Research (AACR), 2007.

Abstract

Inhibitor of growth 4 (ING4) is a candidate tumor suppressor that plays a major role in gene regulation, cell cycle control, apoptosis, and angiogenesis. ING4 expression is down-regulated in glioblastoma cells and head and neck squamous cell carcinoma. Here, we identified liprin α1/PPFIA1, a cytoplasmic protein necessary for focal adhesion formation and axon guidance, as a novel interacting protein with ING4. ING4 and liprin α1 colocalized at lamellipodia in the vicinity of vinculin. Overexpressed ING4 suppressed cell spreading and cell migration. In contrast, overexpressed liprin α1 enhanced cell spreading and cell migration. Knockdown of endogenous ING4 with RNA interference induced cell motility, whereas knockdown of endogenous liprin α1 suppressed cell motility. ING4 also suppressed cell motility that was enhanced by liprin α1. However, ING4 did not further suppress cell motility when liprin α1 was suppressed with RNA interference, suggesting a functional and mechanistic interdependence between these proteins. In addition to its nuclear functions, cytoplasmic ING4 interacts with liprin α1 to regulate cell migration and, with its known antiangiogenic function, may prevent invasion and metastasis. [Cancer Res 2007;67(6):2552–8]

Details

ISSN :
15387445 and 00085472
Volume :
67
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi.dedup.....52b28304b131f175800b3b93aba2b14e
Full Text :
https://doi.org/10.1158/0008-5472.can-06-3870