scholarly journals Targeting the Interaction between the SH3 Domain of Grb2 and Gab2

Cells ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 2435
Author(s):  
Francesca Malagrinò ◽  
Antonio Coluccia ◽  
Marianna Bufano ◽  
Giuseppe La Regina ◽  
Michela Puxeddu ◽  
...  

Gab2 is a scaffolding protein, overexpressed in many types of cancers, that plays a key role in the formation of signaling complexes involved in cellular proliferation, migration, and differentiation. The interaction between Gab2 and the C-terminal SH3 domain of the protein Grb2 is crucial for the activation of the proliferation-signaling pathway Ras/Erk, thus representing a potential pharmacological target. In this study, we identified, by virtual screening, seven potential inhibitor molecules that were experimentally tested through kinetic and equilibrium binding experiments. One compound showed a remarkable effect in lowering the affinity of the C-SH3 domain for Gab2. This inhibitory effect was subsequently validated in cellula by using lung cancer cell lines A549 and H1299. Our results are discussed under the light of previous works on the C-SH3:Gab2 interaction.

2010 ◽  
Vol 9 (6) ◽  
pp. 912-919 ◽  
Author(s):  
Mohammad Pourhassan ◽  
Nosratollah Zarghami ◽  
Mohammad Rahmati ◽  
Abbas Alibakhshi ◽  
Javad Ranjbari

Author(s):  
Soyoung Hwang ◽  
Peter Chang-Whan Lee ◽  
Dong Min Shin ◽  
Jeong Hee Hong

Spinophilin (SPL) is a multifunctional actin-binding scaffolding protein. Although increased research on SPL in cancer biology has revealed a tumor suppressive role, its modulation in cancer biology, and oncological relevance remains elusive. Thus, we determined the role of SPL in the modulation of the junctional network and cellular migration in A549 lung cancer cell line. Knockdown of SPL promoted cancer cell invasion in agarose spot and scratch wound assays. Attenuation of SPL expression also enhanced invadopodia, as revealed by enhanced vinculin spots, and enhanced sodium bicarbonate cotransporter NBC activity without enhancing membranous expression of NBCn1. Disruption of the tubular structure with nocodazole treatment revealed enhanced SPL expression and reduced NBC activity and A549 migration. SPL-mediated junctional modulation and tubular stability affected bicarbonate transporter activity in A549 cells. The junctional modulatory function of SPL in start-up migration, such as remodeling of tight junctions, enhanced invadopodia, and increased NBC activity, revealed here would support fundamental research and the development of an initial target against lung cancer cell migration.


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