The role of the ShcD and RET interaction in neuroblastoma survival and migration

MABRUK, Zeanap A, AHMED, Samrein, THOMAS, Asha Caroline and PRIGENT, Sally A (2018). The role of the ShcD and RET interaction in neuroblastoma survival and migration. Biochemistry and Biophysics Reports, 13, 99-108.

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Official URL: https://www.sciencedirect.com/science/article/pii/...
Open Access URL: https://doi.org/10.1016/j.bbrep.2018.01.007 (Published version)
Link to published version:: https://doi.org/10.1016/j.bbrep.2018.01.007

Abstract

Preliminary screening data showed that the ShcD adaptor protein associates with the proto-oncogene RET receptor tyrosine kinase. In the present study, we aimed to investigate the molecular interaction between ShcD and RET in human neuroblastoma cells and study the functional impact of this interaction. We were able to show that ShcD immunoprecipitated with RET from SK-N-AS neuroblastoma cell lysates upon GDNF treatment. This result was validated by ShcD-RET co-localization, which was visualized using a fluorescence microscope. ShcD-RET coexpression promoted ShcD and RET endosomal localization, resulting in unexpected inhibition of the downstream ERK and AKT pathways. Interestingly, ShcD-RET association reduced the viability and migration of SK-N-AS cells. Although ShcD was previously shown to trigger melanoma cell migration and tumorigenesis, our data showed an opposite role for ShcD in neuroblastoma SK-N-AS cells via its association with RET in GDNF-treated cells. In conclusion, ShcD acts as a switch molecule that promotes contrasting biological responses depending on the stimulus ad cell type.

Item Type: Article
Uncontrolled Keywords: 0601 Biochemistry and Cell Biology; 3101 Biochemistry and cell biology
Identification Number: https://doi.org/10.1016/j.bbrep.2018.01.007
Page Range: 99-108
SWORD Depositor: Symplectic Elements
Depositing User: Symplectic Elements
Date Deposited: 30 Jan 2024 17:02
Last Modified: 30 Jan 2024 17:15
URI: https://shura.shu.ac.uk/id/eprint/33037

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