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bioRxiv · 10.1101/299586

SORLA-driven endosomal trafficking regulates the oncogenic fitness of HER2

Abstract

Human epidermal growth factor receptor 2 (HER2) is an oncogene targeted by several kinase inhibitors and therapeutic antibodies. Endosomal trafficking of many other receptor tyrosine kinases regulates their oncogenic signaling, but the prevailing view is that HER2 is retained on the cell surface. Here we reveal that in cancer cells Sortilin related receptor 1 (SORLA; SORL1) forms a complex with HER2 and regulates its subcellular distribution by promoting recycling of endosomal HER2 back to plasma membrane. Expression of SORLA in cancer cell lines and bladder cancers correlates with HER2 levels. Depletion of SORLA targets HER2 to late endosomal/lysosomal compartments, impairs HER2-driven signaling and in vivo tumor growth. SORLA silencing also disrupts normal lysosome function and sensitizes anti-HER2 therapy sensitive and resistant cancer cells to lysosome-targeting cationic amphiphilic drugs. These findings reveal potentially important SORLA-dependent endosomal trafficking-linked vulnerabilities in HER2-driven cancers.

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BibTeXRIS

Pietila, M., Sahgal, P., Peuhu, E., Jantti, N., Paatero, I., Andersen, O. M., Padzik, A., Blomqvist, M., Saarinen, I., Bostrom, P., Taimen, P., Ivaska, J.. 2018-04-11. SORLA-driven endosomal trafficking regulates the oncogenic fitness of HER2. https://doi.org/10.1101/299586

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