3 years ago

Internalized CD44s splice isoform attenuates EGFR degradation by targeting Rab7A [Medical Sciences]

Internalized CD44s splice isoform attenuates EGFR degradation by targeting Rab7A [Medical Sciences]
Lisa A. Hurley, Chung Kwon Kim, Wei Wang, Bo Hu, Motoo Nagane, Sali Liu, Ryo Nishikawa, Chonghui Cheng, Shi-Yuan Cheng, Alexander H. Stegh, Yilin Xu, Honghong Zhang

CD44 has been postulated as a cell surface coreceptor for augmenting receptor tyrosine kinase (RTK) signaling. However, how exactly CD44 triggers RTK-dependent signaling remained largely unclear. Here we report an unexpected mechanism by which the CD44s splice isoform is internalized into endosomes to attenuate EGFR degradation. We identify a CD44s-interacting small GTPase, Rab7A, and show that CD44s inhibits Rab7A-mediated EGFR trafficking to lysosomes and subsequent degradation. Importantly, CD44s levels correlate with EGFR signature and predict poor prognosis in glioblastomas. Because Rab7A facilitates trafficking of many RTKs to lysosomes, our findings identify CD44s as a Rab7A regulator to attenuate RTK degradation.

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