ROR1 sustains caveolae and survival signalling as a scaffold of cavin-1 and caveolin-1

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Tomoya Yamaguchi
Can Lu
Lisa Ida
Kiyoshi Yanagisawa
Jiro Usukura
Jinglei Cheng
Naoe Hotta
Yukako Shimada
Hisanori Isomura
Motoshi Suzuki
Toyoshi Fujimoto
Takashi Takahashi
机构
[1] Center for Neurological Diseases and Cancer,Division of Molecular Carcinogenesis
[2] Nagoya University Graduate School of Medicine,Division of Integrated Project
[3] EcoTopia Science Institute,Department of Anatomy and Molecular Cell Biology
[4] Nagoya University,undefined
[5] Nagoya University Graduate School of Medicine,undefined
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The receptor tyrosine kinase-like orphan receptor 1 (ROR1) sustains prosurvival signalling directly downstream of the lineage-survival oncogene NKX2-1/TTF-1 in lung adenocarcinoma. Here we report an unanticipated function of this receptor tyrosine kinase (RTK) as a scaffold of cavin-1 and caveolin-1 (CAV1), two essential structural components of caveolae. This kinase-independent function of ROR1 facilitates the interactions of cavin-1 and CAV1 at the plasma membrane, thereby preventing the lysosomal degradation of CAV1. Caveolae structures and prosurvival signalling towards AKT through multiple RTKs are consequently sustained. These findings provide mechanistic insight into how ROR1 inhibition can overcome EGFR–tyrosine kinase inhibitor (TKI) resistance due to bypass signalling via diverse RTKs such as MET and IGF-IR, which is currently a major clinical obstacle. Considering its onco-embryonic expression, inhibition of the scaffold function of ROR1 in patients with lung adenocarcinoma is an attractive approach for improved treatment of this devastating cancer.
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