4.8 Article

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

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NATURE COMMUNICATIONS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms10060

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资金

  1. Japan Society for the Promotion of Science (JSPS)
  2. Programme for Development of Innovative Research on Cancer Therapeutics (P-Direct) from the Japan Agency for Medical Research and Development
  3. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan
  4. Princess Takamatsu Cancer Research Fund
  5. Grants-in-Aid for Scientific Research [26670625, 15H02500, 25250017, 15H05910, 15H05897, 26290051, 25461187] Funding Source: KAKEN

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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 oncoembryonic 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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