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RNF213 knockdown or knockout in HeLa and A549 cells markedly reduces EGFR phosphorylation at key tyrosine sites following EGF and TGF\u03b1 stimulation. In RNF213 knockout cells, HER2 phosphorylation, typically activated through heterodimerization with EGFR, and Src recruitment and\/or phosphorylation are also diminished. Mutations in the RNF213 RING, RZ finger, or AAA+ domains, including the prevalent R4810K mutation in MMD, consistently reduce EGFR phosphorylation. In\u00a0vivo, EGF injections increase EGFR and HER2 phosphorylation in WT but not in RNF213 knockout mice. Despite the reduced phosphorylation levels of these tyrosine kinases in knockout cells, the activation of downstream signals such as AKT, ERK1\/2, and STAT3 remains unaffected, although phosphorylation of PLC\u03b3, a key mediator of Ca<jats:sup>2+<\/jats:sup> release, is selectively reduced by RNF213 knockout. These findings demonstrate that RNF213 modulates EGFR\u2010related pathways and specific downstream signal pathways, possibly affecting physiologic and pathogenic angiogenesis, and may have implications for unraveling the etiology of MMD and for developing cancer therapies that target RNF213.<\/jats:p>","DOI":"10.1111\/gtc.70033","type":"journal-article","created":{"date-parts":[[2025,6,12]],"date-time":"2025-06-12T08:34:14Z","timestamp":1749717254000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["<scp>RNF213<\/scp>\u2010Dependent <scp>EGFR<\/scp> and <scp>HER2<\/scp> Activation Regulates Specific Downstream Signaling Pathways in Human Cancer Cells"],"prefix":"10.1111","volume":"30","author":[{"given":"Intisar M.","family":"Fouad","sequence":"first","affiliation":[{"name":"Laboratory of Molecular Biosciences, Graduate School of Medicine Kyoto University  Kyoto Japan"},{"name":"Laboratory of Molecular Biology of 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