Inappropriate activation of epidermal growth factor receptor (EGFR) plays a causal role in many cancers including colon cancer. The activation of EGFR by phosphorylation is balanced by receptor kinase and protein tyrosine phosphatase activities. However, the mechanisms of negative EGFR regulation by tyrosine phosphatases remain largely unexplored. Our previous results indicate that protein tyrosine phosphatase receptor type O (PTPRO) is down-regulated in a subset of colorectal cancer (CRC) patients with a poor prognosis. Here we identified PTPRO as a phosphatase that negatively regulates SRC by directly dephosphorylating Y416 phosphorylation site. SRC activation triggered by PTPRO down-regulation induces phosphorylation of both EGFR at Y845 and the c-CBL ubiquitin ligase at Y731. Increased EGFR phosphorylation at Y845 promotes its receptor activity, whereas enhanced phosphorylation of c-CBL triggers its degradation promoting EGFR stability. Importantly, hyperactivation of SRC/EGFR signaling triggered by loss of PTPRO leads to high resistance of colon cancer to EGFR inhibitors. Our results not only highlight the PTPRO contribution in negative regulation of SRC/EGFR signaling but also suggest that tumors with low PTPRO expression may be therapeutically targetable by anti-SRC therapies.

• MeSH
• buňky HT-29 MeSH
• Caco-2 buňky MeSH
• chinazoliny farmakologie   MeSH
• epidermální růstový faktor farmakologie   MeSH
• erbB receptory antagonisté a inhibitory   metabolismus   MeSH
• fosforylace MeSH
• gefitinib MeSH
• HCT116 buňky MeSH
• HEK293 buňky MeSH
• inhibitory proteinkinas farmakologie   MeSH
• lidé MeSH
• MAP kinasový signální systém MeSH
• messenger RNA genetika   metabolismus   MeSH
• nádorové buněčné linie MeSH
• nádory tračníku farmakoterapie   enzymologie   genetika   patologie   MeSH
• protoonkogenní proteiny c-cbl metabolismus   MeSH
• signální transdukce MeSH
• skupina kinas odvozených od src-genu metabolismus   MeSH
• tyrosinfosfatasy receptorového typu, třída 3 biosyntéza   genetika   metabolismus   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• CBL protein, human MeSH Prohlížeč
• chinazoliny MeSH
• EGFR protein, human MeSH Prohlížeč
• epidermální růstový faktor MeSH
• erbB receptory MeSH
• gefitinib MeSH
• inhibitory proteinkinas MeSH
• messenger RNA MeSH
• protoonkogenní proteiny c-cbl MeSH
• PTPRO protein, human MeSH Prohlížeč
• skupina kinas odvozených od src-genu MeSH
• tyrosinfosfatasy receptorového typu, třída 3 MeSH