ASBAH, Layka Abbasi, Iria VAZQUEZ, Loredana VECCHIONE, Eva BUDINSKÁ, Veerle DE VRIENDT, Maria Francesca BAIETTI, Mikhail STEKLOV, Bart JACOBS, Nicholas HOE, Sharat SINGH, Naga-Sailaja IMJETI, Pascale ZIMMERMANN, Anna SABLINA a Sabine TEJPAR. The tyrosine phosphatase PTPRO sensitizes colon cancer cells to anti-EGFR therapy through activation of SRC-mediated EGFR signaling. Oncotarget. New York: Impact Journals, roč. 5, č. 20, s. 10070-10083. ISSN 1949-2553. 2014.
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Základní údaje
Originální název The tyrosine phosphatase PTPRO sensitizes colon cancer cells to anti-EGFR therapy through activation of SRC-mediated EGFR signaling
Autoři ASBAH, Layka Abbasi (56 Belgie), Iria VAZQUEZ (56 Belgie), Loredana VECCHIONE (56 Belgie), Eva BUDINSKÁ (703 Slovensko, garant, domácí), Veerle DE VRIENDT (56 Belgie), Maria Francesca BAIETTI (56 Belgie), Mikhail STEKLOV (56 Belgie), Bart JACOBS (56 Belgie), Nicholas HOE (840 Spojené státy), Sharat SINGH (840 Spojené státy), Naga-Sailaja IMJETI (56 Belgie), Pascale ZIMMERMANN (56 Belgie), Anna SABLINA (56 Belgie) a Sabine TEJPAR (56 Belgie).
Vydání Oncotarget, New York, Impact Journals, 2014, 1949-2553.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 6.359
Kód RIV RIV/00216224:14110/14:00078129
Organizační jednotka Lékařská fakulta
UT WoS 000348036500043
Klíčová slova anglicky EGFR; PTPRO; phosphatase; SRC kinase; EGFR inhibitor; colon cancer
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Mgr. Věra Pospíšilíková, učo 9005. Změněno: 24. 4. 2015 14:15.
Anotace
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.
VytisknoutZobrazeno: 19. 4. 2024 19:06