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DERL2 (derlin 2) stabilizes BAG6 (BAG cochaperone 6) in chemotherapy resistance of cholangiocarcinoma
Liu, Luzheng; Wu, Jincai; Yan, Yanggang; Cheng, Shoucai; Yu, Shuyong; Wang, Yong.
Afiliación
  • Liu, Luzheng; The Second Affiliated Hospital of Hainan Medical University. Department of Interventional Radiology and Vascular Surgery. Hainan. China
  • Wu, Jincai; Hainan General Hospital. Department of Hepatobiliary and Pancreatic Surgery. Hainan. China
  • Yan, Yanggang; The Second Affiliated Hospital of Hainan Medical University. Department of Interventional Radiology and Vascular Surgery. Hainan. China
  • Cheng, Shoucai; The Second Affiliated Hospital of Hainan Medical University. Department of Interventional Radiology and Vascular Surgery. Hainan. China
  • Yu, Shuyong; Hainan Cancer Hospital. Department of Gastrointestinal Surgery. Hainan. China
  • Wang, Yong; The Second Affiliated Hospital of Hainan Medical University. Department of Interventional Radiology and Vascular Surgery. Hainan. China
J. physiol. biochem ; 80(1): 81-97, Feb. 2024. ilus, graf
Article en En | IBECS | ID: ibc-EMG-567
Biblioteca responsable: ES1.1
Ubicación: ES15.1 - BNCS
ABSTRACT
DERL2 (derlin 2) is a critical component of the endoplasmic reticulum quality control pathway system whose mutations play an important role in carcinogenesis, including cholangiocarcinoma (CHOL). However, its role and its underlying mechanism have yet to be elucidated. Herein, we revealed that DERL2 was highly expressed in CHOL and considered as an independent prognostic indicator for inferior survival in CHOL. DERL2 ectopically expressed in CHOL cells promoted cell proliferation and colony formation rates, and depleting DERL2 in CHOL cells curbed tumor growth in vitro and in vivo. More interestingly, the knockout of DERL2 augmented the growth-inhibitory effect of gemcitabine chemotherapy on CHOL cells by inducing cell apoptosis. Mechanistically, we discovered that DERL2 interacted with BAG6 (BAG cochaperone 6), thereby extending its half-life and reinforcing the oncogenic role of BAG6 in CHOL progression. (AU)
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Texto completo: 1 Colección: 06-national / ES Banco de datos: IBECS Asunto principal: Colangiocarcinoma / Resistencia a Antineoplásicos / Quimioterapia / Carcinogénesis / Enfermedades Genéticas Congénitas / Trasplante de Hígado / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística / Desnutrición / Sarcopenia Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Adult / Female / Male / Aged País/Región como asunto: Europa / Mexico Idioma: En / Es Revista: J. physiol. biochem / An. pediatr. (2003. Ed. impr.) / Arch. bronconeumol. (Ed. impr.) / Cir. Esp. (Ed. impr.) / Nutr. hosp Año: 2022 / 2023 / 2024 Tipo del documento: Article

Texto completo: 1 Colección: 06-national / ES Banco de datos: IBECS Asunto principal: Colangiocarcinoma / Resistencia a Antineoplásicos / Quimioterapia / Carcinogénesis / Enfermedades Genéticas Congénitas / Trasplante de Hígado / Regulador de Conductancia de Transmembrana de Fibrosis Quística / Fibrosis Quística / Desnutrición / Sarcopenia Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Adult / Female / Male / Aged País/Región como asunto: Europa / Mexico Idioma: En / Es Revista: J. physiol. biochem / An. pediatr. (2003. Ed. impr.) / Arch. bronconeumol. (Ed. impr.) / Cir. Esp. (Ed. impr.) / Nutr. hosp Año: 2022 / 2023 / 2024 Tipo del documento: Article