دورية أكاديمية

Efficacy of CDK4/6 inhibitors in preclinical models of malignant pleural mesothelioma

التفاصيل البيبلوغرافية
العنوان: Efficacy of CDK4/6 inhibitors in preclinical models of malignant pleural mesothelioma
المؤلفون: Aliagas, Elisabet, Alay, Ania, Martínez Iniesta, María, Hernández Madrigal, Miguel, Cordero, David, Gausachs Romero, Mireia, Pros, Eva, Saigí, Maria, Busacca, Sara, Sharkley, Annabel J., Dawson, Alan, Palmero, Ramón, Ruffinelli, José C., Padrones, Susana, Aso, Samantha, Escobar, Ignacio, Ramos, Ricard, Llatjós, Roger, Vidal, August, Dorca, Eduard, Varela, Mar, Sánchez Céspedes, Montserrat, Fennell, Dean, Muñoz Pinedo, Cristina, Villanueva Garatachea, Alberto, Solé, Xavi, Nadal, Ernest
المصدر: Articles publicats en revistes (Patologia i Terapèutica Experimental)
بيانات النشر: Cancer Research UK
سنة النشر: 2021
المجموعة: Dipòsit Digital de la Universitat de Barcelona
مصطلحات موضوعية: Mesotelioma, Immunoteràpia, Pronòstic mèdic, Proliferació cel·lular, Mesothelioma, Immunotheraphy, Prognosis, Cell proliferation
الوصف: Background There is no effective therapy for patients with malignant pleural mesothelioma (MPM) who progressed to platinum-based chemotherapy and immunotherapy. Methods We aimed to investigate the antitumor activity of CDK4/6 inhibitors using in vitro and in vivo preclinical models of MPM. Results Based on publicly available transcriptomic data of MPM, patients with CDK4 or CDK6 overexpression had shorter overall survival. Treatment with abemaciclib or palbociclib at 100 nM significantly decreased cell proliferation in all cell models evaluated. Both CDK4/6 inhibitors significantly induced G1 cell cycle arrest, thereby increasing cell senescence and increased the expression of interferon signalling pathway and tumour antigen presentation process in culture models of MPM. In vivo preclinical studies showed that palbociclib significantly reduced tumour growth and prolonged overall survival using distinct xenograft models of MPM implanted in athymic mice. Conclusions Treatment of MPM with CDK4/6 inhibitors decreased cell proliferation, mainly by promoting cell cycle arrest at G1 and by induction of cell senescence. Our preclinical studies provide evidence for evaluating CDK4/6 inhibitors in the clinic for the treatment of MPM.
نوع الوثيقة: article in journal/newspaper
وصف الملف: 36 p.; application/pdf
اللغة: English
تدمد: 0007-0920
العلاقة: Versió postprint del document publicat a: https://doi.org/10.1038/s41416-021-01547-yTest; British Journal of Cancer, 2021; https://doi.org/10.1038/s41416-021-01547-yTest; info:eu-repo/grantAgreement/EC/H2020/766214/EU//META-CAN; http://hdl.handle.net/2445/180823Test; 715305
الإتاحة: https://doi.org/10.1038/s41416-021-01547-yTest
http://hdl.handle.net/2445/180823Test
حقوق: (c) Aliagas, Elisabet et al., 2021 ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.6B0FFD86
قاعدة البيانات: BASE