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      Synergistic inhibition of pancreatic cancer with anti-PD-L1 and c-Myc inhibitor JQ1

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          ABSTRACT

          Human pancreatic ductal adenocarcinoma (PDAC) exhibits marginal responses to anti-PD-1/PD-L1 immunotherapy and its mechanism remains poorly understood. We have investigated the effect of anti-PD-L1 and c-Myc inhibition in PDAC. Using 87 patients with PDAC from our hospital database we found a significant correlation between the expression of PD-L1 and c-Myc. Moreover, the expression of both PD-L1 and c-Myc was associated with poor overall survival. In addition, we confirmed this finding with the PDAC patients in the TCGA database. Using several PDAC cell lines we demonstrated a significant correlation between the expression of PD-L1 and c-Myc. We also found that expression of PD-L1 correlated with high-grade histology. JQ1, an inhibitor of c-Myc inhibited PD-L1 expression and tumor growth. Using xenograft models, we demonstrated that the combination of JQ1 and anti-PD-L1 antibody exerted synergistic inhibition of PDAC growth. Our data demonstrated that the expression of PD-L1 and c-Myc may be helpful prognostic biomarkers, and their inhibition may potentially serve as an effective treatment for PDAC.

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          Most cited references24

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          Cabozantinib versus everolimus in advanced renal cell carcinoma (METEOR): final results from a randomised, open-label, phase 3 trial.

          Cabozantinib is an oral inhibitor of tyrosine kinases including MET, VEGFR, and AXL. The randomised phase 3 METEOR trial compared the efficacy and safety of cabozantinib versus the mTOR inhibitor everolimus in patients with advanced renal cell carcinoma who progressed after previous VEGFR tyrosine-kinase inhibitor treatment. Here, we report the final overall survival results from this study based on an unplanned second interim analysis.
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            PD-1/PD-L1 and immunotherapy for pancreatic cancer.

            Therapy that targets programmed death 1 or programmed death 1 ligand 1 (PD-1/PD-L1), which are known as immune checkpoints, has been recently rapidly developing as oncotherapy for various carcinomas. However, this therapy has a poor effect on the treatment of pancreatic cancer with PD-1/PD-L1 blockade monotherapy. In this review, the development and limitations of anti-PD-1/PD-L1 monotherapy in pancreatic cancer are discussed. We then consider the underlying mechanism of anti-PD-1/PD-L1 monotherapy failure, combination strategies overcoming resistance to anti-PD-1/PD-L1 immunotherapy and the prospect of targeting PD-1/PD-L1 for the immunotherapy of pancreatic cancer.
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              The MLL1-H3K4me3 Axis-Mediated PD-L1 Expression and Pancreatic Cancer Immune Evasion.

              Pancreatic cancer is one of the cancers where anti-PD-L1/PD-1 immunotherapy has been unsuccessful. What confers pancreatic cancer resistance to checkpoint immunotherapy is unknown. The aim of this study is to elucidate the underlying mechanism of PD-L1 expression regulation in the context of pancreatic cancer immune evasion.
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                Author and article information

                Journal
                Oncoimmunology
                Oncoimmunology
                KONI
                koni20
                Oncoimmunology
                Taylor & Francis
                2162-4011
                2162-402X
                2019
                1 March 2019
                1 March 2019
                : 8
                : 5
                : e1581529
                Affiliations
                [a ]Department of General Surgery, Fujian Medical University Union Hospital , Fuzhou, People’s Republic of China
                [b ]Department of obstetrics and gynecology, 900 Hospital of the Joint Logistics Team , Fuzhou, China
                [c ]College of Bioinformatics Science and Technology, Harbin Medical University , Harbin, China
                [d ]Department of Oncology and Hematology and Division of Research, Kaiser Permanente , Santa Clara, CA, USA
                Author notes
                CONTACT Fengchun Lu fengchun160@ 123456163.com Department of General Surgery, Fujian Medical University Union Hospital , #29 Xinquan Road, Fuzhou 350001, People’s Republic of China
                Heguang Huang heguanghuang22@ 123456163.com Department of General Surgery, Fujian, Medical University Union Hospital , #29 Xinquan Road, Fuzhou 350001, People’s, Republic of China
                [*]

                These authors contributed equally to this work.

                Article
                1581529
                10.1080/2162402X.2019.1581529
                6492971
                31069140
                b11854ed-cfe7-4b63-b4b2-e2754acfab15
                © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

                History
                : 31 October 2018
                : 29 December 2018
                : 6 February 2019
                Page count
                Figures: 7, Tables: 3, References: 43, Pages: 11
                Funding
                Funded by: Medical Talents Training Program of Health and Family Planning Commission of Fujian Province
                Funded by: Joint Funds of Scientific and Technological Innovation Program of Fujian Province
                Award ID: 2017Y9059
                Funded by: The Medical Center of Minimally Invasive Technology of Fujian Province
                Award ID: No. 171
                Award ID: 2017 and No. 4
                Award ID: 2017
                This study was supported by the Medical Talents Training Program of Health and Family Planning Commission of Fujian Province (2016-ZQN-34); The Medical Center of Minimally Invasive Technology of Fujian Province (No. 171, 2017 and No. 4, 2017); Joint Funds of Scientific and Technological Innovation Program of Fujian Province (2017Y9059);Joint Funds of Scientific and Technological Innovation Program of Fujian Province [2017Y9059];The Medical Center of Minimally Invasive Technology of Fujian Province [No. 171, 2017 and No. 4, 2017].
                Categories
                Original Research

                Immunology
                c-myc,pd-l1,jq1,immunotherapy,pancreatic cancer
                Immunology
                c-myc, pd-l1, jq1, immunotherapy, pancreatic cancer

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