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      Micro RNA‐4651 Serves as a Potential Biomarker for Prognosis When Selecting Hepatocellular Carcinoma Patients for Postoperative Adjuvant Transarterial Chemoembolization Therapy

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          Abstract

          Our previous reports have shown that microRNA‐4651 is a potential early diagnostic and prognostic marker for hepatocellular carcinoma. We aimed to investigate whether microRNA‐4651 modified postoperative adjuvant transarterial chemoembolization (pa‐TACE) to improve the prognosis of hepatocellular carcinoma. A hospital‐based retrospective study, including 302 patients with advanced‐stage hepatocellular carcinoma who received tumor resection or tumor resection plus pa‐TACE as an initial therapy, was conducted to assess the effects of microRNA‐4651 on pa‐TACE treatment. MicroRNA‐4651 expression in tumor tissues was tested using the TaqMan‐PCR technique. The sensitivity of tumor cells to doxorubicin (an anticancer drug used in pa‐TACE procedure) was analyzed by the half‐maximal inhibitory concentration (IC50). Upregulated microRNA‐4651 expression in tumor tissues can improve the therapeutic response of patients with hepatocellular carcinoma on pa‐TACE (hazard ratios [95% confidence intervals] = 0.32 [0.22‐0.46] for death risk and 0.39 [0.28‐0.56] for tumor‐recurrence risk, respectively), but downregulated expression cannot. Functional analyses–displayed microRNA‐4651 mimics decreased while its inhibitor increased the IC50 of tumor cells to doxorubicin (0.65 [0.61‐0.69] versus 2.17 [1.98‐2.37] µM). Cytochrome P450 2W1 was shown as a possible target of microRNA‐4651. Additionally, dysregulation of microRNA‐4651 also affected the clinical pathological features of hepatocellular carcinoma and was an independent prognostic factor for this cancer. Conclusion: These results indicate that increasing microRNA‐4651 expression may be beneficial for pa‐TACE in improving hepatocellular carcinoma prognosis.

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          The roles of microRNA in cancer and apoptosis.

          microRNAs (miRNAs) are highly conserved, non-protein-coding RNAs that function to regulate gene expression. In mammals this regulation is primarily carried out by repression of translation. miRNAs play important roles in homeostatic processes such as development, cell proliferation and cell death. Recently the dysregulation of miRNAs has been linked to cancer initiation and progression, indicating that miRNAs may play roles as tumour suppressor genes or oncogenes. The role of miRNAs in apoptosis is not fully understood, however, evidence is mounting that miRNAs are important in this process. The dysregulation of miRNAs involved in apoptosis may provide a mechanism for cancer development and resistance to cancer therapy. This review examines the biosynthesis of miRNA, the mechanisms of miRNA target regulation and the involvement of miRNAs in the initiation and progression of human cancer. It will include miRNAs involved in apoptosis, specifically those miRNAs involved in the regulation of apoptotic pathways and tumour suppressor/oncogene networks. It will also consider emerging evidence supporting a role for miRNAs in modulating sensitivity to anti-cancer therapy.
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            A Review and Update of Treatment Options and Controversies in the Management of Hepatocellular Carcinoma.

            To review the current management, outline recent advances and address controversies in the management of hepatocellular carcinoma (HCC).
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              Serum microRNA panel for early diagnosis of the onset of hepatocellular carcinoma

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                Author and article information

                Contributors
                sjtulongxd@263.net
                Journal
                Hepatol Commun
                Hepatol Commun
                10.1002/(ISSN)2471-254X
                HEP4
                Hepatology Communications
                John Wiley and Sons Inc. (Hoboken )
                2471-254X
                24 September 2018
                October 2018
                : 2
                : 10 ( doiID: 10.1002/hep4.v2.10 )
                : 1259-1273
                Affiliations
                [ 1 ] Department of Pathology the Affiliated Hospital of Youjiang Medical University for Nationalities Baise China
                [ 2 ] Department of Medicine Guangxi Science and Technology University Liuzhou China
                [ 3 ] Department of Medicine the Affiliated Hospital of Youjiang Medical University for Nationalities Baise China
                [ 4 ] Department of Liver Surgery Ren Ji Hospital School of Medicine Shanghai Jiao Tong University Shanghai China
                [ 5 ] Department of Pathology the Affiliated Tumor Hospital, Guangxi Medical University Nanning China
                Author notes
                [*] [* ] Xi‐Dai Long, M.D., Department of Pathology, The Affiliated Hospital of Youjiang Medical University for Nationalities, No. 98, Chengxiang Rd., Baise City, Guangxi Zhuang Autonomous Region 533000, China. E‐mail: sjtulongxd@ 123456263.net , Tel/Fax: +86‐776‐2827661

                [†]

                These authors contributed equally to this work.

                Article
                HEP41245
                10.1002/hep4.1245
                6167067
                30288479
                049d3e29-4141-45c0-94bc-eff9ec181297
                © 2018 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 29 December 2017
                : 19 July 2018
                Page count
                Figures: 7, Tables: 6, Pages: 15, Words: 16467
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 81860489
                Award ID: 81372639
                Award ID: 81472243
                Award ID: 81572353
                Award ID: 81660495
                Award ID: 81760502
                Funded by: Research Program of Guangxi “Zhouyue Scholar”
                Award ID: 2017-38
                Funded by: Natural Science Foundation of Guangxi
                Award ID: 2013GXNSFAA019251
                Award ID: 2014GXNSFAA118144
                Award ID: 2014GXNSFDA118021
                Award ID: 2015GXNSFAA139223
                Award ID: 2016GXNSFDA380003
                Award ID: 2017GXNSFAA198002
                Award ID: 2017GXNSFGA198002
                Funded by: Research Program of Guangxi Clinic Research Center of Hepatobiliary Diseases
                Award ID: AD17129025
                Funded by: Research Program of Guangxi Specially‐invited Expert for Pathology
                Award ID: 2017-6th
                Funded by: Open Research Program from Molecular Immunity Study Room Involving in Acute & Severe Diseases in Guangxi Colleges and Universities
                Award ID: kfkt20160062
                Award ID: kfkt20160063
                Funded by: Innovation Program of Guangxi Municipal Education Department
                Award ID: 201204LX324
                Award ID: 201204LX674
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                hep41245
                October 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.0 mode:remove_FC converted:01.10.2018

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