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      Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals

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          Abstract

          Hepatitis C virus infection is a major cause of hepatocellular carcinoma worldwide. Interferon has been the major antiviral treatment, yielding viral clearance in approximately half of patients. New direct-acting antivirals substantially improved the cure rate to above 90%. However, access to therapies remains limited due to the high costs and under-diagnosis of infection in specific subpopulations, e.g., baby boomers, inmates, and injection drug users, and therefore, hepatocellular carcinoma incidence is predicted to increase in the next decades even in high-resource countries. Moreover, cancer risk persists even after 10 years of viral cure, and thus a clinical strategy for its monitoring is urgently needed. Several risk-predictive host factors, e.g., advanced liver fibrosis, older age, accompanying metabolic diseases such as diabetes, persisting hepatic inflammation, and elevated alpha-fetoprotein, as well as viral factors, e.g., core protein variants and genotype 3, have been reported. Indeed, a molecular signature in the liver has been associated with cancer risk even after viral cure. Direct-acting antivirals may affect cancer development and recurrence, which needs to be determined in further investigation.

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          Most cited references35

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          Epidemiology of hepatocellular carcinoma in the United States: where are we? Where do we go?

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            Awareness of infection, knowledge of hepatitis C, and medical follow-up among individuals testing positive for hepatitis C: National Health and Nutrition Examination Survey 2001-2008.

            Many persons infected with hepatitis C virus (HCV) are unknown to the healthcare system because they may be asymptomatic for years, have not been tested for HCV infection, and only seek medical care when they develop liver-related complications. We analyzed data from persons who tested positive for past or current HCV infection during participation in the National Health and Nutrition Examination Survey (NHANES) from 2001 through 2008. A follow-up survey was conducted 6 months after examination to determine (1) how many participants testing positive for HCV infection were aware of their HCV status before being notified by NHANES, (2) what actions participants took after becoming aware of their first positive test, and (3) participants' knowledge about hepatitis C. Of 30,140 participants tested, 393 (1.3%) had evidence of past or current HCV infection and 170 (43%) could be contacted during the follow-up survey and interviewed. Only 49.7% were aware of their positive HCV infection status before being notified by NHANES, and only 3.7% of these respondents reported that they had first been tested for HCV because they or their doctor thought they were at risk for infection. Overall, 85.4% had heard of hepatitis C; correct responses to questions about hepatitis C were higher among persons 40-59 years of age, white non-Hispanics, and respondents who saw a physician after their first positive HCV test. Eighty percent of respondents indicated they had seen a doctor about their first positive HCV test result. These data indicate that fewer than half of those infected with HCV may be aware of their infection. The findings suggest that more intensive efforts are needed to identify and test persons at risk for HCV infection. Copyright © 2012 American Association for the Study of Liver Diseases.
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              Molecular Liver Cancer Prevention in Cirrhosis by Organ Transcriptome Analysis and Lysophosphatidic Acid Pathway Inhibition.

              Cirrhosis is a milieu that develops hepatocellular carcinoma (HCC), the second most lethal cancer worldwide. HCC prediction and prevention in cirrhosis are key unmet medical needs. Here we have established an HCC risk gene signature applicable to all major HCC etiologies: hepatitis B/C, alcohol, and non-alcoholic steatohepatitis. A transcriptome meta-analysis of >500 human cirrhotics revealed global regulatory gene modules driving HCC risk and the lysophosphatidic acid pathway as a central chemoprevention target. Pharmacological inhibition of the pathway in vivo reduced tumors and reversed the gene signature, which was verified in organotypic ex vivo culture of patient-derived fibrotic liver tissues. These results demonstrate the utility of clinical organ transcriptome to enable a strategy, namely, reverse-engineering precision cancer prevention.
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                Author and article information

                Contributors
                thomas.baumert@unistra.fr
                yujin.hoshida@mssm.edu
                Journal
                BMC Med
                BMC Med
                BMC Medicine
                BioMed Central (London )
                1741-7015
                14 March 2017
                14 March 2017
                2017
                : 15
                : 52
                Affiliations
                [1 ]Inserm, U1110, Institut de Recherche sur les Maladies Virales et Hépatiques, Strasbourg, France
                [2 ]ISNI 0000 0001 2157 9291, GRID grid.11843.3f, , Université de Strasbourg, ; Strasbourg, France
                [3 ]ISNI 0000 0000 8928 6711, GRID grid.413866.e, , Institut Hospitalo-Universitaire, Pôle Hépatodigestif, Nouvel Hôpital Civil, ; Strasbourg, France
                [4 ]ISNI 0000 0001 0670 2351, GRID grid.59734.3c, Division of Liver Diseases, Department of Medicine, Liver Cancer Program, Tisch Cancer Institute, , Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, ; 1470 Madison Ave, Box 1123, New York, NY 10029 USA
                [5 ]ISNI 0000 0000 8711 3200, GRID grid.257022.0, Department of Gastroenterology and Metabolism, Applied Life Sciences, Institute of Biomedical and Health Sciences, , Hiroshima University, ; Hiroshima, Japan
                Article
                815
                10.1186/s12916-017-0815-7
                5348895
                28288626
                1c6fb4db-7dc4-49a2-85cb-e1ec417a7354
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 14 November 2016
                : 10 February 2017
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003768, Université de Strasbourg;
                Award ID: IdEx
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000781, European Research Council;
                Award ID: ERC-2014-AdG-671231 HEPCIR
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000781, European Research Council;
                Award ID: ERC-2014-AdG-671231 HEPCIR
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100007601, Horizon 2020;
                Award ID: H2020-667273-HEPCAR
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003323, Agence Nationale de Recherches sur le Sida et les Hepatites Virales;
                Funded by: FundRef http://dx.doi.org/10.13039/501100004097, Fondation ARC pour la Recherche sur le Cancer;
                Award ID: ARC IHU201301187
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000062, National Institute of Diabetes and Digestive and Kidney Diseases;
                Award ID: R01 DK099558
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100006984, Irma T. Hirschl Trust;
                Funded by: FundRef http://dx.doi.org/10.13039/100000182, Medical Research and Materiel Command;
                Award ID: W81XWH-16-1-0363
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000182, Medical Research and Materiel Command;
                Award ID: W81XWH-16-1-0363
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001665, Agence Nationale de la Recherche;
                Award ID: LABEX ANR-10-LAB28
                Award Recipient :
                Funded by: Fondation Université de Strasbourg
                Categories
                Minireview
                Custom metadata
                © The Author(s) 2017

                Medicine
                hepatitis c virus,hepatocellular carcinoma,interferon,direct-acting antivirals,sustained virologic response

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