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Review



            Recent updates of genetic and genomic alterations in

            hepatocellular carcinoma


            Zhang Zhao, Jian Huang

            Liver Research Center, Experimental Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China



                ABSTRACT
                Hepatocellular carcinoma (HCC) is one of the most common malignant cancers worldwide. However, the molecular
                mechanisms underlining the development and progression of HCC remain unclear. Genetic and genomic alterations are
                common events in various types of cancers including HCC. With the development and application of next generation
                sequencing technology, novel genetic and genomic alterations in HCC have been identified. Here, the article reviews recent
                updates on the genetic and genomic alterations in HCC.
                Key words: Hepatocellular carcinoma; genetics; genomics; next generation sequencing

            Address for correspondence:
            Prof. Jian Huang, Liver Research Center, Beijing Friendship Hospital, Capital Medical University, 95 Yong An Road, Beijing 100050, China.
            E-mail: huangj1966@hotmail.com
            Received: 05-07-2015, Accepted: 01-10-2015



            INTRODUCTION                                       HCC confirmed the important roles of previously
                                                               reported genetic  and genomic  alterations  in  the
            Hepatocellular carcinoma (HCC) is one of the most   development and progression of HCC.  However,
                                                                                                   [2]
            common malignant  neoplasms  worldwide, with       the fact that the most frequently mutated genes were
            a prevalence of more than 50% in China.  Hepatitis   generally previously reported, and that few novel
            B virus  (HBV) or hepatitis  C  virus  (HCV) infection,   mutated genes with high frequency were identified
            ingestion  of food contaminated with  aflatoxin  B1,   by  the  whole-genome  sequencing  suggests  the
            and alcohol  consumption are considered major
            risk factors for HCC development.  Despite  well-  complexity regarding the role of genetic mutations
                                            [1]
            established  risk factors, the  specific molecular   in the pathogenesis of HCC. In this paper, we review
            mechanisms  underlining pathogenesis of HCC        recent updates on genetic mutations and genomic
            remain unclear. Genetic and genomic alterations are   imbalances in HCC.
            common events in various types of cancers including   GENETIC  ALTERATIONS:  MUTATION  AND SINGLE
            HCC, and may be associated with the development
            and progression of cancer. With the development    NUCLEOTIDE POLYMORPHISM
            of the technology of next generation  sequencing,   Somatic mutation
            that  is,  whole-genome  sequencing,  novel genetic
            and genomic alterations have been  identified.     Previous studies have demonstrated that the most
            Recent studies on whole-genome  sequencing  of     significantly mutated genes in HCC include tumor
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             DOI:                                              How to cite this article: Zhao Z, Huang J. Recent updates of genetic
                                                               and genomic alterations in hepatocellular carcinoma.  Hepatoma Res
             10.4103/2394-5079.168446                          2016; 2:31-5.



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