Semin Liver Dis 2014; 34(04): 363-375
DOI: 10.1055/s-0034-1394137
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Molecular Profiling of Liver Tumors: Classification and Clinical Translation for Decision Making

Roser Pinyol
1   HCC Translational Research Laboratory, Barcelona Clinic Liver Cancer Group (BCLC), Liver Unit, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Catalonia, Spain
,
Jean Charles Nault
2   Inserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, IUH, Paris, France
3   Université Paris Descartes, Labex Immuno-Oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France
4   Service d'Hépatologie, Hôpital Jean Verdier, AP-HP, Bondy, et Université Paris 13, Bobigny, France
,
Iris M. Quetglas
1   HCC Translational Research Laboratory, Barcelona Clinic Liver Cancer Group (BCLC), Liver Unit, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Catalonia, Spain
,
Jessica Zucman-Rossi
2   Inserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, IUH, Paris, France
3   Université Paris Descartes, Labex Immuno-Oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France
5   Hopital EGP, AP-HP, Paris, France
,
Josep M. Llovet
1   HCC Translational Research Laboratory, Barcelona Clinic Liver Cancer Group (BCLC), Liver Unit, Hospital Clínic, IDIBAPS, CIBEREHD, University of Barcelona, Barcelona, Catalonia, Spain
6   Mount Sinai Liver Cancer Program, Icahn School of Medicine at Mount Sinai, Mount Sinai School of Medicine, New York, New York
7   Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Catalonia, Spain
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Publikationsdatum:
04. November 2014 (online)

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Abstract

Hepatocellular carcinoma (HCC) is a complex disease with a dismal prognosis. Consequently, a translational approach is required to personalized clinical decision making to improve survival of HCC patients. Molecular signatures from cirrhotic livers and single nucleotide polymorphism have been linked with HCC occurrence. Identification of high-risk populations will be useful to design chemopreventive trials. In addition, molecular signatures derived from tumor and nontumor samples are associated with early tumor recurrence due to metastasis and late tumor recurrence due to de novo carcinogenesis after curative treatment, respectively. Identification of patients with a high risk of relapse will guide adjuvant randomized trials. The genetic landscape drawn by next-generation sequencing has highlighted the genomic diversity of HCC. Genetic drivers recurrently mutated belong to different signaling pathways including telomere maintenance, cell-cycle regulators, chromatin remodeling, Wnt/b-catenin, RAS/RAF/MAPK kinase, and AKT/mTOR pathway. These cancer genes will be ideally targeted by biotherapies as a paradigm of stratified medicine adapted to tumor biology.