Genomic portrait of resectable hepatocellular carcinomas: Implications of <i>RB1</i> and <i>FGF19</i> aberrations for patient stratification

Sung‐Min Ahn(Asan Medical Center), Se Jin Jang(University of Ulsan), Ju Hyun Shim(University of Ulsan), Deokhoon Kim(Asan Medical Center), Seung‐Mo Hong(Ulsan College), Chang Ohk Sung(University of Ulsan), Daehyun Baek(Seoul National University), Farhan Haq(University of Ulsan), Adnan Ahmad Ansari(Gachon University), Sun Young Lee(Ulsan College), Sung‐Min Chun(Asan Medical Center), Seongmin Choi(Namseoul University), Hyun‐Jeung Choi(Asan Medical Center), Jong-Kyu Kim(Seoul National University), Sukjun Kim(Seoul National University), Shin Hwang(University of Ulsan), Young Joo Lee(Ulsan College), Jongeun Lee(DNA Link (South Korea)), Wang‐rim Jung(DNA Link (South Korea)), Hye Yoon Jang(National University of Singapore), Eunho Yang(DNA Link (South Korea)), Wing‐Kin Sung(Genome Institute of Singapore), Nikki P. Lee(Kingdee (China)), Mao Mao(WuXi AppTec (China)), Charles Lee(Jackson Laboratory), Jessica Zucman‐Rossi(Génomique Fonctionnelle des Tumeurs Solides), Eunsil Yu(University of Ulsan), Han Chu Lee(University of Ulsan), Gu Kong(Anyang University)
Hepatology
May 3, 2014
Cited by 413

Abstract

UNLABELLED: Hepatic resection is the most curative treatment option for early-stage hepatocellular carcinoma, but is associated with a high recurrence rate, which exceeds 50% at 5 years after surgery. Understanding the genetic basis of hepatocellular carcinoma at surgically curable stages may enable the identification of new molecular biomarkers that accurately identify patients in need of additional early therapeutic interventions. Whole exome sequencing and copy number analysis was performed on 231 hepatocellular carcinomas (72% with hepatitis B viral infection) that were classified as early-stage hepatocellular carcinomas, candidates for surgical resection. Recurrent mutations were validated by Sanger sequencing. Unsupervised genomic analyses identified an association between specific genetic aberrations and postoperative clinical outcomes. Recurrent somatic mutations were identified in nine genes, including TP53, CTNNB1, AXIN1, RPS6KA3, and RB1. Recurrent homozygous deletions in FAM123A, RB1, and CDKN2A, and high-copy amplifications in MYC, RSPO2, CCND1, and FGF19 were detected. Pathway analyses of these genes revealed aberrations in the p53, Wnt, PIK3/Ras, cell cycle, and chromatin remodeling pathways. RB1 mutations were significantly associated with cancer-specific and recurrence-free survival after resection (multivariate P = 0.038 and P = 0.012, respectively). FGF19 amplifications, known to activate Wnt signaling, were mutually exclusive with CTNNB1 and AXIN1 mutations, and significantly associated with cirrhosis (P = 0.017). CONCLUSION: RB1 mutations can be used as a prognostic molecular biomarker for resectable hepatocellular carcinoma. Further study is required to investigate the potential role of FGF19 amplification in driving hepatocarcinogenesis in patients with liver cirrhosis and to investigate the potential of anti-FGF19 treatment in these patients.


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