Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death worldwide. We sequenced and analyzed the whole genomes of 27 HCCs, 25 of which were associated with hepatitis B or C virus infections, including two sets of multicentric tumors. Although no common somatic mutations were identified in the multicentric tumor pairs, their whole-genome substitution patterns were similar, suggesting that these tumors developed from independent mutations, although their shared etiological backgrounds may have strongly influenced their somatic mutation patterns. Statistical and functional analyses yielded a list of recurrently mutated genes. Multiple chromatin regulators, including ARID1A, ARID1B, ARID2, MLL and MLL3, were mutated in ∼50% of the tumors. Hepatitis B virus genome integration in the TERT locus was frequently observed in a high clonal proportion. Our whole-genome sequencing analysis of HCCs identified the influence of etiological background on somatic mutation patterns and subsequent carcinogenesis, as well as recurrent mutations in chromatin regulators in HCCs.
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The supercomputing resource SHIROKANE was provided by the Human Genome Center at The University of Tokyo. The authors thank T. Urushidate, S. Ohashi, N. Okada, A. Kokubu and H. Shimizu at the National Cancer Center Research Institute and C. Inai, R. Ooishi, and R. Kitada at the RIKEN Center for Genomic Medicine for their technical assistances. This work was supported partially by the Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation (NIBIO), the National Cancer Center Research and Development Fund (23-A-8) and the RIKEN Strategic Research Program for R&D of President's Fund 2011.
The authors declare no competing financial interests.
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Fujimoto, A., Totoki, Y., Abe, T. et al. Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators. Nat Genet 44, 760–764 (2012). https://doi.org/10.1038/ng.2291
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