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      Common Molecular Subtypes among Asian Hepatocellular Carcinoma and Cholangiocarcinoma

      research-article
      1 , 2 , 18 , 1 , 1 , 2 , 2 , 1 , 1 , 1 , 2 , 3 , 4 , 4 , 3 , 5 , 5 , 6 , 7 , 8 , 9 , 10 , 10 , 11 , 12 , 1 , 13 , 13 , 13 , 13 , 13 , 13 , 14 , 15 , 15 , 16 , 17 , 1 , 2 , 2 , 18 , 1
      Cancer cell

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          SUMMARY

          Intrahepatic cholangiocarcinoma (ICC) and hepatocellular carcinoma (HCC) are clinically disparate primary liver cancers with etiological and biological heterogeneity. We identified common molecular subtypes linked to similar prognosis among 199 Thai ICC and HCC patients through systems integration of genomics, transcriptomics, and metabolomics. While ICC and HCC share recurrently mutated genes, including TP53, ARID1A, and ARID2, mitotic checkpoint anomalies distinguish the C1 subtype with key drivers PLK1 and ECT2, whereas the C2 subtype is linked to obesity, T-cell infiltration and bile acid metabolism. These molecular subtypes are found in 582 Asian, but less so in 265 Caucasian patients. Thus, Asian ICC and HCC, while clinically treated as separate entities, share common molecular subtypes with similar actionable drivers to improve precision therapy.

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          Contributors
          On behalf of : on behalf of the TIGER-LC Consortium
          Journal
          101130617
          29778
          Cancer Cell
          Cancer Cell
          Cancer cell
          1535-6108
          1878-3686
          25 May 2017
          22 June 2017
          10 July 2017
          10 July 2018
          : 32
          : 1
          : 57-70.e3
          Affiliations
          [1 ]Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA
          [2 ]Chulabhorn Research Institute, Bangkok, Thailand
          [3 ]Khon Kaen University, Khon Kaen, Thailand
          [4 ]Chiang Mai University, Chiang Mai, Thailand
          [5 ]Chulabhorn Hospital, Bangkok, Thailand
          [6 ]Rajavej hospital, Chiang Mai, Thailand
          [7 ]National Cancer Institute, Bangkok, Thailand
          [8 ]Center for Cancer Research, National Cancer Institute, Bethesda, Maryland
          [9 ]FDA, Bethesda, Maryland, USA
          [10 ]Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA
          [11 ]Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA
          [12 ]Biotech Research and Innovation Centre (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
          [13 ]Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA
          [14 ]Georgetown University Medical Center, Washington, DC, USA
          [15 ]Division of Cancer Genomics, National Cancer Center Research Institute of Tokyo, Tokyo, Japan
          [16 ]Laboratory of Molecular Medicine, Human Genome Center, The institute of Medical Science, The University of Tokyo, Tokyo, Japan
          [17 ]Cancer Inflammation Program, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA
          [18 ]Center of Excellence on Environmental Health and Toxicology, Office of Higher Education Commission, Ministry of Education, Bangkok, Thailand
          Author notes
          [** ]Correspondence and requests for materials should be addressed to C.M and M.R. ( mathuros@ 123456cri.or.th ), or X.W.W. ( xw3u@ 123456nih.gov )
          [*]

          Co-first author

          [19]

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          Article
          PMC5524207 PMC5524207 5524207 nihpa878337
          10.1016/j.ccell.2017.05.009
          5524207
          28648284
          bdff408a-ce30-4f1e-8afd-d14944b021c7
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