4.7 Article

HCC subtypes based on the activity changes of immunologic and hallmark gene sets in tumor and nontumor tissues

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 22, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbaa427

Keywords

hepatocellular carcinoma; immunologic and hallmark gene sets; prognosis; bioinformatic analysis

Funding

  1. National Key Research and Development Program [2018YFC1315400]
  2. Science and Technology Program of Guangzhou, China [201903010039, 201804010474]
  3. R&D Plan of Key Areas in Guangdong Province [2020B1111160003]
  4. National Natural Science Foundation of China [81773176, 81802897, 31401095]
  5. Fundamental Research Funds for the Central Universities [19ykpy18, 20ykpy21]
  6. Science and Technology Planning Project of Guangdong Province, China [2019B020228001]
  7. Sun Yat-sen University Clinical Research 5010 Programme [2016009]

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This study identified three clinically relevant subtypes of HCC based on activity changes of gene sets in tumor and nontumor tissues, improving patient outcomes. The research also revealed the important role of gene sets in both tumor and adjacent nontumor tissues in accurately evaluating prognosis, suggesting consideration of changes in both tissues when selecting HCC treatment modalities, especially post-hepatectomy.
The prognostic role of adjacent nontumor tissue in hepatocellular carcinoma (HCC) patients is still not clear. The activity changes of immunologic and hallmark gene sets in adjacent nontumor tissues may substantially impact on prognosis by affecting proliferation of liver cells and colonization of circulating tumor cells after HCC treatment measures such as hepatectomy. We aimed to identify HCC subtypes and prognostic gene sets based on the activity changes of gene sets in tumor and nontumor tissues, to improve patient outcomes. We comprehensively revealed the activity changes of immunologic and hallmark gene sets in HCC and nontumor samples by gene set variation analysis (GSVA), and identified three clinically relevant subtypes of HCC by nonnegative matrix factorization method (NMF). Patients with subtype 1 had good overall survival, whereas those with subtype 2 and subtype 3 had poor prognosis. Patients with subtype 1 in the validation group also tended to live longer. We also identified three prognostic gene sets in tumor and four prognostic gene sets in nontumor by least absolute shrinkage and selection operator method (LASSO). Interestingly, functional enrichment analysis revealed that in nontumor tissues, genes from four gene sets correlated with immune reaction, cell adhesion, whereas in tumor tissue, genes from three gene sets closely correlated with cell cycle. Our results offer new insights on accurately evaluating prognosis-the important role of gene sets in both tumor and adjacent nontumor tissues, suggesting that when selecting for HCC treatment modality, changes in tumor and nontumor tissues should also be considered, especially after hepatectomy.

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