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Intratumoural immune heterogeneity as a hallmark of tumour evolution and progression in hepatocellular carcinoma.

Phuong H D NguyenSiming MaCheryl Z J PhuaNeslihan Arife KayaHannah L H LaiChun Jye LimJia Qi LimMartin WasserLiyun LaiWai Leong TamTony K H LimWei Keat WanTracy LohWei Qiang LeowYin Huei PangChung Yip ChanSer Yee LeePeng Chung CheowHan Chong TohFlorent GinhouxShridhar IyerAlfred W C KowYock Young DanAlexander ChungGlen K BonneyBrian K P GohSalvatore AlbaniPierce Kah-Hoe ChowWeiwei ZhaiValerie Chew
Published in: Nature communications (2021)
The clinical relevance of immune landscape intratumoural heterogeneity (immune-ITH) and its role in tumour evolution remain largely unexplored. Here, we uncover significant spatial and phenotypic immune-ITH from multiple tumour sectors and decipher its relationship with tumour evolution and disease progression in hepatocellular carcinomas (HCC). Immune-ITH is associated with tumour transcriptomic-ITH, mutational burden and distinct immune microenvironments. Tumours with low immune-ITH experience higher immunoselective pressure and escape via loss of heterozygosity in human leukocyte antigens and immunoediting. Instead, the tumours with high immune-ITH evolve to a more immunosuppressive/exhausted microenvironment. This gradient of immune pressure along with immune-ITH represents a hallmark of tumour evolution, which is closely linked to the transcriptome-immune networks contributing to disease progression and immune inactivation. Remarkably, high immune-ITH and its transcriptomic signature are predictive for worse clinical outcome in HCC patients. This in-depth investigation of ITH provides evidence on tumour-immune co-evolution along HCC progression.
Keyphrases
  • stem cells
  • single cell
  • immune response
  • risk factors
  • dna methylation
  • genome wide
  • prognostic factors