4.8 Article

Trajectory of immune evasion and cancer progression in hepatocellular carcinoma

Journal

NATURE COMMUNICATIONS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-022-29122-w

Keywords

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Funding

  1. National Medical Research Council (NMRC), Singapore [NMRC/TCR/015-NCC/2016, NMRC/CIRG/1460/2016, NMRC/CSA-SI/0013/2017, NMRC/CSA-SI/0018/2017, NMRC/OFLCG/003/2018, NMRC/STaR/020/2013, NMRC/CG/M003/2017, LCG17MAY004, NMRC/OFIRG/0064/2017]
  2. National Research Foundation, Singapore [NRF-NRFF2015-04]

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This study reveals extensive immune remodeling in hepatocellular carcinoma at different stages, indicating a progressive immune evasion of the tumor. The findings provide insights into potential interventions to reverse, prevent or limit the progression of the disease.
Immune evasion is key to cancer initiation and later at metastasis, but its dynamics at intermediate stages, where potential therapeutic interventions could be applied, is undefined. Here we show, using multi-dimensional analyses of resected tumours, their adjacent non-tumour tissues and peripheral blood, that extensive immune remodelling takes place in patients with stage I to III hepatocellular carcinoma (HCC). We demonstrate the depletion of anti-tumoural immune subsets and accumulation of immunosuppressive or exhausted subsets along with reduced tumour infiltration of CD8 T cells peaking at stage II tumours. Corresponding transcriptomic modification occur in the genes related to antigen presentation, immune responses, and chemotaxis. The progressive immune evasion is validated in a murine model of HCC. Our results show evidence of ongoing tumour-immune co-evolution during HCC progression and offer insights into potential interventions to reverse, prevent or limit the progression of the disease. In order to design cancer immune therapies, it is important to understand how tumours evade the immune response that is mounted against them. Authors here analyse the distribution and properties of immune cells in hepatocellular carcinoma and describe a progressive tumour-immune co-evolution programme from early to late stage cancer.

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