4.7 Review

Epigenetic dysregulation of immune-related pathways in cancer: bioinformatics tools and visualization

Journal

EXPERIMENTAL AND MOLECULAR MEDICINE
Volume 53, Issue 5, Pages 761-771

Publisher

SPRINGERNATURE
DOI: 10.1038/s12276-021-00612-z

Keywords

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Funding

  1. Biostatistics and Bioinformatics Shared Resource at the H. Lee Moffitt Cancer Center & Research Institute, an NCI designated Comprehensive Cancer Center [P30-CA076292]

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Bioinformatics tools help identify the evasion of the immune system by cancer, with abnormal genomic chemical modifications playing a crucial role. Immunotherapy is a powerful weapon against cancer, but tumors often evade it by subduing the immune response through epigenetic dysregulation. Tools and resources are available to help decipher the cancer epigenome and potentially lead to better therapies.
Cancer immune evasion is one of the hallmarks of carcinogenesis. Cancer cells employ multiple mechanisms to avoid immune recognition and suppress antitumor immune responses. Recently, accumulating evidence has indicated that immune-related pathways are epigenetically dysregulated in cancer. Most importantly, the epigenetic footprint of immune-related pathways is associated with the patient outcome, underscoring the crucial need to understand this process. In this review, we summarize the current evidence for epigenetic regulation of immune-related pathways in cancer and describe bioinformatics tools, informative visualization techniques, and resources to help decipher the cancer epigenome. Cancer: Bioinformatics helps identify immune system evasion Abnormal patterns of genomic chemical modification help tumors elude immunological destruction, but sophisticated computational tools could help identify and overcome these survival mechanisms. Immunotherapy can be a potent weapon against cancer, but many tumors evolve the ability to protect themselves by subduing the immune response. Sungjune Kim and colleagues at the Moffitt Cancer Center, Tampa, USA, have reviewed efforts to study how chemical alterations to DNA that affect gene expression contribute to this process. Considerable evidence indicates a role for a modification called methylation in this immune evasion, and researchers now have access to vast repositories of tumor-specific gene methylation profiles. The authors describe these data resources, and highlight some of the software tools that are helping oncologists to identify patterns in the data that might lead to better therapies.

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