CircRNAs regulate the crosstalk between inflammation and tumorigenesis: The bilateral association and molecular mechanisms

Mol Ther. 2023 Jun 7;31(6):1514-1532. doi: 10.1016/j.ymthe.2022.12.005. Epub 2022 Dec 14.

Abstract

Inflammation, a hallmark of cancer, has been associated with tumor progression, transition into malignant phenotype and efficacy of the chemotherapeutic agents in cancer. Chronic inflammation provides a favorable environment for tumorigenesis by inducing immunosuppression, whereas acute inflammation prompts tumor suppression by generating anti-tumor immune responses. Inflammatory factors derived from interstitial cells or tumor cells can stimulate cell proliferation and survival by modulating oncogenes and/or tumor suppressors. Recently, a new class of RNAs, i.e., circular RNAs (circRNAs), has been implicated in inflammatory diseases. Although there are reports on circRNAs imparting functions in inflammatory insults, whether these circularized transcripts hold the potential to regulate inflammation-induced cancer or tumor-related inflammation, and modulate the interactions between tumor microenvironment (TME) and the inflammatory stromal/immune cells, awaits further elucidation. Contextually, the current review describes the molecular association between inflammation and cancer, and spotlights the regulatory mechanisms by which circRNAs can moderate TME in response to inflammatory signals/triggers. We also present comprehensive information about the immune cell(s)-specific expression and functions of the circRNAs in TME, modulation of inflammatory signaling pathways to drive tumorigenesis, and their plausible roles in inflammasomes and tumor development. Moreover, the therapeutic potential of these circRNAs in harnessing inflammatory responses in cancer is also discussed.

Keywords: cancer progression; circRNA; circular RNA; immunosuppression; inflammation; inflammatory microenvironment; signal transduction; tumor microenvironment.

Publication types

  • Review

MeSH terms

  • Cell Transformation, Neoplastic / genetics
  • Humans
  • Inflammation / genetics
  • Neoplasms* / genetics
  • RNA / genetics
  • RNA / metabolism
  • RNA, Circular* / genetics
  • Tumor Microenvironment / genetics

Substances

  • RNA, Circular
  • RNA