Immunogenic cell death in colon cancer prevention and therapy

Mol Carcinog. 2020 Jul;59(7):783-793. doi: 10.1002/mc.23183. Epub 2020 Mar 25.

Abstract

Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide. The colonic mucosa constitutes a critical barrier and a major site of immune regulation. The immune system plays important roles in cancer development and treatment, and immune activation caused by chronic infection or inflammation is well-known to increase cancer risk. During tumor development, neoplastic cells continuously interact with and shape the tumor microenvironment (TME), which becomes progressively immunosuppressive. The clinical success of immune checkpoint blockade therapies is limited to a small set of CRCs with high tumor mutational load and tumor-infiltrating T cells. Induction of immunogenic cell death (ICD), a type of cell death eliciting an immune response, can therefore help break the immunosuppressive TME, engage the innate components, and prime T cell-mediated adaptive immunity for long-term tumor control. In this review, we discuss the current understanding of ICD induced by antineoplastic agents, the influence of driver mutations, and recent developments to harness ICD in colon cancer. Mechanism-guided combinations of ICD-inducing agents with immunotherapy and actionable biomarkers will likely offer more tailored and durable benefits to patients with colon cancer.

Keywords: cancer prevention; cancer therapy; colon cancer; immunogenic cell death.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Colonic Neoplasms / immunology*
  • Colonic Neoplasms / prevention & control*
  • Colonic Neoplasms / therapy
  • Humans
  • Immunogenic Cell Death / drug effects
  • Immunogenic Cell Death / immunology*
  • Immunotherapy / methods
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology

Substances

  • Antineoplastic Agents