Immunogenic cell death in anticancer chemotherapy and its impact on clinical studies

Cancer Lett. 2018 Dec 1:438:17-23. doi: 10.1016/j.canlet.2018.08.028. Epub 2018 Sep 11.

Abstract

The traditional view holds that apoptosis is non-immunogenic and does not induce an inflammatory response. However, recent studies have suggested that certain chemotherapeutic drugs that induce tumor cell apoptosis can induce immunogenic cell death (ICD) in cancer cells. This process is characterized by not only up-regulation of a series of signaling molecules in cancer cells, including expose of calreticulin (CRT), secretion of adenosine triphosphate (ATP) and release of high mobility group box 1 (HMGB1). In this review, we summarize recent progress in identifying and classifying ICD inducers; concepts and molecular mechanisms of ICD; and the impact and potential applications of ICD in clinical studies. We also discuss the contributions of ICD inducers in combination with other anticancer drugs in clinical applications.

Keywords: Anti-tumor immunity; Cancer immunogenic cell death; ICD inducers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine Triphosphate / immunology
  • Adenosine Triphosphate / metabolism
  • Animals
  • Antineoplastic Agents / immunology
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Apoptosis / immunology
  • Calreticulin / immunology
  • Calreticulin / metabolism
  • Endoplasmic Reticulum Stress / drug effects
  • Endoplasmic Reticulum Stress / immunology
  • HMGB1 Protein / immunology
  • HMGB1 Protein / metabolism
  • Humans
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • Neoplasms / metabolism
  • Oxaliplatin / immunology
  • Oxaliplatin / pharmacology
  • Reactive Oxygen Species / immunology
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects*
  • Signal Transduction / immunology

Substances

  • Antineoplastic Agents
  • CALR protein, human
  • Calreticulin
  • HMGB1 Protein
  • Reactive Oxygen Species
  • Oxaliplatin
  • Adenosine Triphosphate