The p53 Saga: Early Steps in the Development of Tumor Immunotherapy

J Immunol. 2020 May 1;204(9):2321-2328. doi: 10.4049/jimmunol.1901343.

Abstract

This year marks the 40th anniversary of the initial identification of p53 as a transformation-related Ag, which was the result of our effort to identify an antigenically distinct tumor Ag of a chemically induced mouse tumor and develop a cancer vaccine. Many researchers at the time viewed this effort as folly. Since then, its characterization has progressed from being an attractive cancer vaccine candidate to recognition as a key player in regulating critical pathways controlling the cell cycle and oncogenesis. Advances in molecular immunology and oncology have enhanced the role of p53 in both fields. It is now apparent that p53 plays a critical role in controlling immune recognition and responses in normal tissues as well as the tumor microenvironment. Together with the advances in clinical implementation of p53-based cancer immunotherapy, they highlight the importance of p53 in many areas of basic and translational cancer research.

Publication types

  • Research Support, N.I.H., Intramural
  • Review

MeSH terms

  • Animals
  • Antigens, Neoplasm / immunology
  • Cancer Vaccines / immunology
  • Carcinogenesis / immunology
  • Cell Cycle / immunology
  • Humans
  • Immunotherapy / methods*
  • Neoplasms / immunology
  • Neoplasms / therapy
  • Signal Transduction / immunology
  • Tumor Microenvironment / immunology
  • Tumor Suppressor Protein p53 / immunology*

Substances

  • Antigens, Neoplasm
  • Cancer Vaccines
  • Tumor Suppressor Protein p53