PP2A and tumor radiotherapy

Hereditas. 2020 Aug 26;157(1):36. doi: 10.1186/s41065-020-00149-7.

Abstract

Protein phosphatase 2A (PP2A) is a serine/threonine phosphatase that serves as a key regulator of cellular physiology in the context of apoptosis, mitosis, and DNA damage responses. Canonically, PP2A functions as a tumor suppressor gene. However, recent evidence suggests that inhibiting PP2A activity in tumor cells may represent a viable approach to enhancing tumor sensitivity to chemoradiotherapy as such inhibition can cause cells to enter a disordered mitotic state that renders them more susceptible to cell death. Indeed, there is evidence that inhibiting PP2A can slow tumor growth following radiotherapy in a range of cancer types including ovarian cancer, liver cancer, malignant glioma, pancreatic cancer, and nasopharyngeal carcinoma. In the present review, we discuss current understanding of the role of PP2A in tumor radiotherapy and the potential mechanisms whereby it may influence this process.

Keywords: Conventional tumor radiotherapy; DNA damage response; Protein phosphatase 2A; Radiosensitization effects.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Apoptosis / radiation effects
  • Cell Cycle Checkpoints / genetics
  • Cell Cycle Checkpoints / radiation effects
  • DNA Damage / genetics
  • DNA Damage / radiation effects
  • Humans
  • Mitosis / genetics
  • Mitosis / radiation effects
  • Neoplasms / genetics*
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Neoplasms / radiotherapy
  • Protein Phosphatase 2 / genetics*
  • Protein Phosphatase 2 / metabolism*
  • Radiation Tolerance / genetics
  • Radiotherapy
  • Treatment Outcome

Substances

  • Protein Phosphatase 2