Does particle radiation have superior radiobiological advantages for prostate cancer cells? A systematic review of in vitro studies

Eur J Med Res. 2022 Dec 26;27(1):306. doi: 10.1186/s40001-022-00942-2.

Abstract

Background: Charged particle beams from protons to carbon ions provide many significant physical benefits in radiation therapy. However, preclinical studies of charged particle therapy for prostate cancer are extremely limited. The aim of this study was to comprehensively investigate the biological effects of charged particles on prostate cancer from the perspective of in vitro studies.

Methods: We conducted a systematic review by searching EMBASE (OVID), Medline (OVID), and Web of Science databases to identify the publications assessing the radiobiological effects of charged particle irradiation on prostate cancer cells. The data of relative biological effectiveness (RBE), surviving fraction (SF), standard enhancement ratio (SER) and oxygen enhancement ratio (OER) were extracted.

Results: We found 12 studies met the eligible criteria. The relative biological effectiveness values of proton and carbon ion irradiation ranged from 0.94 to 1.52, and 1.67 to 3.7, respectively. Surviving fraction of 2 Gy were 0.17 ± 0.12, 0.55 ± 0.20 and 0.53 ± 0.16 in carbon ion, proton, and photon irradiation, respectively. PNKP inhibitor and gold nanoparticles were favorable sensitizing agents, while it was presented poorer performance in GANT61. The oxygen enhancement ratio values of photon and carbon ion irradiation were 2.32 ± 0.04, and 1.77 ± 0.13, respectively. Charged particle irradiation induced more G0-/G1- or G2-/M-phase arrest, more expression of γ-H2AX, more apoptosis, and lower motility and/or migration ability than photon irradiation.

Conclusions: Both carbon ion and proton irradiation have advantages over photon irradiation in radiobiological effects on prostate cancer cell lines. Carbon ion irradiation seems to have further advantages over proton irradiation.

Keywords: Charged particle irradiation; In vitro; Prostate cancer; Systematic review.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Carbon
  • DNA Repair Enzymes
  • Dose-Response Relationship, Radiation
  • Gold
  • Humans
  • Male
  • Metal Nanoparticles*
  • Oxygen
  • Phosphotransferases (Alcohol Group Acceptor)
  • Prostatic Neoplasms* / radiotherapy
  • Protons

Substances

  • Protons
  • Gold
  • Carbon
  • Oxygen
  • PNKP protein, human
  • Phosphotransferases (Alcohol Group Acceptor)
  • DNA Repair Enzymes