Hyperthermia Selectively Targets Human Papillomavirus in Cervical Tumors via p53-Dependent Apoptosis

Cancer Res. 2015 Dec 1;75(23):5120-9. doi: 10.1158/0008-5472.CAN-15-0816. Epub 2015 Nov 16.

Abstract

Human papillomavirus (HPV) is associated with cervical cancer, the third most common cancer in women. The high-risk HPV types 16 and 18 are found in over 70% of cervical cancers and produce the oncoprotein, early protein 6 (E6), which binds to p53 and mediates its ubiquitination and degradation. Targeting E6 has been shown to be a promising treatment option to eliminate HPV-positive tumor cells. In addition, combined hyperthermia with radiation is a very effective treatment strategy for cervical cancer. In this study, we examined the effect of hyperthermia on HPV-positive cells using cervical cancer cell lines infected with HPV 16 and 18, in vivo tumor models, and ex vivo-treated patient biopsies. Strikingly, we demonstrate that a clinically relevant hyperthermia temperature of 42 °C for 1 hour resulted in E6 degradation, thereby preventing the formation of the E6-p53 complex and enabling p53-dependent apoptosis and G2-phase arrest. Moreover, hyperthermia combined with p53 depletion restored both the cell-cycle distribution and apoptosis to control levels. Collectively, our findings provide new insights into the treatment of HPV-positive cervical cancer and suggest that hyperthermia therapy could improve patient outcomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Cell Line, Tumor
  • DNA-Binding Proteins / metabolism
  • Female
  • HCT116 Cells
  • HeLa Cells
  • Human papillomavirus 16 / isolation & purification
  • Human papillomavirus 16 / metabolism
  • Human papillomavirus 18 / isolation & purification
  • Human papillomavirus 18 / metabolism
  • Humans
  • Hyperthermia, Induced / methods*
  • Male
  • Mice
  • Mice, Nude
  • Oncogene Proteins, Viral / metabolism
  • Papillomavirus Infections / complications*
  • Papillomavirus Infections / metabolism
  • Papillomavirus Infections / therapy*
  • Papillomavirus Infections / virology
  • Repressor Proteins / metabolism
  • Tumor Suppressor Protein p53 / metabolism*
  • Uterine Cervical Neoplasms / metabolism
  • Uterine Cervical Neoplasms / pathology
  • Uterine Cervical Neoplasms / therapy*
  • Uterine Cervical Neoplasms / virology*
  • Xenograft Model Antitumor Assays

Substances

  • DNA-Binding Proteins
  • E6 protein, Human papillomavirus type 16
  • E6 protein, Human papillomavirus type 18
  • Oncogene Proteins, Viral
  • Repressor Proteins
  • TP53 protein, human
  • Tumor Suppressor Protein p53