Increased expression of SKP2 is an independent predictor of locoregional recurrence in cervical cancer via promoting DNA-damage response after irradiation

Oncotarget. 2016 Jul 12;7(28):44047-44061. doi: 10.18632/oncotarget.10057.

Abstract

Although radiation therapy was known to be effective to cervical cancer, loco-regional recurrences are frequently found in patients. We aimed to identify a molecular marker predicting the response of cervical cancer to radiotherapy. We included the patients (n = 149) with cervical cancer who had undergone radiotherapy from 2004 to 2006. Tumor samples were collected to examine the association between the expression of S-phase kinase-associated protein 2 (SKP2) and prognosis in cervical cancer. We found higher expression of SKP2 associated with recurrence (HRs: 2.52, p < 0.001), death (HRs: 2.01, p < 0.001) and higher locoregional recurrence rate (HRs: 3.76, p < 0.001). Cervical cancer cell lines with higher expression of SKP2 showed higher colony formation, cell survival rate and fewer DNA damages after irradiation. SKP2-C25, an inhibitor for SKP2 activity, dose-dependently decreased cell viability after irradiation and knockdown of SKP2 impaired DNA-damage response and sensitized the cervical cancer cells to irradiation. Our data showed the SKP2 represents a promising tool to identify patients with cervical cancer who have a higher risk of locoregional recurrence after radiotherapy. Targeting SKP2 may serve as a potential radiosensitizer for developing effective therapeutic strategies against cervical cancer.

Keywords: DNA damage; SKP2; cervical cancer; local recurrence; radioresistance.

MeSH terms

  • Cell Line, Tumor
  • Cell Survival / genetics
  • Cell Survival / radiation effects
  • DNA Damage*
  • DNA Repair
  • Female
  • HeLa Cells
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Prognosis
  • RNA Interference
  • S-Phase Kinase-Associated Proteins / biosynthesis*
  • S-Phase Kinase-Associated Proteins / genetics
  • Signal Transduction / genetics
  • Uterine Cervical Neoplasms / genetics
  • Uterine Cervical Neoplasms / metabolism*
  • Uterine Cervical Neoplasms / radiotherapy*

Substances

  • S-Phase Kinase-Associated Proteins