Development and Validation of a 28-gene Hypoxia-related Prognostic Signature for Localized Prostate Cancer

EBioMedicine. 2018 May:31:182-189. doi: 10.1016/j.ebiom.2018.04.019. Epub 2018 Apr 23.

Abstract

Background: Hypoxia is associated with a poor prognosis in prostate cancer. This work aimed to derive and validate a hypoxia-related mRNA signature for localized prostate cancer.

Method: Hypoxia genes were identified in vitro via RNA-sequencing and combined with in vivo gene co-expression analysis to generate a signature. The signature was independently validated in eleven prostate cancer cohorts and a bladder cancer phase III randomized trial of radiotherapy alone or with carbogen and nicotinamide (CON).

Results: A 28-gene signature was derived. Patients with high signature scores had poorer biochemical recurrence free survivals in six of eight independent cohorts of prostatectomy-treated patients (Log rank test P < .05), with borderline significances achieved in the other two (P < .1). The signature also predicted biochemical recurrence in patients receiving post-prostatectomy radiotherapy (n = 130, P = .007) or definitive radiotherapy alone (n = 248, P = .035). Lastly, the signature predicted metastasis events in a pooled cohort (n = 631, P = .002). Prognostic significance remained after adjusting for clinic-pathological factors and commercially available prognostic signatures. The signature predicted benefit from hypoxia-modifying therapy in bladder cancer patients (intervention-by-signature interaction test P = .0026), where carbogen and nicotinamide was associated with improved survival only in hypoxic tumours.

Conclusion: A 28-gene hypoxia signature has strong and independent prognostic value for prostate cancer patients.

Keywords: Gene expression signature; Hypoxia; Prognostic biomarker; Prostate cancer; Radiotherapy.

Publication types

  • Clinical Trial, Phase III
  • Randomized Controlled Trial
  • Validation Study

MeSH terms

  • Disease-Free Survival
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Male
  • Neoplasm Metastasis
  • Prostatic Neoplasms* / genetics
  • Prostatic Neoplasms* / metabolism
  • Prostatic Neoplasms* / mortality
  • Prostatic Neoplasms* / therapy
  • Survival Rate
  • Tumor Hypoxia / genetics*