4.7 Article

Deletion at 6q24.2-26 predicts longer survival of high-grade serous epithelial ovarian cancer patients

Journal

MOLECULAR ONCOLOGY
Volume 9, Issue 2, Pages 422-436

Publisher

WILEY
DOI: 10.1016/j.molonc.2014.09.010

Keywords

HGSOC; CGH; Survival; 6q24.2-26 deletion; Prognosis

Categories

Funding

  1. Fondo de Investigacion Sanitaria (FIS)
  2. Instituto de Salud Carlos III [PS09/01094, PI12/01319]
  3. Institut de Salud Carlos III of the Ministerio Espanol de Sanidad y Consumo (Miguel Servet tipo II Program) [CPII 13/00047]
  4. Fundacion La Caixa
  5. Red Tematica de Inuestigacion Cooperativa en Cancer (RTICC) [RD12/0036/0028, RD12/0036/0037, RD12/0036/0064]
  6. [8102012-40205]

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Standard treatments for advanced high-grade serous ovarian carcinomas (HGSOCs) show significant side-effects and provide only short-term survival benefits due to disease recurrence. Thus, identification of novel prognostic and predictive biomarkers is urgently needed. We have used 42 paraffin-embedded HGSOCs, to evaluate the utility of DNA copy number alterations, as potential predictors of clinical outcome. Copy number-based unsupervised clustering stratified HGSOCs into two clusters of different immunohistopathological features and survival outcome (HR = 0.15, 95%CI = 0.03-0.81; P-adj = 0.03). We found that loss at 6q24.2-26 was significantly associated with the cluster of longer survival independently from other confounding factors (HR = 0.06, 95%CI = 0.01-0.43, P-adj = 0.005). The prognostic value of this deletion was validated in two independent series, one consisting of 36 HGSOCs analyzed by fluorescent in situ hybridization (P = 0.04) and another comprised of 411 HGSOCs from the Cancer Genome Atlas study (TCGA) (HR = 0.67, 95% CI = 0.48-0.93, P-adj = 0.019). In addition, we confirmed the association of low expression of the genes from the region with longer survival in 799 HGSOCs (HR = 0.74, 95% CI = 0.61-0.90, log-rank P = 0.002) and 675 high-FIGO stage HGSOCs (HR = 0.76, 95% CI = 0.61-0.96, log-rank P = 0.02) available from the online tool KM-plotter. Finally, by integrating copy number, RNAseq and survival data of 296 HGSOCs from TCGA we propose a few candidate genes that can potentially explain the association. Altogether our findings indicate that the 6q24.2-26 deletion is an independent marker of favorable outcome in HGSOCs with potential clinical value as it can be analyzed by FISH on tumor sections and guide the selection of patients towards more conservative therapeutic strategies in order to reduce side-effects and improve quality of life. (C) 2014 The Authors. Published by Elsevier B.V. on behalf of Federation of European Biochemical Societies.

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