Combining clinicopathological predictors and molecular biomarkers in the oncogenic K-RAS/Ki67/HIF-1α pathway to predict survival in resectable pancreatic cancer

R. Qin, T. C. Smyrk, N. R. Reed, R. L. Schmidt, T. Schnelldorfer, S. T. Chari, G. M. Petersen, A. H. Tang

Research output: Contribution to journalArticle

27 Scopus citations

Abstract

Background:The dismal prognosis of patients diagnosed with pancreatic cancer points to our limited arsenal of effective anticancer therapies. Oncogenic K-RAS hyperactivation is virtually universal in pancreatic cancer, that confers drug resistance, drives aggressive tumorigenesis and rapid metastasis. Pancreatic tumours are often marked by hypovascularity, increased hypoxia and ineffective drug delivery. Thus, biomarker discovery and developing innovative means of countervailing oncogenic K-RAS activation are urgently needed.Methods:Tumour specimens from 147 pancreatic cancer patients were analysed by immunohistochemical (IHC) staining and tissue microarray (TMA). Statistical correlations between selected biomarkers and clinicopathological predictors were examined to predict survival.Results:We find that heightened hypoxia response predicts poor clinical outcome in resectable pancreatic cancer. SIAH is a tumour-specific biomarker. The combination of five biomarkers (EGFR, phospho-ERK, SIAH, Ki67 and HIF-1α) and four clinicopathological predictors (tumour size, pathological grade, margin and lymph node status) predict patient survival post surgery in pancreatic cancer.Conclusions:Combining five biomarkers in the K-RAS/Ki67/HIF-1α pathways with four clinicopathological predictors may assist to better predict survival in resectable pancreatic cancer.

Original languageEnglish (US)
Pages (from-to)514-522
Number of pages9
JournalBritish journal of cancer
Volume112
Issue number3
DOIs
StatePublished - Feb 3 2015

Keywords

  • clinicopathological predictors
  • hypoxia
  • oncogenic K-RAS signalling pathway
  • pancreatic cancer
  • prognostic biomarkers

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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