Chromodomain-helicase-DNA binding protein 5, 7 and pronecrotic mixed lineage kinase domain-like protein serve as potential prognostic biomarkers in patients with resected pancreatic adenocarcinomas

Crystal S. Seldon, Lauren E. Colbert, William A. Hall, Sarah B. Fisher, David S. Yu, Jerome C. Landry

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Pancreatic cancer is one of the deadliest cancers with a very poor prognosis. Recently, there has been a significantincrease in research directed towards identifying potentialbiomarkers that can be used to diagnose and provideprognostic information for pancreatic cancer. Thesemarkers can be used clinically to optimize and personalizetherapy for individual patients. In this review, we focusedon 3 biomarkers involved in the DNA damage responsepathway and the necroptosis pathway: Chromodomainhelicase-DNA binding protein 5, chromodomain-helicase-DNA binding protein 7, and mixed lineage kinasedomain-like protein. The aim of this article is to reviewpresent literature provided for these biomarkers andcurrent studies in which their effectiveness as prognosticbiomarkers are analyzed in order to determine their futureuse as biomarkers in clinical medicine.

Original languageEnglish (US)
Pages (from-to)358-365
Number of pages8
JournalWorld Journal of Gastrointestinal Oncology
Volume8
Issue number4
DOIs
StatePublished - 2016
Externally publishedYes

Keywords

  • Biomarker
  • Chromodomain-helicase-dna binding protein 5
  • Chromodomain-helicase-dna binding protein 7
  • Mixed lineage kinase domain-like protein
  • Pancreatic adenocarcinoma

ASJC Scopus subject areas

  • Oncology
  • Gastroenterology

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