Evaluation of mRNA by Q-RTPCR and protein expression by AQUA of the M2 subunit of ribonucleotide reductase (RRM2) in human tumors

Cancer Chemother Pharmacol. 2009 Jun;64(1):79-86. doi: 10.1007/s00280-008-0845-0. Epub 2008 Oct 22.

Abstract

Purpose: The purpose of this study was to evaluate baseline RRM2 protein and gene expression in tumors of patients receiving 3-AP.

Methods: Tumor blocks from patients enrolled in phase I and II clinical studies using 3-AP, were evaluated for RRM2 gene and protein expression by quantitative real time polymerase chain reaction (Q-RTPCR) and automated quantitative analysis (AQUA).

Results: Esophageal and gastric cancers overexpressed RRM2 protein when compared to prostate cancer (Z-score, 0.68 +/- 0.94 SD, vs 0.41 +/- 0.84 SD, respectively; p = 0.04). Esophageal and gastric cancers also overexpressed RRM2 mRNA when compared to prostate cancer (relative gene expression 2.56 +/- 1.49 SD, vs 0.29 +/- 0.20 SD, respectively; p = 0.02). Protein and gene expression were moderately associated (Spearman's rank correlation = 0.30; p = 0.12).

Conclusion: RRM2 gene and protein expression varies by tumor type.

Publication types

  • Research Support, N.I.H., Extramural
  • Validation Study

MeSH terms

  • Clinical Trials, Phase I as Topic
  • Clinical Trials, Phase II as Topic
  • Esophageal Neoplasms / drug therapy
  • Esophageal Neoplasms / genetics
  • Gene Expression Regulation, Enzymologic*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Male
  • Polymerase Chain Reaction
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / genetics
  • Protein Subunits
  • Pyridines / pharmacology*
  • RNA, Messenger / metabolism*
  • Ribonucleoside Diphosphate Reductase / genetics
  • Ribonucleoside Diphosphate Reductase / metabolism*
  • Stomach Neoplasms / drug therapy
  • Stomach Neoplasms / genetics
  • Thiosemicarbazones / pharmacology*

Substances

  • Protein Subunits
  • Pyridines
  • RNA, Messenger
  • Thiosemicarbazones
  • 3-aminopyridine-2-carboxaldehyde thiosemicarbazone
  • ribonucleotide reductase M2
  • Ribonucleoside Diphosphate Reductase