Influence of evolution in tumor biobanking on the interpretation of translational research

Cancer Epidemiol Biomarkers Prev. 2008 Dec;17(12):3344-50. doi: 10.1158/1055-9965.EPI-08-0622.

Abstract

Purpose: Translational cancer research increasingly relies on human tissue biospecimens and this has coincided with a shift in tissue biobanking approach. Newer biobanks (post year 2000) deploy standard operating procedures to reduce variability around biospecimen collection. Because current translational research is based on pre-2000 and post-2000 era biospecimens, we consider whether the collection era may influence gene expression data.

Design: We compared the range of breast tumor collection times from pre-2000 and post-2000 era biobanks and compared estrogen receptor (ER) protein expression with collection time. We then collected 10 breast tumor biospecimens under a standardized protocol and examined whether the expression of c-myc and ER was influenced by storage on ice < or = 24 hours.

Results: The range of collection times achieved at a pre-2000 versus post-2000 era biobank differed. Thirty-two percent of biospecimens were cryopreserved within 30 minutes at the pre-2000 era biobank versus 76% at the post-2000 era biobank. Collection time and ER protein level was inversely correlated (r = -0.19, P = 0.025; n = 137). We observed a wide range in initial c-myc and ER mRNA levels (50- versus 130-fold). Although mRNA levels of both genes declined with increasing collection time, the rate of change differed because c-myc was significantly reduced after 24 hours (mean reduction to 79% of initial) versus ER (94% of initial).

Conclusion: The overall shift in biobanking around the year 2000 is reflected in the ranges of collection times associated with pre-2000 and post-2000 era biobanks. Because collection time can differentially alter gene expression, the biospecimen collection era should be considered in gene expression studies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Specimen Banks / trends*
  • Biomedical Research / trends*
  • Blotting, Northern
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • British Columbia
  • Carrier Proteins / metabolism
  • Chi-Square Distribution
  • DNA-Binding Proteins / metabolism
  • Gene Expression
  • Humans
  • Manitoba
  • RNA, Messenger / metabolism
  • Receptors, Estrogen / metabolism
  • Registries
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription Factors / metabolism

Substances

  • Carrier Proteins
  • DNA-Binding Proteins
  • MYCBP protein, human
  • RNA, Messenger
  • Receptors, Estrogen
  • Transcription Factors
  • estrophilin