Extraction of high-integrity RNA suitable for microarray gene expression analysis from long-term stored human thyroid tissues

Pathology. 2006 Jun;38(3):249-53. doi: 10.1080/00313020600696272.

Abstract

Introduction: Isolation of high-quality RNA from fresh-frozen thyroid tissues stored for more than a decade would open novel options for gene expression profiling. Herein, we describe successful extraction of high-integrity RNA from human thyroid tissues that were stored for more than a decade.

Methods: Seventy-nine samples (15 goitres, 20 follicular adenomas, 30 papillary carcinomas, 14 follicular carcinomas) that were shock-frozen in isopentane and stored for a median of 11 years (range 1-16 years) were processed using standard precipitation and column filtration techniques. RNA integrity was assessed by electrophoresis using the RNA integrity number (RIN) algorithm and by gene expression profiling determining the 3'/5' ratio of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene and the percentage of transcripts detected on the Affymetrix U133 2.0 human genome GeneChip.

Results: The median RNA yield was 1.9 microg/mg tissue (papillary carcinoma 2.1 microg/mg, range 0.2-7.2 microg/mg; follicular carcinoma 2.4 microg/mg, range 0.2-3.2 microg/mg; goitre 1.4 microg/mg, range 0.1-5.4 microg/mg; follicular adenoma 1.6 microg/mg, range 0.1-6.2 microg/mg; p = 0.46) with an 8.6 (7.3-9.8) median RIN. The median GAPDH gene 3'/5' ratio was 1.43 (1.34-1.52) and the median percentage of present calls was 48.1% (42.7-52.0%).

Conclusions: Age and entity independent RNA suitable for expression profiling can be extracted from long-term stored fresh-frozen human thyroid tissues.

MeSH terms

  • Adenocarcinoma, Follicular / chemistry
  • Adenocarcinoma, Follicular / genetics
  • Adenocarcinoma, Follicular / pathology
  • Adenoma / chemistry
  • Adenoma / genetics
  • Adenoma / pathology
  • Carcinoma, Papillary / chemistry
  • Carcinoma, Papillary / genetics
  • Carcinoma, Papillary / pathology
  • Gene Expression Profiling*
  • Glyceraldehyde-3-Phosphate Dehydrogenases / genetics
  • Glyceraldehyde-3-Phosphate Dehydrogenases / metabolism
  • Goiter / genetics
  • Goiter / metabolism
  • Goiter / pathology
  • Humans
  • Oligonucleotide Array Sequence Analysis*
  • Organ Preservation
  • RNA / genetics*
  • RNA / isolation & purification
  • Thyroid Gland
  • Thyroid Neoplasms / chemistry
  • Thyroid Neoplasms / genetics*
  • Time Factors

Substances

  • RNA
  • Glyceraldehyde-3-Phosphate Dehydrogenases