A faithful method for PCR-mediated global mRNA amplification and its integration into microarray analysis on laser-captured cells

Biochem Biophys Res Commun. 2003 Jan 24;300(4):915-20. doi: 10.1016/s0006-291x(02)02967-4.

Abstract

Quantitative and qualitative analyses of mRNAs from a small number of cells are extremely important for studies on gene expression in various physiological and pathological conditions in multicellular organisms. We present here an effective method for high-fidelity global mRNA amplification for in vivo gene expression profiling of as few as 100 cells obtained by laser-captured microdissection (LCM). This method, called TALPAT, is based on T7 RNA polymerase-mediated transcription, adaptor ligation, and PCR amplification followed by T7-transcription. More than 80% of genes were commonly identified as a more than 3-fold changed gene among three gastric cancer cell lines using cRNA amplified by both TALPAT and the ordinary in vitro T7-transcription. The reproducibility of TALPAT was validated by microarray analysis on 100 breast cancer cells obtained by LCM. For the application of the LCM-TALPAT method, we successfully obtained expression profiles of gastric cancer cells and the mesenchymal cells, enabling us to understand in vivo cell-to-cell cross-talk in the microenvironment.

Publication types

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

MeSH terms

  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology
  • Female
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation
  • Humans
  • Lasers*
  • Molecular Sequence Data
  • Oligonucleotide Array Sequence Analysis
  • Polymerase Chain Reaction / methods*
  • RNA, Complementary / genetics
  • RNA, Complementary / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Reproducibility of Results
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / pathology
  • Tumor Cells, Cultured

Substances

  • RNA, Complementary
  • RNA, Messenger