A rapid RT-PCR based method for the detection of BCR-ABL translocation

Mol Pathol. 1997 Oct;50(5):266-8. doi: 10.1136/mp.50.5.266.

Abstract

Aims: To optimise a one step reverse transcriptase polymerase chain reaction (RT-PCR) protocol for BCR-ABL chimaera detection.

Methods: Compared with published RT-PCR procedures, this novel approach has at least two advantages. First, the same enzyme is used for both reverse transcription and PCR. Second, amplification of the target (BCR-ABL chimaera) and control gene (ABL) is performed simultaneously in the same tube.

Results: On testing 40 chronic myelogenous leukaemia patients and 10 healthy donors there was a specificity for the newly developed technique. In addition, dilution experiments demonstrated that the protocol was highly sensitive.

Conclusions: The suggested one step PCR strategy is a simple and reliable way to reveal BCR-ABL chimaeras.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • DNA-Directed RNA Polymerases
  • Genes, abl*
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Oncogene Proteins / genetics*
  • Polymerase Chain Reaction / methods*
  • Protein-Tyrosine Kinases*
  • Proto-Oncogene Proteins c-bcr
  • Proto-Oncogene Proteins*
  • Sensitivity and Specificity
  • Time Factors
  • Translocation, Genetic*

Substances

  • Oncogene Proteins
  • Proto-Oncogene Proteins
  • Protein-Tyrosine Kinases
  • BCR protein, human
  • Proto-Oncogene Proteins c-bcr
  • DNA-Directed RNA Polymerases