Myeloperoxidase mRNA detection for lineage determination of leukemic blasts: retrospective analysis

Leukemia. 1995 Jul;9(7):1264-75.

Abstract

Myeloperoxidase (MPO) mRNA is an early myeloid marker; its detection in the morphologically and immunophenotypically primitive blasts of acute undifferentiated leukemia (AUL) establishes myeloid lineage and allows reclassification as acute myelogenous leukemia with minimal differentiation (AML-MO). We have previously reported a procedure for MPO mRNA detection by RT-PCR (reverse transcription-polymerase chain reaction) and an adaptation for use of routine hematology smears. This variant procedure allows retrospective analysis of mRNA and is used in the present study to evaluate the lineage of leukemic blasts in seven cases with morphology and cytochemistry consistent with AUL. All hematology smears used in this study were air-dried, unstained or Wright-stained and stored at room temperature for periods varying between 3 days and 2 years. MPO mRNA was detected in six cases, establishing the myeloid lineage of the blasts and the diagnosis of AML-MO. In the remaining case, the blasts were MPO mRNA negative, confirming the diagnosis of AUL. The RT-PCR procedure for retrospective mRNA analysis is useful in the clinical setting, due to its high specificity and sensitivity, speed (less than 24 h), safety (no radioactivity) and convenient use of routine hematology smears; it is particularly attractive in clinical situations when fresh or frozen specimens are no longer available at the time when the need for molecular diagnostics becomes apparent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Humans
  • Leukemia / diagnosis*
  • Leukemia / enzymology
  • Leukemia, Myeloid, Acute / diagnosis
  • Leukemia, Myeloid, Acute / enzymology
  • Middle Aged
  • Peroxidase / genetics*
  • Polymerase Chain Reaction / methods
  • Predictive Value of Tests
  • RNA, Messenger / blood*
  • Retrospective Studies
  • Sensitivity and Specificity
  • Transcription, Genetic

Substances

  • RNA, Messenger
  • Peroxidase