Abstract
The leukemia-associated ETV6-RUNX1-translocation frequently emerges prenatally. Reverse-transcriptase PCR screening may indicate presence of ETV6-RUNX1 transcripts in random cord blood samples. Subsequent cell enrichment validation finds significantly lower levels than validation applying fluorescence in situ hybridization (FISH) (<10(-5) vs. 10(-3) to 10(-4)). Using three FISH probe sets, we screened 179,000 cells from ETV6-RUNX1-positive dilution series, healthy adults and random cord blood samples. The t(12;21) single fusion extra signal translocation probe and the ETV6 break apart probe gave false positive results mimicking ETV6-RUNX1-positive cell levels of 10(-3). This questions the paradigm that 1% of newborns have ETV6-RUNX1-positive cells at levels of 10(-3) to 10(-4).
Originalsprog | Engelsk |
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Tidsskrift | Pediatric Blood & Cancer |
Vol/bind | 61 |
Udgave nummer | 9 |
Sider (fra-til) | 1704-6 |
Antal sider | 3 |
ISSN | 1545-5009 |
DOI | |
Status | Udgivet - sep. 2014 |