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).
| Original language | English |
|---|---|
| Journal | Pediatric Blood & Cancer |
| Volume | 61 |
| Issue number | 9 |
| Pages (from-to) | 1704-6 |
| Number of pages | 3 |
| ISSN | 1545-5009 |
| DOIs | |
| Publication status | Published - Sept 2014 |
Keywords
- Adult
- Core Binding Factor Alpha 2 Subunit
- Humans
- In Situ Hybridization, Fluorescence
- Infant, Newborn
- Oncogene Proteins, Fusion
- Precursor Cell Lymphoblastic Leukemia-Lymphoma
- Prognosis
- Translocation, Genetic
Fingerprint
Dive into the research topics of 'False positivity of ETV6/RUNX1 detected by FISH in healthy newborns and adults'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS