Abstract
Cellular uptake of clinically important deoxynucleoside analogs is mediated by nucleoside transporters including the human equilibrative nucleoside transporter 1 (hENT1) and the concentrative nucleoside transporter-1 (hCNT1). These transporters are responsible for influx of cytarabine and reduced hENT1 expression is a major resistance mechanism in acute myeloid leukemia. We determined hENT1 and hCNT1 protein expression by immunocytochemistry in 50 diagnostic pediatric acute myeloid leukemia patient samples. All samples expressed hENT1 [9/43 (21%) low; 26/43 (60%) medium and 8/43 (19%) high] and hCNT1 [2/42 (5%) low; 35/42 (83%) medium and 5/42 (12%) high] at the cell membrane and cytoplasm. Statistical analysis showed a non-significant relationship between survival and transporter expression and in vitro drug sensitivity. In conclusion, the nucleoside transporters hENT1 and hCNT1 are broadly expressed in pediatric acute myeloid leukemia at diagnosis.
| Original language | English |
|---|---|
| Pages (from-to) | 1379-1388 |
| Number of pages | 10 |
| Journal | Nucleosides, Nucleotides and Nucleic Acids |
| Volume | 39 |
| Issue number | 10-12 |
| DOIs | |
| Publication status | Published - 2020 |
Keywords
- acute lymphoblastic leukemia (ALL)
- Acute myeloid leukemia (AML)
- bovine serum albumin (BSA)
- cytarabine (Ara-C)
- deoxynucleoside analogs (NAs)
- human concentrative nucleoside transporter-1 (hCNT1)
- human equilibrative nucleoside transporter-1 (hENT1)
- phosphate buffered saline (PBS)
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