# Pretreatment expression of miR-191a may predict response to the induction chemotherapy based on cytarabine in acute myeloid leukemia patients – a single-center pilotal study

**Authors:** Agnieszka Szymczyk, Sylwia Chocholska, Katarzyna Radko, Marek Hus, Monika Podhorecka, Francesco Bertolini, Francesco Bertolini, Francesco Bertolini

PMC · DOI: 10.1371/journal.pone.0324320 · PLOS One · 2025-06-24

## TL;DR

This study suggests that the expression level of miR-191a before treatment can predict how well AML patients will respond to cytarabine-based chemotherapy.

## Contribution

The novel finding is that miR-191a expression is a potential predictor of chemotherapy response in AML patients.

## Key findings

- miR-191a expression was significantly associated with response to induction chemotherapy.
- miR-191 expression was higher in FLT3-ITD negative patients compared to positive ones.
- Low miR-191 expression correlated with higher myeloblast counts in AML patients.

## Abstract

Acute myeloid leukemia (AML) is associated with the accumulation of acquired genetic disorders. Moreorver chromosomal and molecular changes are independent prognostic factors that are taken into account to determine prognosis and treatment. MicroRNAs are novel gene regulators, which have been recognized to play an important role in pathological leukemogenesis. This study is aimed to analyze the possible role of micro RNAs as a markers predicting the outcome to induction chemotherapy based on cytarabine.

The expression of miR-34a, miR-191, miR-199a and miR-199b in previously separated bone marrow cells was assessed at the moment of diagnosis in 44 AML patients with use of qRQ-PCR technique. Assessment of response to induction therapy was based on criteria for response to treatment proposed by European LeukemiaNet (ELN).

Only the expression level of miR-191a out of all analyzed microRNAs was significantly associated with the induction chemotherapy response. We detected also significantly higher expression of miR-191 in FLT3-ITD negative group in comparison to FLT3-ITD positive subjects. For miR-34a, miR-199a and miR-199b, no relationship was found between their expression and FLT3-ITD, NPM1 and CEBPA mutations. It was also shown that in the group of patients with low miR-191 expression, the number of myeloblasts was higher (p < 0.05).

These results may prove an important role of miR-191a expression as a predictor of response to the induction chemotherapy based on cytarabine, even in cases when other risk factors are absent.

## Linked entities

- **Genes:** MIR191A (microRNA mir-191a) [NCBI Gene 100315105], MIR34A (microRNA 34a) [NCBI Gene 407040], MIR199A (microRNA mir-199a) [NCBI Gene 100314809], MIR199B (microRNA 199b) [NCBI Gene 406978], NPM1 (nucleophosmin 1) [NCBI Gene 4869], CEBPA (CCAAT enhancer binding protein alpha) [NCBI Gene 1050]
- **Chemicals:** cytarabine (PubChem CID 6253)
- **Diseases:** acute myeloid leukemia (MONDO:0015667)

## Full-text entities

- **Genes:** MIR34A (microRNA 34a) [NCBI Gene 407040] {aka MIRN34A, miRNA34A, mir-34, mir-34a}, MIR199B (microRNA 199b) [NCBI Gene 406978] {aka MIRN199B, mir-199b}, FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, NPM1 (nucleophosmin 1) [NCBI Gene 4869] {aka B23, NPM}, MIR191 (microRNA 191) [NCBI Gene 406966] {aka MIRN191, miR-191}, CEBPA (CCAAT enhancer binding protein alpha) [NCBI Gene 1050] {aka C/EBP-alpha, CEBP}
- **Diseases:** AML (MESH:D015470), genetic (MESH:D030342)
- **Chemicals:** cytarabine (MESH:D003561)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12186893/full.md

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Source: https://tomesphere.com/paper/PMC12186893