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PMID: 38353109 Published · ppublish English

MIR27A rs895819 TC genotype increases risk of fluoropyrimidine-induced severe toxicity independently of DPYD variations.

Pharmacogenomics ·Vol. 25 ·No. 2 ·2024-01-00

Ragia G, Biziota E, Koukaki T, Amarantidis K, Manolopoulos VG

Abstract

Aim: MicroRNA 27a (miR-27a) regulates post-transcriptionally DPD activity. We have analyzed the association of MIR27A rs895819T>C variation, that modulates miR-27a expression, with fluropyrimidine-induced toxicity. Materials & methods: MIR27A rs895819T>C genotyping was conducted by TaqMan® allelic discrimination assay in 313 FP-treated cancer patients. Results: In overdominance (TC vs TT + CC), TC genotype was associated with grade 3-4 toxicity (p = 0.002), any grade toxicity (p = 0.052), and delayed drug administration or therapy discontinuation (p = 0.038). Odds of grade 3-4 toxicity were increased by both DPYD deficiency (OR: 8.923; p = 0.006) and MIR27A rs895819 TC genotype (OR: 3.865; p = 0.002). Conclusion: MIR27A rs895819 TC genotype is an independent risk factor for fluoropyrimidine-associated toxicity in the Greek population. Thus, MIR27A rs895819TC patients can be closely monitored for fluoropyrimidine-induced severe toxicity.

Keywords
5-fluorouracil DPYD MIR27A capecitabine chemotherapy fluoropyrimidines overdominance pharmacogenomics rs895819 toxicity
Article Info
Journal
Pharmacogenomics
Abbr.
Pharmacogenomics
ISSN
1744-8042
Published
2024-01-00
Language
English
Country/Region
England
NLM ID
100897350
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