# MIRit: an integrative R framework for the identification of impaired miRNA–mRNA regulatory networks in complex diseases

**Authors:** Jacopo Ronchi, Maria Foti

PMC · DOI: 10.1093/bioadv/vbag042 · 2026-02-13

## TL;DR

MIRit is an R package that helps researchers identify disrupted miRNA–mRNA regulatory networks in diseases like cancer and Alzheimer’s, using standardized methods for more accurate insights.

## Contribution

MIRit introduces a flexible and reproducible R framework for analyzing miRNA–mRNA interactions in complex diseases using validated statistical methods.

## Key findings

- MIRit was benchmarked and shown to effectively identify disrupted miRNA–mRNA interactions in three diseases.
- The package supports both matched and unmatched datasets with appropriate statistical tests for each case.
- Functionally relevant disruptions were found consistent with known disease mechanisms in cardiomyopathy, cancer, and Alzheimer’s.

## Abstract

MicroRNAs (miRNAs) play a central role in controlling gene expression, and their abnormal activity is frequently linked to disease. Despite advancements in transcriptomic technologies, elucidating miRNA-mediated mechanisms remains challenging due to methodological limitations and a lack of standardized frameworks.

To overcome these barriers, we developed MIRit, a comprehensive R package designed for the rigorous analysis of miRNA–mRNA interactions. With flexible support for both matched and unmatched datasets, MIRit leverages cutting-edge target identification strategies and applies suitable statistical approaches for each scenario. In this study, we benchmarked the performance of commonly used statistical tests for integrative miRNA analysis and demonstrated the effectiveness of MIRit across three human disease contexts—dilated cardiomyopathy, clear cell renal cell carcinoma, and Alzheimer’s disease—by uncovering functionally relevant miRNA–target disruptions consistent with known disease mechanisms. Through its streamlined pipeline and biologically appropriate methods, MIRit enables more reproducible and accurate insights into the complex landscape of post-transcriptional regulation.

The tool is fully open-source and freely accessible via Bioconductor (https://bioconductor.org/packages/release/bioc/html/MIRit.html), making it readily available to the broader scientific community.

## Linked entities

- **Diseases:** dilated cardiomyopathy (MONDO:0005021), clear cell renal cell carcinoma (MONDO:0005005), Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** MIR141 (microRNA 141) [NCBI Gene 406933] {aka MIRN141, mir-141}, SEMA4A (semaphorin 4A) [NCBI Gene 64218] {aka CORD10, RP35, SEMAB, SEMB}, SLC13A3 (solute carrier family 13 member 3) [NCBI Gene 64849] {aka ARLIAK, NADC3, NaC3, SDCT2}, HOXA7 (homeobox A7) [NCBI Gene 3204] {aka ANTP, HOX1, HOX1.1, HOX1A}, DDX6 (DEAD-box helicase 6) [NCBI Gene 1656] {aka HLR2, IDDILF, P54, RCK, Rck/p54}, TTC39C (tetratricopeptide repeat domain 39C) [NCBI Gene 125488] {aka C18orf17, HsT2697}, MIR142 (microRNA 142) [NCBI Gene 406934] {aka MIRN142, mir-142}, MIR27A (microRNA 27a) [NCBI Gene 407018] {aka MIR27, MIRN27A, mir-27a}, NUP210 (nucleoporin 210) [NCBI Gene 23225] {aka GP210, POM210}, MIR200C (microRNA 200c) [NCBI Gene 406985] {aka MIRN200C, mir-200c}, MIR210 (microRNA 210) [NCBI Gene 406992] {aka MIRN210, mir-210}
- **Diseases:** metastasis (MESH:D009362), hypertrophy (MESH:D006984), myocardial ischemia or infarction (MESH:D009203), VCM (MESH:D002311), coronary artery disease (MESH:D003324), cardiac dysfunction (MESH:D006331), heart failure (MESH:D006333), Clear cell renal cell carcinoma (MESH:D002292), neurodegeneration (MESH:D019636), myocardial disease (MESH:D004194), inflammatory (MESH:D007249), injuries to the myocardium (MESH:D017682), valvular regurgitation (MESH:D006349), tumor (MESH:D009369), AD (MESH:D000544), dyspnea (MESH:D004417), ICM (MESH:D009202), fatigue (MESH:D005221), ventricular dilation (MESH:C566255), SLE (MESH:D008180), kidney cancer (MESH:D007680)
- **Chemicals:** sodium (MESH:D012964)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs2632516

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12961272/full.md

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Source: https://tomesphere.com/paper/PMC12961272