# miR-28-5p and miR-708-5p Share a Common Seed with Different Functions in Lung Cancer Patients

**Authors:** Cristina Alexandra Ciocan, Cecilia Bica, Liviuta Budisan, Lajos Raduly, Sergiu Chira, Claudia-Cristina Burz, Ovidiu Farc, Antonia Harangus, Marioara Simon, Constantin-Ioan Busuioc, Stefan Strilciuc, Cornelia Braicu, Ioana Berindan-Neagoe

PMC · DOI: 10.3390/ijms262110364 · International Journal of Molecular Sciences · 2025-10-24

## TL;DR

This study explores miR-28-5p and miR-708-5p in lung cancer, finding that they share a seed sequence but have different roles, with miR-708-5p showing potential for clinical use.

## Contribution

The study reveals distinct functional roles of two miRNAs with a shared seed sequence in lung cancer.

## Key findings

- miR-28-5p and miR-708-5p are overexpressed in advanced-stage lung cancer tissues.
- miR-708-5p shows consistent overexpression and potential diagnostic value in lung cancer.
- Both miRNAs regulate cancer-related pathways like ECM-receptor interaction and Hippo signaling.

## Abstract

Lung cancer remains the leading cause of cancer-related mortality worldwide, accounting for nearly 1.8 million deaths annually. The present study aimed to investigate the role of miR-28-5p and miR-708-5p in lung cancer and to analyze the relationship between target gene profiles and transcriptional factor regulation. Both miRNAs that share a common seed sequence were found to be overexpressed in a cohort of 32 paired tumor and adjacent normal tissue samples collected from patients diagnosed at advanced stages (III and IV) of disease. Data from the dbDEMC database revealed that miR-28-5p exhibited variable expression across lung cancer subtypes, whereas miR-708-5p showed consistent overexpression, reinforcing its potential clinical diagnostic significance. Using the TransmiR database, we identified complex TF–miRNA regulatory networks, with both shared and distinct transcription factors controlling miR-28-5p and miR-708-5p. Pathway enrichment analysis indicated that these miRNAs regulate several cancer-associated pathways, including ECM–receptor interaction, adherens junctions, and Hippo signaling. Overall, our findings suggest that miR-708-5p may have a potential clinical application in lung cancer.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** MMRN1 (multimerin 1) [NCBI Gene 22915] {aka ECM, EMILIN4, GPIa*, MMRN}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}
- **Diseases:** Lung Cancer (MESH:D008175), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12607647/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12607647/full.md

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Source: https://tomesphere.com/paper/PMC12607647