# Investigation of the Correlation Between Selected miRNAs, Proinflammatory Cytokines, and Serum Trace Elements in Bladder Cancer Development and Progression

**Authors:** Arzu Ay, Nevra Alkanli, Engin Atli, Hakan Gurkan, Pinar Koroglu, Hasan Can Kuvan, Muhidin Hassan Ibrahim, Gokhan Cevik, Necdet Sut

PMC · DOI: 10.3390/cimb48010053 · 2025-12-31

## TL;DR

This study explores how certain miRNAs, cytokines, and trace elements in the blood are linked to bladder cancer development and progression.

## Contribution

The study identifies specific miRNA and cytokine correlations with trace elements in bladder cancer patients.

## Key findings

- miRNA-21 and miRNA-155 levels were significantly higher in bladder cancer patients.
- miRNA-34a levels were significantly lower in bladder cancer patients.
- Copper levels and the copper-to-zinc ratio were elevated in bladder cancer patients.

## Abstract

In our study, we aimed to investigate the relationship between miRNA-21, miRNA-155, miRNA-34a, IL-6, TGF-β, and TNF-α expression levels and serum trace element levels in the development and progression of bladder cancer. RT-PCR was used to establish miRNA-21, miRNA-155, and miRNA-34a expression levels while serum IL-6, TGF-β, and TNF-α levels were determined using the ELISA and measured with an atomic absorption spectrophotometer. In the patient group, miRNA-21 and miRNA-155 expression levels were significantly higher compared with the healthy control group (p < 0.001). Furthermore, in the patient group, miRNA-34a expression was significantly lower compared with the control group (p < 0.001). IL-6, TNF-α, TGF-β, copper levels, and the copper to zinc ratio were significantly higher in the patient group (p < 0.001). Serum iron and zinc levels in the patient group were significantly lower compared with the control group (p < 0.001). There was a significant positive correlation between miRNA-155 and IL-6 and TNF-α (r = 0.279, p = 0.015*; r = 0.325**, p = 0.004). A significant positive correlation was detected between miRNA-34a and IL-6 and TGF-β (r = 0.294*, p = 0.010; r = 0.447**, p < 0.001). By evaluating these important biomarkers together, it might be possible to implement clinical applications for bladder cancer treatment and develop individual therapeutic strategies.

## Linked entities

- **Genes:** MIR21 (microRNA 21) [NCBI Gene 406991], MIR155 (microRNA 155) [NCBI Gene 406947], MIR34A (microRNA 34a) [NCBI Gene 407040]
- **Proteins:** IL6 (interleukin 6), TGFB1 (transforming growth factor beta 1), TNF (tumor necrosis factor)
- **Diseases:** bladder cancer (MONDO:0004986)

## Full-text entities

- **Genes:** MIR155 (microRNA 155) [NCBI Gene 406947] {aka MIRN155, miRNA155, mir-155}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, MIR34A (microRNA 34a) [NCBI Gene 407040] {aka MIRN34A, miRNA34A, mir-34, mir-34a}, MIR21 (microRNA 21) [NCBI Gene 406991] {aka MIRN21, hsa-mir-21, miR-21, miRNA21}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}
- **Diseases:** Bladder Cancer (MESH:D001749)
- **Chemicals:** copper (MESH:D003300), zinc (MESH:D015032), iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12840327/full.md

---
Source: https://tomesphere.com/paper/PMC12840327