# Expression of miR-92a and miR-125b and Their Association with Chemoradiotherapy Response in Locally Advanced Cervical Cancer

**Authors:** Renny Anggia Julianti, Andi Darma Putra, Ahmad Fuady, Laila Nuranna, Gatot Purwoto, Kartiwa Hadi Nuryanto, Muhammad Yurizar Yudhistira

PMC · DOI: 10.3390/ijms27041723 · International Journal of Molecular Sciences · 2026-02-11

## TL;DR

This study shows that high miR-92a and low miR-125b levels in cervical cancer patients are linked to poor treatment response and worse survival, suggesting their potential use in personalized treatment strategies.

## Contribution

The study identifies miR-92a and miR-125b as novel biomarkers for predicting chemoradiotherapy response and survival in locally advanced cervical cancer.

## Key findings

- High miR-92a and low miR-125b expression were significantly associated with poor chemoradiotherapy response.
- Elevated miR-92a and reduced miR-125b levels correlated with shorter overall survival in patients.
- A combined model using BMI, miR-92a, and miR-125b showed good predictive performance for treatment outcomes.

## Abstract

Cervical cancer remains a major cause of morbidity and mortality, with most cases in Indonesia diagnosed at a locally advanced stage. Although concurrent chemoradiotherapy is the standard treatment, response varies. Dysregulation of microRNAs (miRNAs), particularly oncogenic miR-92a and tumor suppressor miR-125b, may contribute to treatment resistance. This study aimed to evaluate the association between miR-92a and miR-125b expression and chemoradiotherapy response in locally advanced cervical cancer. This single-center retrospective cohort study included patients with stage IB3–IVA cervical cancer treated with chemoradiotherapy between 2019 and 2025. miRNA expression levels were measured from pretreatment tumor biopsy specimens. Poor response was defined as incomplete response or disease progression after treatment. Appropriate comparative, predictive, and survival analyses were performed. Sixty-eight patients were included. Poor response was significantly associated with underweight body mass index, elevated miR-92a, and reduced miR-125b expression (p < 0.05). High miR-92a and low miR-125b expression were also associated with shorter overall survival (p < 0.001). A combined model incorporating BMI, miR-92a, and miR-125b showed good predictive performance. Elevated miR-92a and reduced miR-125b are associated with poor treatment response and worse survival. These miRNAs may support risk stratification and treatment personalization in locally advanced cervical cancer.

## Linked entities

- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, FBXW7 (F-box and WD repeat domain containing 7) [NCBI Gene 55294] {aka AGO, CDC4, DEDHIL, FBW6, FBW7, FBX30}, MIR17HG (miR-17-92a-1 cluster host gene) [NCBI Gene 407975] {aka C13orf25, LINC00048, MIHG1, MIRH1, MIRHG1, NCRNA00048}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, FOXO1 (forkhead box O1) [NCBI Gene 2308] {aka FKH1, FKHR, FOXO1A}, MIR9-2 (microRNA 9-2) [NCBI Gene 407047] {aka MIRN9-2, hsa-mir-9-2, miRNA9-2, mir-9-2}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}
- **Diseases:** metabolic disorders (MESH:D008659), hypoxia (MESH:D000860), Squamous cell carcinoma (MESH:D002294), pancreatic, hepatic, colorectal, non-small cell lung cancer (MESH:D002289), lung adenocarcinoma (MESH:D000077192), obese (MESH:D009765), hypoxic (MESH:D002534), overweight (MESH:D050177), cervical carcinogenesis (MESH:D063646), uterine carcinosarcoma (MESH:D002296), Tumor (MESH:D009369), adenocarcinoma (MESH:D000230), T-cell dysfunction (MESH:C536780), injury to (MESH:D014947), inflammation (MESH:D007249), sarcopenia (MESH:D055948), Cervical Cancer (MESH:D002583), ovarian serous cystadenocarcinoma (MESH:D010049), stage (MESH:D062706), adenosquamous carcinoma (MESH:D018196), lymph node metastasis (MESH:D008207), breast invasive carcinoma (MESH:D001943), adiposity (MESH:D018205), underweight (MESH:D013851), FIGO stage III-IV disease (MESH:D007676), gynecologic malignancies (MESH:D005833), infections (MESH:D007239), toxicity (MESH:D064420), metastases (MESH:D009362), Malnourished (MESH:D044342), deaths (MESH:D003643), uterine corpus endometrial carcinoma (MESH:D016889)
- **Chemicals:** paraffin (MESH:D010232), oxygen (MESH:D010100), formalin (MESH:D005557), steroid hormone (MESH:D013256), cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12940580/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940580/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940580/full.md

---
Source: https://tomesphere.com/paper/PMC12940580