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miR-4260 serves as a prognostic biomarker and suppresses thyroid cancer progression

delete2026-01-01
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PRE
AI
X
Xuan, Hongyan
Z
Zhang, Defu
Z
Zhang, Qinghua
L
Liu, Zhao
L
Li, Zhiyong
H
Hou, Xiancun
O
Ouyang, Changli *
L
Li, Xiangwen *
DOI:10.5603/ep.107982delete
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Abstract

Abstract

En 中文
Introduction: MicroRNAs (miRNAs) play critical roles in tumorigenesis and malignant transformation. Studies indicate aberrant expression of miR-4260 in various cancers. However, its specific function and underlying molecular mechanisms in thyroid cancer (TC) remain poorly understood. Material and methods: Paired tumor and adjacent non-tumor tissues were collected from a cohort of 120 TC patients undergoing surgical resection. Real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) quantified miR-4260 expression in clinical specimens and cell lines. The prognostic value of miR-4260 expression was evaluated using Kaplan-Meier survival analysis and multivariate Cox proportional hazards regression. The functional impact of miR-4260 on TC cell proliferation, migration, and invasion was assessed using cell transfection, cell counting kit 8 (CCK-8) assays, and Transwell migration/invasion assays. The regulatory interaction between miR-4260 and its potential target gene was validated by dual-luciferase reporter assay. Results: RT-qPCR analysis revealed significantly elevated miR-4260 expression in TC tissues compared to matched non-tumor tissues. High miR-4260 expression correlated significantly with larger tumor size (p = 0.035), deeper invasion depth (p = 0.038), advanced tumor-node-metastasis (TNM) stage (p = 0.022), and lymph node metastasis (LNM) (p = 0.025) compared to low expression. Multivariate Cox analysis identified high miR-4260 expression as an independent predictor of poor prognosis [hazard ratio (HR) = 3.398, 95% confidence interval (CI): 1.559-7.406, p = 0.002]. Functional experiments demonstrated that inhibiting miR-4260 expression significantly attenuated the proliferative and invasive capacities of TC cells. Dual-luciferase assays validated ANK2 as a direct miR-4260 target. RT-qPCR quantification revealed significantly antagonistic expression patterns between ANK2 and miR-4260 in thyroid carcinoma specimens. Rescue experiments further revealed that miR-4260 modulates the malignant phenotype of TC cells by negatively regulating ANK2, indicating their cooperative involvement in TC progression. Conclusions: miR-4260 is critically implicated in TC advancement and unfavorable patient outcomes, establishing its bifunctional value as a clinically significant prognostic indicator and viable therapeutic candidate. (Endokrynol Pol 2026; 77 (2): 89-97)
Keywords:
miR-4260
thyroid cancer
prognostic biomarkers
ANK2
tumor suppression

Journal

E
Endokrynologia Polska
IF:
2.1
Papers:
31
Citations:
1.4K

Organization

X
xuzhou medical university
Scholars:
1.5W
Papers: 7.2K
Citations: 158
H
Hubei University of Chinese Medicine
Scholars:
3.8K
Papers: 1.6K
Citations: 2.1K
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