The mechanism of miR-204-5p promoting the biological behavior of bladder cancer cells by down-regulating TCF12

  • GAO Wuyue ,
  • ZOU Zhenhai ,
  • ZHANG Shuchao ,
  • WANG Zhongqi ,
  • LIU Jianmin ,
  • WANG Chao ,
  • GUO Yuanyuan
Expand
  • Department of Urology, the First Affiliated Hospital of Bengbu Medical university, Bengbu 233000, China

Received date: 2025-01-13

  Online published: 2025-12-17

Abstract

Objective: To explore the effect of miR-204-5p on the proliferation, migration and invasion of bladder cancer cells by specifically regulating the expression level of TCF12, and to further reveal its mechanism. Methods: The expression levels of miR-204-5p in bladder cancer cells and human urothelial cells, as well as bladder cancer tissues and adjacent tissues were detected by qRT-PCR. CCK-8, Transwell and flow cytometry were used to verify the effect of miR-204-5p on bladder tumor cells. The dual luciferase assay was used to verify the targeting relationship between miR-204-5 p and TCF12. Western-blot and qRT-PCR were used to detect the regulatory effect of miR-204-5p on the expression of TCF12. Results: The expression of miR-204-5p was significantly up-regulated in bladder cancer tissues and cell lines (P<0.05). The overexpression of miR-204-5p was confirmed to promote the progression of bladder cancer in vitro (P<0.05). Studies had confirmed that TCF12 was a potential target gene of miR-204-5p, and down-regulation of TCF12 by miR-204-5p promoted the proliferation, migration and invasion of bladder cancer cells. Overexpression of TCF12 could also reverse the effect of miR-204-5p overexpression on bladder cancer cells. Conclusion: miR-204-5p may promote the proliferation, migration and invasion of bladder cancer cells by targeting TCF12 and down-regulating its expression level. Targeting miR-204-5p / TCF12 may provide a potential therapeutic strategy for bladder cancer.

Cite this article

GAO Wuyue , ZOU Zhenhai , ZHANG Shuchao , WANG Zhongqi , LIU Jianmin , WANG Chao , GUO Yuanyuan . The mechanism of miR-204-5p promoting the biological behavior of bladder cancer cells by down-regulating TCF12[J]. Journal of Baotou Medical College, 2025 , 41(11) : 18 -23 . DOI: 10.16833/j.cnki.jbmc.2025.11.004

References

[1] Mohanty SK, Lobo A, Mishra SK, et al. Precision medicine in bladder cancer: present challenges and future directions[J]. J Pers Med, 2023, 13(5): 756.
[2] Shang RF, Lee S, Senavirathne G, et al. microRNAs in action: biogenesis, function and regulation[J]. Nat Rev Genet, 2023, 24(12): 816-833.
[3] Gu YL, Zhang X, Li Y, et al. miR-204-5p-targeted AP1S2 is necessary for papillary thyroid carcinoma[J]. Mol Cell Endocrinol, 2023, 574: 111993.
[4] Luo HH, Lv WZ, Zhang HY, et al. miR-204-5p inhibits cell proliferation and induces cell apoptosis in esophageal squamous cell carcinoma by regulating Nestin[J]. Int J Med Sci, 2022, 19(3): 472-483.
[5] Gao SN, Bian TT, Zhang YQ, et al. TCF12 overexpression as a poor prognostic factor in ovarian cancer[J]. Pathol Res Pract, 2019, 215(9): 152527.
[6] 郑伟, 蔺雪峰, 韩轩茂, 等. miR-140-3p调节PI3K/Akt通路减轻缺氧复氧心肌细胞损伤的实验研究[J]. 包头医学院学报, 2024, 40(8): 26-31.
[7] Siegel RL, Giaquinto AN, Jemal A. Cancer statistics, 2024[J]. CA A Cancer J Clin, 2024, 74(1): 12-49.
[8] 张宏波, 郭婧, 张琦, 等. miR-15a、miR-466b-3p、miR-328-3p和miR-144-5p对硝酸钕诱导小于胎龄儿绒毛膜细胞凋亡的调控作用[J]. 包头医学院学报, 2024, 40(10): 6-11, 86.
[9] Zou ZH, Cheng Q, Zhang SC, et al. miR-205-3p suppresses bladder cancer progression via GLO1 mediated P38/ERK activation[J]. BMC Cancer, 2023, 23(1): 956.
[10] Dong TF, Zhou HL, Tang JH. The tumor-suppressive role of miR-204-5p through targeting ezrin in breast cancer: experimental evidence from cell lines and clinical samples[J]. Clin Breast Cancer, 2025, 25(5): e588-e596.
[11] 马铁军, 任利, 王燕德. miR-204-5p靶向ZEB1调控EMT途径影响胃癌细胞侵袭转移的机制研究[J]. 现代消化及介入诊疗, 2019, 24(10): 1088-1094.
[12] 郝军舰, 郝丽娟. miR-204-5p通过靶向HMGB1抑制甲状腺乳头状癌K1细胞增殖、侵袭和迁移[J]. 第三军医大学学报, 2019, 41(16): 1559-1565.
[13] Hu Y, Liu L, Chen Y, et al. Cancer-cell-secreted miR-204-5p induces leptin signalling pathway in white adipose tissue to promote cancer-associated Cachexia[J]. Nat Commun, 2023, 14(1): 5179.
[14] 王超. miR-204-5p调控作用促进膀胱癌细胞迁移、侵袭的分子机制研究[D]. 蚌埠: 蚌埠医学院, 2021.
[15] Zheng H, Fang JL, Lu W, et al. TCF12 regulates the TGF-β/Smad2/3 signaling pathway to accelerate the progression of osteoarthritis by targeting CXCR4[J]. J Orthop Transl, 2024, 44: 35-46.
[16] Yang J, Zhang LL, Jiang ZY, et al. TCF12 promotes the tumorigenesis and metastasis of hepatocellular carcinoma via upregulation of CXCR4 expression[J]. Theranostics, 2019, 9(20): 5810-5827.
[17] Wang L, Tang YJ, Wu HY, et al. TCF12 activates MAGT1 expression to regulate the malignant progression of pancreatic carcinoma cells[J]. Oncol Lett, 2022, 23(2): 62.
[18] Zhu G, Yang SR, Wang RL, et al. P53/miR-154 pathway regulates the epithelial-mesenchymal transition in glioblastoma multiforme cells by targeting TCF12[J]. Neuropsychiatr Dis Treat, 2021, 17: 681-693.
[19] Chen YF, Yang CC, Kao SY, et al. microRNA-211 enhances the oncogenicity of carcinogen-induced oral carcinoma by repressing TCF12 and increasing antioxidant activity[J]. Cancer Res, 2016, 76(16): 4872-4886.
[20] Wang ZQ, Zhang CW, Chang JK, et al. LncRNA EMX2OS, regulated by TCF12, interacts with FUS to regulate the proliferation, migration and invasion of prostate cancer cells through the cGMP-PKG signaling pathway[J]. Onco Targets Ther, 2020, 13: 7045-7056.
Outlines

/