The role of miR-92b-3p in notch signaling and monitoring of oral squamous cell carcinoma

被引:0
|
作者
Piao, Yudan [1 ,2 ]
Jung, Seung-Nam [3 ]
Lim, Mi Ae [3 ]
Zheng, Sicong [2 ]
Oh, Chan [2 ]
Jin, Yan Li [2 ]
Shen, Shan [2 ]
Nguyen, Quoc Khanh [2 ]
Park, Se-Hee [2 ]
Kim, Young il [4 ]
Kim, Min-Gyu [5 ]
Kim, Ji Won [6 ]
Ohm, Sun [7 ]
Chang, Jae Won [2 ,3 ]
Won, Ho-Ryun [2 ,3 ]
Koo, Bon Seok [2 ,3 ]
机构
[1] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dent Dept, 3 East Qingchun Rd, Hangzhou 310016, Zhejiang, Peoples R China
[2] Chungnam Natl Univ, Coll Med, Dept Med Sci, Daejeon, South Korea
[3] Chungnam Natl Univ, Coll Med, Dept Otolaryngol Head & Neck Surg, Daejeon, South Korea
[4] Chungnam Natl Univ, Sejong Hosp, Radiat Oncol, Daejeon, South Korea
[5] Chungnam Natl Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Daejeon, South Korea
[6] Chungnam Natl Univ, Sejong Hosp, Dept Otorhinolaryngol Head & Neck Surg, Sejong, South Korea
[7] Temple Univ, Dept Biol, Philadelpha, PA USA
基金
新加坡国家研究基金会;
关键词
BREAST-CANCER; PROGNOSIS; MIR-155; PATHWAY;
D O I
10.1038/s41388-025-03306-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dysregulation of microRNAs (miRNAs) influences diverse hallmarks of cancer, including proliferative signaling, metastasis, and resistance to cell death. We explored the contribution of miR-92b-3p in oral squamous cell carcinoma (OSCC) and its potential as a monitoring biomarker. Analysis of TCGA, GEO, and our own cohort revealed dysregulation of miR-92b-3p in OSCC, which correlated with aggressive tumor characteristics. miR-92b-3p overexpression augmented proliferation and the epithelial-mesenchymal transition in both YD8 and SCC25 cell lines and xenograft models. Mechanically, augmented miR-92b-3p expression suppressed ATXN1 and CPEB3, activating the Notch signaling pathway and thereby promoting metastasis and cisplatin resistance. In our cohort, serum miR-92b-3p expression reflected the disease status, including relapse. Our results suggest that miR-92b-3p might be an onco-miR involved in OSCC through regulating the ATXN1/CPEB3/Notch pathway. These findings provide novel insights for treating and monitoring OSCC.
引用
收藏
页码:1300 / 1311
页数:12
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