PiR-hsa-23533 promotes malignancy in head and neck squamous cell carcinoma via USP7

被引:2
|
作者
Hu, Hanlin [1 ]
Lu, Jingyu [2 ]
Xu, Mingjin [1 ]
Wang, Jie [6 ]
Zhang, Yeling [1 ]
Yang, Shan [1 ]
Wang, Xiaomin [5 ]
Wang, Mengyuan [5 ]
Xie, Wenjie [4 ]
Xu, Wenhua [3 ]
Lu, Haijun [1 ]
机构
[1] Qingdao Univ, Dept Oncol, Affiliated Hosp, Qingdao, Peoples R China
[2] Peking Univ Canc Hosp, Beijing, Peoples R China
[3] Qingdao Univ, Inst Regenerat Med & Lab Technol Innovat, Qingdao, Peoples R China
[4] Linyi Peoples Hosp, Dept Clin Lab, Linyi, Peoples R China
[5] Qingdao Univ, Qingdao, Peoples R China
[6] Qingdao Hiser Hosp, Dept Pharm, Qingdao, Peoples R China
来源
TRANSLATIONAL ONCOLOGY | 2024年 / 45卷
基金
中国国家自然科学基金;
关键词
PiRNA; Head and neck squamous cell carcinoma; USP7; Proliferation; Apoptosis; GERMLINE; PIR-823; CANCER; RNA;
D O I
10.1016/j.tranon.2024.101990
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: With regard to head and neck squamous cell carcinoma (HNSCC), its occurrence and advancement are controlled by genetic and epigenetic anomalies. PIWI-interacting RNAs (piRNAs) are recognized with significance in tumor, but the precise molecular mechanisms of piRNAs in HNSCC largely remain undisclosed. Methods: Differentially expressed piRNAs were identified by RNA sequencing. The expression of piR-hsa-23533 was evaluated using quantitative real-time PCR and RNA in situ hybridization. The impacts of piR-hsa-23533 on the proliferation and apoptosis of HNSCC cells were investigated by a series of in vitro and in vivo assays. Results: piR-hsa-23533 exhibits upregulation within HNSCC cells and tissues. Besides, piR-hsa-23533 overexpression promotes proliferation while inhibiting apoptosis in vitro and in vivo, while piR-hsa-23533 silencing has an opposite function. From the mechanistic perspective, piR-hsa-23533 can bind to Ubiquitin-specific protease 7 (USP7), as shown through RNA pull-down and RNA immunoprecipitation assays, promoting USP7 mRNA and protein expression. Conclusions: These findings highlight the functional importance of piR-hsa-23533 in HNSCC and may assist in the development of anti-HNSCC therapeutic target.
引用
收藏
页数:10
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