Your browser doesn't support javascript.
loading
PiR-hsa-23533 promotes malignancy in head and neck squamous cell carcinoma via USP7.
Hu, Hanlin; Lu, Jingyu; Xu, Mingjin; Wang, Jie; Zhang, Yeling; Yang, Shan; Wang, Xiaomin; Wang, Mengyuan; Xie, Wenjie; Xu, Wenhua; Lu, Haijun.
Affiliation
  • Hu H; Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China.
  • Lu J; Peking University Cancer Hospital, Beijing, China.
  • Xu M; Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China.
  • Wang J; Department of Pharmacy, Qingdao Hiser Hospital, Qingdao, China.
  • Zhang Y; Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China.
  • Yang S; Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China.
  • Wang X; Qingdao University, Qingdao, China.
  • Wang M; Qingdao University, Qingdao, China.
  • Xie W; Department of Clinical Laboratory, Linyi People's Hospital, Linyi, China.
  • Xu W; Institute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, China. Electronic address: qd.wh@163.com.
  • Lu H; Department of Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China. Electronic address: Lhj82920608@163.com.
Transl Oncol ; 45: 101990, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38735270
ABSTRACT

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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transl Oncol Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Transl Oncol Year: 2024 Document type: Article Affiliation country: China