LncRNA MALAT1 promotes growth and metastasis of head and neck squamous cell carcinoma by repressing VHL through a non-canonical function of EZH2

被引:18
作者
Duan, Yuansheng [1 ,2 ]
Yue, Kai [1 ,2 ]
Ye, Beibei [1 ,2 ]
Chen, Peng [1 ,2 ]
Zhang, Jin [3 ]
He, Qinghua [1 ,2 ]
Wu, Yue [1 ,2 ]
Lai, Qingchuan [1 ,2 ]
Li, Hong [1 ,2 ]
Wu, Yansheng [1 ,2 ]
Jing, Chao [1 ,2 ]
Wang, Xudong [1 ,2 ]
机构
[1] Tianjins Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[2] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Dept Maxillofacial & Otorhinolaryngol Oncol, Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[3] Tianjin Med Univ Canc Inst & Hosp, Dept Bone & Soft Tissue Tumors, Tianjin 300060, Peoples R China
基金
中国国家自然科学基金;
关键词
NONCODING RNA MALAT1; EPITHELIAL-MESENCHYMAL TRANSITION; CANCER; BETA; INVASION; TUMORIGENICITY; SURVIVAL; AXIS;
D O I
10.1038/s41419-023-05667-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long non-coding RNAs (LncRNAs) are implicated in malignant progression of human cancers. Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), a well-known lncRNA, has been reported to play crucial roles in multiple malignancies including head and neck squamous cell carcinoma (HNSCC). However, the underlying mechanisms of MALAT1 in HNSCC progression remain to be further investigated. Here, we elucidated that compared with normal squamous epithelium, MALAT1 was notably upregulated in HNSCC tissues, especially in which was poorly differentiated or with lymph nodes metastasis. Moreover, elevated MALAT1 predicted unfavorable prognosis of HNSCC patients. The results of in vitro and in vivo assays showed that targeting MALAT1 could significantly weaken the capacities of proliferation and metastasis in HNSCC. Mechanistically, MALAT1 inhibited von Hippel-Lindau tumor suppressor (VHL) by activating EZH2/STAT3/Akt axis, then promoted the stabilization and activation of beta-catenin and NF-kappa B which could play crucial roles in HNSCC growth and metastasis. In conclusion, our findings reveal a novel mechanism for malignant progression of HNSCC and suggest that MALAT1 might be a promising therapeutic target for HNSCC treatment.
引用
收藏
页数:12
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