LncRNA SOCS2-AS1 promotes the progression of papillary thyroid cancer by destabilizing p53 protein

被引:4
作者
Zhang, Xiaojian [1 ,2 ]
Zhang, Xiaozhou [1 ,2 ]
Yang, Guang [2 ]
Wan, Long [3 ]
Yin, Fengyan [2 ]
Li, Hongqiang [1 ]
Yin, Detao [1 ]
机构
[1] Zhengzhou Univ, Dept Thyroid Surg, Affiliated Hosp 1, 1 Jianshe East Rd, Zhengzhou 450052, Peoples R China
[2] Qingdao Univ, Dept Thyroid Surg, Affiliated Taian City Cent Hosp, Tai An 271000, Peoples R China
[3] Qingdao Univ, Dept Clin Oncol, Affiliated Taian City Cent Hosp, Tai An 271000, Peoples R China
关键词
LncRNA; SOCS2-AS1; Cell proliferation; Fatty acid oxidation; p53; signaling; CARCINOMA;
D O I
10.1016/j.bbrc.2023.05.080
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
Long noncoding RNAs (lncRNAs) have been shown to contribute to tumorigenesis and cancer progres-sion. However, neither the dysregulation nor the functions of anti-sense lncRNAs in papillary thyroid carcinoma (PTC) have been exhaustively studied. In this study, we accessed The Cancer Genome Atlas (TCGA) database and discovered that the natural antisense lncRNA SOCS2-AS1 is highly expressed in PTC and that patients with a higher level of SOCS2-AS1 had a poor prognosis. Furthermore, loss-and gain -function assays demonstrated that SOCS2-AS1 promotes PTC cell proliferation and growth both in vitro and in vivo. In addition, we demonstrated that SOCS2-AS1 regulates the rate of fatty acid oxidation (FAO) in PTC cells. Analysis of the mechanism revealed that SOCS2-AS1 binds to p53 and controls its stability in PTC cell lines. Overall, our findings showed that the natural antisense lncRNA SOCS2-AS1 stimulates the degradation of p53 and enhances PTC cell proliferation and the FAO rate.& COPY; 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 102
页数:8
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