生物
头颈部鳞状细胞癌
基因敲除
基因沉默
下调和上调
癌基因
癌症研究
细胞生长
异位表达
细胞
RNA干扰
细胞周期
细胞凋亡
分子生物学
细胞培养
癌症
核糖核酸
基因
头颈部癌
生物化学
遗传学
作者
Xiaobo Cui,Yali Zhang,Le Zhang,Jiayi Liu,Yunfei Bai,Yanru Cui,Boqian Wang,Shu Zhang,Xin Li
出处
期刊:Gene
[Elsevier]
日期:2022-11-05
卷期号:851: 147033-147033
被引量:2
标识
DOI:10.1016/j.gene.2022.147033
摘要
Lon Peptidase 2, Peroxisomal (LONP2) is a peptidase in peroxisomes that selectively degrades oxidatively damaged proteins in cells and is upregulated in several cancers. In this study, we found both the mRNA and protein level of LONP2 was upregulated in head and neck squamous cell carcinoma (HNSCC) samples. Ectopic overexpressed LONP2 enhanced HNSCC cell growth and migration. Nevertheless, LONP2 silencing suppressed tumor growth in vitro and in vivo. It was also indicated that knockdown of LONP2 also impaired the cell cycle progression and improved apoptosis rate of HNSCC cells. The results of RNA sequencing showed that plastin 3 (PLS3) was heavily downregulated after LONP2 silencing. PLS3 is an actin-bundling protein that functions as an oncogene in several cancers. Furthermore, knockdown of PLS3 inhibited the cell proliferation induced by LONP2 overexpression. In conclusion, we identified an oncogenic effect of LONP2 on cell proliferation and migration in HNSCC via positively regulating the expression of PLS3.
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