MZT2A serves as a prognostic biomarker and promotes the progression of kidney renal clear cell carcinoma

被引:0
|
作者
Cao, Li [1 ,2 ]
Jing, Xintao [2 ]
Liu, Lijuan [1 ]
Wang, Hui [2 ]
Zhu, Jiaqi [2 ]
Zhou, Jing [2 ]
Peng, Hang [1 ,4 ]
Zhang, Jinyuan [2 ]
Li, Fang [2 ]
Wang, Xiaofei [3 ]
Zhao, Le [1 ]
机构
[1] Xi An Jiao Tong Univ, Precis Med Ctr, Affiliated Hosp 1, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Cell Biol & Genet, Xian 710061, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Biomed Expt Ctr, Xian 710061, Shaanxi, Peoples R China
[4] Shaanxi Prov Peoples Hosp, Dept Gen Surg 2, Xian 710068, Shaanxi, Peoples R China
关键词
MZT2A; Prognostic biomarker; Renal cell carcinoma; Proliferation; Apoptosis; COMPLEXES;
D O I
10.1016/j.heliyon.2024.e35695
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MZT2A is a novel core component in the gamma-tubulin ring complex and aberrantly expressed in some types of tumors. However, MZT2A expression pattern across different cancers and its role in kidney renal clear cell carcinoma have not been sufficiently investigated. A thorough analysis of MZT2A expression landscape across 33 cancer types was conducted, utilizing 712 normal samples and 9807 tumor samples from TCGA (version 37.0), as well as 5112 normal samples from the GTEx databases. MZT2A's impact on KIRC cell viability and proliferation were evaluated through BrdU assays and monitored by cell imaging readers in MZT2A-expressing plasmid or siRNAtransfected cells. Additionally, the effects of MZT2A on cell apoptosis and cell cycle were detected using flow cytometry and Western blot. WGCNA analysis was employed to construct a co-expression gene network associated with MZT2A expression in KIRC, and Pearson correlation coefficient was utilized to examine the relationships between pairs of genes. MZT2A is overexpressed in 25 out of 33 types of cancer, including KIRC. In KIRC, high level of MZT2A was associated with higher clinical stage progression and poorer patients' survival. Downregulation of MZT2A decreased KIRC cell proliferation, retarded cell cycle and promoted apoptosis, while upregulation of MZT2A produced the opposite effects. WGCNA analysis and in vitro experiments revealed that MZT2A activated PI3K/AKT signaling pathway in KIRC. In all, MZT2A was overexpressed in most types of tumors. MZT2A served as an oncogene in KIRC and might be a potential target for guiding future treatments.
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页数:14
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