Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features

被引:1
|
作者
Mo, Yingxi [4 ]
Zhao, Jun [1 ,5 ]
Zhao, Ran [1 ,2 ]
Huang, Yiying [1 ]
Liang, Ziyuan [1 ,2 ]
Zhou, Xiaoying [1 ,2 ]
Chu, Jiemei [2 ]
Pan, Xinli [6 ]
Duan, Siyu [2 ]
Chen, Shiman [2 ]
Mo, Liufang [2 ]
Huang, Bizhou [2 ]
Huang, Zhaozhang [2 ]
Wei, Jiale [2 ]
Zheng, Qian [1 ,2 ]
Luo, Wenqi [3 ]
机构
[1] Guangxi Med Univ, Key Lab High Incidence Tumor Prevent & Treatment, Minist Educ, Nanning, Peoples R China
[2] Guangxi Med Univ, Life Sci Inst, 22 Shuangyong Rd, Nanning 530021, Peoples R China
[3] Guangxi Med Univ, Dept Pathol, Canc Hosp, Nanning 530021, Peoples R China
[4] Guangxi Med Univ, Dept Res, Canc Hosp, Nanning, Peoples R China
[5] Guangxi Med Univ, Affiliated Stomatol Hosp, Nanning, Peoples R China
[6] Guangxi Acad Sci, Guangxi Key Lab Marine Nat Prod & Combinatorial Bi, Nanning, Peoples R China
来源
OPEN LIFE SCIENCES | 2023年 / 18卷 / 01期
关键词
clear cell renal cell carcinoma; ACOX1; miR-16-5P; bioinformatics; LIPID-METABOLISM; CANCER; PEROXISOMES; SENSITIVITY; REPRESSION; DIAGNOSIS; BIOMARKER; PATHWAY; MARKER; KIDNEY;
D O I
10.1515/biol-2022-0696
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Clear cell renal cell carcinoma (ccRCC) is a major pathological type of kidney cancer with a poor prognosis due to a lack of biomarkers for early diagnosis and prognosis prediction of ccRCC. In this study, we investigated the aberrant expression of Acyl-coenzyme A oxidase 1 (ACOX1) in ccRCC and evaluated its potential in diagnosis and prognosis. ACOX1 is the first rate-limiting enzyme in the peroxidation beta-oxidation pathway and is involved in the regulation of fatty acid oxidative catabolism. The mRNA and protein levels of ACOX1 were significantly downregulated in ccRCC, and its downregulation was closely associated with the tumor-node-metastasis stage of patients. The ROC curves showed that ACOX1 possesses a high diagnostic value for ccRCC. The OS analysis suggested that lower expression of ACOX1 was closely related to the worse outcome of patients. In addition, gene set enrichment analysis suggested that expression of ACOX1 was positively correlated with CDH1, CDH2, CDKL2, and EPCAM, while negatively correlated with MMP9 and VIM, which strongly indicated that ACOX1 may inhibit the invasion and migration of ccRCC by reversing epithelial-mesenchymal transition. Furthermore, we screened out that miR-16-5p is upregulated at the mRNA transcript level in ccRCC and negatively correlated with ACOX1. In conclusion, our results showed that ACOX1 is abnormally low expressed in ccRCC, suggesting that it could serve as a diagnostic and prognostic biomarker for ccRCC. Overexpression of miR-16-5p may be responsible for the inactivation of ACOX1.
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页数:12
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