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

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 eval...

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Autores principales: Mo, Yingxi, Zhao, Jun, Zhao, Ran, Huang, Yiying, Liang, Ziyuan, Zhou, Xiaoying, Chu, Jiemei, Pan, Xinli, Duan, Siyu, Chen, Shiman, Mo, Liufang, Huang, Bizhou, Huang, Zhaozhang, Wei, Jiale, Zheng, Qian, Luo, Wenqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505341/
https://www.ncbi.nlm.nih.gov/pubmed/37724116
http://dx.doi.org/10.1515/biol-2022-0696
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author Mo, Yingxi
Zhao, Jun
Zhao, Ran
Huang, Yiying
Liang, Ziyuan
Zhou, Xiaoying
Chu, Jiemei
Pan, Xinli
Duan, Siyu
Chen, Shiman
Mo, Liufang
Huang, Bizhou
Huang, Zhaozhang
Wei, Jiale
Zheng, Qian
Luo, Wenqi
author_facet Mo, Yingxi
Zhao, Jun
Zhao, Ran
Huang, Yiying
Liang, Ziyuan
Zhou, Xiaoying
Chu, Jiemei
Pan, Xinli
Duan, Siyu
Chen, Shiman
Mo, Liufang
Huang, Bizhou
Huang, Zhaozhang
Wei, Jiale
Zheng, Qian
Luo, Wenqi
author_sort Mo, Yingxi
collection PubMed
description 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 β-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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spelling pubmed-105053412023-09-18 Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features Mo, Yingxi Zhao, Jun Zhao, Ran Huang, Yiying Liang, Ziyuan Zhou, Xiaoying Chu, Jiemei Pan, Xinli Duan, Siyu Chen, Shiman Mo, Liufang Huang, Bizhou Huang, Zhaozhang Wei, Jiale Zheng, Qian Luo, Wenqi Open Life Sci Research Article 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 β-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. De Gruyter 2023-09-08 /pmc/articles/PMC10505341/ /pubmed/37724116 http://dx.doi.org/10.1515/biol-2022-0696 Text en © 2023 the author(s), published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
Mo, Yingxi
Zhao, Jun
Zhao, Ran
Huang, Yiying
Liang, Ziyuan
Zhou, Xiaoying
Chu, Jiemei
Pan, Xinli
Duan, Siyu
Chen, Shiman
Mo, Liufang
Huang, Bizhou
Huang, Zhaozhang
Wei, Jiale
Zheng, Qian
Luo, Wenqi
Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title_full Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title_fullStr Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title_full_unstemmed Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title_short Loss of ACOX1 in clear cell renal cell carcinoma and its correlation with clinical features
title_sort loss of acox1 in clear cell renal cell carcinoma and its correlation with clinical features
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505341/
https://www.ncbi.nlm.nih.gov/pubmed/37724116
http://dx.doi.org/10.1515/biol-2022-0696
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