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LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway

Clear cell renal cell carcinoma (ccRCC) accounts for 60-70% of renal cell carcinoma (RCC) cases. It is an urgent mission to find more therapeutic targets for advanced ccRCC. Leucine-rich a-2-glycoprotein 1 (LRG1) is a secreted protein associated with a variety of malignancies. Our study focused on t...

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Detalles Bibliográficos
Autores principales: Hong, Quan, Wang, Shuqiang, Liu, Shuxin, Chen, Xiangmei, Cai, Guangyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149433/
https://www.ncbi.nlm.nih.gov/pubmed/32337221
http://dx.doi.org/10.1155/2020/1285068
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author Hong, Quan
Wang, Shuqiang
Liu, Shuxin
Chen, Xiangmei
Cai, Guangyan
author_facet Hong, Quan
Wang, Shuqiang
Liu, Shuxin
Chen, Xiangmei
Cai, Guangyan
author_sort Hong, Quan
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) accounts for 60-70% of renal cell carcinoma (RCC) cases. It is an urgent mission to find more therapeutic targets for advanced ccRCC. Leucine-rich a-2-glycoprotein 1 (LRG1) is a secreted protein associated with a variety of malignancies. Our study focused on the expression and mechanism of LRG1 in ccRCC based on data from The Cancer Genome Atlas (TCGA) and provided primary verification including LRG1 expression detection, LRG1 gene methylation detection, and downstream signaling detection. We found that LRG1 was overexpressed in ccRCC kidney tissue samples, and the methylation level of LRG1 gene was significantly decreased in ccRCC. Moreover, the expression of LRG1 was negatively related to patient survival. Based on our previous study and the verification reported in this article, we propose that demethylation-induced overexpression of LRG1 is likely to accelerate ccRCC progression via the TGF-β pathway.
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spelling pubmed-71494332020-04-24 LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway Hong, Quan Wang, Shuqiang Liu, Shuxin Chen, Xiangmei Cai, Guangyan Biomed Res Int Research Article Clear cell renal cell carcinoma (ccRCC) accounts for 60-70% of renal cell carcinoma (RCC) cases. It is an urgent mission to find more therapeutic targets for advanced ccRCC. Leucine-rich a-2-glycoprotein 1 (LRG1) is a secreted protein associated with a variety of malignancies. Our study focused on the expression and mechanism of LRG1 in ccRCC based on data from The Cancer Genome Atlas (TCGA) and provided primary verification including LRG1 expression detection, LRG1 gene methylation detection, and downstream signaling detection. We found that LRG1 was overexpressed in ccRCC kidney tissue samples, and the methylation level of LRG1 gene was significantly decreased in ccRCC. Moreover, the expression of LRG1 was negatively related to patient survival. Based on our previous study and the verification reported in this article, we propose that demethylation-induced overexpression of LRG1 is likely to accelerate ccRCC progression via the TGF-β pathway. Hindawi 2020-03-28 /pmc/articles/PMC7149433/ /pubmed/32337221 http://dx.doi.org/10.1155/2020/1285068 Text en Copyright © 2020 Quan Hong et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hong, Quan
Wang, Shuqiang
Liu, Shuxin
Chen, Xiangmei
Cai, Guangyan
LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title_full LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title_fullStr LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title_full_unstemmed LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title_short LRG1 May Accelerate the Progression of ccRCC via the TGF-β Pathway
title_sort lrg1 may accelerate the progression of ccrcc via the tgf-β pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149433/
https://www.ncbi.nlm.nih.gov/pubmed/32337221
http://dx.doi.org/10.1155/2020/1285068
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