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Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma
Lactate dehydrogenase (LDH) is an enzyme involved in anaerobic glycolysis and is associated with the prognosis of patients with renal cell carcinoma (RCC). The human genome has four LDH genes: LDHA, LDHB, LDHC and LDHD. In order to determine which of these four LDH genes may predict clear cell RCC (...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019897/ https://www.ncbi.nlm.nih.gov/pubmed/29963157 http://dx.doi.org/10.3892/ol.2018.8782 |
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author | Wang, Yue Li, Gaoxiang Wan, Fangning Dai, Bo Ye, Dingwei |
author_facet | Wang, Yue Li, Gaoxiang Wan, Fangning Dai, Bo Ye, Dingwei |
author_sort | Wang, Yue |
collection | PubMed |
description | Lactate dehydrogenase (LDH) is an enzyme involved in anaerobic glycolysis and is associated with the prognosis of patients with renal cell carcinoma (RCC). The human genome has four LDH genes: LDHA, LDHB, LDHC and LDHD. In order to determine which of these four LDH genes may predict clear cell RCC (ccRCC), a total of 509 patients with ccRCC from The Cancer Genome Atlas (TCGA) cohort and 192 patients with ccRCC from the Fudan University Shanghai Cancer Centre (FUSCC) cohort were enrolled in the present study. The expression profiles of LDHD genes in the TCGA cohort were obtained from the TCGA RNAseq database. The Cox proportional hazards regression model and Kaplan-Meier curves were used to assess relative factors. The LDH family genes that were revealed to have an association with overall survival (OS) were further validated in the FUSCC cohort. In the TCGA cohort, following Cox proportional hazards analysis, LDHD expression (P=0.0400; hazard ratio, 0.872; 95% confidence interval, 0.764–0.994) was revealed to be predictive of the prognosis of patients with ccRCC. Further analysis revealed that low LDHD expression (P<0.0001) was significantly associated with a poor prognosis in terms of OS. Additionally, the expression of LDHD (P<0.0001) was significantly different in patients with ccRCC compared with paired controls. In the FUSCC cohort, low LDHD expression was also associated with a poor OS (P=0.0103), and the tumour pathological T stage was a factor that influenced the expression of LDHD (P=0.0120). Furthermore, the expression of LDHD influenced the serum LDH level (P=0.0126). The downregulation of LDHD expression may be a predictor of poor prognosis in patients with ccRCC. |
format | Online Article Text |
id | pubmed-6019897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60198972018-06-29 Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma Wang, Yue Li, Gaoxiang Wan, Fangning Dai, Bo Ye, Dingwei Oncol Lett Articles Lactate dehydrogenase (LDH) is an enzyme involved in anaerobic glycolysis and is associated with the prognosis of patients with renal cell carcinoma (RCC). The human genome has four LDH genes: LDHA, LDHB, LDHC and LDHD. In order to determine which of these four LDH genes may predict clear cell RCC (ccRCC), a total of 509 patients with ccRCC from The Cancer Genome Atlas (TCGA) cohort and 192 patients with ccRCC from the Fudan University Shanghai Cancer Centre (FUSCC) cohort were enrolled in the present study. The expression profiles of LDHD genes in the TCGA cohort were obtained from the TCGA RNAseq database. The Cox proportional hazards regression model and Kaplan-Meier curves were used to assess relative factors. The LDH family genes that were revealed to have an association with overall survival (OS) were further validated in the FUSCC cohort. In the TCGA cohort, following Cox proportional hazards analysis, LDHD expression (P=0.0400; hazard ratio, 0.872; 95% confidence interval, 0.764–0.994) was revealed to be predictive of the prognosis of patients with ccRCC. Further analysis revealed that low LDHD expression (P<0.0001) was significantly associated with a poor prognosis in terms of OS. Additionally, the expression of LDHD (P<0.0001) was significantly different in patients with ccRCC compared with paired controls. In the FUSCC cohort, low LDHD expression was also associated with a poor OS (P=0.0103), and the tumour pathological T stage was a factor that influenced the expression of LDHD (P=0.0120). Furthermore, the expression of LDHD influenced the serum LDH level (P=0.0126). The downregulation of LDHD expression may be a predictor of poor prognosis in patients with ccRCC. D.A. Spandidos 2018-07 2018-05-22 /pmc/articles/PMC6019897/ /pubmed/29963157 http://dx.doi.org/10.3892/ol.2018.8782 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Yue Li, Gaoxiang Wan, Fangning Dai, Bo Ye, Dingwei Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title | Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title_full | Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title_fullStr | Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title_full_unstemmed | Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title_short | Prognostic value of D-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
title_sort | prognostic value of d-lactate dehydrogenase in patients with clear cell renal cell carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019897/ https://www.ncbi.nlm.nih.gov/pubmed/29963157 http://dx.doi.org/10.3892/ol.2018.8782 |
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