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Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma

BACKGROUND: Accumulating evidence has suggested that Nei-like DNA glycosylase 3 (NEIL3) is associated with human tumors. However, there are few studies on the role of NEIL3 in hepatocellular carcinoma (HCC). The aim of this study was to investigate the expression profile of NEIL3 and its clinical re...

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Autores principales: Wu, Dongyu, Zhang, Guangcong, Ma, Jiamei, Wu, Hongfen, Xiong, Ju, Huang, Xiaoxi, Tian, Yuanyuan, Deng, Taozhi, Han, Xiangyang, Sun, Xiaoning, Xiang, Tian, Yu, Xiangnan, Jiang, Xuemei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519696/
https://www.ncbi.nlm.nih.gov/pubmed/34659404
http://dx.doi.org/10.1155/2021/1301671
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author Wu, Dongyu
Zhang, Guangcong
Ma, Jiamei
Wu, Hongfen
Xiong, Ju
Huang, Xiaoxi
Tian, Yuanyuan
Deng, Taozhi
Han, Xiangyang
Sun, Xiaoning
Xiang, Tian
Yu, Xiangnan
Jiang, Xuemei
author_facet Wu, Dongyu
Zhang, Guangcong
Ma, Jiamei
Wu, Hongfen
Xiong, Ju
Huang, Xiaoxi
Tian, Yuanyuan
Deng, Taozhi
Han, Xiangyang
Sun, Xiaoning
Xiang, Tian
Yu, Xiangnan
Jiang, Xuemei
author_sort Wu, Dongyu
collection PubMed
description BACKGROUND: Accumulating evidence has suggested that Nei-like DNA glycosylase 3 (NEIL3) is associated with human tumors. However, there are few studies on the role of NEIL3 in hepatocellular carcinoma (HCC). The aim of this study was to investigate the expression profile of NEIL3 and its clinical relevance in HCC. MATERIALS AND METHODS: A total of 130 HCC and corresponding nontumor tissues were collected to perform immunohistochemistry (IHC). The clinical relevance and prognostic value of NEIL3 in HCC were analyzed by the chi-square test, Kaplan–Meier analysis, the Cox proportional hazard model, and nomogram. RESULTS: IHC showed that the NEIL3 protein level was remarkably upregulated in tumor tissues compared with nontumor tissues (fold change = 1.24; P < 0.001). High NEIL3 expression was significantly correlated with BCLC stage (P=0.004) and TNM stage (P=0.005). Overall survival (OS) and disease-free survival (DFS) rates in the high NEIL3 expression group were significantly worse than those in the low NEIL3 expression group (P=0.007 and P=0.004, respectively). Furthermore, subgroup analysis showed that high NEIL3 expression predicted worse OS and DFS for HCC patients with advanced TNM stage, poorly differentiated tumor, HBsAg positive, or cirrhosis. Multivariate analysis and the prognostic nomograms revealed that tumor NEIL3 level may serve as a promising prognostic indicator for OS and DFS in HCC patients. CONCLUSION: Our findings suggested that NEIL3 might be a potential prognosis assessment marker and therapeutic target for HCC patients.
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spelling pubmed-85196962021-10-16 Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma Wu, Dongyu Zhang, Guangcong Ma, Jiamei Wu, Hongfen Xiong, Ju Huang, Xiaoxi Tian, Yuanyuan Deng, Taozhi Han, Xiangyang Sun, Xiaoning Xiang, Tian Yu, Xiangnan Jiang, Xuemei J Oncol Research Article BACKGROUND: Accumulating evidence has suggested that Nei-like DNA glycosylase 3 (NEIL3) is associated with human tumors. However, there are few studies on the role of NEIL3 in hepatocellular carcinoma (HCC). The aim of this study was to investigate the expression profile of NEIL3 and its clinical relevance in HCC. MATERIALS AND METHODS: A total of 130 HCC and corresponding nontumor tissues were collected to perform immunohistochemistry (IHC). The clinical relevance and prognostic value of NEIL3 in HCC were analyzed by the chi-square test, Kaplan–Meier analysis, the Cox proportional hazard model, and nomogram. RESULTS: IHC showed that the NEIL3 protein level was remarkably upregulated in tumor tissues compared with nontumor tissues (fold change = 1.24; P < 0.001). High NEIL3 expression was significantly correlated with BCLC stage (P=0.004) and TNM stage (P=0.005). Overall survival (OS) and disease-free survival (DFS) rates in the high NEIL3 expression group were significantly worse than those in the low NEIL3 expression group (P=0.007 and P=0.004, respectively). Furthermore, subgroup analysis showed that high NEIL3 expression predicted worse OS and DFS for HCC patients with advanced TNM stage, poorly differentiated tumor, HBsAg positive, or cirrhosis. Multivariate analysis and the prognostic nomograms revealed that tumor NEIL3 level may serve as a promising prognostic indicator for OS and DFS in HCC patients. CONCLUSION: Our findings suggested that NEIL3 might be a potential prognosis assessment marker and therapeutic target for HCC patients. Hindawi 2021-10-08 /pmc/articles/PMC8519696/ /pubmed/34659404 http://dx.doi.org/10.1155/2021/1301671 Text en Copyright © 2021 Dongyu Wu et al. https://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
Wu, Dongyu
Zhang, Guangcong
Ma, Jiamei
Wu, Hongfen
Xiong, Ju
Huang, Xiaoxi
Tian, Yuanyuan
Deng, Taozhi
Han, Xiangyang
Sun, Xiaoning
Xiang, Tian
Yu, Xiangnan
Jiang, Xuemei
Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title_full Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title_fullStr Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title_full_unstemmed Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title_short Upregulation of Nei-Like DNA Glycosylase 3 Predicts Poor Prognosis in Hepatocellular Carcinoma
title_sort upregulation of nei-like dna glycosylase 3 predicts poor prognosis in hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519696/
https://www.ncbi.nlm.nih.gov/pubmed/34659404
http://dx.doi.org/10.1155/2021/1301671
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