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

Author:

Wu Dongyu1ORCID,Zhang Guangcong2ORCID,Ma Jiamei3ORCID,Wu Hongfen4ORCID,Xiong Ju5ORCID,Huang Xiaoxi3ORCID,Tian Yuanyuan1ORCID,Deng Taozhi1ORCID,Han Xiangyang1ORCID,Sun Xiaoning6ORCID,Xiang Tian7ORCID,Yu Xiangnan2ORCID,Jiang Xuemei1ORCID

Affiliation:

1. Department of Gastroenterology, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570100, China

2. Department of Gastroenterology and Hepatology, Zhongshan Hospital of Fudan University, Shanghai 200030, China

3. Department of Gastroenterology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, Haikou 570100, China

4. Department of Gastroenterology, Sanya People’s Hospital, Sanya 572000, China

5. Department of General Surgery, People’s Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, China

6. Hainan Medical University, Haikou 570100, China

7. Medical Examination, School of Tropical Medicine and Laboratory Medicine, Hainan Medical University, Haikou 570100, China

Abstract

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.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Oncology

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