| Literature DB >> 30426509 |
Ai-Ping Fang1,2, Pei-Yan Chen1, Xiao-Yan Wang1, Zhao-Yan Liu1, Dao-Ming Zhang1, Yun Luo1, Gong-Cheng Liao1, Jing-An Long1, Rong-Huan Zhong1, Zhong-Guo Zhou3,4, Yan-Jun Xu5, Xiao-Jun Xu5, Wen-Hua Ling1,2, Min-Shan Chen3,4, Yao-Jun Zhang3,4, Hui-Lian Zhu1,2.
Abstract
Copper and zinc are essential micronutrients, whose imbalance may be involved in the development and progression of cancer. However, the role of copper and/or zinc imbalance in the prognosis of hepatocellular carcinoma (HCC) is currently unclear. Our objective was to investigate the association between serum levels of copper, zinc and their ratio (copper/zinc) at diagnosis with HCC survival. We included 989 patients with incident HCC in this prospective cohort study, who were enrolled in the Guangdong Liver Cancer Cohort (GLCC) study within 30 days of diagnosis between September 2013 and February 2017. Serum copper and zinc were measured using inductively coupled plasma mass spectrometry. Primary outcomes were liver cancer-specific survival (LCSS) and overall survival (OS). Cox proportional hazards models were used to calculate the multivariable hazard ratios (HRs) and 95% confidence interval (CI). Higher serum copper levels were strongly associated with worse LCSS (Q4 vs. Q1: HR = 1.87, 95% CI: 1.22-2.86; p < 0.01 for trend) and OS (Q4 vs. Q1: HR = 2.06, 95% CI: 1.36-3.11; p < 0.01 for trend). The calculated copper/zinc ratio was positively associated with LCSS (Q4 vs. Q1: HR = 1.31, 95% CI: 0.89-1.92; P = 0.04 for trend) and OS (Q4 vs. Q1: HR = 1.43, 95% CI: 0.99-2.08; P = 0.01 for trend). No overall associations were observed between serum zinc levels and LCSS or OS in the entire cohort. The results suggest that higher serum copper and copper in relation to zinc levels (i.e., higher copper/zinc ratio) may be associated with worse HCC survival, but serum zinc levels may be not associated with HCC survival.Entities:
Keywords: copper; hepatocellular carcinoma; prospective cohort; survival; zinc
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Year: 2019 PMID: 30426509 DOI: 10.1002/ijc.31991
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396