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本文引用的文献

1
Oxidative Stress and Liver Cancer: Etiology and Therapeutic Targets.氧化应激与肝癌:病因学及治疗靶点
Oxid Med Cell Longev. 2016;2016:7891574. doi: 10.1155/2016/7891574. Epub 2016 Nov 10.
2
Dose-response association between hepatitis B surface antigen levels and liver cancer risk in Chinese men and women.中国男性和女性乙肝表面抗原水平与肝癌风险之间的剂量反应关联。
Int J Cancer. 2016 Jul 15;139(2):355-62. doi: 10.1002/ijc.30086. Epub 2016 Mar 30.
3
Role of Sex Hormones in the Development and Progression of Hepatitis B Virus-Associated Hepatocellular Carcinoma.性激素在乙型肝炎病毒相关肝细胞癌发生发展中的作用
Int J Endocrinol. 2015;2015:854530. doi: 10.1155/2015/854530. Epub 2015 Sep 27.
4
Cohort Profile: The Shanghai Men's Health Study.队列简介:上海男性健康研究。
Int J Epidemiol. 2015 Jun;44(3):810-8. doi: 10.1093/ije/dyv013. Epub 2015 Mar 2.
5
Global cancer statistics, 2012.全球癌症统计数据,2012 年。
CA Cancer J Clin. 2015 Mar;65(2):87-108. doi: 10.3322/caac.21262. Epub 2015 Feb 4.
6
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.全球癌症发病与死亡:GLOBOCAN 2012 数据源、方法与主要模式。
Int J Cancer. 2015 Mar 1;136(5):E359-86. doi: 10.1002/ijc.29210. Epub 2014 Oct 9.
7
Estrogens increase cystathionine-γ-lyase expression and decrease inflammation and oxidative stress in the myocardium of ovariectomized rats.雌激素增加卵巢切除大鼠心肌中胱硫醚-γ-裂解酶的表达,减少炎症和氧化应激。
Menopause. 2013 Oct;20(10):1084-91. doi: 10.1097/GME.0b013e3182874732.
8
Is mitochondrial DNA content a potential biomarker of mitochondrial dysfunction?线粒体 DNA 含量是否是线粒体功能障碍的潜在生物标志物?
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9
Oxidative DNA damage correlates with cell immortalization and mir-92 expression in hepatocellular carcinoma.氧化 DNA 损伤与肝癌细胞永生化和 mir-92 表达相关。
BMC Cancer. 2012 May 15;12:177. doi: 10.1186/1471-2407-12-177.
10
The tumor microenvironment in hepatocellular carcinoma (review).肝细胞癌的肿瘤微环境(综述)。
Int J Oncol. 2012 Jun;40(6):1733-47. doi: 10.3892/ijo.2012.1408. Epub 2012 Mar 22.

诊断前尿液中 15-F-异前列烷水平与肝癌风险:来自上海女性和男性健康研究的结果。

Pre-diagnostic urinary 15-F -isoprostane level and liver cancer risk: Results from the Shanghai Women's and Men's Health Studies.

机构信息

State Key Laboratory of Oncogene and Related Genes & Department of Epidemiology, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medicine Center, Nashville, TN.

出版信息

Int J Cancer. 2018 Oct 15;143(8):1896-1903. doi: 10.1002/ijc.31591. Epub 2018 Aug 10.

DOI:10.1002/ijc.31591
PMID:29756347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6158048/
Abstract

Oxidative stress has been hypothesized to affect cancer development via various mechanisms, but the evidence from human is limited and inconclusive. 15-F -isoprostane (15-F -IsoP) is an accurate marker of oxidative stress in humans. Recent studies showed that the evidence of urinary 15-F -IsoP level correlating cancer risk is conflicting. We conducted a case-control study nested within two population-based cohort studies. Pre-diagnosis urine samples, collected at cohort enrollment, from 363 incident liver cancer cases and 725 individually matched controls, were used to determine the level of 15-F -IsoP by enzyme-linked immunosorbent assay. Conditional logistic regression model was used to estimate the odds ratio to measure the association between the urinary 15-F -IsoP level and liver cancer risk. We found that higher pre-diagnostic urinary 15-F -IsoP level was associated with an increased liver cancer risk, with an adjusted OR in males (OR  = 8.84, 95% CI 2.74-28.60), which was significantly higher than those in females (OR  = 1.75, 95% CI 0.70-4.42). HBsAg carriers with higher 15-F -IsoP had a significantly increased liver cancer risk (OR  = 59.04, 95% CI 12.26, 284.30; OR  = 92.55, 95% CI 34.83, 245.96) compared to non-carriers with lower 15-F -IsoP. High urinary 15-F -IsoP level was associated with high liver cancer risk, suggesting that 15-F -IsoP may be a promising biomarker for liver cancer risk. The result suggests that people with sero-positive HBsAg and higher level of 15-F -IsoP might be given a higher priority on future surveillance program of liver cancer.

摘要

氧化应激被认为通过多种机制影响癌症的发展,但来自人类的证据有限且不确定。15-F-同型前列腺素(15-F-IsoP)是人类氧化应激的准确标志物。最近的研究表明,尿液 15-F-IsoP 水平与癌症风险相关的证据相互矛盾。我们进行了一项病例对照研究,该研究嵌套在两项基于人群的队列研究中。使用酶联免疫吸附试验(ELISA)测定 363 例肝癌新发病例和 725 例个体匹配对照者在队列入组时收集的前瞻性尿液样本中 15-F-IsoP 的水平。条件逻辑回归模型用于估计比值比以衡量尿液 15-F-IsoP 水平与肝癌风险之间的关联。我们发现,较高的预诊断尿液 15-F-IsoP 水平与肝癌风险增加相关,男性的调整比值比(OR=8.84,95%CI2.74-28.60)明显高于女性(OR=1.75,95%CI0.70-4.42)。与低 15-F-IsoP 的非携带者相比,高 15-F-IsoP 的 HBsAg 携带者的肝癌风险显著增加(OR=59.04,95%CI12.26-284.30;OR=92.55,95%CI34.83-245.96)。高尿 15-F-IsoP 水平与高肝癌风险相关,表明 15-F-IsoP 可能是肝癌风险的有前途的生物标志物。该结果表明,HBsAg 血清阳性和 15-F-IsoP 水平较高的人群可能在未来的肝癌监测计划中得到更高的优先级。