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本文引用的文献

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Biomarker-based MicroRNA Therapeutic Strategies for Hepatocellular Carcinoma.基于生物标志物的微小 RNA 治疗策略治疗肝细胞癌。
J Clin Transl Hepatol. 2014 Dec;2(4):253-8. doi: 10.14218/JCTH.2014.00020. Epub 2014 Dec 15.
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Alterations of Wnt/β-catenin signaling pathway in hepatocellular carcinomas associated with hepatitis C virus.丙型肝炎病毒相关肝细胞癌中Wnt/β-连环蛋白信号通路的改变
Pol J Pathol. 2015 Mar;66(1):9-21. doi: 10.5114/pjp.2015.51148.
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Glypican-3 as a specific biomarker for hepatocellular carcinoma.磷脂酰肌醇蛋白聚糖-3作为肝细胞癌的特异性生物标志物。
Hepatobiliary Pancreat Dis Int. 2015 Apr;14(2):122-3. doi: 10.1016/s1499-3872(15)60350-2.
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Novel molecular targets for diagnosis and treatment of hepatocellular carcinoma.肝细胞癌诊断与治疗的新型分子靶点
Discov Med. 2015 Jan;19(102):7-14.
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Abnormal nuclear expression of Pygopus-2 in human primary hepatocellular carcinoma correlates with a poor prognosis.Pygopus-2 的核表达异常与人类原发性肝细胞癌的不良预后相关。
Histopathology. 2015 Aug;67(2):176-84. doi: 10.1111/his.12637. Epub 2015 Feb 12.
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Encouraging microRNA-based Therapeutic Strategies for Hepatocellular Carcinoma.鼓励基于微小RNA的肝细胞癌治疗策略。
Anticancer Agents Med Chem. 2015;15(4):453-60. doi: 10.2174/1871520615666141216150135.
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Cytoplasmic and/or nuclear expression of β-catenin correlate with poor prognosis and unfavorable clinicopathological factors in hepatocellular carcinoma: a meta-analysis.β-连环蛋白的细胞质和/或细胞核表达与肝细胞癌的不良预后及不利的临床病理因素相关:一项荟萃分析。
PLoS One. 2014 Nov 17;9(11):e111885. doi: 10.1371/journal.pone.0111885. eCollection 2014.
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Molecular profiling of liver tumors: classification and clinical translation for decision making.肝脏肿瘤的分子图谱分析:用于决策的分类及临床转化
Semin Liver Dis. 2014 Nov;34(4):363-75. doi: 10.1055/s-0034-1394137. Epub 2014 Nov 4.
9
CLDN3 inhibits cancer aggressiveness via Wnt-EMT signaling and is a potential prognostic biomarker for hepatocellular carcinoma.紧密连接蛋白3通过Wnt-上皮-间质转化信号通路抑制癌症侵袭性,是肝细胞癌潜在的预后生物标志物。
Oncotarget. 2014 Sep 15;5(17):7663-76. doi: 10.18632/oncotarget.2288.
10
The direct and indirect roles of HBV in liver cancer: prospective markers for HCC screening and potential therapeutic targets.HBV 在肝癌中的直接和间接作用:HCC 筛查的前瞻性标志物和潜在治疗靶点。
J Pathol. 2015 Jan;235(2):355-67. doi: 10.1002/path.4434.

致癌性Wnt3a表达作为肝细胞癌的一种可评估的预后标志物。

Oncogenic Wnt3a expression as an estimable prognostic marker for hepatocellular carcinoma.

作者信息

Pan Liu-Hong, Yao Min, Cai Yin, Gu Juan-Juan, Yang Xu-Li, Wang Li, Yao Deng-Fu

机构信息

Liu-Hong Pan, Deng-Fu Yao, Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu Province, China.

出版信息

World J Gastroenterol. 2016 Apr 14;22(14):3829-36. doi: 10.3748/wjg.v22.i14.3829.

DOI:10.3748/wjg.v22.i14.3829
PMID:27076768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4814746/
Abstract

AIM

To investigate member 3a of Wingless-type MMTV integration site family (Wnt3a) expression in cancerous and surrounding tissues and the relationship between clinicopathologic features of hepatocellular carcinoma (HCC) and Wnt3a expression.

METHODS

Wnt3a expression and cellular distribution and clinicopathologic characteristics in cancerous tissue and matched surrounding tissues were analyzed in 80 HCC patients from January 2006 to August 2008 by tissue microarrays and immunohistochemistry. The overall and disease-free survival rates were estimated using the Kaplan-Meier method and compared with the log-rank test. The prognostic analysis was carried out with univariate and multivariate Cox regressions models.

RESULTS

The incidence of oncogenic Wnt3a expression in the cancerous group was up to 96.25% (77 of 80), which was significantly higher (χ(2) = 48.818, P < 0.001) than that in the surrounding group (46.25%, 37 of 80). Brown Wnt3a staining gradually increased with clinical staging that showed very strong staining in advanced HCC. The clinicopathologic features of high Wnt3a expression in HCC were related to poorly-differentiated grade (χ(2) = 20.211, P < 0.001), liver cirrhosis (χ(2) = 8.467, P < 0.004), hepatitis B virus (HBV) infection (χ(2) = 12.957, P < 0.001), higher tumor-node-metastasis stage (χ(2) = 22.960, P < 0.001), and 5-year survival rate (χ(2) = 15.469, P < 0.001).

CONCLUSION

Oncogenic Wnt3a expression associated with HBV infection and cirrhotic liver might be an independent prognostic factor for HCC.

摘要

目的

研究无翅型MMTV整合位点家族成员3a(Wnt3a)在肝癌组织及其癌旁组织中的表达情况,以及肝细胞癌(HCC)的临床病理特征与Wnt3a表达之间的关系。

方法

采用组织芯片和免疫组化方法,分析2006年1月至2008年8月期间80例HCC患者癌组织及其配对癌旁组织中Wnt3a的表达、细胞分布及临床病理特征。采用Kaplan-Meier法估计总生存率和无病生存率,并通过对数秩检验进行比较。采用单因素和多因素Cox回归模型进行预后分析。

结果

癌组织中致癌性Wnt3a表达发生率高达96.25%(80例中的77例),显著高于癌旁组织(46.25%,80例中的37例)(χ(2)=48.818,P<0.001)。Wnt3a棕色染色随临床分期逐渐增加,在晚期HCC中显示出非常强的染色。HCC中Wnt3a高表达的临床病理特征与低分化程度(χ(2)=20.211,P<0.001)、肝硬化(χ(2)=8.467,P<0.004)、乙型肝炎病毒(HBV)感染(χ(2)=12.957,P<0.001)、较高的肿瘤-淋巴结-转移分期(χ(2)=22.960,P<0.001)和5年生存率(χ(2)=15.469,P<0.001)有关。

结论

与HBV感染和肝硬化肝脏相关的致癌性Wnt3a表达可能是HCC的一个独立预后因素。