孤儿核受体TR3/Nur77在慢性肝病中的表达及临床意义

Yingling Zeng, Xiaoguang Ye, Degui Liao, Shizhang Huang, Huinan Mao, Dezheng Zhao, Huiyan Zeng
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引用次数: 1

摘要

目的:虽然癌症治疗取得了巨大的成功,但目前的癌症治疗方法,包括抗肿瘤和抗血管生成,仍然面临着疗效不足、耐药和内在难治性的问题,以及毒副作用。有必要确定可以阻断的其他靶标,以关闭大多数(如果不是全部的话)途径的下游影响。我们的研究表明孤儿核受体TR3(人)/Nur77(小鼠)就是这样一个靶点。最近,我们报道了TR3/Nur77在人肝癌组织中的表达与肿瘤进展密切相关,这表明TR3是肝癌的特异性治疗靶点。然而,TR3/Nur77在肝细胞癌(HCC)中表达与慢性肝炎的相关性尚未研究。方法:采用免疫组化染色法对病历完整的人原发性肝癌标本中TR3/Nur77的表达进行分析。采用统计学方法分析TR3在肿瘤组织、肝硬化组织和慢性肝炎组织(伴和不伴乙型肝炎病毒感染的HBV(+)和HBV(-))中表达的意义。结果:TR3/Nur77在肝细胞癌、癌性肝硬化和慢性肝炎中的表达阳性率分别为66.67%、30%和20%,差异均有统计学意义(p)结论:TR3/Nur77在肝细胞癌中的表达阳性率高于慢性肝炎和肝硬化。肝细胞癌中TR3/Nur77表达阳性率在HBV感染组高于未感染组。我们的研究结果提示,TR3/Nur77在慢性肝炎的进展和HCC的发生发展中起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expressions of Orphan Nuclear Receptor TR3/Nur77 in Chronic Hepatopathy and Its Clinical Significance.

Objective: Although great success has been achieved in cancer treatment, current cancer therapies, including anti-tumorigenesis and anti-angiogenesis, still face the problems of insufficient efficacy, resistance and intrinsic refractoriness, in addition to their toxic side effects. There is a demand to identify additional targets that can be blocked to turn off the downstream effects of most, if not all, pathways. Our studies suggest that orphan nuclear receptor TR3 (human)/Nur77 (mouse) is such a target. Most recently, we reported that TR3/Nur77 expression in human hepatic cancer tissues correlates well with tumor progress, suggesting that TR3 is a specific therapeutic target for hepatic cancers. However, the correlation of TR3/Nur77 expression in hepatocellular carcinoma (HCC) with chronic hepatitis has not been studied.

Methods: The expression of TR3/Nur77 was analyzed in human primary hepatic cancer specimens from patients that have complete medical records with Immunohistochemically staining. The statistical analysis was used to access the significance of TR3 expression in tumor tissues, cirrhosis tissues and chronic hepatitis tissues with and without hepatitis B virus infection (HBV(+) and HBV(-)), which were obtained from para-tumor tissues.

Results: The positive rates of TR3/Nur77 expression in hepatocellular carcinoma, cancerous liver cirrhosis and chronic hepatitis are 66.67%, 30%, and 20%, respectively, which are statistic significant (p<0.05). The positive rates of TR3/Nur77 expression in hepatocellular carcinoma are statistic significant (p<0.05) with 81.25% and 20% in HBV (+) or HBV (-), respectively.

Conclusion: The positive expression rate of TR3/Nur77 in hepatocellular carcinoma is higher than that in chronic hepatitis and cirrhosis. The positive rate of TR3/Nur77 expression in hepatocellular carcinoma is higher with HBV infection than that without infection. Our results suggest that TR3/Nur77 plays an important role in the progression of chronic hepatitis, and the occurrence and development of HCC.

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