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本文引用的文献

1
Viral hepatocarcinogenesis.病毒性肝癌发生机制。
Oncogene. 2010 Apr 22;29(16):2309-24. doi: 10.1038/onc.2010.36. Epub 2010 Mar 15.
2
Aflatoxin exposure and viral hepatitis in the etiology of liver cirrhosis in the Gambia, West Africa.西非冈比亚肝硬化病因中的黄曲霉毒素暴露与病毒性肝炎
Environ Health Perspect. 2008 Nov;116(11):1553-7. doi: 10.1289/ehp.11661. Epub 2008 Jul 10.
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Foxp3 expression in human cancer cells.人类癌细胞中的Foxp3表达。
J Transl Med. 2008 Apr 22;6:19. doi: 10.1186/1479-5876-6-19.
4
The regulatory T cell-associated transcription factor FoxP3 is expressed by tumor cells.调节性T细胞相关转录因子FoxP3由肿瘤细胞表达。
Cancer Res. 2008 Apr 15;68(8):3001-9. doi: 10.1158/0008-5472.CAN-07-5664.
5
FOXP3 is a novel transcriptional repressor for the breast cancer oncogene SKP2.FOXP3是一种针对乳腺癌致癌基因SKP2的新型转录抑制因子。
J Clin Invest. 2007 Dec;117(12):3765-73. doi: 10.1172/JCI32538.
6
Foxp3 expression in pancreatic carcinoma cells as a novel mechanism of immune evasion in cancer.胰腺癌细胞中Foxp3的表达作为癌症免疫逃逸的一种新机制。
Cancer Res. 2007 Sep 1;67(17):8344-50. doi: 10.1158/0008-5472.CAN-06-3304.
7
FOXP3 is an X-linked breast cancer suppressor gene and an important repressor of the HER-2/ErbB2 oncogene.FOXP3是一种X连锁的乳腺癌抑制基因,也是HER-2/ErbB2癌基因的重要抑制因子。
Cell. 2007 Jun 29;129(7):1275-86. doi: 10.1016/j.cell.2007.04.034. Epub 2007 Jun 14.
8
FOXP3+ regulatory T cells affect the development and progression of hepatocarcinogenesis.FOXP3+调节性T细胞影响肝癌发生的发展与进程。
Clin Cancer Res. 2007 Feb 1;13(3):902-11. doi: 10.1158/1078-0432.CCR-06-2363.
9
Foxp3 occupancy and regulation of key target genes during T-cell stimulation.T细胞刺激过程中Foxp3对关键靶基因的占据及调控
Nature. 2007 Feb 22;445(7130):931-5. doi: 10.1038/nature05478. Epub 2007 Jan 21.
10
Transcriptional regulation by Foxp3 is associated with direct promoter occupancy and modulation of histone acetylation.Foxp3介导的转录调控与直接的启动子占据及组蛋白乙酰化的调节相关。
J Biol Chem. 2006 Dec 1;281(48):36828-34. doi: 10.1074/jbc.M608848200. Epub 2006 Oct 6.

FOXP3 表达与肝细胞癌的临床特征。

FOXP3 expression and clinical characteristics of hepatocellular carcinoma.

机构信息

National Center for Safety Evaluation of Drugs, National Institute for the Control of Pharmaceutical and Biological Products, Beijing 100050, China.

出版信息

World J Gastroenterol. 2010 Nov 21;16(43):5502-9. doi: 10.3748/wjg.v16.i43.5502.

DOI:10.3748/wjg.v16.i43.5502
PMID:21086571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2988246/
Abstract

AIM

To study the biological and clinical characteristics of transcription factor forkhead box protein 3 (FOXP3) in hepatocellular carcinoma (HCC).

METHODS

We analyzed the expression and localization of FOXP3 in HCC tissues and cell lines to evaluate its biological features. The relationship between FOXP3 staining and clinical risk factors of HCC was assessed to identify the clinical characteristics of FOXP3 in HCC.

RESULTS

The mRNA and protein expression of FOXP3 were found in some hepatoma cell lines. Immunohistochemical (IHC) analysis of HCC sections revealed that 48% of HCC displayed FOXP3 staining, but we did not find any FOXP3 staining in normal liver tissues and para-tumor tissues. IHC and Confocal analysis showed that the expressions of FOXP3 were mainly present in the nucleus and cytoplasm of tumor cells in tissues or cell lines. In HCC, the distribution of FOXP3 was similar to that of the cirrhosis, but not to the hepatitis B virus. Those findings implicate that FOXP3 staining seems to be associated with the high risk of HCC.

CONCLUSION

The clinical characteristics of FOXP3 in HCC warrants further studies to explore its functions and roles in the cirrhosis and development of HCC.

摘要

目的

研究转录因子叉头框蛋白 3(FOXP3)在肝细胞癌(HCC)中的生物学和临床特征。

方法

我们分析了 FOXP3 在 HCC 组织和细胞系中的表达和定位,以评估其生物学特征。评估 FOXP3 染色与 HCC 临床危险因素之间的关系,以确定 FOXP3 在 HCC 中的临床特征。

结果

在一些肝癌细胞系中发现了 FOXP3 的 mRNA 和蛋白表达。对 HCC 切片的免疫组织化学(IHC)分析显示,48%的 HCC 显示 FOXP3 染色,但我们在正常肝组织和癌旁组织中未发现任何 FOXP3 染色。IHC 和共聚焦分析显示,FOXP3 的表达主要存在于组织或细胞系中肿瘤细胞的核和细胞质中。在 HCC 中,FOXP3 的分布与肝硬化相似,但与乙型肝炎病毒无关。这些发现表明,FOXP3 染色似乎与 HCC 的高风险相关。

结论

FOXP3 在 HCC 中的临床特征需要进一步研究,以探讨其在肝硬化和 HCC 发展中的功能和作用。