Expression of angiopoietin-2 gene and its receptor Tie2 in hepatocellular carcinoma.

L Chen, Z Yang, G Wang, C Wang
{"title":"Expression of angiopoietin-2 gene and its receptor Tie2 in hepatocellular carcinoma.","authors":"L Chen, Z Yang, G Wang, C Wang","doi":"10.1007/BF02886437","DOIUrl":null,"url":null,"abstract":"<p><p>To explore the relationship of angiogenesis-related angiopoietin-2 gene and its receptor Tie2 with angiogenesis and the biology of hepatocellular carcinoma (HCC), angiopoietin-2 gene, Tie2 and CD34 protein expression in 22 resected HCC, 8 cirrhotic and 8 control liver specimens were investigated by in situ hybridization and immunohistochemistry respectively, and the level of angiopoietin-2 and Tie2 expression in HCC were compared in terms of tumor biological parameters. It was found that CD34 was not expressed in control liver, expressed scarcely in cirrhotic liver (17.8 +/- 13.5/HP), but intensively expressed in HCC (86.3 +/- 34.8/HP, P < 0.01). Tie2 receptor was not expressed in controls, expressed at low level in cirrhotic liver (11.3 +/- 8.7/HP), while strongly positive in the microvascular endothelia of HCC (52.4 +/- 16.7/HP, P < 0.01). The level of Tie2 receptor expression in HCC was closely related with tumor diameter, angiogenesis and portal invasion. Angiopoietin-2 gene was not expressed in control liver, expressed mildly in cirrhotic liver (11.2 +/- 9.7/HP), but extensively in tumor zone (36.4 +/- 17.5/HP), the level of angiopoietin-2 expression was closely related with angiogenesis, portal invasion and histological grading of HCC. It is concluded that angiogenesis is increased in HCC; angiopoietin-2/Tie2 expression in human hepatic carcinoma is closely related with angiogenesis, which are probably involved in the HCC angiogenesis regulation, promoting the development and metastasis of human hepatic cancer.</p>","PeriodicalId":73995,"journal":{"name":"Journal of Tongji Medical University = Tong ji yi ke da xue xue bao","volume":"21 3","pages":"228-30, 235"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Tongji Medical University = Tong ji yi ke da xue xue bao","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/BF02886437","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

To explore the relationship of angiogenesis-related angiopoietin-2 gene and its receptor Tie2 with angiogenesis and the biology of hepatocellular carcinoma (HCC), angiopoietin-2 gene, Tie2 and CD34 protein expression in 22 resected HCC, 8 cirrhotic and 8 control liver specimens were investigated by in situ hybridization and immunohistochemistry respectively, and the level of angiopoietin-2 and Tie2 expression in HCC were compared in terms of tumor biological parameters. It was found that CD34 was not expressed in control liver, expressed scarcely in cirrhotic liver (17.8 +/- 13.5/HP), but intensively expressed in HCC (86.3 +/- 34.8/HP, P < 0.01). Tie2 receptor was not expressed in controls, expressed at low level in cirrhotic liver (11.3 +/- 8.7/HP), while strongly positive in the microvascular endothelia of HCC (52.4 +/- 16.7/HP, P < 0.01). The level of Tie2 receptor expression in HCC was closely related with tumor diameter, angiogenesis and portal invasion. Angiopoietin-2 gene was not expressed in control liver, expressed mildly in cirrhotic liver (11.2 +/- 9.7/HP), but extensively in tumor zone (36.4 +/- 17.5/HP), the level of angiopoietin-2 expression was closely related with angiogenesis, portal invasion and histological grading of HCC. It is concluded that angiogenesis is increased in HCC; angiopoietin-2/Tie2 expression in human hepatic carcinoma is closely related with angiogenesis, which are probably involved in the HCC angiogenesis regulation, promoting the development and metastasis of human hepatic cancer.

肝细胞癌中血管生成素-2 基因及其受体 Tie2 的表达。
为探讨血管生成相关的血管生成素-2基因及其受体Tie2与血管生成和肝细胞癌(HCC)生物学的关系,采用原位杂交和免疫组化方法分别检测了22例切除的HCC肝标本、8例肝硬化肝标本和8例对照肝标本中血管生成素-2基因、Tie2和CD34蛋白的表达,并将HCC中血管生成素-2和Tie2的表达水平与肿瘤生物学指标进行了比较。结果发现,CD34在对照组肝脏中不表达,在肝硬化肝脏中表达较少(17.8 +/- 13.5/HP),但在HCC中表达较多(86.3 +/- 34.8/HP,P < 0.01)。Tie2 受体在对照组中不表达,在肝硬化肝脏中低水平表达(11.3 +/- 8.7/HP),而在 HCC 的微血管内皮中强阳性表达(52.4 +/- 16.7/HP,P <0.01)。Tie2 受体在 HCC 中的表达水平与肿瘤直径、血管生成和门静脉侵犯密切相关。血管生成素-2基因在对照肝中不表达,在肝硬化肝中轻度表达(11.2 +/- 9.7/HP),但在肿瘤区广泛表达(36.4 +/- 17.5/HP),血管生成素-2的表达水平与血管生成、门静脉侵犯和HCC的组织学分级密切相关。结论:HCC中血管生成增加;血管生成素-2/Tie2在人类肝癌中的表达与血管生成密切相关,可能参与了HCC血管生成的调控,促进了人类肝癌的发展和转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信