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[人直肠腺癌淋巴管内皮细胞上细胞间黏附分子(ICAM-1)的转录调控]

[Transcription regulation of intercellular adhesion molecule (ICAM-1) on lymphatic endothelial cells of rectum adenocarcinoma of human].

作者信息

Chen Y, Liu Z, Li R, Jin S

机构信息

Department of Anatomy, School of Basic Medical Sciences, WCUMS, Chengdu 610041.

出版信息

Hua Xi Yi Ke Da Xue Xue Bao. 2000 Sep;31(3):315-8.

Abstract

This study inquired into the mechanism of cancer lymphatic metastasis. The immunohistochemistry method and DNA hybridization in situ were employed in examining the peritumoral rectum tissues and metastatic lymph nodes from 8 rectum carcinoma patients and the rectum tissues and lymph nodes from 5 normal subjects. The results showed that the proteins of ICAM-1 and nuclear factor kappa B (NF kappa Bp65) were expressed on the lymphatic endothelial cells of the rectum adenocarcinoma patients, and there was a NF kappa B binding consensus sequences on ICAM-1 promoter in lymphatic endothelial cells of rectum adenocarcinoma patients. When DIG-AKP labeled 38 bp oligonucleotide probe was used, there was no the expression of ICAM-1 and NF kappa Bp65 on the lymphatic endothelial cells of the normal human lymph node and rectum tissues. It is suggested that the activation of ICAM-1 promoter may critically depend on NF kappa Bp65 homodimers or heterodimers binding to a variant kappa B site on the lymphatic endothelial cells of the rectum adencarcinoma of human. These observations may indicate the potential roles of NF kappa B in cancer metastasis, thus giving clues to facilitate the development of a novel anti-metastasis strategy, that is obstruction the NF kappa B-activation pathways.

摘要

本研究探讨了癌症淋巴转移的机制。采用免疫组织化学方法和原位DNA杂交技术,对8例直肠癌患者的肿瘤周围直肠组织和转移淋巴结以及5例正常受试者的直肠组织和淋巴结进行检测。结果显示,ICAM-1蛋白和核因子κB(NFκBp65)在直肠腺癌患者的淋巴管内皮细胞上表达,且在直肠腺癌患者淋巴管内皮细胞的ICAM-1启动子上存在NFκB结合共有序列。当使用地高辛碱性磷酸酶(DIG-AKP)标记的38 bp寡核苷酸探针时,正常人淋巴结和直肠组织的淋巴管内皮细胞上未检测到ICAM-1和NFκBp65的表达。提示ICAM-1启动子的激活可能关键取决于NFκBp65同二聚体或异二聚体与人类直肠腺癌淋巴管内皮细胞上一个变异κB位点的结合。这些观察结果可能表明NFκB在癌症转移中的潜在作用,从而为促进新型抗转移策略的开发提供线索,即阻断NFκB激活途径。

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