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肿瘤转移抑制基因KAI1的表达由p53直接激活。

The expression of the KAI1 gene, a tumor metastasis suppressor, is directly activated by p53.

作者信息

Mashimo T, Watabe M, Hirota S, Hosobe S, Miura K, Tegtmeyer P J, Rinker-Shaeffer C W, Watabe K

机构信息

Department of Medical Microbiology and Immunology, School of Medicine, Southern Illinois University, Springfield, IL 62702, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11307-11. doi: 10.1073/pnas.95.19.11307.

Abstract

KAI1 is a tumor metastasis suppressor gene that is capable of inhibiting the metastatic process in animals. The expression of the KAI1 gene also is found to be down-regulated during the tumor progression of prostate, breast, lung, bladder, and pancreatic cancers in humans, and this down-regulation appears to be at or posttranscription level. We have found that the tumor suppressor gene p53 can directly activate the KAI1 gene by interacting with the 5' upstream region. The p53 responding region is located at approximately 860 bases upstream of the transcriptional initiation site, and it contains a typical tandem repeat of the p53 consensus-binding sequence. A gel-shift mobility analysis showed that this sequence indeed had the ability to bind to the purified p53 protein. Mutations of this sequence abolished the responsiveness to p53 and also the binding ability to the p53 protein. Furthermore, immunohistochemical analysis of 177 samples of human prostate tumors revealed that the expression of the KAI1 gene was correlated strongly to that of the p53 gene and that the loss of these two markers resulted in poor survivals of patients. Our data indicate a direct relationship between p53 and KAI1 genes and suggest that the loss of p53 function, which is commonly observed in many types of cancer, leads to the down-regulation of the KAI1 gene, which may result in the progression of metastasis.

摘要

KAI1是一种肿瘤转移抑制基因,能够抑制动物体内的转移过程。研究发现,在人类前列腺癌、乳腺癌、肺癌、膀胱癌和胰腺癌的肿瘤进展过程中,KAI1基因的表达也会下调,而且这种下调似乎发生在转录水平或转录后水平。我们发现,肿瘤抑制基因p53可通过与5'上游区域相互作用直接激活KAI1基因。p53反应区域位于转录起始位点上游约860个碱基处,包含一个典型的p53共有结合序列串联重复。凝胶迁移率分析表明,该序列确实能够与纯化的p53蛋白结合。该序列的突变消除了对p53的反应性以及与p53蛋白的结合能力。此外,对177例人类前列腺肿瘤样本的免疫组织化学分析显示,KAI1基因的表达与p53基因的表达密切相关,这两种标志物的缺失会导致患者生存率降低。我们的数据表明p53基因与KAI1基因之间存在直接关系,并表明在许多类型的癌症中常见的p53功能丧失会导致KAI1基因下调,这可能会导致转移进展。

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