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Differential transformation of primary human embryo retinal cells by adenovirus E1 regions and combinations of E1A + ras.

作者信息

Byrd P J, Grand R J, Gallimore P H

机构信息

Department of Cancer Studies, Medical School, Birmingham, UK.

出版信息

Oncogene. 1988 May;2(5):477-84.

PMID:2967455
Abstract

The efficiency of transformation of primary human embryo retinal (HER) cells by the adenovirus E1 region (E1A + E1B) depended on the virus serotype whereas transformation by E1A alone was a rare event regardless of serotype. Activated human c-Ha-ras and N-ras genes co-operated differentially with different E1As for HER transformation but were ineffective without E1A. Ras + E1A co-transformants containing Ad 12 E1A established directly from foci, in contrast to those containing Ad 2 or Ad 5 E1A. A spectrum of activated ras gene expression was found in stable co-transformants with mRNA and protein levels being lower in Ad 12 E1A + N-ras than Ad 2 E1A + N-ras cell lines. Down regulation of E1A transcription in the absence of E1B was found in Ad 2 E1A + Ha-ras transformants only but E1A protein levels were similar to those in Ad 2 E1A + N-ras or Ad 5 E1A + E1B cell lines. HER cell transformants which contained Ad 12 E1A were more tumourigenic than those which contained the Ad 2 or Ad 5 E1A. This unique transformation system shows that stable malignant transformation of primary human cells in vitro is a complex process requiring the combined activities of two or more types of genes.

摘要

相似文献

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Oncogene. 1988 May;2(5):477-84.
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引用本文的文献

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Adenovirus 5 E1A enhances histone deacetylase inhibitors-induced apoptosis through Egr-1-mediated Bim upregulation.腺病毒 5 E1A 通过 Egr-1 介导的 Bim 上调增强组蛋白去乙酰化酶抑制剂诱导的细胞凋亡。
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Downregulation of microRNA miR-520h by E1A contributes to anticancer activity.
E1A 通过下调 microRNA miR-520h 发挥抗癌活性。
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Recruitment of CBP/p300, TATA-binding protein, and S8 to distinct regions at the N terminus of adenovirus E1A.CBP/p300、TATA结合蛋白和S8被招募至腺病毒E1A N端的不同区域。
J Virol. 2005 May;79(9):5594-605. doi: 10.1128/JVI.79.9.5594-5605.2005.
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Mol Cell Biol. 1999 Dec;19(12):8075-82. doi: 10.1128/MCB.19.12.8075.
6
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