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Overexpression of the prostaglandin E2 receptor EP2 results in enhanced skin tumor development.前列腺素E2受体EP2的过表达会导致皮肤肿瘤发展加剧。
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Selective evolution of stromal mesenchyme with p53 loss in response to epithelial tumorigenesis.响应上皮肿瘤发生,p53缺失导致基质间充质的选择性进化。
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Modulation of the angiogenesis response through Ha-ras control, placenta growth factor, and angiopoietin expression in mouse skin carcinogenesis.通过在小鼠皮肤癌发生过程中对Ha-ras的调控、胎盘生长因子和血管生成素表达来调节血管生成反应。
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Mice deficient in the Rac activator Tiam1 are resistant to Ras-induced skin tumours.缺乏Rac激活剂Tiam1的小鼠对Ras诱导的皮肤肿瘤具有抗性。
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IKKalpha provides an essential link between RANK signaling and cyclin D1 expression during mammary gland development.在乳腺发育过程中,IKKα在RANK信号传导与细胞周期蛋白D1表达之间提供了关键联系。
Cell. 2001 Dec 14;107(6):763-75. doi: 10.1016/s0092-8674(01)00599-2.
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IKKalpha controls formation of the epidermis independently of NF-kappaB.IKKα独立于核因子κB调控表皮的形成。
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In vivo detection of human vascular endothelial growth factor promoter activity in transgenic mouse skin.转基因小鼠皮肤中人类血管内皮生长因子启动子活性的体内检测。
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Characterization of loricrin regulation in vitro and in transgenic mice.体外及转基因小鼠中loricrin调节的特征分析
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IκB激酶α在人类和小鼠鳞状细胞癌发生发展中起关键作用。

A critical role for I kappaB kinase alpha in the development of human and mouse squamous cell carcinomas.

作者信息

Liu Bigang, Park Eunmi, Zhu Feng, Bustos Tracie, Liu Jinsong, Shen Jianjun, Fischer Susan M, Hu Yinling

机构信息

Department of Carcinogenesis, University of Texas M D Anderson Cancer Center, Smithville, TX 78957, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17202-7. doi: 10.1073/pnas.0604481103. Epub 2006 Nov 1.

DOI:10.1073/pnas.0604481103
PMID:17079494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1859910/
Abstract

IKK (I kappaB kinase) alpha is essential for embryonic skin development in mice. Mice deficient in IKKalpha display markedly hyperplasic epidermis that lacks terminal differentiation, and they die because of this severely impaired skin. However, the function of IKKalpha in human skin diseases remains largely unknown. To shed light on the role of IKKalpha in human skin diseases, we examined IKKalpha expression and Ikkalpha mutations in human squamous cell carcinomas (SCCs). We found a marked reduction in IKKalpha expression in poorly differentiated human SCCs and identified Ikkalpha mutations in exon 15 of Ikkalpha in eight of nine human SCCs, implying that IKKalpha is involved in development of this human skin cancer. Furthermore, in a chemical carcinogen-induced skin carcinogenesis setting, mice overexpressing human IKKalpha in the epidermis under the control of a truncated loricrin promoter developed significantly fewer SCCs and metastases than did wild-type mice. The IKKalpha transgene altered the skin microenvironment conditions, leading to elevated terminal differentiation in the epidermis, reduced mitogenic activity in the epidermis, and decreased angiogenic activity in the skin stroma. Thus, overexpression of IKKalpha in the epidermis antagonized chemical carcinogen-induced mitogenic and angiogenic activities, repressing tumor progression and metastases.

摘要

IKK(IκB激酶)α对小鼠胚胎皮肤发育至关重要。IKKα缺陷的小鼠表现出明显增生的表皮,缺乏终末分化,并且因严重受损的皮肤而死亡。然而,IKKα在人类皮肤疾病中的功能仍 largely未知。为了阐明IKKα在人类皮肤疾病中的作用,我们检测了人类鳞状细胞癌(SCC)中IKKα的表达及Ikkα突变。我们发现低分化人类SCC中IKKα表达显著降低,并在9例人类SCC中的8例中鉴定出Ikkα第15外显子的Ikkα突变,这意味着IKKα参与了这种人类皮肤癌的发生发展。此外,在化学致癌物诱导的皮肤癌发生模型中,在截短的loricrin启动子控制下在表皮中过表达人类IKKα的小鼠比野生型小鼠发生的SCC和转移明显更少。IKKα转基因改变了皮肤微环境条件,导致表皮终末分化增加、表皮有丝分裂活性降低以及皮肤基质血管生成活性降低。因此,表皮中IKKα的过表达拮抗了化学致癌物诱导的有丝分裂和血管生成活性,抑制了肿瘤进展和转移。