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IκB激酶α在胚胎皮肤发育和皮肤癌发生中的关键作用。

Critical role of IkappaB kinase alpha in embryonic skin development and skin carcinogenesis.

作者信息

Zhu Feng, Park Eunmi, Liu Bigang, Xia Xiaojun, Fischer Susan M, Hu Yinling

机构信息

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

出版信息

Histol Histopathol. 2009 Feb;24(2):265-71. doi: 10.14670/HH-24.265.

Abstract

IkappaB kinase alpha (IKKalpha), IKKbeta, and IKKgamma/NEMO form the IKK complex, which is essential for NF-kappaB activation. However, genetic studies have shown that the role of IKKalpha is distinct from that of IKKbeta or IKKgamma in the development of the mouse embryonic skin. Loss of IKKalpha has been shown to cause epidermal hyperplasia, prevent keratinocyte terminal differentiation, and impair the formation of the skin, resulting in the deaths of IKKalpha-deficient (Ikkalpha-/-) mice soon after birth. Recent experimental data from several laboratories have revealed that IKKalpha functions as a tumor suppressor in human squamous cell carcinomas (SCCs) of skin, lungs, and head and neck. Chemical carcinogenesis studies using mice have shown that reduction in IKKalpha expression increases the number and size of Ras-initiated skin tumors and promotes their progression, indicating that reduced IKKalpha expression provides a selective growth advantage that cooperates with Ras activity to promote skin carcinogenesis. In this review, we will summarize these findings from our and other studies on the role that IKKalpha plays in development of the mouse embryonic skin and skin carcinogenesis.

摘要

IκB激酶α(IKKα)、IKKβ和IKKγ/NEMO组成IKK复合物,这对于NF-κB激活至关重要。然而,遗传学研究表明,在小鼠胚胎皮肤发育过程中,IKKα的作用与IKKβ或IKKγ不同。已表明IKKα缺失会导致表皮增生、阻止角质形成细胞终末分化并损害皮肤形成,导致IKKα缺陷(Ikkα-/-)小鼠出生后不久死亡。来自多个实验室的最新实验数据表明,IKKα在人类皮肤、肺和头颈部鳞状细胞癌(SCC)中起肿瘤抑制作用。使用小鼠进行的化学致癌研究表明,IKKα表达降低会增加Ras引发的皮肤肿瘤的数量和大小,并促进其进展,表明IKKα表达降低提供了一种选择性生长优势,与Ras活性协同促进皮肤癌发生。在本综述中,我们将总结我们和其他研究中关于IKKα在小鼠胚胎皮肤发育和皮肤癌发生中所起作用的这些发现。

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