Liu Bigang, Park Eunmi, Zhu Feng, Bustos Tracie, Liu Jinsong, Shen Jianjun, Fischer Susan M, Hu Yinling
Department of Carcinogenesis, University of Texas M D Anderson Cancer Center, Smithville, TX 78957, USA.
Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17202-7. doi: 10.1073/pnas.0604481103. Epub 2006 Nov 1.
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.
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。