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bcl-2拮抗剂bak在炎症性和肿瘤性皮肤病中的表达。

Expression of bcl-2 antagonist bak in inflammatory and neoplastic skin diseases.

作者信息

Tomková H, Fujimoto W, Arata J

机构信息

Department of Dermatology, Okayama University Medical School, Japan.

出版信息

Br J Dermatol. 1997 Nov;137(5):703-8.

PMID:9415228
Abstract

Bak (bcl-2 homologous antagonist/killer) is a proapoptotic member of the ever-expanding bcl-2 gene family, a recently described category of oncogenes that is critical for the regulation of programmed cell death. We investigated the expression of bak in several inflammatory and neoplastic skin diseases in comparison with normal skin. Immunohistochemical analysis revealed positive bak staining in epidermal keratinocytes of normal skin, with the granular layer being stained slightly more strongly than the basal and spinous layers, and in psoriasis vulgaris, lichen planus, actinic keratosis, keratoacanthoma and squamous cell carcinoma. We demonstrated the expression of bak in the follicular infundibulum in contrast to the outer root sheath of the lower follicle, which showed only negative to weak bak expression. Seventeen of 20 basal cell carcinomas examined showed negative immunostaining for bak, and the remaining three basal cell carcinomas showed only partial weak positivity, mainly in the palisading layers of some tumour formations. Immunoblot analysis using cultured normal human epidermal keratinocytes revealed the presence of bak protein in both undifferentiated and differentiated keratinocytes. The results of our study suggest that the loss of bak expression, in conjunction with the previously reported overexpression of bcl-2, might contribute to the pathogenesis of basal cell carcinoma.

摘要

Bak(bcl-2同源拮抗剂/杀手)是不断扩大的bcl-2基因家族中的促凋亡成员,bcl-2基因家族是最近描述的一类癌基因,对程序性细胞死亡的调节至关重要。我们研究了bak在几种炎症性和肿瘤性皮肤病中的表达,并与正常皮肤进行比较。免疫组织化学分析显示,在正常皮肤的表皮角质形成细胞中bak染色呈阳性,颗粒层染色略强于基底层和棘层,在寻常型银屑病、扁平苔藓、光化性角化病、角化棘皮瘤和鳞状细胞癌中也呈阳性。我们证明了bak在毛囊漏斗部表达,而下段毛囊外根鞘仅呈阴性至弱阳性表达。在检测的20例基底细胞癌中,17例对bak免疫染色呈阴性,其余3例基底细胞癌仅呈部分弱阳性,主要在一些肿瘤结构的栅栏状层。使用培养的正常人表皮角质形成细胞进行免疫印迹分析显示,未分化和分化的角质形成细胞中均存在bak蛋白。我们的研究结果表明,bak表达缺失,与先前报道的bcl-2过表达一起,可能有助于基底细胞癌的发病机制。

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