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四跨膜蛋白CD9在皮肤基底细胞癌、鳞状细胞癌及光化性角化病中的差异表达

Differential expression of tetraspanin CD9 in basal cell and squamous cell carcinomas of the skin and actinic keratosis.

作者信息

Ach Thomas, Ziemer Mirjana, Dawczynski Jens, Strobel Jürgen, Sauer Georg, Deissler Helmut

机构信息

Department of Ophthalmology, University Hospital Heidelberg, Heidelberg.

出版信息

Oncol Lett. 2010 Jan;1(1):37-40. doi: 10.3892/ol_00000006. Epub 2010 Jan 1.

Abstract

Tetraspanins are potentially useful molecular markers that differentiate between tumour classes and subtypes, since members of this protein family were often found to be altered during malignant conversion and tumour progression. In this study, we analysed expression of the tetraspanin CD9 in the frequent cutaneous neoplasms basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and actinic keratosis (AK), which is considered a precursor lesion (carcinoma in situ) from which an invasive SCC can develop. A moderate to strong CD9-specific staining of the tumour cells' plasma membranes was uniquely observed in all BCCs, SCCs and AKs. All SCCs showed additional intracellular CD9 which was rarely (20%) seen in AKs. Semi-quantitative assessment of CD9 present in the plasma membranes of tumour cells of BCCs (mean staining intensity 1.91) and SCCs (3.64) reflected the different CD9 expression of normal precursor cells from which these tumours most likely originate. Although considered an intermediate stage in the development of SCCs, AKs did not show intense staining of the plasma membranes typical of normal keratinocytes or invasive SCCs (p=0.011) but only moderate intensity (mean 1.63). In BCCs, significantly (p=0.0005, n=56) stronger CD9-specific immunoreactivity was seen in the inner regions of the tumours than at their sites of expansion. In summary, our results point to an important role of CD9 at the front of tumour expansion in BCCs and SCCs, and in the pathogenesis of invasive SCCs.

摘要

四跨膜蛋白是潜在有用的分子标志物,可区分肿瘤类别和亚型,因为该蛋白家族的成员在恶性转化和肿瘤进展过程中常发生改变。在本研究中,我们分析了四跨膜蛋白CD9在常见皮肤肿瘤基底细胞癌(BCC)、鳞状细胞癌(SCC)和光化性角化病(AK)中的表达情况,AK被认为是一种前驱病变(原位癌),可发展为浸润性SCC。在所有BCC、SCC和AK中均独特地观察到肿瘤细胞质膜有中度至强的CD9特异性染色。所有SCC均显示有额外的细胞内CD9,而在AK中很少见(20%)。对BCC(平均染色强度1.91)和SCC(3.64)肿瘤细胞质膜中CD9的半定量评估反映了这些肿瘤最可能起源的正常前驱细胞的不同CD9表达。尽管AK被认为是SCC发展的中间阶段,但其质膜并未显示出正常角质形成细胞或浸润性SCC典型的强烈染色(p = 0.011),而只有中度强度(平均1.63)。在BCC中,肿瘤内部区域的CD9特异性免疫反应性明显(p = 0.0005,n = 56)强于其扩展部位。总之,我们的结果表明CD9在BCC和SCC的肿瘤扩展前沿以及浸润性SCC的发病机制中起重要作用。

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