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本文引用的文献

1
Tspan-1 is a tetraspanin preferentially expressed by mucinous and endometrioid subtypes of human ovarian carcinomas.四跨膜蛋白-1是一种四跨膜蛋白,优先表达于人卵巢癌的黏液性和子宫内膜样亚型中。
Cancer Lett. 2009 Mar 18;275(2):198-203. doi: 10.1016/j.canlet.2008.10.014. Epub 2008 Nov 18.
2
Targeting of tetraspanin proteins--potential benefits and strategies.四跨膜蛋白的靶向作用——潜在益处与策略
Nat Rev Drug Discov. 2008 Sep;7(9):747-58. doi: 10.1038/nrd2659.
3
Epidemiology of melanoma and nonmelanoma skin cancer--the role of sunlight.黑色素瘤和非黑色素瘤皮肤癌的流行病学——阳光的作用
Adv Exp Med Biol. 2008;624:89-103. doi: 10.1007/978-0-387-77574-6_8.
4
Tetraspanin CD9 is involved in the migration of retinal microvascular endothelial cells.四跨膜蛋白CD9参与视网膜微血管内皮细胞的迁移。
Int J Mol Med. 2007 Nov;20(5):643-52.
5
Management of nonmelanoma skin cancer in 2007.2007年非黑素瘤皮肤癌的管理
Nat Clin Pract Oncol. 2007 Aug;4(8):462-9. doi: 10.1038/ncponc0883.
6
Reliability of the histopathologic diagnosis of keratinocyte carcinomas.角质形成细胞癌组织病理学诊断的可靠性
J Am Acad Dermatol. 2007 Aug;57(2):279-84. doi: 10.1016/j.jaad.2007.03.021. Epub 2007 May 7.
7
Tetraspanin functions and associated microdomains.四跨膜蛋白的功能及相关微结构域。
Nat Rev Mol Cell Biol. 2005 Oct;6(10):801-11. doi: 10.1038/nrm1736.
8
Motility-related protein-1 (MRP-1/CD9) expression can predict disease-free survival in patients with squamous cell carcinoma of the head and neck.运动相关蛋白-1(MRP-1/CD9)的表达可预测头颈部鳞状细胞癌患者的无病生存期。
Br J Cancer. 2004 Jan 26;90(2):471-5. doi: 10.1038/sj.bjc.6601542.
9
Progression of cervical carcinomas is associated with down-regulation of CD9 but strong local re-expression at sites of transendothelial invasion.宫颈癌的进展与CD9的下调有关,但在跨内皮侵袭部位有强烈的局部重新表达。
Clin Cancer Res. 2003 Dec 15;9(17):6426-31.
10
Motility-related protein-1/CD9 expression in head and neck squamous cell carcinoma.头颈鳞状细胞癌中与运动相关蛋白-1/CD9的表达
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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.

DOI:10.3892/ol_00000006
PMID:22966252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3436406/
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。