首页> 美国卫生研究院文献>Journal of Histochemistry and Cytochemistry >Expression of the Ly6/uPAR-Domain Proteins C4.4A and Haldisin in Non-Invasive and Invasive Skin Lesions
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Expression of the Ly6/uPAR-Domain Proteins C4.4A and Haldisin in Non-Invasive and Invasive Skin Lesions

机译:Ly6 / uPAR域蛋白C4.4A和Haldisin在非侵袭性和侵袭性皮肤病变中的表达

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摘要

C4.4A and Haldisin belong to the Ly6/uPAR/α-neurotoxin protein domain family. They exhibit highly regulated expression profiles in normal epidermis, where they are confined to early (C4.4A) and late (Haldisin) squamous differentiation. We have now explored if dysregulated expressions occur in non-invasive and invasive skin lesions. In non-invasive lesions, their expression signatures were largely maintained as defined by that of normal epidermis. The scenario was, however, markedly different in the progression towards invasive squamous cell carcinomas. In its non-invasive stage (carcinoma in situ), a pronounced attenuation of C4.4A expression was observed, but upon transition to malignant invasive squamous cell carcinomas, the invasive fronts regained high expression of C4.4A. A similar progression was observed for the early stages of benign infiltrating keratoacanthomas. Interestingly, this transition was accompanied by a shift in the predominant association of C4.4A expression with CK1/10 in the normal epidermis to CK5/14 in the invasive lesions. In contrast, Haldisin expression maintained its confinement to the most-differentiated cells and was hardly expressed in the invasive lesions. Because this altered expression of C4.4A was seen in the invasive front of benign (keratoacanthomas) and malignant (squamous cell carcinomas) neoplasms, we propose that this transition of expression is primarily related to the invasive process.
机译:C4.4A和Haldisin属于Ly6 / uPAR /α-神经毒素蛋白结构域家族。它们在正常表皮中表现出高度调节的表达特征,它们局限于早期(C4.4A)和晚期(Haldisin)鳞状分化。现在我们已经研究了非侵入性和侵入性皮肤损伤中是否发生表达失调。在非侵入性病变中,它们的表达特征在很大程度上被正常表皮所定义。然而,在向浸润性鳞状细胞癌发展的过程中,情况截然不同。在其非侵入性阶段(原位癌)中,观察到C4.4A表达的明显减弱,但是在转变为恶性浸润性鳞状细胞癌后,浸润性前沿恢复了C4.4A的高表达。良性浸润性角棘层瘤的早期观察到相似的进展。有趣的是,这种转变伴随着正常表皮中C4.4A表达与CK1 / 10的主要关联向浸润性病变中的CK5 / 14的转变。相比之下,Haldisin的表达维持在分化最严重的细胞中,并且在侵袭性病变中几乎不表达。因为在良性(角质层棘层瘤)和恶性(鳞状细胞癌)肿瘤的浸润前部可见到C4.4A的这种表达改变,所以我们建议这种表达的转变主要与浸润过程有关。

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