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首页> 外文期刊>The 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结构域蛋白C4.4a和Haldisin在非侵入性和侵袭性皮肤病变中的表达

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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 and late 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 , 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 and malignant 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-神经毒素蛋白质结构域系列。它们在正常表皮中表现出高度调节的表达谱,其中它们被限制在早期和晚期鳞状区分中。我们现在已经探索了非侵入性和侵袭性皮肤病因的表达表达。在非侵入性损伤中,它们的表达签名大致如正常表皮所定义的。然而,这种情况在侵袭性鳞状细胞癌的进展中显着不同。在其非侵入性阶段,观察到C4.4a表达的明显衰减,但在过渡到恶性侵袭性鳞状细胞癌后,侵入性前线将重新表达C4.4a。对于良性渗透角膜囊孢子的早期阶段,观察到类似的进展。有趣的是,这种转变伴随着在正常表皮中的CK1 / 10在侵袭性病变中的CK1 / 10中的CK1 / 10表达的主要关联的转变。相反,Haldisin表达将其限制保持对最分化的细胞,并且在侵入性病变中几乎没有表达。因为在良性和恶性肿瘤的侵袭性前面看到了这种改变的C4.4a表达,所以我们提出这种表达的转变主要与侵入过程有关。

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