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N 端缺失型 E-钙黏蛋白在乳腺浸润性小叶癌中的表达。

Expression of N-Terminal-Deficient E-Cadherin Protein in Invasive Lobular Carcinoma of the Breast.

机构信息

Division of Pathology, Shizuoka Cancer Center, Shizuoka.

Department of Pathology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

Am J Surg Pathol. 2022 Mar 1;46(3):383-391. doi: 10.1097/PAS.0000000000001822.

Abstract

Invasive lobular carcinoma (ILC) of the breast is characterized by the discohesive growth of tumor cells, which is mainly associated with the complete loss of E-cadherin (E-cad) expression. However, some aberrant expression patterns of E-cad protein that are inconsistent with their morphologies have been reported in ILC. We report herein ILC cases expressing a new type of abnormal E-cad protein that lacks the N-terminal domain, but conserves the C-terminal domain on the cell membrane. Immunohistochemical staining of 299 ILC cases using specific antibodies against the N-terminal or C-terminal region of E-cad revealed that 227 (76%) cases showed loss of the membranous expression of both terminuses (N-/C-) and 72 (24%) cases showed expression of only the C-terminus (N-/C+). In all cases, the expression of p120-catenin and β-catenin coincided with the expression of the C-terminus of E-cad. Clinicopathologic analysis revealed that N-/C+ expression in ILC cells was significantly associated with the histologic subtype (especially mixed-type ILC with another histologic type) and immunohistochemical molecular subtype (especially the triple-negative subtype), but not with prognostic factors (pT or pN). In addition, 12 of 15 cases (80%) with aberrant cytoplasmic localization of the N-terminal of E-cad showed diffuse membranous expression of the C-terminal domain. Additional immunohistochemistry using an antibody recognizing the extracellular juxtamembrane region showed that 28 (39%) of the N-/C+ cases had lost membranous expression, suggesting diversity in the deletion pattern of the N-terminal region. Our findings provide a novel mechanism for the loss of E-cad function because of N-terminal-deficient E-cad protein in ILC.

摘要

乳腺浸润性小叶癌(ILC)的特征是肿瘤细胞的离散生长,这主要与 E-钙黏蛋白(E-cad)表达的完全缺失有关。然而,在 ILC 中已经报道了一些与形态不一致的 E-钙蛋白异常表达模式。我们在此报告了表达新型异常 E-钙蛋白的 ILC 病例,该蛋白缺乏 N 端结构域,但在细胞膜上保留 C 端结构域。使用针对 E-cad 的 N 端或 C 端区域的特异性抗体对 299 例 ILC 病例进行免疫组织化学染色,结果显示 227 例(76%)病例均表现为两个末端(N-/C-)的膜表达缺失,72 例(24%)病例仅表现为 C 端(N-/C+)表达。在所有病例中,p120-连环蛋白和β-连环蛋白的表达与 E-cad 的 C 端表达一致。临床病理分析显示,ILC 细胞中的 N-/C+表达与组织学亚型(尤其是另一种组织学类型的混合性 ILC)和免疫组织化学分子亚型(尤其是三阴性亚型)显著相关,但与预后因素(pT 或 pN)无关。此外,15 例异常 E-cad 胞质内定位的病例中有 12 例(80%)显示 C 端的弥漫膜表达。使用识别细胞外连接膜区的抗体进行的额外免疫组织化学分析显示,28 例(39%)N-/C+病例丧失了膜表达,表明 N 端区域缺失模式存在多样性。我们的发现提供了一个新的机制,即 ILC 中 N 端缺失的 E-cad 蛋白导致 E-cad 功能丧失。

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