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核 β-连环蛋白定位与 CTNNB1 基因突变:一种依赖于上下文的关联。

Nuclear β-catenin localization and mutation of the CTNNB1 gene: a context-dependent association.

机构信息

Department of Pathology and Laboratory Medicine, LAC+USC Medical Center/Keck School of Medicine of University of Southern California, Los Angeles, CA, USA.

Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Mod Pathol. 2018 Oct;31(10):1553-1559. doi: 10.1038/s41379-018-0080-0. Epub 2018 May 24.

Abstract

Although the majority of low-grade, early-stage endometrial cancer patients have good survival with surgery alone, patients who recur tend to do poorly. Identification of patients at high risk of recurrence who would benefit from adjuvant treatment or more extensive surgical staging would help optimize individualized care of endometrial cancer patients. CTNNB1 (encodes β-catenin) mutations identify a subset of low-grade, early-stage endometrial cancer patients at high risk of recurrence. Mutation of CTNNB1 exon 3 is classically associated with translocation of the β-catenin protein from the membrane to the nucleus and activation of Wnt/β-catenin signaling. Given the clinical utility of identifying endometrial carcinomas with CTNNB1 mutation, the purpose of this study was to determine if immunohistochemistry could act as a surrogate for CTNNB1 gene sequencing. Next-generation sequencing was performed on 345 endometrial carcinomas. Immunohistochemical localization of β-catenin was determined for 53/63 CTNNB1 exon 3 mutant tumors for which tissue was available and a subset of wild-type tumors. Nuclear localization of β-catenin had 100% specificity in distinguishing CTNNB1 mutant from wild type, but sensitivity was lower (84.9%). Nearly half of CTNNB1 mutant cases had only 5-10% of tumor cells with β-catenin nuclear localization. The concordance between pathologists blinded to mutation status in assessing nuclear localization was 100%. The extent of β-catenin nuclear localization was not associated with specific CTNNB1 gene mutation, tumor grade, presence of non-endometrioid component, or specific concurrent gene mutations in the tumor. For comparison, nuclear localization of β-catenin was more diffuse in desmoid fibromatosis, a tumor also associated with CTNNB1 mutation. Thus, nuclear localization of β-catenin assessed by immunohistochemistry does not detect all endometrial cancers with CTNNB1 gene mutation. The extent of nuclear localization may be tumor type dependent. For endometrial cancer, immunohistochemistry could be an initial screen, with CTNNB1 sequencing employed when nuclear localization of β-catenin is absent.

摘要

尽管大多数低级别、早期子宫内膜癌患者仅通过手术即可获得良好的生存,但复发的患者预后往往较差。识别出复发风险较高、受益于辅助治疗或更广泛手术分期的患者,有助于优化子宫内膜癌患者的个体化治疗。CTNNB1(编码β-连环蛋白)突变可识别出一组低级别、早期子宫内膜癌患者,这些患者复发风险较高。CTNNB1 外显子 3 的突变与β-连环蛋白蛋白从膜转位到核内以及 Wnt/β-连环蛋白信号通路激活有关。鉴于识别具有 CTNNB1 突变的子宫内膜癌的临床实用性,本研究旨在确定免疫组化是否可作为 CTNNB1 基因测序的替代方法。对 345 例子宫内膜癌进行了下一代测序。对 53/63 例 CTNNB1 外显子 3 突变肿瘤(有组织可用)和部分野生型肿瘤进行了β-连环蛋白免疫组化定位。β-连环蛋白核定位在区分 CTNNB1 突变型和野生型方面具有 100%的特异性,但敏感性较低(84.9%)。几乎一半的 CTNNB1 突变病例中,仅有 5-10%的肿瘤细胞存在β-连环蛋白核定位。对β-连环蛋白核定位评估的病理学家对突变状态的评估具有 100%的一致性。β-连环蛋白核定位的程度与特定 CTNNB1 基因突变、肿瘤分级、非子宫内膜样成分的存在或肿瘤中特定的同时存在的基因突变无关。相比之下,β-连环蛋白核定位在纤维瘤病中更为弥散,纤维瘤病也是一种与 CTNNB1 突变相关的肿瘤。因此,免疫组化评估的β-连环蛋白核定位并不能检测到所有具有 CTNNB1 基因突变的子宫内膜癌。核定位的程度可能与肿瘤类型有关。对于子宫内膜癌,免疫组化可以作为初始筛查方法,当β-连环蛋白核定位缺失时,可采用 CTNNB1 测序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b930/6168348/806d504e2fdd/nihms958873f1.jpg

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