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定义第一个用于鉴定 SMARCA4 缺陷型、未分化肿瘤的真正细胞模型。

Defining the first bona fide cell model for SMARCA4-deficient, undifferentiated tumor.

机构信息

Department of Biochemistry and Molecular Biology I, Faculty of Sciences, University of Granada, Granada, Spain.

GENYO, Centre for Genomics and Oncological Research: Pfizer/University of Granada/Andalusian Regional Government, Granada, Spain.

出版信息

J Pathol. 2023 Sep;261(1):5-10. doi: 10.1002/path.6141. Epub 2023 Jun 23.

Abstract

The World Health Organization's tumor classification guidelines are frequently updated and renewed as knowledge of cancer biology advances. For instance, in 2021, a novel lung tumor subtype named SMARCA4-deficient, undifferentiated tumor (SMARCA4-dUT, code 8044/3) was included. To date, there is no defined cell model for SMARCA4-dUT that could be used to help thoracic clinicians and researchers in the study of this newly defined tumor type. As this tumor type was recently described, it is feasible that some cell models formerly classified as lung adenocarcinoma (LUAD) could now be better classified as SMARCA4-dUT. Thus, in this work, we aimed to identify a bona fide cell model for the experimental study of SMARCA4-dUT. We compared the differential expression profiles of 36 LUAD-annotated cell lines and 38 cell lines defined as rhabdoid in repositories. These comparative results were integrated with the mutation and expression profiles of the SWI/SNF complex members, and they were surveyed for the presence of the SMARCA4-dUT markers SOX2, SALL4, and CD34, measured by RT-qPCR and western blotting. Finally, the cell line with the paradigmatic SMARCA4-dUT markers was engrafted into immunocompromised mice to assess the histological morphology of the formed tumors and compare them with those formed by a bona fide LUAD cancer cell line. NCI-H522, formerly classified as LUAD, displayed expression profiles nearer to rhabdoid tumors than LUAD tumors. Furthermore, NCI-H522 has most of the paradigmatic features of SMARCA4-dUT: hemizygous inactivating mutation of SMARCA4, severe SMARCA2 downregulation, and high-level expression of stem cell markers SOX2 and SALL4. In addition, the engrafted tumors of NCI-H522 did not display a typical differentiated glandular structure as other bona fide LUAD cell lines (A549) do but had rather a largely undifferentiated morphology, characteristic of SMARCA4-dUT. Thus, we propose the NCI-H522 as the first bona fide cell line model of SMARCA4-dUT. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

摘要

世界卫生组织的肿瘤分类指南随着癌症生物学知识的进步而经常更新和修订。例如,在 2021 年,纳入了一种新的肺肿瘤亚型,命名为 SMARCA4 缺陷型、未分化肿瘤(SMARCA4-dUT,代码 8044/3)。迄今为止,尚无针对 SMARCA4-dUT 的明确细胞模型,可用于帮助胸科临床医生和研究人员研究这种新定义的肿瘤类型。由于这种肿瘤类型是最近描述的,因此一些以前被归类为肺腺癌(LUAD)的细胞模型现在可能被更好地归类为 SMARCA4-dUT。因此,在这项工作中,我们旨在为 SMARCA4-dUT 的实验研究确定一个真正的细胞模型。我们比较了 36 个 LUAD 注释细胞系和 38 个在存储库中定义为横纹肌样的细胞系的差异表达谱。这些比较结果与 SWI/SNF 复合物成员的突变和表达谱相结合,并通过 RT-qPCR 和 Western blot 测量来调查 SMARCA4-dUT 标志物 SOX2、SALL4 和 CD34 的存在情况。最后,将具有典型 SMARCA4-dUT 标志物的细胞系植入免疫缺陷小鼠中,以评估形成的肿瘤的组织形态,并将其与真正的 LUAD 癌细胞系形成的肿瘤进行比较。NCI-H522 以前被归类为 LUAD,其表达谱比 LUAD 肿瘤更接近横纹肌样肿瘤。此外,NCI-H522 具有 SMARCA4-dUT 的大多数典型特征:SMARCA4 半合子失活突变、SMARCA2 严重下调以及干细胞标志物 SOX2 和 SALL4 的高表达。此外,NCI-H522 植入的肿瘤没有表现出其他真正的 LUAD 细胞系(A549)所具有的典型分化腺结构,而是具有很大程度的未分化形态,这是 SMARCA4-dUT 的特征。因此,我们建议 NCI-H522 作为 SMARCA4-dUT 的第一个真正的细胞系模型。

© 2023 作者。约翰威立父子公司代表英国和爱尔兰的病理学学会出版的《病理学杂志》。

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