通常间质性肺炎相关肺腺癌中癌症相关成纤维细胞标志物特征和基质组成:使用蛋白质组免疫组织化学方法的分析

IF 3.1 3区 医学 Q1 PATHOLOGY
Chihiro Inoue, Yasuhiro Miki, Tetsuya Fukuda, Yoshinori Okada, Hironobu Sasano, Takashi Suzuki
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引用次数: 0

摘要

肺腺癌(LUAD)合并常规间质性肺炎(UIP)与肺腺癌相比具有明显的特征。因此,我们的目标是通过关注癌症相关成纤维细胞(CAFs)和基质组成,用UIP来表征LUAD的肿瘤微环境。对32例LUAD样本(含和不含UIP各16例)进行免疫组化,评估CAF标志物表达和淋巴细胞浸润情况。随后进行了激光显微解剖基质区域的蛋白质组学分析和公开可用的单细胞RNA测序数据的再分析。在纤维间质检测的CAF标志物中,与未患UIP的LUAD相比,合并UIP的LUAD具有更高水平的足平面蛋白和胶原三螺旋重复含1 (CTHRC1)免疫反应性,炎症细胞浸润增加,CD8 +和Foxp3 +淋巴细胞计数更高。蛋白质组学分析显示,LUAD患者间质中聚集蛋白(ACAN)、透明质酸和蛋白多糖连接蛋白1 (HAPLN1)水平升高,随后通过免疫组织化学证实了这一点。单细胞RNA测序也支持ACAN和HAPLN1在CAFs子集中的表达。UIP患者LUAD的肿瘤微环境具有明显的特征,包括CAF标志物的改变和基质成分中炎症细胞浸润的增加。新的基质蛋白如ACAN和HAPLN1可能在LUAD合并UIP的发病机制中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cancer-associated fibroblast marker signatures and stromal composition in usual interstitial pneumonia-associated lung adenocarcinoma: an analysis using a proteomic-immunohistochemical approach.

Lung adenocarcinoma (LUAD) associated with usual interstitial pneumonia (UIP) harbours distinct features compared to lung adenocarcinoma without UIP. Therefore, we aimed to characterise the tumour microenvironment of LUAD with UIP by focusing on cancer-associated fibroblasts (CAFs) and stromal composition. Immunohistochemistry was performed on 32 LUAD samples (16 each with and without UIP) to evaluate CAF marker expression and lymphocyte infiltration. Proteomic analysis of laser-microdissected stromal regions and reanalysis of publicly available single-cell RNA sequencing data were subsequently performed. LUAD with UIP had higher levels of podoplanin and collagen triple helix repeat containing 1 (CTHRC1) immunoreactivity, among the CAF markers examined in the fibrous stroma, increased inflammatory cell infiltration, and higher CD8 + and Foxp3 + lymphocyte counts than LUAD without UIP. The proteomic analysis revealed elevated aggrecan (ACAN) and hyaluronan and proteoglycan link protein 1 (HAPLN1) levels in the stroma of LUAD patients with UIP tissues, which was subsequently confirmed by immunohistochemistry. Single-cell RNA sequencing also supported ACAN and HAPLN1 expression in a subset of CAFs based on public data. The tumour microenvironment of LUAD in patients with UIP harbours distinct characteristics, including altered CAF markers and increased inflammatory cell infiltration in stromal components. Novel stromal proteins such as ACAN and HAPLN1 may play a role in the pathogenesis of LUAD with UIP.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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