SMARCA4 as a support for the differential diagnosis of poorly differentiated lung carcinomas.

IF 4.4 Q1 PATHOLOGY PATHOLOGICA Pub Date : 2023-06-01 DOI:10.32074/1591-951X-847
Martina Panozzi, Greta Alì, Agnese Proietti, Franca Melfi, Carmelina C Zirafa, Marco Lucchi, Gabriella Fontanini
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Abstract

Among non-small cell lung cancers (NSCLCs), sarcomatoid carcinomas account for 3%. They are rare tumours with a poor prognosis, classified into three subgroups, namely pleomorphic carcinoma, pulmonary blastoma and carcinosarcoma. In the 5th edition of WHO Classification of Thoracic Tumours more space is given to SMARC4-deficient lung cancers. Although studies on SMARCA4-deficient lung tumours are limited, a small percentage of SMARCA4 loss is present within NSCLCs. This finding is clinically relevant, as the loss of the SMARCA4 gene is associated with a worse prognosis. In our study, we analysed the presence of the main catalytic subunit of the SMARCA4 gene, the BRG1 protein, in 60 sarcomatoid lung tumours. The results of our study show that 5.3% of sarcomatoid carcinomas have BRG1-loss in tumour cells, proving that a non-negligible amount of lung sarcomatoid carcinomas are SMARCA4-deficient. These data open the debate on the necessity of including the detection of SMARCA4 within a standardised immunohistochemical panel.

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SMARCA4作为低分化肺癌鉴别诊断的支持。
在非小细胞肺癌(nsclc)中,肉瘤样癌占3%。它们是一种预后不良的罕见肿瘤,可分为3个亚组,即多形性癌、肺母细胞瘤和癌肉瘤。在第5版WHO胸椎肿瘤分类中,对smarc4缺陷型肺癌给予了更多的空间。尽管对缺乏SMARCA4的肺肿瘤的研究有限,但在非小细胞肺癌中存在一小部分SMARCA4缺失。这一发现具有临床相关性,因为SMARCA4基因的缺失与较差的预后相关。在我们的研究中,我们分析了60例肉瘤样肺肿瘤中SMARCA4基因的主要催化亚基BRG1蛋白的存在。我们的研究结果显示,5.3%的肉瘤样癌肿瘤细胞中存在brg1缺失,这证明了不可忽视的数量的肺肉瘤样癌是缺乏smarca4的。这些数据开启了关于在标准化免疫组织化学小组中包括SMARCA4检测的必要性的辩论。
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来源期刊
PATHOLOGICA
PATHOLOGICA PATHOLOGY-
CiteScore
5.90
自引率
5.70%
发文量
108
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