SMARCA4 deficiency in small cell lung cancer: A case report and narrative review of the literature.

0 MEDICINE, RESEARCH & EXPERIMENTAL Biomolecules & biomedicine Pub Date : 2025-01-27 DOI:10.17305/bb.2024.11154
Andreas M Matthaiou, Ioannis Tomos, Nikoleta Bizymi, Ioannis Vamvakaris, Nektarios Anagnostopoulos, Aikaterini Papadopoulou, Kalliopi Angelou, Grigoris Stratakos, Adamantia Liapikou
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Abstract

SWItch/sucrose non-fermentable (SWI/SNF) is a large protein complex with a central role in chromatin remodeling and genome transcription. The catalytic subunits of the SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 (SWI/SNF SMARCA2; also called BRM) and SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 (SMARCA4; also called BRG1) are encoded by the SMARCA2 and SMARCA4 genes, respectively, and are mutually exclusive. Loss of either SMARCA2 and/or SMARCA4 has been previously reported in several types of malignant solid tumors of the gastrointestinal and genitourinary tract. So far, their absence in non-small cell lung cancer (SCLC) has been observed in a series of studies involving primary tumors and cell lines, where it is associated with loss of differentiation and heightened tumorigenic potential leading to an unfavorable prognosis. SMARCA2 and SMARCA4 deficiency is frequent in solid predominant adenocarcinomas and tumors with low levels of bronchial epithelial markers, including thyroid transcription factor 1. A rare case of SMARCA4 deficiency in SCLC is described. A 57-year-old male patient, with no medical history of past illness, was admitted to our center for the investigation and management of a space-occupying lesion in the right upper lung lobe with tracheal and mediastinal infiltration. Biopsy of a lymph node in the right supraclavicular region was diagnostic for SCLC with regional loss of SMARCA4. The patient demonstrated progressive respiratory failure and clinical deterioration and eventually deceased despite intubation and transfer to the intensive care unit. This case indicates that SMARCA4-deficient SCLC may present with an aggressively deteriorating phenotype with poor outcomes for the patients.

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小细胞肺癌中SMARCA4缺乏:1例报告及文献综述
开关/蔗糖不可发酵蛋白(SWI/SNF)是一种大型蛋白复合物,在染色质重塑和基因组转录中起核心作用。SWI/SNF相关BAF染色质重塑复合物亚基ATPase 2 (SWI/SNF SMARCA2;也称为BRM)和SWI/SNF相关BAF染色质重塑复合物亚基ATPase 4 (SMARCA4;也称为BRG1)分别由SMARCA2和SMARCA4基因编码,并且是互斥的。SMARCA2和/或SMARCA4的缺失在胃肠道和泌尿生殖系统的几种恶性实体瘤中已有报道。到目前为止,在一系列涉及原发肿瘤和细胞系的研究中观察到它们在非小细胞肺癌(SCLC)中的缺失,这与分化丧失和致瘤潜力增加有关,导致预后不良。SMARCA2和SMARCA4缺乏症在实体显性腺癌和支气管上皮标志物(包括甲状腺转录因子1)水平低的肿瘤中很常见。本文报道了一例罕见的SCLC中SMARCA4缺乏的病例。患者男,57岁,既往无病史,因右上肺叶占位性病变伴气管及纵隔浸润而入院治疗。右侧锁骨上区淋巴结活检诊断SCLC伴有SMARCA4的区域性缺失。患者表现出进行性呼吸衰竭和临床恶化,尽管插管并转移到重症监护病房,但最终死亡。该病例表明,smarca4缺陷的SCLC可能表现为严重恶化的表型,患者预后较差。
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