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胸段SMARCA4缺陷型未分化肿瘤。

Thoracic SMARCA4-deficient undifferentiated tumor.

作者信息

Jiang Jiapeng, Chen Zhixin, Gong Jiali, Han Na, Lu Hongyang

机构信息

The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, 310053, People's Republic of China.

Zhejiang Key Laboratory of Diagnosis & Treatment Technology on Thoracic Oncology (Lung and Esophagus), Zhejiang Cancer Hospital, Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences, Hangzhou, 310022, China.

出版信息

Discov Oncol. 2023 Apr 28;14(1):51. doi: 10.1007/s12672-023-00639-w.

DOI:10.1007/s12672-023-00639-w
PMID:37115343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10147882/
Abstract

Thoracic SMARCA4-deficient undifferentiated tumor (SMARCA4-UT) is a recently described smoking-related malignancy. The pathogenesis of SMARCA4-UT is the mutational inactivation and loss of expression of a subunit encoding the mammalian switch/sucrose nonfermenting ATPase-dependent chromatin remodeling complex (which can be mobilized using adenosine triphosphate hydrolysis nucleosomes and regulate other cellular processes including development, differentiation, proliferation, and apoptosis), in particular SMARCA4 and SMARCA2. The dynamic activity of this complex plays an important role in regulating the activation and repression of gene expression programs. SMARCA4-UT exhibits morphological features similar to the malignant rhabdoid tumor (MRT), small cell carcinoma of the ovary of the hypercalcemic type (SCCOHT), and INI1-deficient tumor, but SMARCA4-UT differs from SCCOHT and MRT from a genomic perspective. SMARCA4-UT mainly involves the mediastinum and lung parenchyma, and appears as a large infiltrative mass that easily compresses surrounding tissues. At present, chemotherapy is a common treatment, but its efficacy is not clear. Moreover, the inhibitor of the enhancer of zeste homolog 2 showed promising efficacy in some patients with SMARCA4-UT. This study aimed to review the clinical characteristics, diagnosis, treatment, and prognosis of SMARCA4-UT.

摘要

胸段SMARCA4缺陷型未分化肿瘤(SMARCA4-UT)是一种最近描述的与吸烟相关的恶性肿瘤。SMARCA4-UT的发病机制是编码哺乳动物开关/蔗糖非发酵ATP酶依赖性染色质重塑复合物(可利用三磷酸腺苷水解核小体动员并调节包括发育、分化、增殖和凋亡在内的其他细胞过程)的一个亚基发生突变失活和表达缺失,特别是SMARCA4和SMARCA2。该复合物的动态活性在调节基因表达程序的激活和抑制中起重要作用。SMARCA4-UT表现出与恶性横纹肌样瘤(MRT)、高钙血症型卵巢小细胞癌(SCCOHT)和INI1缺陷型肿瘤相似的形态学特征,但从基因组角度来看,SMARCA4-UT与SCCOHT和MRT不同。SMARCA4-UT主要累及纵隔和肺实质,表现为一个易于压迫周围组织的大浸润性肿块。目前,化疗是常见的治疗方法,但其疗效尚不清楚。此外,zeste同源物2增强子抑制剂在一些SMARCA4-UT患者中显示出有前景的疗效。本研究旨在综述SMARCA4-UT的临床特征、诊断、治疗和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8139/10147882/f160ec1d3716/12672_2023_639_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8139/10147882/f160ec1d3716/12672_2023_639_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8139/10147882/f160ec1d3716/12672_2023_639_Fig1_HTML.jpg

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本文引用的文献

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: Implications of an Altered Chromatin-Remodeling Gene for Cancer Development and Therapy.: 染色质重塑基因改变与癌症发生和治疗的关系。
Mol Cancer Ther. 2021 Dec;20(12):2341-2351. doi: 10.1158/1535-7163.MCT-21-0433. Epub 2021 Oct 12.
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Ipilimumab and Pembrolizumab Mixed Response in a 41-Year-Old Patient with SMARCA4-Deficient Thoracic Sarcoma: An Interdisciplinary Case Study.41岁SMARCA4缺陷型胸壁肉瘤患者使用伊匹单抗和帕博利珠单抗的混合反应:一项跨学科病例研究
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Recent updates in thoracic SMARCA4-deficient undifferentiated tumor.
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Oncologist. 2025 May 8;30(5). doi: 10.1093/oncolo/oyaf121.
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Retrospective Insights into the Clinicopathological Features and Treatment Outcomes of Thoracic SMARCA4-Deficient Tumors.胸段SMARCA4缺陷型肿瘤临床病理特征及治疗结果的回顾性分析
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