Huh Seok Jae, Oh Sung Yong, Lee Suee, Lee Ji Hyun, Kim Sung Hyun, Pak Min Kyung, Kim Hyo-Jin
Department of Internal Medicine, Dong-A University College of Medicine, Seo-gu, Busan 49201, Republic of Korea.
Department of Pathology, Dong-A University College of Medicine, Seo-gu, Busan 49201, Republic of Korea.
Oncol Lett. 2020 Nov;20(5):205. doi: 10.3892/ol.2020.12068. Epub 2020 Sep 8.
Extranodal marginal zone lymphoma is a type of low-grade B-cell lymphoma that can be classified as a mucosal-associated lymphoid tissue (MALT) lymphoma. Recently, second-generation or next-generation sequencing (NGS), which allows simultaneous sequencing of hundreds to billions of DNA strands, has been a focus of attention and is rapidly being adopted in various fields. In the present study, paraffin-embedded tissue samples of gastric MALT lymphoma (n=1) and small intestine MALT lymphoma (n=4) were selected, and DNA was extracted from the tissue samples. After performing quality control, NGS was performed using HemaSCAN™, a custom panel of 426 genes, including essential blood cancer genes. NGS revealed single nucleotide variations (SNVs), short insertions and deletions (InDels) and copy number variations (CNVs). These genomic variants were reported as annotated, known or novel variants. An annotated variant, an erb-b2 receptor tyrosine kinase 2 gene amplification, was observed in one patient. Known and novel variants, including SNVs of SET binding protein 6 (SETBP6), Runt-related transcription factor 1 and Kelch-like ECH-associated protein 1 genes, InDel of the marker of proliferation Ki-67 gene, and CNVs of the zinc finger protein 703 and NOTCH1 genes, were observed in ≥2 patients. Additionally, InDels with frameshift mutations were identified in the B-cell lymphoma/leukemia 10, DEAD-box helicase 3 X-linked, forkhead box O3 and mucin 2, oligomeric mucus/gel-forming genes in one patient. Since few NGS studies have been performed on MALT lymphoma, the current results were unable to determine if the different mutations that were identified are 'actionable' (that is, potentially responsive to a targeted therapy) Further studies are required to determine the associations between genetic mutations and the development of MALT lymphoma.
结外边缘区淋巴瘤是一种低度B细胞淋巴瘤,可归类为黏膜相关淋巴组织(MALT)淋巴瘤。最近,第二代或新一代测序(NGS)能够同时对数以百计到数十亿的DNA链进行测序,已成为关注焦点,并正在各个领域迅速得到应用。在本研究中,选取了胃MALT淋巴瘤(n = 1)和小肠MALT淋巴瘤(n = 4)的石蜡包埋组织样本,并从组织样本中提取DNA。在进行质量控制后,使用HemaSCAN™进行NGS,HemaSCAN™是一个包含426个基因的定制检测板,包括重要的血液癌症基因。NGS揭示了单核苷酸变异(SNV)、短插入和缺失(InDel)以及拷贝数变异(CNV)。这些基因组变异被报告为注释变异、已知变异或新变异。在一名患者中观察到一个注释变异,即erb-b2受体酪氨酸激酶2基因扩增。在≥2名患者中观察到已知和新变异,包括SET结合蛋白6(SETBP6)、Runt相关转录因子1和Kelch样ECH相关蛋白1基因的SNV,增殖标志物Ki-67基因的InDel,以及锌指蛋白703和NOTCH1基因的CNV。此外,在一名患者的B细胞淋巴瘤/白血病10、DEAD盒解旋酶3 X连锁、叉头盒O3和黏蛋白2、寡聚黏液/凝胶形成基因中鉴定出具有移码突变的InDel。由于对MALT淋巴瘤进行的NGS研究较少,目前的结果无法确定所鉴定的不同突变是否“可操作”(即可能对靶向治疗有反应)。需要进一步研究以确定基因突变与MALT淋巴瘤发生之间的关联。