首页> 外文期刊>Genes, Chromosomes and Cancer >Establishment of a novel MALT lymphoma cell line, ma-1, from a patient with t(14;18)(q32;q21)-positive Helicobacter pylori-independent gastric MALT lymphoma.
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Establishment of a novel MALT lymphoma cell line, ma-1, from a patient with t(14;18)(q32;q21)-positive Helicobacter pylori-independent gastric MALT lymphoma.

机译:从t(14; 18)(q32; q21)阳性幽门螺杆菌非依赖性胃MALT淋巴瘤患者中建立新型MALT淋巴瘤细胞系ma-1。

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摘要

Although t(11;18)(q21;q21), t(1;14)(p22;q32), and a few other genetic mutations are specific markers for the Helicobacter pylori (HP)-independent status of gastric mucosa-associated lymphoid tissue (MALT) lymphoma, the molecular mechanisms responsible for HP-independence of gastric MALT lymphoma without such translocations and mutations remain uncharacterized. In the present study, we describe the establishment and characterization of a novel MALT lymphoma cell line, MA-1, which was derived from a gastric MALT lymphoma which was negative for both t(11;18)(q21;q21) and t(1;14)(p22;q32); the patient had failed HP eradication therapy and chemotherapy. The cell morphology and the immunophenotype of this cell line were similar to that of the original gastric MALT lymphoma. Comparative genomic hybridization analysis showed no significant gene copy number changes. Spectral karyotyping displayed a near-diploid chromosome content (48 < 2n>XY), with at least 13 chromosome structural abnormalities. Furthermore, fluorescence in situ hybridization analyses disclosed the existence of three sub-clones, characterized by t(14;18)(q32;q21)/IGH-BCL2, t(14;18)(q32;q21)/IGH-MALT1, and the presence of both chromosomal translocations in the same cell, respectively; whereas amplification of the genes CRAD9, TRAF2, and BCL10 were not found. In conclusion, we have established the first human gastric MALT lymphoma cell line, which is characterized by unusual and complex chromosome translocations and will be useful to explore further the molecular mechanisms of HP-independence in gastric MALT lymphoma.
机译:尽管t(11; 18)(q21; q21),t(1; 14)(p22; q32)和其他一些遗传突变是胃黏膜相关淋巴样细胞不依赖幽门螺杆菌(HP)状态的特异性标记组织(MALT)淋巴瘤,没有这种易位和突变的胃MALT淋巴瘤独立于HP的分子机制仍未鉴定。在本研究中,我们描述了一种新型MALT淋巴瘤细胞系MA-1的建立和表征,该细胞系来源于胃MALT淋巴瘤,而t(11; 18)(q21; q21)和t( 1; 14)(p22; q32);该患者的HP根除疗法和化学疗法失败。该细胞系的细胞形态和免疫表型与原始胃MALT淋巴瘤相似。比较基因组杂交分析显示没有明显的基因拷贝数变化。光谱核型分析显示接近二倍体的染色体含量(48 2n> XY),至少有13个染色体结构异常。此外,荧光原位杂交分析揭示了三个亚克隆的存在,其特征在于t(14; 18)(q32; q21)/ IGH-BCL2,t(14; 18)(q32; q21)/ IGH-MALT1,在同一个细胞中分别存在两个染色体易位;而未发现基因CRAD9,TRAF2和BCL10的扩增。总之,我们已经建立了第一个人类胃MALT淋巴瘤细胞系,其特征是异常和复杂的染色体易位,将有助于进一步探索胃MALT淋巴瘤中HP依赖性的分子机制。

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