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首页> 外文期刊>Journal of Thoracic Disease >Recent studies move closer to answering questions about sequential therapy for anaplastic lymphoma kinase-rearranged non-small cell lung cancer
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Recent studies move closer to answering questions about sequential therapy for anaplastic lymphoma kinase-rearranged non-small cell lung cancer

机译:最近的研究更接近于回答有关间变性淋巴瘤激酶重排非小细胞肺癌序贯治疗的问题

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Anaplastic lymphoma kinase ( AL K) fusion gene resulting from gene rearrangement was first identified in anaplastic large-cell lymphoma ( ALCL ) and is characterized by the fusion of nucleophosmin (NPM) and ALK genes (1). Subsequently, this type of fusion gene was described for the first time in lung cancer by Soda et al. through cDNA expression screening of surgically resected specimens from lung adenocarcinoma patients (2). Unlike the fusion gene in ALCL, this gene results from a fusion between echinoderm microtubule-associated protein-like 4 ( EML4 ) and ALK . The two genes are positioned in opposite directions on the short arm of chromosome 2, and the inversion of this region orients the genes in the same direction leading to the formation of the EML4-ALK fusion cancer gene (2).
机译:由基因重排产生的间变性淋巴瘤激酶(AL K)融合基因首先在间变性大细胞淋巴瘤(ALCL)中鉴定,其特征是核磷脂(NPM)和ALK基因融合(1)。随后,Soda等在肺癌中首次描述了这种融合基因。通过对肺腺癌患者手术切除的标本进行cDNA表达筛选(2)。与ALCL中的融合基因不同,该基因来自棘皮动物微管相关蛋白样4(EML4)和ALK的融合。这两个基因在2号染色体的短臂上位于相反的方向,该区域的倒置使这些基因在同一方向上定向,从而导致EML4-ALK融合癌基因的形成(2)。

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