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EML4-ALK转录本而非融合蛋白可在反应性和肿瘤性淋巴组织中表达。

The EML4-ALK transcript but not the fusion protein can be expressed in reactive and neoplastic lymphoid tissues.

作者信息

Sozzi Gabriella, Martelli Maria Paola, Conte Davide, Modena Piergiorgio, Pettirossi Valentina, Pileri Stefano A, Falini Brunangelo

机构信息

Istituto Nazionale Tumori, Milan, Italy.

出版信息

Haematologica. 2009 Sep;94(9):1307-11. doi: 10.3324/haematol.2009.008045.

Abstract

Rearrangements involving the ALK gene define two distinct entities in the new 2008 WHO classification of lymphoid neoplasms, i.e. ALK+ anaplastic large cell lymphoma and a rare subset of ALK+ diffuse large B-cell lymphoma. Recently, rearrangements involving ALK and the echinoderm microtubule associated protein-like 4 (EML4) gene were described as a specific genetic alteration in about 6% of non-small cell lung cancer (NSCLC). We investigated the expression of EML4-ALK mRNA and protein in 51 reactive and 58 neoplastic lymphoid tissues. EML4-ALK transcripts were detected in 3/51 (5.9%) of reactive lymphoid tissues and 12/58 (20.7%) of lymphomas of different categories, including follicular lymphoma, diffuse large B-cell lymphoma and Hodgkin's disease. Notably, none of these cases expressed the EML4-ALK fusion protein at Western blotting samples and immunohistochemistry. These results indicate that EML4-ALK rearrangements are not specific of NSCLC and raise yet unsolved questions about their role in promoting human neoplasms.

摘要

在2008年世界卫生组织淋巴样肿瘤新分类中,涉及ALK基因的重排定义了两个不同的实体,即ALK阳性间变性大细胞淋巴瘤和ALK阳性弥漫性大B细胞淋巴瘤的一个罕见亚组。最近,涉及ALK和棘皮动物微管相关蛋白样4(EML4)基因的重排被描述为约6%的非小细胞肺癌(NSCLC)中的一种特异性基因改变。我们研究了51例反应性和58例肿瘤性淋巴组织中EML4-ALK mRNA和蛋白的表达。在3/51(5.9%)的反应性淋巴组织和12/58(20.7%)的不同类型淋巴瘤(包括滤泡性淋巴瘤、弥漫性大B细胞淋巴瘤和霍奇金病)中检测到EML4-ALK转录本。值得注意的是,在蛋白质印迹样本和免疫组织化学检测中,这些病例均未表达EML4-ALK融合蛋白。这些结果表明,EML4-ALK重排并非NSCLC所特有,并引发了关于其在促进人类肿瘤发生中作用的尚未解决的问题。

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A mouse model for EML4-ALK-positive lung cancer.一种EML4-ALK阳性肺癌的小鼠模型。
Proc Natl Acad Sci U S A. 2008 Dec 16;105(50):19893-7. doi: 10.1073/pnas.0805381105. Epub 2008 Dec 8.
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ALK is not expressed in Hodgkin disease.
Blood. 2001 Mar 15;97(6):1901-2. doi: 10.1182/blood.v97.6.1901.

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