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本文引用的文献

1
Biochemical detection of novel anaplastic lymphoma kinase proteins in tissue sections of anaplastic large cell lymphoma.间变性大细胞淋巴瘤组织切片中新型间变性淋巴瘤激酶蛋白的生化检测
Am J Pathol. 1999 Jun;154(6):1657-63. doi: 10.1016/S0002-9440(10)65421-1.
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ALK expression defines a distinct group of T/null lymphomas ("ALK lymphomas") with a wide morphological spectrum.ALK表达定义了一组具有广泛形态谱的独特T/null淋巴瘤(“ALK淋巴瘤”)。
Am J Pathol. 1998 Sep;153(3):875-86. doi: 10.1016/S0002-9440(10)65629-5.
3
Nucleolar localization of the nucleophosmin-anaplastic lymphoma kinase is not required for malignant transformation.恶性转化并不需要核磷蛋白-间变性淋巴瘤激酶的核仁定位。
Cancer Res. 1998 Mar 1;58(5):1057-62.
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ALK-positive lymphoma: a single disease with a broad spectrum of morphology.ALK阳性淋巴瘤:一种具有广泛形态学谱的单一疾病。
Blood. 1998 Mar 15;91(6):2076-84.
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Retrovirus-mediated gene transfer of NPM-ALK causes lymphoid malignancy in mice.逆转录病毒介导的NPM-ALK基因转移可导致小鼠发生淋巴恶性肿瘤。
Blood. 1997 Oct 15;90(8):2901-10.
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Oncogenic transcription factors in the human acute leukemias.人类急性白血病中的致癌转录因子。
Science. 1997 Nov 7;278(5340):1059-64. doi: 10.1126/science.278.5340.1059.
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ALK, the chromosome 2 gene locus altered by the t(2;5) in non-Hodgkin's lymphoma, encodes a novel neural receptor tyrosine kinase that is highly related to leukocyte tyrosine kinase (LTK).间变性淋巴瘤激酶(ALK)是2号染色体上的基因位点,在非霍奇金淋巴瘤中因t(2;5)而发生改变,它编码一种新型神经受体酪氨酸激酶,与白细胞酪氨酸激酶(LTK)高度相关。
Oncogene. 1997 May 8;14(18):2175-88. doi: 10.1038/sj.onc.1201062.
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Biology and genetics of human neuroblastomas.
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Role of the nucleophosmin (NPM) portion of the non-Hodgkin's lymphoma-associated NPM-anaplastic lymphoma kinase fusion protein in oncogenesis.非霍奇金淋巴瘤相关的核磷蛋白(NPM)-间变性淋巴瘤激酶融合蛋白中的核磷蛋白(NPM)部分在肿瘤发生中的作用。
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间变性淋巴瘤激酶(ALK)酪氨酸激酶基因在神经母细胞瘤中的表达。

Expression of the ALK tyrosine kinase gene in neuroblastoma.

作者信息

Lamant L, Pulford K, Bischof D, Morris S W, Mason D Y, Delsol G, Mariamé B

机构信息

Department of Pathology, Centre Hospitalo-Universitaire Purpan, Toulouse, France.

出版信息

Am J Pathol. 2000 May;156(5):1711-21. doi: 10.1016/S0002-9440(10)65042-0.

DOI:10.1016/S0002-9440(10)65042-0
PMID:10793082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1876934/
Abstract

ALK (anaplastic lymphoma kinase) is a tyrosine kinase receptor, expressed as part of the chimeric NPM-ALK protein, in anaplastic large cell lymphomas (ALCLs) exhibiting the t(2;5)(p23;q35) translocation. As a result of this translocation, the NPM (nucleophosmin) gene is fused to the portion of the ALK gene encoding its intracytoplasmic segment. In normal mouse tissues, mRNA encoding the Alk receptor has been found only in neural cells, suggesting involvement of this receptor in the development of the nervous system. The purpose of the present study was to examine the presence of ALK transcripts and protein in normal human tissues and a variety of cell lines and human tumors. Emphasis was placed on neuroblastomas because other tyrosine kinase receptors are expressed in human neuroblastomas. Fifty-six cell lines, including 29 lines of neural origin, and lymphoid and nonlymphoid tissue specimens, including 24 neuroblastomas, were investigated for ALK expression, using reverse transcriptase-polymerase chain reaction, Western blotting, and immunohistochemistry. The results confirmed that mRNA encoding ALK protein was not detectable in any normal or neoplastic hematopoietic tissue tested, except for t(2;5)-positive ALCL. The salient finding was that 13 of the 29 cell lines of neural origin and 22 of 24 neuroblastomas were found to express ALK transcripts and ALK protein. However, no correlation was evident between any known prognostic factors and the level of ALK expression.

摘要

间变性淋巴瘤激酶(ALK)是一种酪氨酸激酶受体,在表现出t(2;5)(p23;q35)易位的间变性大细胞淋巴瘤(ALCL)中作为嵌合NPM-ALK蛋白的一部分表达。由于这种易位,核仁磷酸蛋白(NPM)基因与ALK基因编码其胞浆内片段的部分融合。在正常小鼠组织中,仅在神经细胞中发现了编码Alk受体的mRNA,这表明该受体参与了神经系统的发育。本研究的目的是检测ALK转录本和蛋白在正常人体组织、多种细胞系及人类肿瘤中的存在情况。由于其他酪氨酸激酶受体在人类神经母细胞瘤中表达,因此重点研究了神经母细胞瘤。使用逆转录聚合酶链反应、蛋白质印迹法和免疫组织化学,对56种细胞系(包括29种神经源性细胞系)以及淋巴和非淋巴组织标本(包括24例神经母细胞瘤)进行了ALK表达检测。结果证实,除了t(2;5)阳性的ALCL外,在任何测试的正常或肿瘤性造血组织中均未检测到编码ALK蛋白的mRNA。显著的发现是,在29种神经源性细胞系中有13种以及24例神经母细胞瘤中有22例被发现表达ALK转录本和ALK蛋白。然而,任何已知的预后因素与ALK表达水平之间均无明显相关性。