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c-myc编码区的突变在获得性免疫缺陷综合征相关淋巴瘤中频繁发生。

Mutations in the coding region of c-myc occur frequently in acquired immunodeficiency syndrome-associated lymphomas.

作者信息

Bhatia K, Spangler G, Gaidano G, Hamdy N, Dalla-Favera R, Magrath I

机构信息

Lymphoma Biology Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Blood. 1994 Aug 1;84(3):883-8.

PMID:8043869
Abstract

We have analyzed 30 cases of high- and intermediate-grade acquired immunodeficiency syndrome-associated non-Hodgkin's lymphoma (AIDS-NHL) for mutations in the c-myc coding region. In addition, in these same tumors, we have sought the presence of mutations in a regulatory region within the first c-myc intron defined by the binding to a factor that inhibits c-myc transcription (MYC intron factor, or mif). Mutations in the c-myc coding region were present in 10 of 16 small noncleaved cell lymphoma (SNCL), but in only 3 of 14 other histologic subtypes tested (0/3 large non-cleaved cell, 2/8 immunoblastic, and 1/3 anaplastic large cell lymphomas). Nineteen of the AIDS-NHLs analyzed contained a c-myc rearrangement and in 10 of these the c-myc gene was mutated in its coding region. In contrast, we could detect a mutation in the coding region in only 2 of 8 AIDS-NHL without a c-myc rearrangement. Mutations in the mif region were detected in 5 of 16 SNCL. Among AIDS-NHL carrying mutations in the c-myc coding region, only 4 carried mutations in the regulatory region. These results suggest that the mutations in the coding region of the c-myc protein may either be a consequence of the translocations involving c-myc, or may be necessary only in tumors where c-myc is deregulated as a result of a c-myc/lg translocation.

摘要

我们分析了30例高级别和中级别获得性免疫缺陷综合征相关非霍奇金淋巴瘤(AIDS-NHL)的c-myc编码区突变情况。此外,在这些相同的肿瘤中,我们还探寻了第一个c-myc内含子内一个调控区域的突变情况,该区域由与一种抑制c-myc转录的因子(MYC内含子因子,或mif)的结合所定义。c-myc编码区的突变存在于16例小无裂细胞淋巴瘤(SNCL)中的10例,但在其他14种检测的组织学亚型中仅3例存在(3例大无裂细胞淋巴瘤中0例、8例免疫母细胞淋巴瘤中2例、3例间变性大细胞淋巴瘤中1例)。所分析的19例AIDS-NHL含有c-myc重排,其中10例c-myc基因在其编码区发生突变。相比之下,在8例无c-myc重排的AIDS-NHL中,仅2例在编码区检测到突变。在16例SNCL中的5例检测到mif区域的突变。在c-myc编码区携带突变的AIDS-NHL中,仅有4例在调控区域携带突变。这些结果表明,c-myc蛋白编码区的突变可能要么是涉及c-myc的易位的结果,要么可能仅在因c-myc/Ig易位导致c-myc失调的肿瘤中才是必需的。

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