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茶碱诱导分化为伯基特淋巴瘤中c-myc的失调提供了直接证据,并提示免疫球蛋白增强子序列参与其中。

Theophylline induced differentiation provides direct evidence for the deregulation of c-myc in Burkitt's lymphoma and suggests participation of immunoglobulin enhancer sequences.

作者信息

Sandlund J T, Neckers L M, Schneller H E, Woodruff L S, Magrath I T

机构信息

Pediatric Branch, National Cancer Institute, NIH, Bethesda, Maryland 20892.

出版信息

Cancer Res. 1993 Jan 1;53(1):127-32.

PMID:8416737
Abstract

Most of the evidence that supports the hypothesis that the c-myc gene is abnormally regulated in Burkitt's lymphoma (BL) is indirect. The putative abnormal expression of c-myc is likely, at least in part, to be a consequence of the usurpation of its regulatory sequences by immunoglobulin enhancer elements, which are invariably juxtaposed to c-myc by the translocations associated with this tumor (C. M. Croce, J. Erikson, A. Ar-Rushdi, D. Aden, and K. Nishikura, Proc. Natl. Acad. Sci. USA, 81: 3170-3174, 1984). We have developed a differentiation induction model system to examine this issue more directly. In a variety of non-BL cell lines, differentiation induction results in the down-regulation of c-myc (G. P. Studzinski, A. K. Bhandal, and Z. S. Brelvi, Proc. Soc. Exp. Biol. Med., 179: 288-295, 1985; Y. Matsui, R. Takahasi, K. Minara, T. Nakagawa, T. Koizumi, Y. Nakao, T. Sugiyama, and T. Fugita, Cancer Res., 49: 1366-1371, 1985; T. Mitchell, E. Sariban, and D. Kufe, Mol. Pharmacol., 30: 398-402, 1986; Z. S. Brelvi, and G. P. Studzinski, J. Cell. Physiol., 128: 171-179, 1986). Since BL is of B-cell origin, differentiation is associated with persistent or increased expression of immunoglobulin genes. Therefore, if c-myc and c-mu are coregulated in BL via immunoglobulin enhancer sequences, persistent or increased expression of the c-myc gene, rather than down-regulation, should occur in differentiated BL cells. Differentiation was induced in four BL cell lines with theophylline (7 x 10(-3) M), and mRNA was examined by Northern blot analysis. In all four BL lines studied (JD38, AG876, KK124, and Daudi), there was persistent or increased expression of both c-mu and c-myc genes (detected with a third exon c-myc probe), in contrast to the decreased expression of the c-myc gene observed in the three Epstein-Barr virus transformed lines studied (A3317, TC84, and CB34). In the BL cell line, JD38, the c-myc gene is truncated (the second and third exons are translocated to chromosome 14 while the first exon remains on chromosome 8). In this line, we demonstrated that theophylline induced differentiation results in down-regulation of the first exon while the level of expression of the translocated second and third exons remains unchanged or increases.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

大多数支持c-myc基因在伯基特淋巴瘤(BL)中受到异常调控这一假说的证据都是间接的。c-myc假定的异常表达可能至少部分是免疫球蛋白增强子元件篡夺其调控序列的结果,这些增强子元件总是通过与该肿瘤相关的易位与c-myc并列(C.M.克罗齐、J.埃里克森、A.阿尔-鲁什迪、D.阿登和K.西久良,《美国国家科学院院刊》,81: 3170 - 3174, 1984)。我们开发了一个分化诱导模型系统来更直接地研究这个问题。在多种非BL细胞系中,分化诱导导致c-myc下调(G.P.斯塔津斯基、A.K.班达尔和Z.S.布雷尔维,《实验生物学与医学学会会刊》,179: 288 - 295, 1985;松井洋、高桥隆、水无濑健、中川彻、小泉彻、中尾洋、杉山智和藤田富,《癌症研究》,49: 1366 - 1371, 1985;T.米切尔、E.萨里班和D.库费,《分子药理学》,30: 398 - 402, 1986;Z.S.布雷尔维和G.P.斯塔津斯基,《细胞生理学杂志》,128: 171 - 179, 1986)。由于BL起源于B细胞,分化与免疫球蛋白基因的持续或增加表达相关。因此,如果c-myc和c-mu在BL中通过免疫球蛋白增强子序列共同调控,那么在分化的BL细胞中应该出现c-myc基因的持续或增加表达,而不是下调。用茶碱(7×10⁻³ M)诱导四种BL细胞系分化,并通过Northern印迹分析检测mRNA。在所有研究的四种BL细胞系(JD38、AG876、KK124和Daudi)中,c-mu和c-myc基因均持续或增加表达(用c-myc第三外显子探针检测),这与在研究的三种爱泼斯坦-巴尔病毒转化细胞系(A3317、TC84和CB34)中观察到的c-myc基因表达降低形成对比。在BL细胞系JD38中,c-myc基因被截断(第二和第三外显子易位到14号染色体,而第一外显子保留在8号染色体上)。在该细胞系中,我们证明茶碱诱导的分化导致第一外显子下调,而易位的第二和第三外显子的表达水平保持不变或增加。(摘要截于400字)

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