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在γ射线诱导的小鼠胸腺淋巴瘤中,Notch1和Notch2的表达缺陷与c-Myc和Ikaros的改变有关。

Defective expression of Notch1 and Notch2 in connection to alterations of c-Myc and Ikaros in gamma-radiation-induced mouse thymic lymphomas.

作者信息

López-Nieva P, Santos J, Fernández-Piqueras J

机构信息

Laboratorio de Genetica Molecular Humana, Departamento de Biologia, Facultad de Ciencias, Universidad Autonoma de Madrid, E-28049 Madrid, Espana.

出版信息

Carcinogenesis. 2004 Jul;25(7):1299-304. doi: 10.1093/carcin/bgh124. Epub 2004 Feb 19.

Abstract

Gamma-radiation-induced thymic lymphomas constitute a heterogeneous group of T-cell lymphomas. Some tumour suppressor genes and oncogenes have been shown to be defective in a fraction of such lymphomas, yet a considerable number of these remain elusive in terms of gene alterations. In the present work we present evidence that gamma-radiation-induced thymic lymphomas in (C57BL/6 J x BALB/c) F1 hybrid mice often exhibit increased levels of Notch1 expression, but, contrary to what was expected, they also exhibit a clearly reduced Notch2 mRNA expression, suggesting a cooperative antagonism of these genes. These results represent the first reported instance for the involvement of Notch2 inactivation in the development of thymic primary tumours while confirming the role of Notch1 as an activated oncogene. Additional analyses revealed that c-Myc over-expression and partial inactivation of Znfn1a1/Ikaros appear to be relevant events some how coupled to alterations in Notch genes inducing these kinds of tumours.

摘要

γ射线诱导的胸腺淋巴瘤构成了一组异质性的T细胞淋巴瘤。一些肿瘤抑制基因和癌基因已被证明在部分此类淋巴瘤中存在缺陷,但其中相当一部分在基因改变方面仍不清楚。在本研究中,我们提供证据表明,(C57BL/6 J×BALB/c)F1杂交小鼠中γ射线诱导的胸腺淋巴瘤通常表现出Notch1表达水平升高,但与预期相反,它们还表现出Notch2 mRNA表达明显降低,提示这些基因存在协同拮抗作用。这些结果代表了首次报道Notch2失活参与胸腺原发性肿瘤发生,同时证实了Notch1作为激活癌基因的作用。进一步分析表明,c-Myc过表达和Znfn1a1/Ikaros部分失活似乎是与Notch基因改变相关的事件,这些改变诱导了此类肿瘤的发生。

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