Heilman Susan A, Kuo Ya-Huei, Goudswaard Chantal S, Valk Peter J, Castilla Lucio H
Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Cancer Res. 2006 Dec 1;66(23):11214-8. doi: 10.1158/0008-5472.CAN-06-0959.
The gene encoding for core-binding factor beta (CBFbeta) is altered in acute myeloid leukemia samples with an inversion in chromosome 16, expressing the fusion protein CBFbeta-SMMHC. Previous studies have shown that this oncoprotein interferes with hematopoietic differentiation and proliferation and participates in leukemia development. In this study, we provide evidence that Cbfbeta modulates the oncogenic function of this fusion protein. We show that Cbfbeta plays an important role in proliferation of hematopoietic progenitors expressing Cbfbeta-SMMHC in vitro. In addition, Cbfbeta-SMMHC-mediated leukemia development is accelerated in the absence of Cbfbeta. These results indicate that the balance between Cbfbeta and Cbfbeta-SMMHC directly affects leukemia development, and suggest that CBF-specific therapeutic molecules should target CBFbeta-SMMHC function while maintaining CBFbeta activity.
在16号染色体发生倒位的急性髓系白血病样本中,编码核心结合因子β(CBFβ)的基因发生改变,表达融合蛋白CBFβ-SMMHC。先前的研究表明,这种癌蛋白会干扰造血分化和增殖,并参与白血病的发展。在本研究中,我们提供证据表明Cbfβ可调节这种融合蛋白的致癌功能。我们发现,Cbfβ在体外表达Cbfβ-SMMHC的造血祖细胞增殖中发挥重要作用。此外,在缺乏Cbfβ的情况下,Cbfβ-SMMHC介导的白血病发展会加速。这些结果表明,Cbfβ与Cbfβ-SMMHC之间的平衡直接影响白血病的发展,并提示CBF特异性治疗分子应在维持Cbfβ活性的同时靶向Cbfβ-SMMHC的功能。