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G(1)期加速与核心结合因子β-平滑肌肌球蛋白重链协同作用诱导小鼠急性白血病。

Acceleration of G(1) cooperates with core binding factor beta-smooth muscle myosin heavy chain to induce acute leukemia in mice.

作者信息

Yang Yandan, Wang Weihua, Cleaves Rebecca, Zahurak Marianna, Cheng Linzhao, Civin Curt I, Friedman Alan D

机构信息

Department of Oncology, Cancer Research Building, Johns Hopkins University, 1650 Orleans Street, Baltimore, MD 21231, USA.

出版信息

Cancer Res. 2002 Apr 15;62(8):2232-5.

Abstract

The genes encoding the AML1 (RUNX1) or CBFbeta subunits of core binding factor (CBF) are commonly altered by translocation or mutation in human leukemias. Because CBF oncoproteins slow G(1), we sought to determine whether mutations that accelerate G(1) potentiate their ability to induce transformation. Wild-type or p16(INK4a)p19(ARF) (-/-) marrow cells transduced with CBFbeta-smooth muscle myosin heavy chain (SMMHC) were transplanted into wild-type, syngeneic recipients. CBFbeta-SMMHC significantly increased the development of acute leukemias from marrow lacking the overlapping p16p19 genes, based on analysis of Kaplan-Meier event-time distributions. Wild-type marrow was also transduced with vectors expressing either E7 alone or both E7 and CBFbeta-SMMHC. Combining oncogenes again increased leukemia formation. Exposing mice transplanted with CBFbeta-SMMHC-transduced cells to a mutagen, ethylnitrosourea, markedly accelerated leukemogenesis compared to expressing CBFbeta-SMMHC with loss of p16p19, indicating the need for multiple "hits" for transformation. The INV/p16p19 and INV/E7 leukemias were lymphoid and were clonal and retransplantable. Overall, these findings indicate that CBF mutations cooperate with genetic alterations that accelerate G(1) to induce acute leukemia.

摘要

编码核心结合因子(CBF)的AML1(RUNX1)或CBFβ亚基的基因在人类白血病中常因易位或突变而发生改变。由于CBF癌蛋白会减缓G1期进程,我们试图确定加速G1期进程的突变是否会增强其诱导转化的能力。将转导了CBFβ-平滑肌肌球蛋白重链(SMMHC)的野生型或p16(INK4a)p19(ARF)(-/-)骨髓细胞移植到同基因的野生型受体中。基于Kaplan-Meier事件时间分布分析,CBFβ-SMMHC显著增加了缺乏重叠p16p19基因的骨髓中急性白血病的发生。野生型骨髓也用单独表达E7或同时表达E7和CBFβ-SMMHC的载体进行转导。联合癌基因再次增加了白血病的形成。与表达缺失p16p19的CBFβ-SMMHC相比,将移植了CBFβ-SMMHC转导细胞的小鼠暴露于诱变剂乙基亚硝基脲中,显著加速了白血病的发生,表明转化需要多个“打击”。INV/p16p19和INV/E7白血病为淋巴细胞性,具有克隆性且可再次移植。总体而言,这些发现表明CBF突变与加速G1期进程的基因改变协同作用以诱导急性白血病。

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