Comer A R, Liebl E C, Hoffmann F M
McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706, USA.
J Lab Clin Med. 1995 Jun;125(6):686-91.
Translocations affecting the structure of the c-abl proto-oncogene are involved in the development or progression of chronic myelogenous leukemia (CML) and acute lymphocytic leukemia (ALL). Leukemic cells from patients with CML show alterations in adhesive properties that may play a part in the pathology of these diseases. Mutations in the Drosophila Abl homolog are lethal and indicate that Abl may mediate processes involving differential cell adhesion. These observations suggest that Abl may regulate similar adhesive processes in human beings and Drosophila. Genetic analysis of Abl function in Drosophila has identified novel proteins that function in Abl-related processes. Analysis of the functions of these new molecules may provide insight into mechanisms by which oncogenic abl proteins participate in the etiology of CML and ALL.
影响c-abl原癌基因结构的易位与慢性粒细胞白血病(CML)和急性淋巴细胞白血病(ALL)的发生或进展有关。CML患者的白血病细胞显示出黏附特性的改变,这可能在这些疾病的病理过程中起作用。果蝇Abl同源物中的突变是致死性的,这表明Abl可能介导涉及差异细胞黏附的过程。这些观察结果表明,Abl可能在人类和果蝇中调节相似的黏附过程。对果蝇中Abl功能的遗传分析已经鉴定出在与Abl相关过程中起作用的新蛋白质。对这些新分子功能的分析可能有助于深入了解致癌性abl蛋白参与CML和ALL病因的机制。