Ikeda H, Kanakura Y, Tamaki T, Kuriu A, Kitayama H, Ishikawa J, Kanayama Y, Yonezawa T, Tarui S, Griffin J D
Second Department of Internal Medicine, Osaka University Medical School, Japan.
Blood. 1991 Dec 1;78(11):2962-8.
The c-kit proto-oncogene encodes a receptor tyrosine kinase that is thought to play an important role in hematopoiesis. In a series of human acute myeloblastic leukemia (AML), the expression of the c-kit proto-oncogene and its product was studied by means of Northern blot and immunoblot analyses. The c-kit mRNA was expressed in 20 of 25 cases of AML, and in those cases the product of the c-kit proto-oncogene was detected by immunoblotting with anti-c-kit antibody. The expression of c-kit transcripts and protein was barely detectable in normal bone marrow cells as a control. The expression of c-kit transcript did not correlate with the French-American-British classification nor clinical manifestations. In 6 of 11 cases that expressed c-kit product, AML cells were found to proliferate in response to recombinant human stem cell factor (rhSCF), the ligand for c-kit, and the synergistic stimulation of AML cells was observed by rhSCF and granulocyte-macrophage colony-stimulating factor. Immunoblotting with anti-phosphotyrosine antibody showed that the c-kit receptor protein was detectably phosphorylated in 7 of 12 cases tested before the stimulation with rhSCF, while the rhSCF treatment resulted in an increased tyrosine phosphorylation of c-kit in AML cells. These results indicate that c-kit proto-oncogene is expressed in most cases of AML and is functional in terms of supporting proliferation.
原癌基因c-kit编码一种受体酪氨酸激酶,被认为在造血过程中发挥重要作用。在一系列人类急性髓细胞白血病(AML)中,通过Northern印迹和免疫印迹分析研究了原癌基因c-kit及其产物的表达。c-kit mRNA在25例AML中的20例中表达,在这些病例中,用抗c-kit抗体通过免疫印迹检测到原癌基因c-kit的产物。作为对照,在正常骨髓细胞中几乎检测不到c-kit转录本和蛋白质的表达。c-kit转录本的表达与法美英分类及临床表现均无相关性。在表达c-kit产物的11例病例中的6例中,发现AML细胞对重组人干细胞因子(rhSCF)(c-kit的配体)有增殖反应,并且观察到rhSCF和粒细胞-巨噬细胞集落刺激因子对AML细胞有协同刺激作用。用抗磷酸酪氨酸抗体进行免疫印迹显示,在12例接受检测的病例中,有7例在rhSCF刺激前可检测到c-kit受体蛋白磷酸化,而rhSCF处理导致AML细胞中c-kit的酪氨酸磷酸化增加。这些结果表明,原癌基因c-kit在大多数AML病例中表达,并且在支持增殖方面具有功能。