Gabillot-Carré Marion, Lepelletier Yves, Humbert Martine, de Sepuvelda Paulo, Hamouda Nadine Ben, Zappulla Jean Pierre, Liblau Roland, Ribadeau-Dumas Antoine, Machavoine François, Letard Sébastien, Baude Cédric, Hermant Aurélie, Yang Ying, Vargaftig Jacques, Bodemer Christine, Morelon Emmanuel, Lortholary Olivier, Recher Christian, Laurent Guy, Dy Michel, Arock Michel, Dubreuil Patrice, Hermine Olivier
CNRS UMR-8147, Université René Descartes Paris V, Hôpital Necker, 161 rue de Sèvres, 75743 Paris cedex 15, France.
Blood. 2006 Aug 1;108(3):1065-72. doi: 10.1182/blood-2005-06-2433. Epub 2006 Apr 4.
Two classes of oncogenic mutations of the c-kit tyrosine kinase have been described: the juxtamembrane domain V560G mutation, which is preferentially found in gastrointestinal stromal tumors (GISTs), and the kinase domain D816V mutation, which is highly representative of systemic mastocytosis (SM). Here we show that both mutations constitutively activate the mammalian target of rapamycin (mTOR) signaling pathway. Surprisingly, the mTOR inhibitor rapamycin induces only apoptosis in HMC-1 cells bearing the D816V but not the V560G mutation. In support of this unexpected selectivity, rapamycin inhibits the phosphorylation of 4E-BP1, a downstream substrate of the mTOR pathway, but only in D816V HMC-1 cells. Importantly, D816V mast cells isolated from SM patients or from transgenic mice are sensitive to rapamycin whereas normal human or mouse mast cells are not. Thus, rapamycin inhibition appears specific to the D816V mutation. At present there is no effective cure for SM patients with the D816V mutation. The data presented here provide a rationale to test whether rapamycin could be a possible treatment for SM and other hematologic malignancies with the D816V mutation.
已描述了两类c-kit酪氨酸激酶的致癌突变:近膜结构域V560G突变,其优先见于胃肠道间质瘤(GISTs);以及激酶结构域D816V突变,其是系统性肥大细胞增多症(SM)的高度代表性突变。在此我们表明,这两种突变均组成性激活雷帕霉素哺乳动物靶标(mTOR)信号通路。令人惊讶的是,mTOR抑制剂雷帕霉素仅在携带D816V而非V560G突变的HMC-1细胞中诱导凋亡。为支持这种意外的选择性,雷帕霉素抑制mTOR通路的下游底物4E-BP1的磷酸化,但仅在D816V HMC-1细胞中。重要的是,从SM患者或转基因小鼠分离的D816V肥大细胞对雷帕霉素敏感,而正常人类或小鼠肥大细胞则不敏感。因此,雷帕霉素抑制似乎对D816V突变具有特异性。目前,对于具有D816V突变的SM患者尚无有效的治愈方法。此处呈现的数据为测试雷帕霉素是否可能成为治疗具有D816V突变的SM和其他血液系统恶性肿瘤的一种疗法提供了理论依据。