Aix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Marseille, France.
Unité de Biostatistique et de Méthodologie, Département de la Recherche Clinique et de l'Innovation, Institut Paoli-Calmettes, Marseille, France.
Cancer Res. 2017 Dec 1;77(23):6627-6640. doi: 10.1158/0008-5472.CAN-17-1223. Epub 2017 Sep 28.
Acute myeloid leukemia (AML) originates from hematopoietic stem and progenitor cells that acquire somatic mutations, leading to disease and clonogenic evolution. AML is characterized by accumulation of immature myeloid cells in the bone marrow and phenotypic cellular heterogeneity reflective of normal hematopoietic differentiation. Here, we show that JAM-C expression defines a subset of leukemic cells endowed with leukemia-initiating cell activity (LIC). Stratification of AML patients at diagnosis based on JAM-C-expressing cells frequencies in the blood served as an independent prognostic marker for disease outcome. Using publicly available leukemic stem cell (LSC) gene expression profiles and gene expression data generated from JAM-C-expressing leukemic cells, we defined a single cell core gene expression signature correlated to JAM-C expression that reveals LSC heterogeneity. Finally, we demonstrated that JAM-C controls Src family kinase (SFK) activation in LSC and that LIC with exacerbated SFK activation was uniquely found within the JAM-C-expressing LSC compartment. .
急性髓系白血病 (AML) 起源于获得体细胞突变的造血干/祖细胞,导致疾病和克隆进化。AML 的特征是骨髓中不成熟髓系细胞的积累和反映正常造血分化的表型细胞异质性。在这里,我们表明 JAM-C 的表达定义了具有白血病起始细胞 (LIC) 活性的白血病细胞亚群。基于血液中 JAM-C 表达细胞的频率对 AML 患者进行诊断分层,是疾病结局的独立预后标志物。利用公开的白血病干细胞 (LSC) 基因表达谱和从 JAM-C 表达的白血病细胞中生成的基因表达数据,我们定义了一个与 JAM-C 表达相关的单细胞核心基因表达特征,该特征揭示了 LSC 的异质性。最后,我们证明 JAM-C 控制 LSC 中的Src 家族激酶 (SFK) 激活,并且在 JAM-C 表达的 LSC 隔室中唯一发现了具有增强的 SFK 激活的 LIC。