外周血单个核细胞
骨髓
骨髓增生异常综合症
菌落形成单位
CFU-GM
粒细胞集落刺激因子
医学
癌症研究
干细胞
免疫学
内科学
祖细胞
生物
化疗
体外
细胞生物学
生物化学
细菌
遗传学
作者
Junya Kuroda,Ayumi Kodama,Yoshiaki Chinen,Yuji Shimura,Shinsuke Mizutani,Hisao Nagoshi,Tsutomu Kobayashi,Yosuke Matsumoto,Yohei Nakaya,Ayako Tamura,Yutaka Kobayashi,Hiroshi Naito,Masafumi Taniwaki
标识
DOI:10.1016/j.leukres.2014.03.001
摘要
JAK2/STAT signaling promotes survival and expansion of myelodysplastic syndrome (MDS) clones, but little is known about the potential of JAK2/STAT as a therapeutic target in MDS. We investigated the effect of NS-018, a novel antagonist for JAK2, on the colony-forming ability of bone marrow mononuclear cells (BMMNCs) from high-risk MDS patients. NS-018 decreased colony-forming unit-granulocyte/macrophage (CFU-GM) colony numbers from MDS-derived BMMNCs in a dose-dependent manner, and this effect was significantly more potent than against normal BMMNCs. In addition, NS-018 suppressed the phosphorylation of STAT3 in colony-forming cells from MDS patients. Collectively, NS-018 could be a new therapeutic option for high-risk MDS.
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