首页> 外文OA文献 >Rapid and selective death of leukemia stem and progenitor cells induced by the compound 4-benzyl, 2-methyl, 1,2,4-thiadiazolidine, 3,5 dione (TDZD-8)
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Rapid and selective death of leukemia stem and progenitor cells induced by the compound 4-benzyl, 2-methyl, 1,2,4-thiadiazolidine, 3,5 dione (TDZD-8)

机译:化合物4-苄基,2-甲基,1,2,4-噻二唑烷,3,5二酮(TDZD-8)诱导的白血病干细胞和祖细胞快速选择性死亡

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摘要

Leukemia is thought to arise from malignant stem cells, which have been described for acute and chronic myeloid leukemia (AML and CML) and for acute lymphoblastic leukemia (ALL). Leukemia stem cells (LSCs) are relatively resistant to current chemotherapy and likely contribute to disease relapse and progression. Consequently, the identification of drugs that can efficiently eradicate LSCs is an important priority. In the present study, we investigated the antileukemia activity of the compound TDZD-8. Analysis of primary AML, blast crisis CML (bcCML), ALL, and chronic lymphoblastic leukemia (CLL) specimens showed rapid induction of cell death upon treatment with TDZD-8. In addition, for myeloid leukemias, cytotoxicity was observed for phenotypically primitive cells, in vitro colony-forming progenitors, and LSCs as defined by xenotransplantation assays. In contrast, no significant toxicity was observed for normal hematopoietic stem and progenitor cells. Notably, cell death was frequently evident within 2 hours or less of TDZD-8 exposure. Cellular and molecular studies indicate that the mechanism by which TDZD-8 induces cell death involves rapid loss of membrane integrity, depletion of free thiols, and inhibition of both the PKC and FLT3 signaling pathways. We conclude that TDZD-8 uses a unique and previously unknown mechanism to rapidly target leukemia cells, including malignant stem and progenitor populations.
机译:白血病被认为是由恶性干细胞引起的,恶性干细胞已被描述为急性和慢性骨髓性白血病(AML和CML)以及急性淋巴细胞性白血病(ALL)。白血病干细胞(LSC)对目前的化学疗法有相对的抵抗力,并可能导致疾病的复发和进展。因此,鉴定能够有效根除LSC的药物是重要的优先事项。在本研究中,我们研究了化合物TDZD-8的抗白血病活性。对原发性AML,高危CML(bcCML),ALL和慢性淋巴细胞性白血病(CLL)标本的分析显示,用TDZD-8处理后,细胞死亡迅速诱导。此外,对于骨髓性白血病,通过异种移植测定法可以观察到表型原始细胞,体外集落形成祖细胞和LSC的细胞毒性。相反,对于正常的造血干细胞和祖细胞没有观察到明显的毒性。值得注意的是,在TDZD-8暴露后2小时或更短时间内,细胞死亡常常很明显。细胞和分子研究表明,TDZD-8诱导细胞死亡的机制涉及膜完整性的快速丧失,游离硫醇的耗竭以及对PKC和FLT3信号通路的抑制。我们得出的结论是,TDZD-8使用独特且以前未知的机制快速靶向白血病细胞,包括恶性干细胞和祖细胞。

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