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首页> 外文期刊>Japanese Journal of Cancer Research >Human T cell leukemia cell death by apoptosis-inducing nucleosides from CD57(+) HLA-DR(bright) natural suppressor cell line.
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Human T cell leukemia cell death by apoptosis-inducing nucleosides from CD57(+) HLA-DR(bright) natural suppressor cell line.

机译:人类T细胞白血病细胞死亡的凋亡诱导从CD57(+)HLA-DR(明亮)自然抑制细胞系的核苷。

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摘要

Apoptosis-inducing nucleosides (AINs) released from CD57( +) HLA-DR(bright) natural suppressor (57.DR-NS) cell line, derived from human decidual tissue, were isolated from 57.DR-NS cell culture supernatant by the combination of thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC). Apoptotic cell death was strongly induced in human T cell leukemia Molt4 cells treated with AINs, absolutely depending on DNA strand breaks, with activation of the caspase cascade, especially caspase-3. The administration of AINs to Molt4 tumor-bearing severe combined immunodeficiency (SCID) mice resulted in drastic suppression of tumor growth, with a decrease of tumor size and the appearance of apoptotic signals in tumor tissue. Thus, AINs are candidates for development as anticancer agents.
机译:从人蜕膜组织的CD57(+)HLA-DR(亮)自然抑制物(57.DR-NS)细胞系释放的诱导细胞凋亡的核苷(AINs)从57.DR-NS细胞培养上清液中分离得到。薄层色谱(TLC)和高效液相色谱(HPLC)的组合。在人T细胞白血病中,用AINs强烈诱导凋亡细胞死亡,这完全取决于DNA链断裂,并激活caspase级联反应,尤其是caspase-3。对携带Molt4肿瘤的严重联合免疫缺陷(SCID)小鼠施用AINs会导致肿瘤生长的显着抑制,肿瘤大小减小,肿瘤组织中出现凋亡信号。因此,AINs有望成为抗癌药。

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