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抑制丝氨酸/苏氨酸磷酸酶PPM1D可诱导HL-60细胞向中性粒细胞分化。

Inhibition of Ser/Thr phosphatase PPM1D induces neutrophil differentiation in HL-60 cells.

作者信息

Kamada Rui, Kudoh Fuki, Yoshimura Fumihiko, Tanino Keiji, Sakaguchi Kazuyasu

机构信息

Laboratory of Biological Chemistry, Department of Chemistry, Faculty of Science, Hokkaido University, North10, West8, Kita-ku, Sapporo 060-0810, Japan.

Laboratory of Organic Chemistry II, Department of Chemistry, Faculty of Science, Hokkaido University, North10, West8, Kita-ku, Sapporo 060-0810, Japan.

出版信息

J Biochem. 2017 Oct 1;162(4):303-308. doi: 10.1093/jb/mvx032.

Abstract

Protein phosphatase Magnesium-dependent 1, Delta (PPM1D) is a wild-type p53-inducible Ser/Thr phosphatase that acts as a negative regulator of the p53 tumor suppressor. Gene amplification and overexpression of PPM1D have been reported in various cancers including leukemia and neuroblastoma. Therefore, PPM1D is a promising target in cancer therapy. It has been reported that PPM1D knockout mice exhibit neutrophilia in blood and show a defective immune response. Here, we found that inhibition of PPM1D induced neutrophil differentiation of human promyelocytic leukemia cell line HL-60. The combination of a PPM1D inhibitor and all-trans retinoic acid significantly increased their differentiation efficiency. The PPM1D inhibitor also induced G1 arrest in HL-60 cells. Our results suggest that PPM1D may be a potential therapeutic target for blood cell diseases including leukemia.

摘要

蛋白磷酸酶镁依赖1δ(PPM1D)是一种野生型p53诱导的丝氨酸/苏氨酸磷酸酶,作为p53肿瘤抑制因子的负调节因子。PPM1D的基因扩增和过表达已在包括白血病和神经母细胞瘤在内的多种癌症中被报道。因此,PPM1D是癌症治疗中一个有前景的靶点。据报道,PPM1D基因敲除小鼠血液中出现嗜中性粒细胞增多,并表现出免疫反应缺陷。在此,我们发现抑制PPM1D可诱导人早幼粒细胞白血病细胞系HL-60向中性粒细胞分化。PPM1D抑制剂与全反式维甲酸联合使用可显著提高其分化效率。PPM1D抑制剂还可诱导HL-60细胞G1期阻滞。我们的结果表明,PPM1D可能是包括白血病在内的血细胞疾病的潜在治疗靶点。

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