Department of Hematology, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, P. R. China.
Divisions of Pathology and Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, OH, USA.
Am J Chin Med. 2021;49(2):461-485. doi: 10.1142/S0192415X2150021X. Epub 2021 Feb 25.
Traditional Chinese Medicine (TCM) is a practical medicine based on thousands of years of medical practice in China. Arsenic dispensing powder (ADP) has been used as a treatment for MDS patients with a superior efficacy on anemia at Xiyuan Hospital of China Academy of Chinese Medical Sciences. In this study, we retrospectively analyzed MDS patients that received ADP treatment in the past 9 years and confirmed that ADP improves patients' anemia and prolongs overall survival in intermediate-risk MDS patients. Then, we used the MDS transgenic mice model and cell line to explore the drug mechanism. In normal and MDS cells, ADP does not show cellular toxicity but promotes differentiation. In mouse MDS models, we observed that ADP showed significant efficacy on promoting erythropoiesis. In the BFU-E and CFU-E assays, ADP could promote erythropoiesis not only in normal clones but also in MDS clones. Mechanistically, we found that ADP could downregulate HIF1A in MDS clones through upregulation of VHL, P53 and MDM2, which is involved in two parallel pathways to downregulate HIF1A. We also confirmed that ADP upregulates GATA factors in normal clones. Thus, our clinical and experimental studies indicate that ADP is a promising drug to promote erythropoiesis in both MDS and normal clones with a superior outcome than current regular therapies. ADP promotes erythropoiesis in myelodysplastic syndromes via downregulation of HIF1A and upregulation of GATA factors.
中药(TCM)是一门基于中国几千年医学实践的实用医学。砷剂散剂(ADP)已被用于治疗中国中医科学院西苑医院 MDS 患者的贫血症,疗效优于常规疗法。在本研究中,我们回顾性分析了过去 9 年接受 ADP 治疗的 MDS 患者,证实 ADP 可改善患者的贫血症状并延长中危 MDS 患者的总生存期。然后,我们使用 MDS 转基因小鼠模型和细胞系来探索药物机制。在正常和 MDS 细胞中,ADP 不表现出细胞毒性,反而促进分化。在小鼠 MDS 模型中,我们观察到 ADP 对促进红细胞生成具有显著疗效。在 BFU-E 和 CFU-E 检测中,ADP 不仅可以促进正常克隆的红细胞生成,还可以促进 MDS 克隆的红细胞生成。在机制上,我们发现 ADP 通过上调 VHL、P53 和 MDM2 下调 MDS 克隆中的 HIF1A,这涉及两条平行的途径来下调 HIF1A。我们还证实 ADP 可上调正常克隆中的 GATA 因子。因此,我们的临床和实验研究表明,ADP 是一种很有前途的药物,可促进 MDS 和正常克隆中的红细胞生成,其疗效优于目前的常规疗法。ADP 通过下调 HIF1A 和上调 GATA 因子促进骨髓增生异常综合征中的红细胞生成。