对骨髓增生异常综合症或骨髓增生性肿瘤患者进行冻干黑树莓甲基化功能试验性临床研究。

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2022-06-30 DOI:10.15430/JCP.2022.27.2.129
Athena Dong, Xiaoqing Pan, Chien-Wei Lin, Yi-Wen Huang, Hayden Krause, Pan Pan, Arielle Baim, Michael J Thomas, Xiao Chen, Jianhua Yu, Laura Michaelis, Pengyuan Liu, Li-Shu Wang, Ehab Atallah
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引用次数: 0

摘要

骨髓增生异常综合征(MDS)和骨髓增生异常/骨髓增生性肿瘤(MDS/MPN)是以细胞减少和发展为急性髓系白血病为特征的骨髓疾病。低甲基化药物(HMAs)是美国食品和药物管理局批准的治疗 MDS 和 MDS/MPN 患者的药物。与其他疗法相比,HMAs 可提高患者的生存率和生活质量。虽然 HMAs 对 MDS 和 MDS/MPN 患者有效,但它们也有明显的毒性,给患者带来了沉重的负担。我们的目标是从天然产品中开发出更安全、更有效的 HMA。我们以前曾报道过,黑树莓(BRBs)在小鼠的结肠、血液、脾脏和骨髓中具有低甲基化作用。此外,黑树莓还对结肠直肠癌和家族性腺瘤性息肉病患者产生了低甲基化作用。在本研究中,我们进行了一项试验性临床试验,以评估BRB对低风险MDS或MDS/MPN患者的低甲基化作用。在BRB干预三个月之前和之后,我们分离了外周血单核细胞(PBMC)。从外周血单核细胞(PBMC)中分离出 CD45+ 细胞,使用还原代表亚硫酸氢盐测序法进行甲基化分析。每位患者都作为自己的匹配对照,他们在干预前的测量结果为干预后的结果提供了基线。临床数据显示,BRBs 的耐受性良好,没有副作用。结合甲基化数据,BRBs 对 477 个启动子区域的甲基化水平有显著影响。通路分析表明,BRB 诱导的基因内低甲基化推动了白细胞的分化。在低风险 MDS 或 MDS/MPN 患者中使用 BRB 的随机安慰剂对照临床试验是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Pilot Clinical Study to Investigate the Hypomethylating Properties of Freeze-dried Black Raspberries in Patients with Myelodysplastic Syndrome or Myeloproliferative Neoplasm.

Myelodysplastic syndromes (MDS) and myelodysplastic/myeloproliferative neoplasms (MDS/MPN) are bone marrow disorders characterized by cytopenias and progression to acute myeloid leukemia. Hypomethylating agents (HMAs) are Food and Drug Administration-approved therapies for MDS and MDS/MPN patients. HMAs have improved patients' survival and quality of life when compared with other therapies. Although HMAs are effective in MDS and MDS/MPN patients, they are associated with significant toxicities that place a large burden on patients. Our goal is to develop a safer and more effective HMA from natural products. We previously reported that black raspberries (BRBs) have hypomethylating effects in the colon, blood, spleen, and bone marrow of mice. In addition, BRBs exert hypomethylating effects in patients with colorectal cancer and familial adenomatous polyposis. In the current study, we conducted a pilot clinical trial to evaluate the hypomethylating effects of BRBs in patients with low-risk MDS or MDS/MPN. Peripheral blood mononuclear cells (PBMCs) were isolated before and after three months of BRB intervention. CD45+ cells were isolated from PBMCs for methylation analysis using a reduced-representation bisulfite sequencing assay. Each patient served as their own matched control, with their measurements assessed before intervention providing a baseline for post-intervention results. Clinically, our data showed that BRBs were well-tolerated with no side effects. When methylation data was combined, BRBs significantly affected methylation levels of 477 promoter regions. Pathway analysis suggests that BRB-induced intragenic hypomethylation drives leukocyte differentiation. A randomized, placebo-controlled clinical trial of BRB use in low-risk MDS or MDS/MPN patients is warranted.

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