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

被引:6
作者
Dong, Athena [1 ]
Pan, Xiaoqing [2 ]
Lin, Chien-Wei [3 ]
Huang, Yi-Wen [4 ]
Krause, Hayden [1 ]
Pan, Pan [1 ]
Baim, Arielle [1 ]
Thomas, Michael J. [5 ]
Chen, Xiao [1 ]
Yu, Jianhua [6 ]
Michaelis, Laura [1 ]
Liu, Pengyuan [7 ]
Wang, Li-Shu [1 ]
Atallah, Ehab [1 ]
机构
[1] Med Coll Wisconsin, Dept Med, Div Hematol & Oncol, Milwaukee, WI 53226 USA
[2] Shanghai Normal Univ, Dept Math, Shanghai, Peoples R China
[3] Med Coll Wisconsin, Div Biostat, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Obstet & Gynecol, Milwaukee, WI 53226 USA
[5] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[6] City Hope Natl Med Ctr, Comprehens Canc Ctr, Dept Hematol & Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
[7] Med Coll Wisconsin, Dept Physiol, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA
关键词
Words Rubus; Myelodysplastic syndromes; Leukocytes; mononuclear; Peripheral blood stem cells; Clinical trial; DNA METHYLATION; VALPROIC ACID; DECITABINE; COMBINATION; GENES;
D O I
10.15430/JCP.2022.27.2.129
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:129 / 138
页数:10
相关论文
共 24 条
[1]   Treatment strategies in myelodysplastic syndromes [J].
Atallah, Ehab ;
Garcia-Manero, Guillermo .
CANCER INVESTIGATION, 2008, 26 (02) :208-216
[2]   Phase I study of decitabine alone or in combination with valproic acid in acute myeloid leukemia [J].
Blum, William ;
Klisovic, Rebecca B. ;
Hackanson, Bjoern ;
Liu, Zhongfa ;
Liu, Shujun ;
Devine, Hollie ;
Vukosavljevic, Tamara ;
Huynh, Lenguyen ;
Lozanski, Gerard ;
Kefauver, Cheryl ;
Plass, Christoph ;
Devine, Steven M. ;
Heerema, Nyla A. ;
Murgo, Anthony ;
Chan, Kenneth K. ;
Grever, Michael R. ;
Byrd, John C. ;
Marcucci, Guido .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (25) :3884-3891
[3]   Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: a randomised, open-label, phase III study [J].
Fenaux, Pierre ;
Mufti, Ghulam J. ;
Hellstrom-Lindberg, Eva ;
Santini, Valeria ;
Finelli, Carlo ;
Giagounidis, Aristoteles ;
Schoch, Robert ;
Gattermann, Norbert ;
Sanz, Guillermo ;
List, Alan ;
Gore, Steven D. ;
Seymour, John F. ;
Bennett, John M. ;
Byrd, John ;
Backstrom, Jay ;
Zimmerman, Linda ;
McKenzie, David ;
Beach, C. L. ;
Silverman, Lewis R. .
LANCET ONCOLOGY, 2009, 10 (03) :223-232
[4]   Review of Functional and Pharmacological Activities of Berries [J].
Golovinskaia, Oksana ;
Wang, Chin-Kun .
MOLECULES, 2021, 26 (13)
[5]   International scoring system for evaluating prognosis in myelodysplastic syndromes [J].
Greenberg, P ;
Cox, C ;
LeBeau, MM ;
Fenaux, P ;
Morel, P ;
Sanz, G ;
Sanz, M ;
Vallespi, T ;
Hamblin, T ;
Oscier, D ;
Ohyashiki, K ;
Toyama, K ;
Aul, C ;
Mufti, G ;
Bennett, J .
BLOOD, 1997, 89 (06) :2079-2088
[6]   Erythroid response to treatment with G-CSF plus erythropoietin for the anaemia of patients with myelodysplastic syndromes: proposal for a predictive model [J].
HellstromLindberg, E ;
Negrin, R ;
Stein, R ;
Krantz, S ;
Lindberg, G ;
Vardiman, J ;
Ost, A ;
Greenberg, P .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 99 (02) :344-351
[7]   CELLULAR-DIFFERENTIATION, CYTIDINE ANALOGS AND DNA METHYLATION [J].
JONES, PA ;
TAYLOR, SM .
CELL, 1980, 20 (01) :85-93
[8]   metilene: fast and sensitive calling of differentially methylated regions from bisulfite sequencing data [J].
Juehling, Frank ;
Kretzmer, Helene ;
Bernhart, Stephan H. ;
Otto, Christian ;
Stadler, Peter F. ;
Hoffmann, Steve .
GENOME RESEARCH, 2016, 26 (02) :256-262
[9]   BSMAP: whole genome bisulfite sequence MAPping program [J].
Li, Yuanxin ;
Li, Wei .
BMC BIOINFORMATICS, 2009, 10
[10]   Myelodysplastic syndromes - Incidence and survival in the United States [J].
Ma, Xiaomei ;
Does, Monique ;
Raza, Azra ;
Mayne, Susan T. .
CANCER, 2007, 109 (08) :1536-1542