Casiopeina III-Ea, a copper-containing small molecule, inhibits the in vitro growth of primitive hematopoietic cells from chronic myeloid leukemia

被引:13
作者
Chavez-Gonzalez, Antonieta [1 ]
Centeno-Llanos, Sandra [1 ]
Moreno-Lorenzana, Dafne [1 ]
Angel Sandoval-Esquivel, Miguel [1 ]
Aviles-Vazquez, Socrates [1 ]
Bravo-Gomez, Maria Elena [2 ]
Ruiz-Azuara, Lena [3 ]
Ayala-Sanchez, Manuel [4 ]
Torres-Martinez, Hector [5 ]
Mayani, Hector [1 ]
机构
[1] Mexican Inst Social Secur IMSS, Natl Med Ctr, Oncol Hosp, Oncol Res Unit, Mexico City, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Sch Med, Mexico City, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Natl Autonomous Univ Mexico, Inorgan & Nucl Chem Dept, Mexico City, DF, Mexico
[4] IMSS, La Raza Med Ctr, Dept Hematol, Mexico City, DF, Mexico
[5] IMSS, Villa Coapa Gen Hosp, Dept Hip Surg, Mexico City, DF, Mexico
关键词
Chronic myeloid leukemia; Leukemic stem cells elimination; Casiopeinas; COMPARATIVE GENOMIC HYBRIDIZATION; STEM-CELLS; MIXED CHELATE; COMPLEXES CASIOPEINAS(R); INDUCE APOPTOSIS; INDEPENDENT MECHANISMS; SITU HYBRIDIZATION; PROGENITOR CELLS; TUMOR-CELLS; BCR-ABL;
D O I
10.1016/j.leukres.2016.11.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Several novel compounds have been developed for the treatment of different types of leukemia. In the present study, we have assessed the in vitro effects of Casiopeina III-Ea, a copper-containing small molecule, on cells from patients with Chronic Myeloid Leukemia (CML). We included primary CD34(+) Lineage-negative (Lin(-)) cells selected from CML bone marrow, as well as the K562 and MEG01 cell lines. Bone marrow cells obtained from normal individuals - both total mononuclear cells as well as CD34(+) Lin(-) cells- were used as controls. IC50 corresponded to 0.5 mu M for K562 cells, 0.63M for MEG01 cells, 0.38M for CML CD34(+) lin(-) cells, and 1.0 mu M for normal CD34(+) lin(-) cells. Proliferation and expansion were also inhibited to significantly higher extents in cultures of CML cells as compared to their normal counterparts. All these effects seemed to occur via a bcr-abl transcription-independent mechanism that involved a delay in cell division, an increase in cell death, generation of Reactive Oxygen Species and changes in cell cycle. Our results demonstrate that Casiopeina III-Ea possesses strong antileukemic activity in vitro, and warrant further preclinical (animal) studies to assess such effects in vivo. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8 / 19
页数:12
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