Cheloni Giulia, Tanturli Michele
Department of Experimental and Clinical Biomedical Sciences "Mario Serio", Section of Experimental and Clinical Oncology, Università degli Studi di Firenze, viale GB Morgagni, 50-50134, Florence, Italy.
Department of Experimental and Clinical Biomedical Sciences "Mario Serio", Section of Clinical Physiopathology, viale G. Pieraccini, 6-50139, Florence, Italy.
Methods Mol Biol. 2016;1465:73-85. doi: 10.1007/978-1-4939-4011-0_7.
Chronic myeloid leukemia (CML) is a stem cell-driven disorder caused by the BCR/Abl oncoprotein, a constitutively active tyrosine kinase (TK). Chronic-phase CML patients are treated with impressive efficacy with TK inhibitors (TKi) such as imatinib mesylate (IM). However, rather than definitively curing CML, TKi induces a state of minimal residual disease, due to the persistence of leukemia stem cells (LSC) which are insensitive to this class of drugs. LSC persistence may be due to different reasons, including the suppression of BCR/Abl oncoprotein. It has been shown that this suppression follows incubation in low oxygen under appropriate culture conditions and incubation times.Here we describe the culture repopulation ability (CRA) assay, a non-clonogenic assay capable - together with incubation in low oxygen - to reveal in vitro stem cells endowed with marrow repopulation ability (MRA) in vivo. The CRA assay can be used, before moving to animal tests, as a simple and reliable method for the prescreening of drugs potentially active on CML and other leukemias with respect to their activity on the more immature leukemia cell subsets.
慢性粒细胞白血病(CML)是一种由BCR/Abl癌蛋白驱动的干细胞疾病,BCR/Abl癌蛋白是一种组成型活性酪氨酸激酶(TK)。慢性期CML患者使用甲磺酸伊马替尼(IM)等TK抑制剂治疗,疗效显著。然而,TK抑制剂并非能彻底治愈CML,而是会诱导出微小残留病状态,这是由于白血病干细胞(LSC)持续存在,而这类细胞对这类药物不敏感。LSC持续存在可能有不同原因,包括BCR/Abl癌蛋白的抑制。研究表明,在适当的培养条件和培养时间下,低氧孵育后会出现这种抑制。在此,我们描述了培养再增殖能力(CRA)检测方法,这是一种非克隆性检测方法,与低氧孵育一起,能够在体外揭示具有体内骨髓再增殖能力(MRA)的干细胞。在进行动物试验之前,CRA检测可作为一种简单可靠的方法,用于预筛选对CML和其他白血病中更不成熟的白血病细胞亚群有潜在活性的药物。