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首页> 外文期刊>Leukemia >Effective killing of Gleevec-resistant CML cells with T315I mutation by a natural compound PEITC through redox-mediated mechanism
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Effective killing of Gleevec-resistant CML cells with T315I mutation by a natural compound PEITC through redox-mediated mechanism

机译:天然化合物PEITC通过氧化还原介导的机制有效杀死具有T315I突变的格列卫耐药性CML细胞

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Mutation of Bcr-Abl is an important mechanism by which chronic myelogenous leukemia (CML) cells become resistant to Gleevec. The T315I mutation is clinically significant since CML cells harboring this mutation are insensitive to Gleevec and other Bcr-Abl-targeted drugs. Identification of new agents capable of effectively killing CML cells with T315I mutation would have important therapeutic implications in Gleevec-resistant CML. Here, we showed that -phenylethyl isothiocyanate (PEITC), a natural compound found in vegetables, is effective in killing CML cells expressing T315I BCR-ABL. Treatment of leukemia cell lines harboring wild-type or mutant Bcr-Abl with 10M PEITC resulted in an elevated ROS stress and a redox-mediated degradation of the BCR-ABL protein, leading to massive death of the leukemia cells. Antioxidant NAC attenuated the PEITC-induced oxidative stress in CML cells and prevented the degradation of BCR-ABL, caspase-3 activation and cell death. We further showed that the ROS-induced degradation of BCR-ABL was mediated partially by caspase-3 and the proteasome pathway. The ability of PEITC to effectively kill T315I-positive CML cells was further confirmed using primary leukemia cells isolated from CML patients. Our results suggest that PEITC is a promising compound capable of killing Gleevec-resistant CML cells through a ROS-mediated mechanism and warrants further investigations.
机译:Bcr-Abl的突变是慢性骨髓性白血病(CML)细胞对格列卫产生耐药性的重要机制。 T315I突变具有重要的临床意义,因为具有此突变的CML细胞对格列卫和其他Bcr-Abl靶向药物不敏感。鉴定能够有效杀死具有T315I突变的CML细胞的新药物在耐格列卫的CML中具有重要的治疗意义。在这里,我们证明了-苯基乙基异硫氰酸酯(PEITC)是一种在蔬菜中发现的天然化合物,可有效杀死表达T315I BCR-ABL的CML细胞。用10M PEITC处理具有野生型或突变型Bcr-Abl的白血病细胞系会导致ROS应激升高和氧化还原介导的BCR-ABL蛋白降解,从而导致白血病细胞大量死亡。抗氧化剂NAC可减轻PEITC诱导的CML细胞氧化应激,并防止BCR-ABL降解,caspase-3活化和细胞死亡。我们进一步表明,ROS诱导的BCR-ABL降解部分由caspase-3和蛋白酶体途径介导。使用从CML患者中分离出的原发性白血病细胞,进一步证实了PEITC有效杀死T315I阳性CML细胞的能力。我们的结果表明,PEITC是一种有望通过ROS介导的机制杀死耐Gleevec的CML细胞的化合物,值得进一步研究。

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