首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Betulinic acid induces apoptosis in human chronic myelogenous leukemia (CML) cell line K-562 without altering the levels of Bcr-Abl.
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Betulinic acid induces apoptosis in human chronic myelogenous leukemia (CML) cell line K-562 without altering the levels of Bcr-Abl.

机译:桦木酸可诱导人慢性粒细胞白血病(CML)细胞K-562凋亡,而不会改变Bcr-Abl的水平。

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摘要

Betulinic acid (BA), a plant derived triterpenoid, isolated from various sources shows cytotoxicity in cell lines of melanoma, neuroectodermal and malignant brain tumors. Chronic myelogenous leukemia (CML) is characterized by Philadelphia chromosome (Bcr-Abl), a molecular abnormality leading to the intrinsic tyrosine kinase activity that provides growth and survival advantage to the cells. Present study describes the cytotoxicity of BA on human CML cell line K-562, positive for Bcr-Abl. The decrease in the viability of K-562 cells treated with BA at different concentrations and time intervals was assessed using MTT assay. Cell death induced by BA was determined to be apoptotic as measured by FACS analysis of PI stained nuclei, PS externalization by Annexin-V fluorescence and characteristic DNA fragmentation. DiOC6(3) fluorescent probe determined alterations in the mitochondrial membrane potential (MMP). RT-PCR confirmed the expression levels of Bcr-Abl in controls and K-562 cells treated with BA. The rapid loss of MMP of K-562 cells upon treatment with BA shows the direct activation of apoptosis at the level of mitochondria, overcoming the resistance of the high levels of expression of Bcr-Abl.
机译:桦木酸(BA)是一种植物来源的三萜类化合物,从多种来源中分离出来,在黑素瘤,神经外胚层和恶性脑肿瘤的细胞系中显示出细胞毒性。慢性粒细胞性白血病(CML)的特征是费城染色体(Bcr-Abl),这是一种分子异常,导致固有的酪氨酸激酶活性,从而为细胞提供了生长和生存优势。本研究描述了BA对Bcr-Abl阳性的人CML细胞K-562的细胞毒性。使用MTT测定法评估了在不同浓度和时间间隔下用BA处理的K-562细胞活力的降低。通过PI染色的核的FACS分析,膜联蛋白-V荧光的PS外在化和特征性DNA片段化,通过BAS诱导的BA细胞死亡被确定为是凋亡的。 DiOC6(3)荧光探针确定线粒体膜电位(MMP)的变化。 RT-PCR证实Bcr-Abl在BA处理的对照组和K-562细胞中的表达水平。 BA处理后,K-562细胞的MMP迅速丧失,表明线粒体水平上的细胞凋亡被直接激活,克服了Bcr-Abl高表达水平的耐药性。

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