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首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer
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The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer

机译:促红细胞生成素作为抑制乳腺癌的可能选择的抗癌剂活性

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Recombinant human erythropoietin (Epo) is an effective and convenient treatment for cancer-related anaemia. In our study for the first time, we evaluated the effect of simultaneous use of Epo and Bruton’s tyrosine kinase (BTK) inhibitor LFM-A13 on the viability and tumour development of breast cancer cells. The results demonstrated that Epo significantly intensifies the anticancer activity of LFM-A13 in MCF-7 and MDA-MB-231. The featured therapeutic scheme efficiently blocked the tumour development in zebrafish experimental cancer model. Epo and LFM-A13 administered together resulted in effective cell killing, accompanied by attenuation of the BTK signalling pathways, loss of mitochondrial membrane potential (MMP), accumulation of apoptotic breast cancer cells with externalised PS, a slight increase in phase G0/G1 and a reduction in cyclin D1 expression. Simultaneous use of Epo with LFM-A13 inhibited early stages of tumour progression. This therapeutic scheme may be rationale for further possible research.
机译:重组人促红细胞生成素(EPO)是对癌症相关贫血的有效且方便的治疗方法。在我们第一次研究中,我们评估了同时使用EPO和Bruton的酪氨酸激酶(BTK)抑制剂LFM-A13对乳腺癌细胞的活力和肿瘤发育的影响。结果表明,EPO显着加剧了MCF-7和MDA-MB-231中LFM-A13的抗癌活性。特色治疗方案有效地阻断了斑马鱼实验癌症模型中的肿瘤发育。一起给予EPO和LFM-A13导致有效的细胞杀灭,伴随着BTK信号传导途径的衰减,线粒体膜电位(MMP)的丧失,凋亡乳腺癌细胞的积累,外部PS,阶段G0 / G1的略微增加Cyclin D1表达的减少。用LFM-A13同时使用EPO抑制肿瘤进展的早期阶段。这种治疗方案可能是进一步可能的研究的理由。

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