[含有稀土元素、胆固醇和发光染料的正钒酸盐杂化纳米复合物处理埃利希癌细胞后的功能活性]。

A. Goltsev, N. Babenko, A. Gaevskaya, O. Chelombitko, N. Bondarovich, T. Dubrava, M. Ostankov, V. Klochkov, N. Kavok, Y. Malyukin
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引用次数: 0

摘要

肿瘤的发展是具有无限自我维持潜力的低分化细胞群体扩大的结果,即癌症干细胞(CSCs)。应用新型纳米复合材料结合CSCs并诱导肿瘤破坏是治疗该病理的一个重要方向。已经开发出了含有稀土正钒酸盐GdYVO4:Eu³+、胆固醇和发光染料Dil的杂化纳米配合物的方法。利用CD44、CD24、CD117和Sca-1标记物单克隆抗体免疫荧光法,建立了杂交纳米复合物治疗普通埃利希癌(EC)后不同分化水平肿瘤祖细胞比例的变化。最具致瘤性的CD44high细胞的浓度明显降低,同时CD117 +细胞的数量增加,导致CD44high/CD117 +比值指数增加。研究表明,应用杂化纳米复合物可抑制肿瘤生长近80%。不同表型标志的细胞在肿瘤部位的合作相互作用的价值已被证明。CD44high/CD117 +比值指标可作为使用不同类型抗肿瘤治疗时肿瘤过程发生和失活率的诊断和预后参数之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[FUNCTIONAL ACTIVITY OF EHRLICH CARCINOMA CELLS AFTER TREATMENT WITH HYBRID NANOCOMPLEXES CONTAINING ORTHOVANADATES OF RARE-EARTH ELEMENTS, CHOLESTEROL AND LUMINESCENT DYE].
Tumor development is the consequence of expanding the population of low differentiated cells with unlimited self-maintenance potential, i.e. cancer stem cells (CSCs). Application of new forms of nanocomposites capable of binding to CSCs and inducing the tumor destruction is perspective direction for treating this pathology. There have been developed the methods of obtaining hybrid nanocomplexes containing rare-earth orthovanadates GdYVO4:Eu³⁺, cholesterol and luminescent dye Dil. By immune fluorescence method using monoclonal antibodies to CD44, CD24, CD117 and Sca-1 markers there has been established the change in the ratio of tumor progenitors of various differentiation levels in a general pool of Ehrlich carcinoma (EC) after treatment with hybrid nanocomplexes. Essential reduction in the concentration of the most tumorogenic CD44high cells with simultaneous rise in the number of CD117⁺-cells resulted in an increased index of CD44high/CD117⁺ ratio. It has been demonstrated that application of hybrid nanocomplexes suppressed the tumor growth almost by 80%. The value of cooperative interactions of the cells with different phenotype signs in tumor sites has been proved. The index of CD44high/CD117⁺ ratio can be used as one of diagnostic and prognostic parameters of development and inactivation rate of tumor process when using different types of anti-tumor therapy.
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