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Combined antitumor effects of bee venom and cisplatin on human cervical and laryngeal carcinoma cells and their drug resistant sublines

机译:蜂毒和顺铂对人宫颈癌和喉癌细胞及其耐药亚系的联合抗肿瘤作用

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摘要

In the present study, we investigated the possible combined anticancer ability of bee venom (BV) and cisplatin towards two pairs of tumour cell lines: parental cervical carcinoma HeLa cells and their cisplatin-resistant HeLa CK subline, as well as laryngeal carcinoma HEp-2 cells and their cisplatin-resistant CK2 subline. Additionally, we identified several peptides of BV in the BV sample used in the course of the study and determined the exact concentration of MEL. BV applied alone in concentrations of 30 to 60 μg ml-1 displayed dose-dependent cytotoxicity against all cell lines tested. Cisplatin-resistant cervical carcinoma cells were more sensitive to BV than their parental cell lines (IC50 values were 52.50 μg ml-1 for HeLa vs. 47.64 μg ml-1 for HeLa CK cells), whereas opposite results were obtained for cisplatin-resistant laryngeal carcinoma cells (IC50 values were 51.98 μg ml-1 for HEp-2 vs. 60.00 μg ml-1 for CK2 cells). Treatment with BV alone induced a necrotic type of cell death, as shown by characteristic morphological features, fast staining with ethidium-bromide and a lack of cleavage of apoptotic marker poly (ADP-ribose) polymerase (PARP) on Western blot. Combined treatment of BV and cisplatin induced an additive and/or weak synergistic effect towards tested cell lines, suggesting that BV could enhance the killing effect of selected cells when combined with cisplatin. Therefore, a greater anticancer effect could be triggered if BV was used in the course of chemotherapy. Our results suggest that combined treatment with BV could be useful from the point of minimizing the cisplatin concentration during chemotherapy, consequently reducing and/or postponing the development of cisplatin resistance.
机译:在本研究中,我们研究了蜂毒(BV)和顺铂对两对肿瘤细胞系可能的联合抗癌能力:亲代宫颈癌HeLa细胞及其顺铂耐药性HeLa CK亚系,以及喉癌HEp-2细胞及其耐顺铂CK2亚系。此外,我们在研究过程中鉴定了BV样品中的BV几种肽,并确定了MEL的准确浓度。单独以30至60μgml-1的浓度施用BV对所有测试的细胞系均表现出剂量依赖性的细胞毒性。耐顺铂子宫颈癌细胞对BV的敏感性高于其亲本细胞系(HeLa的IC50值为52.50μgml-1,而HeLa CK细胞的IC50值为47.64μgml-1),而耐顺铂的喉癌获得了相反的结果癌细胞(HEp-2的IC50值为51.98μgml-1,而CK2细胞的IC50值> 60.00μgml-1)。单用BV处理可导致坏死类型的细胞死亡,如特征性形态学特征,溴乙锭快速染色以及在Western blot上缺乏凋亡标记多聚(ADP-核糖)聚合酶(PARP)的裂解所示。 BV和顺铂的联合治疗对被测细胞系诱导了加性和/或弱协同作用,这表明BV与顺铂结合可以增强所选细胞的杀伤作用。因此,如果在化疗过程中使用BV,可能会引发更大的抗癌作用。我们的结果表明,从使化疗期间顺铂浓度降至最低,从而降低和/或推迟顺铂耐药性的发展角度出发,BV联合治疗可能是有用的。

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