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首页> 外文期刊>British Journal of Cancer >Synergistic cytotoxicity of bcl-2 antisense oligodeoxynucleotides and etoposide, doxorubicin and cisplatin on small-cell lung cancer cell lines
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Synergistic cytotoxicity of bcl-2 antisense oligodeoxynucleotides and etoposide, doxorubicin and cisplatin on small-cell lung cancer cell lines

机译:bcl-2反义寡聚脱氧核苷酸与依托泊苷,阿霉素和顺铂对小细胞肺癌细胞系的协同细胞毒性

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Expression of Bcl-2 is life-sustaining for small-cell lung cancer cells and associated with drug resistance. In the present study, the interactions between the bcl-2 antisense oligodeoxynucleotide 2009 and the chemotherapeutic agents etoposide, doxorubicin and cisplatin were investigated on small-cell lung cancer cell lines to search for synergistic combinations. The cell lines NCI-H69, SW2 and NCI-H82 express high, intermediate-high and low basal levels of Bcl-2, respectively, which are inversely correlated with the sensitivities of the cell lines to treatment with oligodeoxynucleotide 2009 and the chemotherapeutic agents alone. Moreover, differences were found in the responsiveness of the cell lines to treatment with combinations of oligodeoxynucleotide 2009 and the chemotherapeutic agents. In the cell lines NCI-H69 and SW2, all combinations resulted in synergistic cytotoxicity. In NCI-H69 cells, maximum synergy with a combination index of 0.2 was achieved with the combination of oligodeoxynucleotide 2009 and etoposide. In SW2 cells, the combination of oligodeoxynucleotide 2009 and doxorubicin was the most effective (combination index = 0.5). In the cell line NCI-H82, which expresses a low basal level of Bcl-2, most of the combinations were slightly antagonistic. Our data suggest the use of oligodeoxynucleotide 2009 in combination with chemotherapy for the treatment of small-cell lung cancer that overexpresses Bcl-2.
机译:Bcl-2的表达对于小细胞肺癌细胞是维持生命的,并且与耐药性有关。在本研究中,在小细胞肺癌细胞系上研究了bcl-2反义寡聚脱氧核苷酸2009与化疗剂依托泊苷,阿霉素和顺铂之间的相互作用,以寻找协同作用的组合。细胞系NCI-H69,SW2和NCI-H82分别表达高,中-高和低基础水平的Bcl-2,这与细胞系对寡聚脱氧核苷酸2009和单独的化学治疗剂的敏感性呈负相关。此外,发现细胞系对寡聚脱氧核苷酸2009和化学治疗剂的组合的反应性的差异。在细胞系NCI-H69和SW2中,所有组合均导致协同的细胞毒性。在NCI-H69细胞中,寡聚脱氧核苷酸2009和依托泊苷的组合可达到0.2的最大协同作用。在SW2细胞中,寡聚脱氧核苷酸2009和阿霉素的组合最为有效(组合指数= 0.5)。在表达低基础水平的Bcl-2的NCI-H82细胞系中,大多数组合都具有轻微的拮抗作用。我们的数据表明,将寡聚脱氧核苷酸2009与化学疗法联合用于治疗过表达Bcl-2的小细胞肺癌。

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