Sooman Linda, Gullbo Joachim, Bergqvist Michael, Bergström Stefan, Lennartsson Johan, Ekman Simon
Department of Immunology, Genetics and Pathology (former Radiation, Oncology and Radiation Science), Section of Oncology, Rudbeck Laboratory, Uppsala University, Dag Hammarskjölds väg 20, 751 85, Uppsala, Sweden.
Department of Medical Sciences, Division of Clinical Pharmacology, Uppsala University Hospital, 751 85, Uppsala, Sweden.
BMC Res Notes. 2017 Nov 2;10(1):544. doi: 10.1186/s13104-017-2842-z.
The prognosis for patients with disseminated lung cancer is poor and current treatments have limited survival benefit as resistance often occurs, and is often associated with significant toxicity. A possible strategy to improve treatment and evade chemoresistance may be to find new combinations of drugs. The aim of this study was to analyze the potential of combining proteasome inhibitors (PIs) with chemotherapeutic drugs used in the routine treatment for lung cancer patients.
The median-effect method was applied to the Fluorometric Microculture Cytotoxicity Assay (FMCA) to evaluate effects of combining two different PIs (bortezomib and b-AP15) with clinically used chemotherapeutic drugs representing different mechanisms of action (cisplatin, gefitinib, gemcitabine and vinorelbine) in two lung cancer cell lines (one sensitive and one resistant). Proteasome inhibition in combination with cisplatin, gemcitabine or vinorelbine had synergistic effects in at least one of the tested cell lines. Furthermore, the effect of gefitinib appeared strongly potentiated by the PI in the least resistant lung cancer cell line, although the level of synergy could not be determined with the median-effect method.
Combining PIs with cisplatin, gefitinib, gemcitabine or vinorelbine show potential as new combination chemotherapy for the treatment of lung cancer.
弥漫性肺癌患者的预后较差,目前的治疗方法对生存期的改善有限,因为常常会出现耐药性,且往往伴有显著的毒性。改善治疗并规避化疗耐药性的一种可能策略是寻找新的药物组合。本研究的目的是分析蛋白酶体抑制剂(PIs)与肺癌患者常规治疗中使用的化疗药物联合使用的潜力。
采用中位效应法对荧光微量培养细胞毒性试验(FMCA)进行分析,以评估两种不同的蛋白酶体抑制剂(硼替佐米和b-AP15)与代表不同作用机制的临床常用化疗药物(顺铂、吉非替尼、吉西他滨和长春瑞滨)在两种肺癌细胞系(一种敏感细胞系和一种耐药细胞系)中的联合效果。蛋白酶体抑制与顺铂、吉西他滨或长春瑞滨联合在至少一种受试细胞系中具有协同作用。此外,在耐药性最低的肺癌细胞系中,蛋白酶体抑制剂对吉非替尼的效果有显著增强作用,尽管用中位效应法无法确定协同作用的程度。
蛋白酶体抑制剂与顺铂、吉非替尼、吉西他滨或长春瑞滨联合使用显示出作为肺癌新联合化疗方案的潜力。