Sigounas George, Sallah Sabah, Sigounas Vaia Y
Department of Internal Medicine, Brody School of Medicine, East Carolina University, Hem/Onc Section, Brody Bldg, Rm 3E-102, 600 Moye Blvd, Greenville, NC 27858, USA.
Cancer Lett. 2004 Oct 28;214(2):171-9. doi: 10.1016/j.canlet.2004.06.009.
In this study, we assessed the ability of erythropoietin (EPO) to synergize with various chemotherapeutic agents and suppress the growth and metastasis of solid tumors. Animals were inoculated with Lewis lung carcinoma (LLC) cells and treated with EPO alone, the designated chemotherapeutic drug (cisplatin, mitomycin C or cyclophoshamide) alone, or EPO and the drug. Tumor volume was monitored daily. Thirteen days following cell injection, tumor mass was determined. In addition, the number of the metastatic foci in the lungs was determined. Cisplatin alone was capable of inducing a 7-fold decrease in final tumor volume compared to tumor-bearing animals injected with saline. However, when EPO was combined with cisplatin, the animals experienced an 11-fold reduction in final tumor volume compared to saline-injected animals (P<0.001). A 2.5-fold reduction in tumor mass was observed in animals treated with cisplatin, compared to the saline-injected groups. Furthermore, injections of EPO and cisplatin induced a 4-fold reduction in tumor mass (P<0.001). Blood analysis indicated that a significant increase of more than 30% in WBC was found in animals injected concurrently with cisplatin and EPO, as compared to saline-injected mice (P<0.03). When EPO and mitomycin C were injected together, tumor mass was further reduced by 14% compared to that seen in mice treated with mitomycin C alone. However, this difference was not statistically significant. We conclude from this study that EPO can synergize with chemotherapeutic agents to further suppress the growth of tumors. The level of synergism is drug related.
在本研究中,我们评估了促红细胞生成素(EPO)与各种化疗药物协同作用并抑制实体瘤生长和转移的能力。将动物接种Lewis肺癌(LLC)细胞,并分别用单独的EPO、指定的化疗药物(顺铂、丝裂霉素C或环磷酰胺)或EPO与药物进行治疗。每天监测肿瘤体积。细胞注射13天后,测定肿瘤质量。此外,还测定了肺内转移灶的数量。与注射生理盐水的荷瘤动物相比,单独使用顺铂能够使最终肿瘤体积减少7倍。然而,当EPO与顺铂联合使用时,与注射生理盐水的动物相比,最终肿瘤体积减少了11倍(P<0.001)。与注射生理盐水的组相比,接受顺铂治疗的动物肿瘤质量减少了2.5倍。此外,注射EPO和顺铂导致肿瘤质量减少了4倍(P<0.001)。血液分析表明,与注射生理盐水的小鼠相比,同时注射顺铂和EPO的动物白细胞显著增加了30%以上(P<0.03)。当EPO和丝裂霉素C一起注射时,与单独用丝裂霉素C治疗的小鼠相比,肿瘤质量进一步减少了14%。然而,这种差异无统计学意义。我们从这项研究得出结论,EPO可以与化疗药物协同作用,进一步抑制肿瘤生长。协同作用水平与药物有关。