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Combinatory cytotoxic effects produced by E1B-55kDa-deleted adenoviruses and chemotherapeutic agents are dependent on the agents in esophageal carcinoma

机译:由E1B-55kDa缺失的腺病毒和化疗药物产生的联合细胞毒作用取决于食道癌中的药物

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摘要

We examined possible combinatory antitumor effects of replication-competent type 5 adenoviruses (Ad) lacking E1B-55kDa molecules (Ad-delE1B55) and chemotherapeutic agents in nine human esophageal carcinoma cells. Ad-delE1B55 produced cytotoxic effects on all the carcinoma cells and the cytotoxicity is not directly linked with the p53 status of the tumors or with the infectivity to respective tumors. A combinatory treatment with Ad-delE1B55 and an anticancer agent, 5-fluorouracil (5-FU), mitomycin C or etoposide, produced greater cytotoxic effects than that with either the Ad or the agent. Administration of 5-FU could minimally inhibit the viral replication and a simultaneous treatment with the Ad and 5-FU achieved better cytotoxicity than sequential treatments. We also confirmed the antitumor effects by the combination of Ad-delE1B55 with 5-FU in vivo. Cisplatin, however, did not achieve the combinatory effects in most of the cells tested. These data indicate that the Ad-delE1B55 produce combinatory antitumor effects with a chemotherapeutic agent irrespective of the administration schedule, but the effects depend on an agent in esophageal carcinoma.
机译:我们检查了具有复制能力的5型腺病毒(Ad)缺乏E1B-55kDa分子(Ad-delE1B55)和化学治疗剂在9例人食道癌细胞中的可能的组合抗肿瘤作用。 Ad-delE1B55对所有癌细胞产生细胞毒性作用,而细胞毒性与肿瘤的p53状态或与对各个肿瘤的感染性没有直接关系。 Ad-delE1B55和抗癌药5-氟尿嘧啶(5-FU),丝裂霉素C或依托泊苷的联合治疗产生的细胞毒性作用比Ad或药剂更大。施用5-FU可以最小程度地抑制病毒复制,同时使用Ad和5-FU进行治疗比连续治疗具有更好的细胞毒性。我们还证实了Ad-delE1B55与5-FU在体内的组合具有抗肿瘤作用。然而,顺铂在大多数测试细胞中均未达到组合作用。这些数据表明,与给药方案无关,Ad-delE1B55与化学治疗剂产生联合的抗肿瘤作用,但是该作用取决于食道癌中的作用剂。

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