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联合光动力疗法与药物对体外培养肿瘤细胞大分子合成影响的研究。

Studies of the effects of associated photodynamic therapy and drugs on macromolecular synthesis of tumoral cells grown in vitro.

作者信息

Dima V F, Mihăilescu I N, Dima S V, Chivu L, Stirbeţ M, Udrea M, Popa A

机构信息

Cantacuzino Institute, Bucharest, Romania.

出版信息

Arch Roum Pathol Exp Microbiol. 1990 Apr-Jun;49(2):155-75.

PMID:2129279
Abstract

HeLa S3 tumoral cells were used as an experimental model for studying the association of photodynamic therapy (PDT) and antitumoral agents. Tumoral monolayer cultures were incubated 18 hours at 37 degrees C with Photofrin II, trypsinized and suspended in Eagle medium supplemented with 10% FCS and then treated with antitumoral agents 90 minutes before He-Ne laser exposure. The tumoral cells were exposed to antitumoral agents in the following concentrations (equivalent to ED70): adriamycin (0.0297 micrograms); mitomycin C (0.0199 micrograms); 5-FU (0.4937 micrograms) and vinblastine (0.0109 micrograms) per 10(5) cells. Macromolecular syntheses (DNA, RNA and proteins) were investigated by use of radioactive precursors: 3H-thymidine, 3H-uridine and 3H-leucine, as expressed in percent referring to Photofrin II-pretreated controls; they were exposed to He-Ne laser but not treated with antitumoral agents. All experiments were followed for 72 hours incubation at 37 degrees C. The conclusions of the results of PDT associated with antitumoral agents sustain the following aspects: a) the antitumoral agents activity (adriamycin, mitomycin C, 5-FU, vinblastine) was more noticeable when applied 90 minutes before He-Ne laser irradiation; b) inhibition of radioactive precursors uptake in DNA, RNA and proteins was accompanied by suppression of in vitro tumoral cells development and c) PDT association with antitumoral agents could manifest at least three positive effects upon animals; 1) PDT potentiating effects with antitumoral agents; 2) suppressing effects on tumoral macromolecular synthesis; 3) antitumoral agents cytotoxic elimination (due to the low doses used).

摘要

HeLa S3肿瘤细胞被用作研究光动力疗法(PDT)与抗肿瘤药物关联的实验模型。肿瘤单层培养物在37℃下与卟吩姆钠II孵育18小时,胰蛋白酶消化后悬浮于补充有10%胎牛血清的伊格尔培养基中,然后在氦氖激光照射前90分钟用抗肿瘤药物处理。肿瘤细胞暴露于以下浓度(相当于ED70)的抗肿瘤药物:每10⁵个细胞中阿霉素(0.0297微克)、丝裂霉素C(0.0199微克)、5-氟尿嘧啶(0.4937微克)和长春碱(0.0109微克)。通过使用放射性前体3H-胸腺嘧啶核苷、3H-尿苷和3H-亮氨酸研究大分子合成(DNA、RNA和蛋白质),以相对于经卟吩姆钠II预处理的对照的百分比表示;它们暴露于氦氖激光但未用抗肿瘤药物处理。所有实验在37℃下孵育72小时。PDT与抗肿瘤药物联合使用的结果结论支持以下方面:a)在氦氖激光照射前90分钟应用时,抗肿瘤药物活性(阿霉素、丝裂霉素C、5-氟尿嘧啶、长春碱)更显著;b)DNA、RNA和蛋白质中放射性前体摄取的抑制伴随着体外肿瘤细胞发育的抑制;c)PDT与抗肿瘤药物联合使用对动物可表现出至少三种积极作用:1)PDT与抗肿瘤药物的增效作用;2)对肿瘤大分子合成的抑制作用;3)抗肿瘤药物的细胞毒性消除(由于使用的剂量较低)。

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