Powell C B, Horuchi T, Kao M S, Collins J L
Department of Obstetrics and Gynecology, University of California at San Francisco 94117.
Am J Obstet Gynecol. 1993 Sep;169(3):661-7. doi: 10.1016/0002-9378(93)90640-5.
Our purpose was to examine the in vitro cytolytic potential of interferon alfa for human cervical and ovarian carcinoma cell lines.
The lytic potential of interferon alfa alone and in the presence the protein synthesis inhibitors actinomycin D and emetine was determined in the human cervical carcinoma cell lines ME-180, MS751, SiHa, HT-3, and C-33A and the ovarian carcinoma cell lines Caov-3, NIH:OVCAR-3, SK-OV-3 carcinoma cell lines by means of an 18-hour chromium 51 release assay.
Exposure of these cell lines to interferon alfa alone did not result in lysis. Similarly, when cells were simultaneously exposed to interferon alfa and either actinomycin D or emetine there was no additional increase in lysis above that seen with actinomycin D or emetine alone. Pretreatment of cells with interferon alfa (10(3), 10(4), or 10(5) U/ml) followed by protein synthesis inhibition by actinomycin D or emetine resulted in a synergistic increase in lysis.
The ability to reveal the lytic potential of interferon alfa when protein synthesis is subsequently inhibited could have practical applications for the treatment of gynecologic malignancies.
我们的目的是检测干扰素α对人宫颈癌细胞系和卵巢癌细胞系的体外细胞溶解潜力。
通过18小时的铬51释放试验,测定干扰素α单独以及与蛋白质合成抑制剂放线菌素D和依米丁共同作用时,对人宫颈癌细胞系ME-180、MS751、SiHa、HT-3和C-33A以及卵巢癌细胞系Caov-3、NIH:OVCAR-3、SK-OV-3的溶解潜力。
这些细胞系单独暴露于干扰素α不会导致细胞溶解。同样,当细胞同时暴露于干扰素α和放线菌素D或依米丁时,与单独使用放线菌素D或依米丁相比,细胞溶解没有额外增加。先用干扰素α(10³、10⁴或10⁵ U/ml)预处理细胞,随后用放线菌素D或依米丁抑制蛋白质合成,会导致细胞溶解协同增加。
当随后抑制蛋白质合成时,揭示干扰素α细胞溶解潜力的能力可能对妇科恶性肿瘤的治疗具有实际应用价值。