Ohmura K, Tsukamoto T
Department of Urology, Sapporo Medical College.
Hinyokika Kiyo. 1989 May;35(5):737-47.
With human tumor clonogenic assay, the direct antiproliferative activity of recombinant human leukocyte interferon alpha (IFN-alpha) was investigated on human renal cell carcinomas (RCCs), which consisted of a human RCC cell line (ACHN), two human RCC xenografts and fifteen primary RCCs. The combination effect of IFN-alpha with a cancer chemotherapeutic agent was studied, as well, with the assay system. IFN-alpha showed a dose-dependent antiproliferative activity against the human RCCs. The clonal growth of ACHN cell line was inhibited by less than 50% at the concentration of 1,000 IU/ml. Two xenografts had a different sensitivity to IFN-alpha, in which the percent colony formation was less than 20% in RCC-3 at the concentration of 100-100,000 IU/ml, while in RCC-4 more than 50% even at the high concentration of 10,000 IU/ml. In 15 primary tumors obtained at surgery, two types of response to IFN-alpha were demonstrated. One was the response in which the colony formation was inhibited in a dose-dependent manner as an increment of IFN-alpha concentration, and the other in which the colony formation was not sufficiently inhibited even at the high concentration of IFN-alpha. The dose-dependent inhibition of colony formation was demonstrated in 10 out of 15 specimens (66.7%). When the colony formation suppressed to less than 50% of control was considered to be sensitive to IFN-alpha, 6.7% of these 15 primary tumors were sensitive to IFN-alpha at 100 IU/ml, 20.0% at 1,000 IU/ml and 20.0% at 10,000 IU/ml. Combination effects of IFN-alpha and with each of four different cancer chemotherapeutic agents (vinblastine, adriamycin, methotrexate, 5-fluorouracil) were investigated on the ACHN cell line. Every combination type produced a subadditive or synergistic combination effect. In particular, the combination of IFN-alpha with vinblastine of more than 0.1 microgram/ml concentration yielded a combination effect of statistical significance (p less than 0.001). Even against premary tumors, the combination of IFN-alpha with vinblastine showed a synergistic effect in one out of every three tumors. These results suggested that the combination of IFN-alpha with a cancer chemotherapeutic agent would enhance the clinical effect of IFN-alpha alone in only a certain situation.
采用人肿瘤克隆形成试验,研究重组人白细胞α干扰素(IFN-α)对人肾细胞癌(RCC)的直接抗增殖活性,人肾细胞癌包括一株人RCC细胞系(ACHN)、两个人RCC异种移植瘤和15例原发性RCC。还利用该试验系统研究了IFN-α与一种癌症化疗药物的联合效应。IFN-α对人RCC显示出剂量依赖性抗增殖活性。在1000 IU/ml浓度时,ACHN细胞系的克隆生长被抑制不到50%。两种异种移植瘤对IFN-α的敏感性不同,在100 - 100000 IU/ml浓度下,RCC - 3的集落形成百分比小于20%,而在RCC - 4中,即使在10000 IU/ml的高浓度下,集落形成百分比仍超过50%。在手术获取的15例原发性肿瘤中,显示出对IFN-α的两种反应类型。一种是随着IFN-α浓度增加,集落形成呈剂量依赖性抑制的反应,另一种是即使在IFN-α高浓度下集落形成也未得到充分抑制的反应。15个标本中有10个(66.7%)显示出集落形成的剂量依赖性抑制。当集落形成抑制至对照的50%以下被认为对IFN-α敏感时,这15例原发性肿瘤中,6.7%在100 IU/ml时对IFN-α敏感,20.0%在1000 IU/ml时敏感,20.0%在10000 IU/ml时敏感。研究了IFN-α与四种不同癌症化疗药物(长春碱、阿霉素、甲氨蝶呤、5-氟尿嘧啶)分别联合对ACHN细胞系的效应。每种联合类型均产生亚相加或协同联合效应。特别是,IFN-α与浓度超过0.1微克/毫升的长春碱联合产生了具有统计学意义的联合效应(p < 0.001)。即使针对原发性肿瘤,IFN-α与长春碱联合在每三个肿瘤中就有一个显示出协同效应。这些结果表明,IFN-α与癌症化疗药物联合仅在特定情况下会增强IFN-α单独的临床效果。