Brambilla Giovanni, Martelli Antonietta
Department of Internal Medicine, Division of Clinical Pharmacology and Toxicology, University of Genoa, Viale Benedetto XV, 2, I-16132 Genoa, Italy.
Mutat Res. 2006 Mar;612(2):115-49. doi: 10.1016/j.mrrev.2005.12.002. Epub 2006 Feb 7.
This survey is a compendium of genotoxicity and carcinogenicity information of antihypertensive drugs. Data from 164 marketed drugs were collected. Of the 164 drugs, 65 (39.6%) had no retrievable genotoxicity or carcinogenicity data; this group was comprised largely of drugs marketed in a limited number of countries. The remaining 99 (60.4%) had at least one genotoxicity or carcinogenicity test result. Of these 99, 48 (48.5%) had at least one positive finding: 32 tested positive in at least one genotoxicity assay, 26 in at least one carcinogenicity assay, and 10 gave a positive result in both at least one genotoxicity assay and at least one carcinogenicity assay. In terms of correlation between results of the various genotoxicity assays and absence of carcinogenic activity in both mice and rats 2 of 44 non-carcinogenic drugs tested positive in the in vitro bacterial mutagenesis assay, 2 of 9 tested positive in the mouse lymphoma assay, none of 14 tested positive for gene mutation at the hprt locus, 5 of 25 tested positive in in vitro cytogenetic assays, none of 31 in in vivo cytogenetic assays, and none of 14 in inducing DNA damage and/or repair in in vitro and/or in vivo assays. Concerning the predictivity of genetic toxicology findings for long-term carcinogenesis assays, 75 drugs had both genotoxicity and carcinogenicity data; of these 37 (49.3%) were neither genotoxic nor carcinogenic, 14 (18.7%) were non-carcinogens which tested positive in at least one genotoxicity assay, 14 (18.7%) were carcinogenic in at least one sex of mice or rats but tested negative in genotoxicity assays, and 10 (13.3%) were both genotoxic and carcinogenic. Only 42 of the 164 marketed antihypertensives (25.6%) had all data required by the guidelines for testing of pharmaceuticals.
本调查是抗高血压药物遗传毒性和致癌性信息的汇编。收集了164种已上市药物的数据。在这164种药物中,65种(39.6%)没有可检索到的遗传毒性或致癌性数据;这一组主要由在少数国家上市的药物组成。其余99种(60.4%)至少有一项遗传毒性或致癌性测试结果。在这99种药物中,48种(48.5%)至少有一项阳性结果:32种在至少一项遗传毒性试验中呈阳性,26种在至少一项致癌性试验中呈阳性,10种在至少一项遗传毒性试验和至少一项致癌性试验中均呈阳性。就各种遗传毒性试验结果与小鼠和大鼠无致癌活性之间的相关性而言,44种非致癌药物中有2种在体外细菌诱变试验中呈阳性,9种中有2种在小鼠淋巴瘤试验中呈阳性,14种中无一在hprt基因座的基因突变检测中呈阳性,25种中有5种在体外细胞遗传学试验中呈阳性,31种中无一在体内细胞遗传学试验中呈阳性,14种中无一在体外和/或体内试验中诱导DNA损伤和/或修复呈阳性。关于遗传毒理学研究结果对长期致癌试验的预测性,75种药物同时有遗传毒性和致癌性数据;其中37种(49.3%)既无遗传毒性也无致癌性,14种(18.7%)是非致癌物,但在至少一项遗传毒性试验中呈阳性,14种(18.7%)在至少一种性别小鼠或大鼠中具有致癌性,但在遗传毒性试验中呈阴性,10种(13.3%)既有遗传毒性又有致癌性。164种已上市的抗高血压药物中只有42种(25.6%)具备药品测试指南要求的所有数据。