Health Services Vocational College, 52950Çanakkale Onsekiz Mart University, Canakkale, Turkey.
Hum Exp Toxicol. 2021 Dec;40(12_suppl):S158-S163. doi: 10.1177/09603271211036126. Epub 2021 Aug 1.
Tetrachlorvinphos is an organophosphate that is classified as a carcinogen in humans by several authorities. Due to very limited data regarding the genotoxic potential, we aimed to comprehensively investigate in vitro genotoxic potential of tetrachlorvinphos. We performed our study by applying the cytokinesis-block micronucleus cytome and sister chromatid exchange (SCE) assays to human peripheral blood lymphocytes. We evaluated micronucleus (MN) and SCE frequencies and cytokinesis-block proliferation index in both exposed and non-exposed lymphocytes. We also calculated the chromosomal instability level in response to exposure by combining the results of MN and SCE. We found that MN frequency did not increase with exposure to tetrachlorvinphos (0-50 µg/ml). In contrast, we observed that SCE frequencies significantly increased with exposure to ≥5 µg/ml tetrachlorvinphos. Furthermore, exposure to tetrachlorvinphos at concentrations of 50 µg/ml induced a significant increase in chromosomal instability level ( < 0.05). Cytokinesis-block proliferation index level did not significantly decrease in response to tetrachlorvinphos exposure. Our findings reveal that tetrachlorvinphos resulted in different DNA damages that were measured by two assays. Furthermore, our findings suggested that exposure to tetrachlorvinphos increased chromosomal instability that is a hallmark of many malignancies. We conclude that although tetrachlorvinphos does not significantly increase the MN level, the significant increase of both SCE and CIN frequencies indicates the genotoxic potential of tetrachlorvinphos in human peripheral lymphocytes. Additionally, tetrachlorvinphos is not cytotoxic in the range of tested concentrations.
四氯苯膦是一种有机磷化合物,被多个权威机构归类为人类致癌物。由于关于其遗传毒性潜力的资料非常有限,我们旨在全面研究四氯苯膦的体外遗传毒性潜力。我们通过应用细胞分裂阻断微核细胞遗传学和姐妹染色单体交换(SCE)试验来研究人类外周血淋巴细胞。我们评估了暴露和未暴露淋巴细胞中的微核(MN)和 SCE 频率以及细胞分裂阻断增殖指数。我们还通过结合 MN 和 SCE 的结果来计算染色体不稳定性水平,以响应暴露。我们发现 MN 频率不会随着四氯苯膦(0-50μg/ml)的暴露而增加。相反,我们观察到 SCE 频率随着暴露于≥5μg/ml 的四氯苯膦而显著增加。此外,在 50μg/ml 的四氯苯膦浓度下暴露会导致染色体不稳定性水平显著增加(<0.05)。细胞分裂阻断增殖指数水平不会因四氯苯膦暴露而显著降低。我们的研究结果表明,四氯苯膦通过两种试验导致了不同的 DNA 损伤。此外,我们的研究结果表明,暴露于四氯苯膦会增加染色体不稳定性,这是许多恶性肿瘤的标志。我们得出结论,尽管四氯苯膦不会显著增加 MN 水平,但 SCE 和 CIN 频率的显著增加表明四氯苯膦在人类外周血淋巴细胞中的遗传毒性潜力。此外,在测试浓度范围内,四氯苯膦没有细胞毒性。