薤白试验:探索博莱霉素诱导的细胞遗传毒性和根尖分生组织细胞周期动力学的改变

IF 1.5 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Ria Das, Sanjib Ray
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引用次数: 0

摘要

博莱霉素常用于治疗霍奇金淋巴瘤和睾丸癌,具有严重的肺毒性。虽然已有多项研究评估了化疗药物对水生和陆生环境的毒性影响,但有关博莱霉素影响的数据却十分有限,尤其是对高等植物的影响。为了填补这一空白,我们利用在评估化学和生化制剂毒性影响方面享有盛誉的薤白试验来研究博莱霉素对陆地生态系统的影响。我们的研究旨在评估博莱霉素在最低浓度(10-40 μg mL-1)和不同暴露时间(2、4、6和24小时)下对牛肝菌根尖细胞的细胞遗传毒性作用。博莱霉素处理过的牛肝菌根尖细胞核和有丝分裂异常情况分析,以及吖啶橙-噻啶溴化物双重染色检测,揭示了博莱霉素对细胞活力的影响。此外,琼脂糖凝胶电泳测定了该药物的 DNA 降解潜力,揭示了细胞遗传毒性的潜在机制。研究结果还显示,随着博莱霉素浓度和暴露时间的增加,有丝分裂指数会下降,各种细胞遗传毒性异常现象的发生频率也会升高,包括染色体粘连、染色体断裂、染色体落后、桥接、极性偏离、核病变和色素沉着。研究结果表明,即使在低浓度和短时间接触博莱霉素的情况下,它也具有潜在风险,会对植物的遗传物质产生严重不良影响,可能导致细胞死亡。因此,这项研究揭示了博莱霉素对高等植物系统的细胞遗传毒性作用,强调了其对陆地生态系统的威胁,尤其是在长期和不受监控的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allium cepa tests: Exploring bleomycin induced cyto-genotoxicity and altered cell cycle kinetics in root tips meristematic cells

Bleomycin, commonly employed in treating Hodgkin’s lymphoma and testicular cancer, is associated with significant pulmonary toxicity. While various studies have assessed the toxic impact of chemotherapeutic agents on aquatic and terrestrial environments, limited data exist on bleomycin's effects, especially concerning higher plants. To address this gap, we utilized the Allium cepa assays, renowned for evaluating chemical and biochemical agents' toxic effects, to investigate bleomycin's impact on the terrestrial ecosystem. Our study aimed to assess bleomycin's cyto-genotoxic effects on A. cepa root tip cells at minimal concentrations (10–40 μg mL−1) and varied exposure durations (2, 4, 6, and 24 h). Analysis of nuclear and mitotic abnormalities in bleomycin-treated A. cepa root tip cells, alongside an acridine orange-ethidium bromide double staining assay, illuminated its influence on cell viability. Additionally, agarose gel electrophoresis determined the drug's potential for DNA degradation, unveiling the underlying mechanisms of cyto-genotoxicity. Results also demonstrated a decline in the mitotic index with increased bleomycin concentrations and exposure time, elevated frequencies of various cyto-genotoxic abnormalities, including sticky chromosomes, chromatid breaks, laggards, bridges, polar deviations, nuclear lesions, and hyperchromasia. The study indicated the potential risks of bleomycin even at low concentrations and brief exposures, highlighting its severe adverse effects on genetic material of plant, potentially contributing to cell death. Consequently, this investigation unveils bleomycin's cyto-genotoxic effects on higher plant system, underscoring its threat to terrestrial ecosystems, particularly upon chronic and unmonitored exposure.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
24
审稿时长
51 days
期刊介绍: Mutation Research (MR) provides a platform for publishing all aspects of DNA mutations and epimutations, from basic evolutionary aspects to translational applications in genetic and epigenetic diagnostics and therapy. Mutations are defined as all possible alterations in DNA sequence and sequence organization, from point mutations to genome structural variation, chromosomal aberrations and aneuploidy. Epimutations are defined as alterations in the epigenome, i.e., changes in DNA methylation, histone modification and small regulatory RNAs. MR publishes articles in the following areas: Of special interest are basic mechanisms through which DNA damage and mutations impact development and differentiation, stem cell biology and cell fate in general, including various forms of cell death and cellular senescence. The study of genome instability in human molecular epidemiology and in relation to complex phenotypes, such as human disease, is considered a growing area of importance. Mechanisms of (epi)mutation induction, for example, during DNA repair, replication or recombination; novel methods of (epi)mutation detection, with a focus on ultra-high-throughput sequencing. Landscape of somatic mutations and epimutations in cancer and aging. Role of de novo mutations in human disease and aging; mutations in population genomics. Interactions between mutations and epimutations. The role of epimutations in chromatin structure and function. Mitochondrial DNA mutations and their consequences in terms of human disease and aging. Novel ways to generate mutations and epimutations in cell lines and animal models.
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