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Assessment of drug induced genotoxicity in gastric cancer patients

机译:胃癌患者药物性遗传毒性的评估

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The aim of this study was to evaluate the frequency and severity of chromosomal damage during chemotherapy treatment, to understand the role of chemotherapeutic agents inducing genetic damage and to understand the phenomenon of acquiring drug resistance. Blood samples were collected from gastric cancer patients receiving chemotherapy with the cytotoxic drugs epirubicin, cisplatin and 5-fluorouracil, and 100 controls from recognized cancer hospitals under the supervision of an oncologist. Cytogenetic studies were carried out in peripheral blood lymphocytes of study population by adopting standard cytogenetic protocols such as (a) chromosomal aberrations (CA) and (b) sister chromatid exchanges (SCE). Student t- test was adopted to analyze the statistical significance. An increased pattern in the frequency of chromosomal aberrations was observed in the patients that received chemotherapy 10.14 ± 0.77 followed by 7.13 ± 0.48 without chemotherapy as against 3.70 ± 0.32 in control subjects (p<0.001). In conclusion, our results clearly reveal as a whole, the obvious effects of anticarcinogenic agents on the level of chromosomal aberrations in gastric cancer patients receiving therapy with respect to the genetic material.
机译:这项研究的目的是评估化学疗法治疗过程中染色体损伤的频率和严重程度,以了解化学治疗剂诱导遗传损伤的作用并了解获得耐药性的现象。在接受胃癌治疗的胃癌患者中,从细胞毒药物表柔比星,顺铂和5-氟尿嘧啶中抽取血样,并在肿瘤学家的监督下从公认的癌症医院中​​抽取100名对照。通过采用标准的细胞遗传学方案,例如(a)染色体畸变(CA)和(b)姐妹染色单体交换(SCE),在研究人群的外周血淋巴细胞中进行细胞遗传学研究。采用学生t检验分析统计学意义。在接受化学疗法的患者中,染色体畸变频率的模式增加了,分别为10.14±0.77和7.13±0.48,而未接受化学疗法的患者则为3.70±0.32(对照组)(p <0.001)。总之,我们的研究结果从整体上清楚地揭示了抗癌剂对接受基因治疗的胃癌患者的染色体畸变水平的明显影响。

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