Arsenic Exposure and the Risk of Cancer

I. Pizarro
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Abstract

It is known that exposure to environmental chemicals increases the risk of cancerous and non-cancerous pathologies. Geomedical and anthropic evidence indicates that there is a close relationship between increased morbidities from cardiovascular diseases and cancer among the population in the Antofagasta Region and the etiology of exposure to arsenic. The most commonly used drugs with chemotherapy are platinum-based. The present work characterizes short-term urinary evacuation, that is, the pooled urine excreted 24 hours after the first cycle of treatments of cancer patients with cisplatin or carboplatin. The inorganic biochemical status and behavior of excreted As, Se and Pt administered to and evacuated by patients could be involved in the post-treatment quality of life of the patients and the evolution and final outcome of the disease. There were 90 patients in the group, 32 with lung cancer and 58 with different cancers termed “other types of cancer”, as well as 10 patients untreated with platinum-based drugs. Platinum and selenium were determined by ICP-OES and As by HGAAS. The detection limits were 7.7, 5.4 and 0.2 (ng/mL), respectively. The decreasing tendency of the administered Pt followed the order: carboplatin (other types of cancer) >cisplatin (lung cancer) >cisplatin (other types of cancer); the short-term urinary excretion of Pt was low. The decreasing tendency of the quantities of excreted Se was: carboplatin (other types of cancer) >cisplatin (other types of cancer) ≈ cisplatin (lung cancer); and the tendency of decreasing quantities of excreted As was cisplatin (other types of cancer) >carboplatin (other types of cancer) >cisplatin (lung cancer).The quantities of excreted Pt did not present significant differences among the cases of patients with lung cancer or with other cancers treated with cisplatin, despite significant variations in the quantities of Pt administered by the drug. The tendency in quantities of excreted Pt was similar to that of selenium and arsenic, but the evacuation of selenium was greater than that of arsenic, including in the group of patients with “other types of cancer” treated with drugs without Pt. The results of the study could arise from the subtle participation of antagonist mechanisms among Se, As and Pt that are involved in apoptotic and autophagic events in homeostasis, which could indicate the presence of cancer in patients from areas with chronic exposure to arsenic, as is the case of the Antofagasta Region in Chile.
砷暴露与癌症风险
众所周知,接触环境中的化学物质会增加患癌症和非癌症疾病的风险。地质医学和人类活动证据表明,安托法加斯塔地区人口中心血管疾病和癌症发病率的增加与接触砷的病因之间存在密切关系。化疗中最常用的药物是铂类药物。本研究的特点是短期尿排出,即顺铂或卡铂治疗癌症患者第一个周期后24小时排出的尿。患者给药和排出的砷、硒、铂的无机生化状态和行为可能关系到患者治疗后的生活质量以及疾病的演变和最终结局。该组有90名患者,其中32名患有肺癌,58名患有被称为“其他类型癌症”的不同癌症,以及10名未经铂类药物治疗的患者。铂和硒采用ICP-OES测定,砷采用HGAAS测定。检出限分别为7.7、5.4和0.2 (ng/mL)。给药铂的下降趋势为:卡铂(其他类型癌症)>顺铂(肺癌)>顺铂(其他类型癌症);尿中铂的短期排出量较低。硒排泄量的下降趋势为:卡铂(其他类型癌症)>顺铂(其他类型癌症)≈顺铂(肺癌);排As量减少的趋势为顺铂(其他类型癌症)>卡铂(其他类型癌症)>顺铂(肺癌)。在接受顺铂治疗的肺癌或其他癌症患者中,Pt的排泄量没有显著差异,尽管药物给药的Pt量有显著差异。Pt排泄量的趋势与硒和砷相似,但硒的排出量大于砷,包括在不使用Pt的药物治疗的“其他类型癌症”患者组。研究结果可能是由于硒、砷和Pt之间的拮抗剂机制的微妙参与,这些机制参与了稳态中的凋亡和自噬事件。这可能表明来自长期接触砷的地区的患者存在癌症,比如智利的安托法加斯塔地区。
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