The dynamic face of cadmium-induced Carcinogenesis: Mechanisms, emerging trends, and future directions

IF 2.9 Q2 TOXICOLOGY
Mohamed Ali Hussein , Abishek Kamalakkannan , Kamyab Valinezhad , Jhishnuraj Kannan , Nikhila Paleati , Rama Saad , André Kajdacsy-Balla , Gnanasekar Munirathinam
{"title":"The dynamic face of cadmium-induced Carcinogenesis: Mechanisms, emerging trends, and future directions","authors":"Mohamed Ali Hussein ,&nbsp;Abishek Kamalakkannan ,&nbsp;Kamyab Valinezhad ,&nbsp;Jhishnuraj Kannan ,&nbsp;Nikhila Paleati ,&nbsp;Rama Saad ,&nbsp;André Kajdacsy-Balla ,&nbsp;Gnanasekar Munirathinam","doi":"10.1016/j.crtox.2024.100166","DOIUrl":null,"url":null,"abstract":"<div><p>Cadmium (Cd) is a malleable element with odorless, tasteless characteristics that occurs naturally in the earth’s crust, underground water, and soil. The most common reasons for the anthropological release of Cd to the environment include industrial metal mining, smelting, battery manufacturing, fertilizer production, and cigarette smoking. Cadmium-containing products may enter the environment as soluble salts, vapor, or particle forms that accumulate in food, soil, water, and air. Several epidemiological studies have highlighted the association between Cd exposure and adverse health outcomes, especially renal toxicity, and the impact of Cd exposure on the development and progression of carcinogenesis. Also highlighted is the evidence for early-life and even maternal exposure to Cd leading to devastating health outcomes, especially the risk of cancer development in adulthood. Several mechanisms have been proposed to explain how Cd mediates carcinogenic transformation, including epigenetic alteration, DNA methylation, histone posttranslational modification, dysregulated non-coding RNA, DNA damage in the form of DNA mutation, strand breaks, and chromosomal abnormalities with double-strand break representing the most common DNA form of damage. Cd induces an indirect genotoxic effect by reducing p53′s DNA binding activity, eventually impairing DNA repair, inducing downregulation in the expression of DNA repair genes, which might result in carcinogenic transformation, enhancing lipid peroxidation or evasion of antioxidant interference such as catalase, superoxide dismutase, and glutathione. Moreover, Cd mediates apoptosis evasion, autophagy activation, and survival mechanisms. In this review, we decipher the role of Cd mediating carcinogenic transformation in different models and highlight the interaction between various mechanisms. We also discuss diagnostic markers, therapeutic interventions, and future perspectives.</p></div>","PeriodicalId":11236,"journal":{"name":"Current Research in Toxicology","volume":"6 ","pages":"Article 100166"},"PeriodicalIF":2.9000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666027X24000197/pdfft?md5=c08f999a224581b582db3eea858bbc40&pid=1-s2.0-S2666027X24000197-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666027X24000197","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Cadmium (Cd) is a malleable element with odorless, tasteless characteristics that occurs naturally in the earth’s crust, underground water, and soil. The most common reasons for the anthropological release of Cd to the environment include industrial metal mining, smelting, battery manufacturing, fertilizer production, and cigarette smoking. Cadmium-containing products may enter the environment as soluble salts, vapor, or particle forms that accumulate in food, soil, water, and air. Several epidemiological studies have highlighted the association between Cd exposure and adverse health outcomes, especially renal toxicity, and the impact of Cd exposure on the development and progression of carcinogenesis. Also highlighted is the evidence for early-life and even maternal exposure to Cd leading to devastating health outcomes, especially the risk of cancer development in adulthood. Several mechanisms have been proposed to explain how Cd mediates carcinogenic transformation, including epigenetic alteration, DNA methylation, histone posttranslational modification, dysregulated non-coding RNA, DNA damage in the form of DNA mutation, strand breaks, and chromosomal abnormalities with double-strand break representing the most common DNA form of damage. Cd induces an indirect genotoxic effect by reducing p53′s DNA binding activity, eventually impairing DNA repair, inducing downregulation in the expression of DNA repair genes, which might result in carcinogenic transformation, enhancing lipid peroxidation or evasion of antioxidant interference such as catalase, superoxide dismutase, and glutathione. Moreover, Cd mediates apoptosis evasion, autophagy activation, and survival mechanisms. In this review, we decipher the role of Cd mediating carcinogenic transformation in different models and highlight the interaction between various mechanisms. We also discuss diagnostic markers, therapeutic interventions, and future perspectives.

Abstract Image

镉诱导致癌的动态面貌:机制、新趋势和未来方向
镉(Cd)是一种可塑元素,具有无臭、无味的特性,天然存在于地壳、地下水和土壤中。人类向环境排放镉的最常见原因包括工业金属开采、冶炼、电池制造、化肥生产和吸烟。含镉产品可能以可溶性盐、蒸汽或颗粒形式进入环境,在食物、土壤、水和空气中积累。一些流行病学研究强调了镉暴露与不良健康后果(尤其是肾毒性)之间的联系,以及镉暴露对致癌的发生和发展的影响。有证据表明,早年甚至母体接触镉会导致破坏性的健康后果,特别是成年后罹患癌症的风险。人们提出了几种机制来解释镉如何介导致癌转化,包括表观遗传学改变、DNA 甲基化、组蛋白翻译后修饰、非编码 RNA 失调、DNA 变异形式的 DNA 损伤、链断裂和染色体异常,其中双链断裂是最常见的 DNA 损伤形式。镉会降低 p53 的 DNA 结合活性,最终损害 DNA 修复,诱导 DNA 修复基因表达下调,从而可能导致癌变,增强脂质过氧化或逃避过氧化氢酶、超氧化物歧化酶和谷胱甘肽等抗氧化剂的干扰,从而诱导间接的基因毒性效应。此外,镉还能介导凋亡逃避、自噬激活和生存机制。在这篇综述中,我们解读了镉在不同模型中介导癌变的作用,并强调了各种机制之间的相互作用。我们还讨论了诊断标记、治疗干预和未来展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信