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本文引用的文献

1
Integrin α4 up-regulation activates the hedgehog pathway to promote arsenic and benzo[α]pyrene co-exposure-induced cancer stem cell-like property and tumorigenesis.整合素 α4 的上调激活了 hedgehog 通路,促进了砷和苯并[a]芘共同暴露诱导的癌症干细胞样特性和肿瘤发生。
Cancer Lett. 2020 Nov 28;493:143-155. doi: 10.1016/j.canlet.2020.08.015. Epub 2020 Aug 26.
2
Deubiquitinase USP7-mediated MCL-1 up-regulation enhances Arsenic and Benzo(a)pyrene co-exposure-induced Cancer Stem Cell-like property and Tumorigenesis.去泛素化酶 USP7 介导的 MCL-1 上调增强了砷和苯并[a]芘共暴露诱导的癌症干细胞样特性和肿瘤发生。
Theranostics. 2020 Jul 11;10(20):9050-9065. doi: 10.7150/thno.47897. eCollection 2020.
3
Relationship between exposure to mixtures of persistent, bioaccumulative, and toxic chemicals and cancer risk: A systematic review.持久性、生物累积性和毒性化学物质混合物暴露与癌症风险的关系:系统评价。
Environ Res. 2020 Sep;188:109787. doi: 10.1016/j.envres.2020.109787. Epub 2020 Jun 14.
4
Metals and molecular carcinogenesis.金属与分子致癌作用。
Carcinogenesis. 2020 Sep 24;41(9):1161-1172. doi: 10.1093/carcin/bgaa076.
5
A Positive Feedback Loop Between c-Myc Upregulation, Glycolytic Shift, and Histone Acetylation Enhances Cancer Stem Cell-like Property and Tumorigenicity of Cr(VI)-transformed Cells.c-Myc 上调、糖酵解转换和组蛋白乙酰化之间的正反馈循环增强了 Cr(VI)转化细胞的癌症干细胞样特性和致瘤性。
Toxicol Sci. 2020 Sep 1;177(1):71-83. doi: 10.1093/toxsci/kfaa086.
6
ToxPoint: Dissecting Functional RNA Modifications in Responses to Environmental Exposure-Mechanistic Toxicology Research Enters a New Era.ToxPoint:剖析对环境暴露反应中的功能性RNA修饰——机制毒理学研究进入新时代。
Toxicol Sci. 2020 Mar 1;174(1):1-2. doi: 10.1093/toxsci/kfz252.
7
Arsenic and benzo[a]pyrene co-exposure acts synergistically in inducing cancer stem cell-like property and tumorigenesis by epigenetically down-regulating SOCS3 expression.砷和苯并[a]芘共同暴露通过表观遗传下调SOCS3表达,在诱导癌症干细胞样特性和肿瘤发生方面具有协同作用。
Environ Int. 2020 Apr;137:105560. doi: 10.1016/j.envint.2020.105560. Epub 2020 Feb 18.
8
Toxicity assessment due to prenatal and lactational exposure to lead, cadmium and mercury mixtures.产前和哺乳期暴露于铅、镉和汞混合物的毒性评估。
Environ Int. 2019 Dec;133(Pt B):105192. doi: 10.1016/j.envint.2019.105192. Epub 2019 Oct 19.
9
Chronic Hexavalent Chromium Exposure Induces Cancer Stem Cell-Like Property and Tumorigenesis by Increasing c-Myc Expression.六价铬慢性暴露通过增加 c-Myc 表达诱导癌症干细胞样特性和肿瘤发生。
Toxicol Sci. 2019 Dec 1;172(2):252-264. doi: 10.1093/toxsci/kfz196.
10
Effects of single and combined toxic exposures on the gut microbiome: Current knowledge and future directions.单一和联合毒性暴露对肠道微生物组的影响:现有知识和未来方向。
Toxicol Lett. 2019 Sep 15;312:72-97. doi: 10.1016/j.toxlet.2019.04.014. Epub 2019 Apr 27.

砷和苯并(a)芘联合暴露协同致肺肿瘤作用的机制。

Mechanisms of the synergistic lung tumorigenic effect of arsenic and benzo(a)pyrene combined- exposure.

机构信息

Division of Cancer Biology, Department of Medicine, MetroHealth Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH, 44109, USA.

出版信息

Semin Cancer Biol. 2021 Nov;76:156-162. doi: 10.1016/j.semcancer.2021.05.002. Epub 2021 May 7.

DOI:10.1016/j.semcancer.2021.05.002
PMID:33971262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9000133/
Abstract

Humans are often exposed to mixtures of environmental pollutants especially environmental chemical carcinogens, representing a significant environmental health issue. However, our understanding on the carcinogenic effects and mechanisms of environmental carcinogen mixture exposures is limited and mostly relies on the findings from studying individual chemical carcinogens. Both arsenic and benzo(a)pyrene (BaP) are among the most common environmental carcinogens causing lung cancer and other types of cancer in humans. Millions of people are exposed to arsenic via consuming arsenic-contaminated drinking water and even more people are exposed to BaP via cigarette smoking and consuming BaP-contaminated food. Thus arsenic and BaP combined-exposure in humans is common. Previous epidemiology studies indicated that arsenic-exposed people who were cigarette smokers had significantly higher lung cancer risk than those who were non-smokers. Since BaP is one of the major carcinogens in cigarette smoke, it has been speculated that arsenic and BaP combined-exposure may play important roles in the increased lung cancer risk observed in arsenic-exposed cigarette smokers. In this review, we summarize important findings and inconsistencies about the co-carcinogenic effects and underlying mechanisms of arsenic and BaP combined-exposure and propose new areas for future studies. A clear understanding on the mechanism of co-carcinogenic effects of arsenic and BaP combined exposure may identify novel targets to more efficiently treat and prevent lung cancer resulting from arsenic and BaP combined-exposure.

摘要

人类经常暴露于环境污染物混合体中,尤其是环境化学致癌物,这是一个重大的环境健康问题。然而,我们对环境致癌物混合物暴露的致癌作用和机制的理解是有限的,并且主要依赖于研究个别化学致癌物的发现。砷和苯并(a)芘(BaP)都是最常见的环境致癌物之一,可导致人类肺癌和其他类型的癌症。数百万人通过饮用受砷污染的饮用水接触砷,更多的人通过吸烟和食用受 BaP 污染的食物接触 BaP。因此,人类同时接触砷和 BaP 是很常见的。先前的流行病学研究表明,暴露于砷的吸烟者患肺癌的风险明显高于不吸烟者。由于 BaP 是香烟烟雾中的主要致癌物之一,因此有人推测,砷和 BaP 的联合暴露可能在观察到的砷暴露吸烟者肺癌风险增加中起重要作用。在这篇综述中,我们总结了砷和 BaP 联合暴露的协同致癌作用及其潜在机制的重要发现和不一致之处,并提出了未来研究的新领域。对砷和 BaP 联合暴露协同致癌作用机制的清晰认识,可能为更有效地治疗和预防由砷和 BaP 联合暴露引起的肺癌提供新的靶点。