Epigenetic Applications in Adverse Outcome Pathways and Environmental Risk Evaluation

被引:29
作者
Angrish, Michelle M. [1 ]
Allard, Patrick [2 ]
McCullough, Shaun D. [3 ]
Druwe, Ingrid L. [1 ]
Chadwick, Lisa Helbling [4 ]
Hines, Erin [1 ]
Chorley, Brian N. [2 ]
机构
[1] US EPA, Natl Ctr Environm Assessment, ORD, Res Triangle Pk, NC 27711 USA
[2] Univ Calif Los Angeles, Inst Soc & Genet, Los Angeles, CA USA
[3] US EPA, Natl Hlth & Environm Effects Res Lab, ORD, Res Triangle Pk, NC 27711 USA
[4] NIEHS, Div Extramural Res & Training, NIH, Dept Hlth & Human Serv, POB 12233, Res Triangle Pk, NC 27709 USA
关键词
DEVELOPMENTAL EXPOSURE; TRANSGENERATIONAL INHERITANCE; HISTONE MODIFICATIONS; EVALUATION CRITERIA; CHROMATIN-STRUCTURE; ARSENIC EXPOSURE; DOWN-REGULATION; CIRCULAR RNAS; SKIN-CANCER; DNA;
D O I
10.1289/EHP2322
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: The epigenome may be an important nterface between environmental chemical exposures and human health. However, the links between epigenetic modifications and health outcomes are often correlative and do not distinguish between cause and effect or common-cause relationships. The Adverse Outcome Pathway (AOP) framework has the potential to demonstrate, by way of an inference-and science-based analysis, the causal relationship between chemical exposures, epigenome, and adverse health outcomes, OBJECTIVE: The objective of this work is to discuss the epigenome as a modifier of exposure effects and risk, perspectives for integrating toxicoepigenetic data into an AOP framework, tools for the exploration of epigenetic toxicity, and integration of AOP-guided epigenetic information into science and risk-assessment processes. DISCUSSION: Organizing epigenetic information into the topology of a qualitative AOP network may help describe how a system will respond to epigenetic modifications caused by environmental chemical exposures. However, understanding the biological plausibility, linking epigenetic effects to short-and long-term health outcomes, and including epigenetic studies in the risk assessment process is met by substantive challenges. These obstacles include understanding the complex range of epigenetic modifications and their combinatorial effects, the large number of environmental chemicals to he tested, and the lack of data that quantitatively evaluate the epigenetic effects of environmental exposure. CONCLUSION: We anticipate that epigenetic information organized into AOP frameworks can he consistently used to support biological plausibility and to identify data gaps that will accelerate the pace at which epigenetic information is applied in chemical evaluation and risk-assessment paradigms.
引用
收藏
页码:045001 / 1
页数:12
相关论文
共 105 条
[1]   Reporting and evaluation criteria as means towards a transparent use of ecotoxicity data for environmental risk assessment of pharmaceuticals [J].
Agerstrand, M. ;
Kuester, A. ;
Bachmann, J. ;
Breitholtz, M. ;
Ebert, I. ;
Rechenberg, B. ;
Ruden, C. .
ENVIRONMENTAL POLLUTION, 2011, 159 (10) :2487-2492
[2]   ADVERSE OUTCOME PATHWAYS: A CONCEPTUAL FRAMEWORK TO SUPPORT ECOTOXICOLOGY RESEARCH AND RISK ASSESSMENT [J].
Ankley, Gerald T. ;
Bennett, Richard S. ;
Erickson, Russell J. ;
Hoff, Dale J. ;
Hornung, Michael W. ;
Johnson, Rodney D. ;
Mount, David R. ;
Nichols, John W. ;
Russom, Christine L. ;
Schmieder, Patricia K. ;
Serrrano, Jose A. ;
Tietge, Joseph E. ;
Villeneuve, Daniel L. .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2010, 29 (03) :730-741
[3]  
[Anonymous], 2009, SCI DEC ADV RISK ASS, DOI DOI 10.17226/12209
[4]  
[Anonymous], 2013, Revised guidance document on developing and assessing adverse outcome pathways
[5]   Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma [J].
Arroyo, Jason D. ;
Chevillet, John R. ;
Kroh, Evan M. ;
Ruf, Ingrid K. ;
Pritchard, Colin C. ;
Gibson, Donald F. ;
Mitchell, Patrick S. ;
Bennett, Christopher F. ;
Pogosova-Agadjanyan, Era L. ;
Stirewalt, Derek L. ;
Tait, Jonathan F. ;
Tewari, Muneesh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (12) :5003-5008
[6]   Arsenic and the Epigenome: Interindividual Differences in Arsenic Metabolism Related to Distinct Patterns of DNA Methylation [J].
Bailey, Kathryn A. ;
Wu, Michael C. ;
Ward, William O. ;
Smeester, Lisa ;
Rager, Julia E. ;
Garcia-Vargas, Gonzalo ;
Del Razo, Luz-Maria ;
Drobna, Zuzana ;
Styblo, Miroslav ;
Fry, Rebecca C. .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2013, 27 (02) :106-115
[7]   A novel ATAC-seq approach reveals lineage-specific reinforcement of the open chromatin landscape via cooperation between BAF and p63 [J].
Bao, Xiaomin ;
Rubin, Adam J. ;
Qu, Kun ;
Zhang, Jiajing ;
Giresi, Paul G. ;
Chang, Howard Y. ;
Khavari, Paul A. .
GENOME BIOLOGY, 2015, 16
[8]   miR-190-Mediated Downregulation of PHLPP Contributes to Arsenic-Induced Akt Activation and Carcinogenesis [J].
Beezhold, Kevin ;
Liu, Jia ;
Kan, Hong ;
Meighan, Terry ;
Castranova, Vince ;
Shi, Xianglin ;
Chen, Fei .
TOXICOLOGICAL SCIENCES, 2011, 123 (02) :411-420
[9]   The complex language of chromatin regulation during transcription [J].
Berger, Shelley L. .
NATURE, 2007, 447 (7143) :407-412
[10]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326