Pathways of Toxicity

被引:74
作者
Kleensang, Andre [1 ]
Maertens, Alexandra [1 ]
Rosenberg, Michael [2 ]
Fitzpatrick, Suzanne [3 ]
Lamb, Justin [4 ]
Auerbach, Scott [5 ]
Brennan, Richard [6 ]
Crofton, Kevin M. [7 ]
Gordon, Ben [8 ]
Fornace, Albert J., Jr. [9 ,10 ]
Gaido, Kevin [3 ]
Gerhold, David [11 ]
Haw, Robin [12 ]
Henney, Adrian [13 ]
Ma'ayan, Avi [14 ]
McBride, Mary [2 ]
Monti, Stefano [15 ]
Ochs, Michael F. [16 ]
Pandey, Akhilesh [17 ,18 ,19 ,20 ]
Sharan, Roded [21 ]
Stierum, Rob [22 ]
Tugendreich, Stuart [23 ]
Willett, Catherine [24 ]
Wittwehr, Clemens [25 ]
Xia, Jianguo [26 ]
Patton, Geoffrey W. [27 ]
Arvidson, Kirk [27 ]
Bouhifd, Mounir [1 ]
Hogberg, Helena T. [1 ]
Luechtefeld, Thomas [1 ]
Smirnova, Lena [1 ]
Zhao, Liang [1 ]
Adeleye, Yeyejide [28 ]
Kanehisa, Minoru [29 ]
Carmichael, Paul [28 ]
Andersen, Melvin E. [30 ]
Hartung, Thomas [1 ,31 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing, Baltimore, MD USA
[2] Agilent Technol, Santa Clara, CA USA
[3] US FDA, Ctr Food Safety & Appl Nutr, College Pk, MD USA
[4] Genometry Inc, Cambridge, MA USA
[5] NIEHS, Div Natl Toxicol Program, NIH, Res Triangle Pk, NC 27709 USA
[6] Thomson Reuters Inc, Carlsbad, CA USA
[7] US EPA, Off Res & Dev, Natl Ctr Computat Toxicol, Res Triangle Pk, NC 27711 USA
[8] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[9] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Washington, DC USA
[10] Georgetown Univ, Lombardi Comprehens Canc Ctr, Washington, DC USA
[11] NIH, Natl Ctr Adv Translat Sci, Rockville, MD USA
[12] Ontario Inst Canc Res, Reactome, Toronto, ON, Canada
[13] Heidelberg Univ, German Virtual Liver Network, Heidelberg, Germany
[14] Icahn Sch Med Mt Sinai, Dept Pharmacol & Syst Therapeut, New York, NY USA
[15] Boston Univ, Sch Med, Sect Computat Biomed, Boston, MA 02118 USA
[16] Johns Hopkins Univ, Sch Med, Ctr Oncol, Baltimore, MD 21205 USA
[17] Johns Hopkins Univ, Sch Med, Inst Med Genet, Baltimore, MD USA
[18] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[19] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[20] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[21] Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
[22] TNO Hlth Living Microbiol & Syst Biol, Zeist, Netherlands
[23] Ingenu Syst Inc, Redwood City, CA USA
[24] Humane Soc United States, Washington, DC USA
[25] Commiss European Communities, Joint Res Ctr, Syst Toxicol Unit, I-21020 Ispra, Italy
[26] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V5Z 1M9, Canada
[27] US FDA, Ctr Food Safety & Appl Nutr, Off Food Addit Safety, College Pk, MD USA
[28] Unilever, Safety & Environm Assurance Ctr, Sharnbrook, Beds, England
[29] Kyoto Univ, Inst Chem Res, Kyoto 606, Japan
[30] Hamner Inst Hlth Sci, Res Triangle Pk, NC USA
[31] Univ Konstanz, CAAT Europe, Constance, Germany
关键词
systems toxicology; pathways of toxicity; adverse outcome pathways; in vitro toxicology; human toxome; TOXICOLOGY; THOUGHT; FOOD; 21ST-CENTURY; TOXICOGENOMICS; INTEGRATION; VALIDATION; DOSIMETRY; EVOLUTION; RESPONSES;
D O I
10.14573/altex.1309261
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Despite wide-spread consensus on the need to transform toxicology and risk assessment in order to keep pace with technological and computational changes that have revolutionized the life sciences, there remains much work to be done to achieve the vision of toxicology based on a mechanistic foundation. A workshop was organized to explore one key aspect of this transformation the development of Pathways of Toxicity (PoT) as a key tool for hazard identification based on systems biology. Several issues were discussed in depth in the workshop: The first was the challenge of formally defining the concept of a PoT as distinct from, but complementary to, other toxicological pathway concepts such as mode of action (MoA). The workshop came up with a preliminary definition of PoT as "A molecular definition of cellular processes shown to mediate adverse outcomes of toxicants". It is further recognized that normal physiological pathways exist that maintain homeostasis and these, sufficiently perturbed, can become PoT. Second, the workshop sought to define the adequate public and commercial resources for PoT information, including data, visualization, analyses, tools, and use-cases, as well as the kinds of efforts that will be necessary to enable the creation of such a resource. Third, the workshop explored ways in which systems biology approaches could inform pathway annotation, and which resources are needed and available that can provide relevant PoT information to the diverse user communities.
引用
收藏
页码:53 / 61
页数:9
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