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      SkinSensDB: a curated database for skin sensitization assays

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          Abstract

          Skin sensitization is an important toxicological endpoint for chemical hazard determination and safety assessment. Prediction of chemical skin sensitizer had traditionally relied on data from rodent models. The development of the adverse outcome pathway (AOP) and associated alternative in vitro assays have reshaped the assessment of skin sensitizers. The integration of multiple assays as key events in the AOP has been shown to have improved prediction performance. Current computational models to predict skin sensitization mainly based on in vivo assays without incorporating alternative in vitro assays. However, there are few freely available databases integrating both the in vivo and the in vitro skin sensitization assays for development of AOP-based skin sensitization prediction models. To facilitate the development of AOP-based prediction models, a skin sensitization database named SkinSensDB has been constructed by curating data from published AOP-related assays. In addition to providing datasets for developing computational models, SkinSensDB is equipped with browsing and search tools which enable the assessment of new compounds for their skin sensitization potentials based on data from structurally similar compounds. SkinSensDB is publicly available at http://cwtung.kmu.edu.tw/skinsensdb.

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          Development of a peptide reactivity assay for screening contact allergens.

          Allergic contact dermatitis resulting from skin sensitization is a common occupational and environmental health problem. In recent years, the local lymph node assay (LLNA) has emerged as a practical option for assessing the skin sensitization potential of chemicals. In addition to accurate identification of skin sensitizers, the LLNA can also provide a reliable measure of relative sensitization potency; information that is pivotal in successful management of human health risks. However, even with the significant animal welfare benefits provided by the LLNA, there is still interest in the development of nonanimal test methods for skin sensitization testing. One characteristic of a chemical allergen is its ability to react with proteins prior to the induction of skin sensitization. The majority of chemical allergens is electrophilic and as such reacts with nucleophilic amino acids like cysteine or lysine. In order to determine if reactivity correlates with sensitization potential, 38 chemicals representing allergens of different potencies (weak to extreme) and nonsensitizers were evaluated for their ability to react with glutathione or three synthetic peptides containing either cysteine, lysine, or histidine. Following a 15-min reaction time for glutathione or a 24 h reaction period for the three synthetic peptides, the samples were analyzed by HPLC. UV detection was used to monitor the depletion of glutathione or the peptide following reaction. The results demonstrate that a significant correlation (Spearman correlation) exists between allergen potency and the depletion of glutathione (p = 0.001), lysine (p = 0.025), and cysteine (p = 0.020), but not histidine. The peptide with the highest sensitivity was cysteine (80.8%) whereas histidine was the least sensitive (11.5%). The data presented show that measuring peptide reactivity has utility for screening chemicals for their skin sensitization potency and thus potential for reducing our reliance on animal test methods.
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            Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects

            Contact allergies are complex diseases, and one of the important challenges for public health and immunology. The German ‘Federal Institute for Risk Assessment’ hosted an ‘International Workshop on Contact Dermatitis’. The scope of the workshop was to discuss new discoveries and developments in the field of contact dermatitis. This included the epidemiology and molecular biology of contact allergy, as well as the development of new in vitro methods. Furthermore, it considered regulatory aspects aiming to reduce exposure to contact sensitisers. An estimated 15–20% of the general population suffers from contact allergy. Workplace exposure, age, sex, use of consumer products and genetic predispositions were identified as the most important risk factors. Research highlights included: advances in understanding of immune responses to contact sensitisers, the importance of autoxidation or enzyme-mediated oxidation for the activation of chemicals, the mechanisms through which hapten-protein conjugates are formed and the development of novel in vitro strategies for the identification of skin-sensitising chemicals. Dendritic cell cultures and structure-activity relationships are being developed to identify potential contact allergens. However, the local lymph node assay (LLNA) presently remains the validated method of choice for hazard identification and characterisation. At the workshop the use of the LLNA for regulatory purposes and for quantitative risk assessment was also discussed.
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              Performance of a novel keratinocyte-based reporter cell line to screen skin sensitizers in vitro.

              In vitro tests are needed to replace animal tests to screen for the skin sensitization potential of chemicals. Skin sensitizers are electrophilic molecules and the Nrf2-electrophile-sensing pathway comprising the repressor protein Keap1, the transcription factor Nrf2 and the antioxidant response element (ARE) is emerging as a toxicity pathway induced by skin sensitizers. Previously, we screened a large set of chemicals in the reporter cell line AREc32, which contains an eight-fold repeat of the rat GSTA2 ARE-sequence upstream of a luciferase reporter gene in the human breast cancer cell line MCF7. This approach was now further developed to bring it closer to the conditions in the human skin and to propose a fully standardized assay. To this end, a luciferase reporter gene under control of a single copy of the ARE-element of the human AKR1C2 gene was stably inserted into HaCaT keratinocytes. A standard operating procedure was developed whereby chemicals are routinely tested at 12 concentrations in triplicate for significant induction of gene activity. We report results from this novel assay on (i) a list of reference chemicals published by ECVAM, (ii) the ICCVAM list of chemicals for validation of alternative endpoints in the LLNA and (iii) on a more general list of 67 chemicals derived from the ICCVAM database. For comparison, peptide reactivity data are presented for the same chemicals. The results indicate a good predictive value of this approach for hazard identification. Its technical simplicity, the high-throughput format and the good predictivity may make this assay a candidate for rapid validation to meet the tight deadline to replace animal tests for skin sensitization by 2013 set by the European authorities. Copyright 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                chiachiwang@kmu.edu.tw
                yclin@kmu.edu.tw
                shanwang332@gmail.com
                nowiznesh4113@gmail.com
                complexhui@gmail.com
                +886-7-3121101 , cwtung@kmu.edu.tw
                Journal
                J Cheminform
                J Cheminform
                Journal of Cheminformatics
                Springer International Publishing (Cham )
                1758-2946
                31 January 2017
                31 January 2017
                2017
                : 9
                : 5
                Affiliations
                [1 ]ISNI 0000 0000 9476 5696, GRID grid.412019.f, School of Pharmacy, , Kaohsiung Medical University, ; 100 Shih-Chuan 1st Road, Kaohsiung, 80708 Taiwan
                [2 ]ISNI 0000 0000 9476 5696, GRID grid.412019.f, PhD Program in Toxicology, , Kaohsiung Medical University, ; Kaohsiung, 80708 Taiwan
                [3 ]ISNI 0000000406229172, GRID grid.59784.37, National Institute of Environmental Health Sciences, , National Health Research Institutes, ; Miaoli County, 35053 Taiwan
                [4 ]ISNI 0000 0004 0531 9758, GRID grid.412036.2, Institute of Environmental Engineering, , National Sun Yat-sen University, ; Kaohsiung, 80424 Taiwan
                [5 ]ISNI 0000 0000 9476 5696, GRID grid.412019.f, Research Center for Environmental Medicine, , Kaohsiung Medical University, ; Kaohsiung, 80708 Taiwan
                Author information
                http://orcid.org/0000-0003-3011-8440
                Article
                194
                10.1186/s13321-017-0194-2
                5285290
                6d9d4c27-a0e3-424a-9575-cff4b0043b6e
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 22 October 2016
                : 23 January 2017
                Funding
                Funded by: National Health Research Institutes of Taiwan
                Award ID: NHRI-105A1-PDCO-0316164
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004663, Ministry of Science and Technology, Taiwan;
                Award ID: MOST104-2221-E-037-001-MY3
                Award ID: MOST104-2320-B-037-032-MY2
                Award Recipient :
                Funded by: Kaohsiung Medical University Research Foundation
                Award ID: KMU-M105005
                Award Recipient :
                Funded by: NSYSU-KMU Joint Research Project
                Award ID: NSYSUKMU105-I007
                Funded by: Research Center for Environmental Medicine
                Award ID: KMU-TP104A25
                Award Recipient :
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                © The Author(s) 2017

                Chemoinformatics
                Chemoinformatics

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