A development of a graph-based ensemble machine learning model for skin sensitization hazard and potency assessment

被引:6
作者
Jeon, Byoungjun [1 ]
Lim, Min Hyuk [2 ]
Choi, Tae Hyun [3 ]
Kang, Byeong-Cheol [4 ,5 ]
Kim, Sungwan [6 ,7 ]
机构
[1] Seoul Natl Univ, Grad Sch, Interdisciplinary Program Bioengn, Seoul, South Korea
[2] Seoul Natl Univ Hosp, Dept Biomed Engn, Seoul, South Korea
[3] Thenevus Plast Surg Clin, Seoul, South Korea
[4] Seoul Natl Univ Hosp, Biomed Res Inst, Dept Expt Anim Res, Seoul 03080, South Korea
[5] Seoul Natl Univ, Coll Med, Grad Sch Translat Med, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Biomed Engn, Seoul 03080, South Korea
[7] Seoul Natl Univ, Inst Bioengn, Seoul, South Korea
关键词
defined approach; direct peptide reactivity assay; graph neural network; human cell line activation test; integrated testing strategy; KeratinoSens (TM); machine learning; risk assessment; skin sensitization; PEPTIDE REACTIVITY ASSAY; LINE ACTIVATION TEST; RISK-ASSESSMENT; PREDICTION;
D O I
10.1002/jat.4361
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Many defined approaches (DAs) for skin sensitization assessment based on the adverse outcome pathway (AOP) have been developed to replace animal testing because the European Union has banned animal testing for cosmetic ingredients. Several DAs have demonstrated that machine learning models are beneficial. In this study, we have developed an ensemble prediction model utilizing the graph convolutional network (GCN) and machine learning approach to assess skin sensitization. The model integrates in silico parameters and data from alternatives to animal testing of well-defined AOP to improve DA predictivity. Multiple ensemble models were created using the probability produced by the GCN with six physicochemical properties, direct peptide reactivity assay, KeratinoSens (TM), and human cell line activation test (h-CLAT), using a multilayer perceptron approach. Models were evaluated by predicting the testing set's human hazard class and three potency classes (strong, weak, and non-sensitizer). When the GCN feature was used, 11 models out of 16 candidates showed the same or improved accuracy in the testing set. The ensemble model with the feature set of GCN, KeratinoSens (TM), and h-CLAT produced the best results with an accuracy of 88% for assessing human hazards. The best three-class potency model was created with the feature set of GCN and all three assays, resulting in 64% accuracy. These results from the ensemble approach indicate that the addition of the GCN feature could provide an improved predictivity of skin sensitization hazard and potency assessment.
引用
收藏
页码:1832 / 1842
页数:11
相关论文
共 28 条
[1]   Prevalence of contact allergy in the general population: A systematic review and meta-analysis [J].
Alinaghi, Farzad ;
Bennike, Niels H. ;
Egeberg, Alexander ;
Thyssen, Jacob P. ;
Johansen, Jeanne D. .
CONTACT DERMATITIS, 2019, 80 (02) :77-85
[2]  
[Anonymous], 2010, Test No. 429: Skin Sensitisation: Local Lymph Node Assay, DOI [10.1787/9789264071100-en, DOI 10.1787/9789264071100-EN]
[3]   Unsupervised data base clustering based on Daylight's fingerprint and Tanimoto similarity: A fast and automated way to cluster small and large data sets [J].
Butina, D .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1999, 39 (04) :747-750
[4]   The rise of deep learning in drug discovery [J].
Chen, Hongming ;
Engkvist, Ola ;
Wang, Yinhai ;
Olivecrona, Marcus ;
Blaschke, Thomas .
DRUG DISCOVERY TODAY, 2018, 23 (06) :1241-1250
[5]  
European Commission, 2009, OFFICIAL J EUROPEAN
[6]   Development of an artificial neural network model for risk assessment of skin sensitization using human cell line activation test, direct peptide reactivity assay, KeratinoSens and in silico structure alert parameter [J].
Hirota, Morihiko ;
Ashikaga, Takao ;
Kouzuki, Hirokazu .
JOURNAL OF APPLIED TOXICOLOGY, 2018, 38 (04) :514-526
[7]   Evaluation of combinations of in vitro sensitization test descriptors for the artificial neural network-based risk assessment model of skin sensitization [J].
Hirota, Morihiko ;
Fukui, Shiho ;
Okamoto, Kenji ;
Kurotani, Satoru ;
Imai, Noriyasu ;
Fujishiro, Miyuki ;
Kyotani, Daiki ;
Kato, Yoshinao ;
Kasahara, Toshihiko ;
Fujita, Masaharu ;
Toyoda, Akemi ;
Sekiya, Daisuke ;
Watanabe, Shinichi ;
Seto, Hirokazu ;
Takenouchi, Osamu ;
Ashikaga, Takao ;
Miyazawa, Masaaki .
JOURNAL OF APPLIED TOXICOLOGY, 2015, 35 (11) :1333-1347
[8]   Non-animal methods to predict skin sensitization (I): the Cosmetics Europe database [J].
Hoffmann, Sebastian ;
Kleinstreuer, Nicole ;
Alepee, Nathalie ;
Allen, David ;
Api, Anne Marie ;
Ashikaga, Takao ;
Clouet, Elodie ;
Cluzel, Magalie ;
Desprez, Bertrand ;
Gellatly, Nichola ;
Goebel, Carsten ;
Kern, Petra S. ;
Klaric, Martina ;
Kuehnl, Jochen ;
Lalko, Jon F. ;
Martinozzi-Teissier, Silvia ;
Mewes, Karsten ;
Miyazawa, Masaaki ;
Parakhia, Rahul ;
van Vliet, Erwin ;
Zang, Qingda ;
Petersohn, Dirk .
CRITICAL REVIEWS IN TOXICOLOGY, 2018, 48 (05) :344-358
[9]   Bayesian integrated testing strategy (ITS) for skin sensitization potency assessment: a decision support system for quantitative weight of evidence and adaptive testing strategy [J].
Jaworska, Joanna S. ;
Natsch, Andreas ;
Ryan, Cindy ;
Strickland, Judy ;
Ashikaga, Takao ;
Miyazawa, Masaaki .
ARCHIVES OF TOXICOLOGY, 2015, 89 (12) :2355-2383
[10]   Could graph neural networks learn better molecular representation for drug discovery? A comparison study of descriptor-based and graph-based models [J].
Jiang, Dejun ;
Wu, Zhenxing ;
Hsieh, Chang-Yu ;
Chen, Guangyong ;
Liao, Ben ;
Wang, Zhe ;
Shen, Chao ;
Cao, Dongsheng ;
Wu, Jian ;
Hou, Tingjun .
JOURNAL OF CHEMINFORMATICS, 2021, 13 (01)