Literature DB >> 20020921

Understanding genetic toxicity through data mining: the process of building knowledge by integrating multiple genetic toxicity databases.

C Yang1, C H Hasselgren, S Boyer, K Arvidson, S Aveston, P Dierkes, R Benigni, R D Benz, J Contrera, N L Kruhlak, E J Matthews, X Han, J Jaworska, R A Kemper, J F Rathman, A M Richard.   

Abstract

ABSTRACT Genetic toxicity data from various sources were integrated into a rigorously designed database using the ToxML schema. The public database sources include the U.S. Food and Drug Administration (FDA) submission data from approved new drug applications, food contact notifications, generally recognized as safe food ingredients, and chemicals from the NTP and CCRIS databases. The data from public sources were then combined with data from private industry according to ToxML criteria. The resulting "integrated" database, enriched in pharmaceuticals, was used for data mining analysis. Structural features describing the database were used to differentiate the chemical spaces of drugs/candidates, food ingredients, and industrial chemicals. In general, structures for drugs/candidates and food ingredients are associated with lower frequencies of mutagenicity and clastogenicity, whereas industrial chemicals as a group contain a much higher proportion of positives. Structural features were selected to analyze endpoint outcomes of the genetic toxicity studies. Although most of the well-known genotoxic carcinogenic alerts were identified, some discrepancies from the classic Ashby-Tennant alerts were observed. Using these influential features as the independent variables, the results of four types of genotoxicity studies were correlated. High Pearson correlations were found between the results of Salmonella mutagenicity and mouse lymphoma assay testing as well as those from in vitro chromosome aberration studies. This paper demonstrates the usefulness of representing a chemical by its structural features and the use of these features to profile a battery of tests rather than relying on a single toxicity test of a given chemical. This paper presents data mining/profiling methods applied in a weight-of-evidence approach to assess potential for genetic toxicity, and to guide the development of intelligent testing strategies.

Entities:  

Year:  2008        PMID: 20020921     DOI: 10.1080/15376510701857502

Source DB:  PubMed          Journal:  Toxicol Mech Methods        ISSN: 1537-6516            Impact factor:   2.987


  6 in total

Review 1.  How accurate is in vitro prediction of carcinogenicity?

Authors:  Richard Maurice Walmsley; Nicholas Billinton
Journal:  Br J Pharmacol       Date:  2011-03       Impact factor: 8.739

Review 2.  Bioinformatics opportunities for identification and study of medicinal plants.

Authors:  Vivekanand Sharma; Indra Neil Sarkar
Journal:  Brief Bioinform       Date:  2012-05-15       Impact factor: 11.622

Review 3.  Genetic toxicology in the 21st century: reflections and future directions.

Authors:  Brinda Mahadevan; Ronald D Snyder; Michael D Waters; R Daniel Benz; Raymond A Kemper; Raymond R Tice; Ann M Richard
Journal:  Environ Mol Mutagen       Date:  2011-04-28       Impact factor: 3.216

Review 4.  The Salmonella mutagenicity assay: the stethoscope of genetic toxicology for the 21st century.

Authors:  Larry D Claxton; Gisela de A Umbuzeiro; David M DeMarini
Journal:  Environ Health Perspect       Date:  2010-11       Impact factor: 9.031

5.  Development of a New Threshold of Toxicological Concern Database of Non-cancer Toxicity Endpoints for Industrial Chemicals.

Authors:  Takashi Yamada; Masayuki Kurimoto; Akihiko Hirose; Chihae Yang; James F Rathman
Journal:  Front Toxicol       Date:  2021-03-23

Review 6.  Chemistry in Times of Artificial Intelligence.

Authors:  Johann Gasteiger
Journal:  Chemphyschem       Date:  2020-09-28       Impact factor: 3.102

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.