| Literature DB >> 19743944 |
Annie M Jarabek1, Lynn H Pottenger, Larry S Andrews, Daniel Casciano, Michelle R Embry, James H Kim, R Julian Preston, M Vijayaraj Reddy, Rita Schoeny, David Shuker, Julie Skare, James Swenberg, Gary M Williams, Errol Zeiger.
Abstract
The assessment of human cancer risk from chemical exposure requires the integration of diverse types of data. Such data involve effects at the cell and tissue levels. This report focuses on the specific utility of one type of data, namely DNA adducts. Emphasis is placed on the appreciation that such DNA adduct data cannot be used in isolation in the risk assessment process but must be used in an integrated fashion with other information. As emerging technologies provide even more sensitive quantitative measurements of DNA adducts, integration that establishes links between DNA adducts and accepted outcome measures becomes critical for risk assessment. The present report proposes an organizational approach for the assessment of DNA adduct data (e.g., type of adduct, frequency, persistence, type of repair process) in concert with other relevant data, such as dosimetry, toxicity, mutagenicity, genotoxicity, and tumor incidence, to inform characterization of the mode of action. DNA adducts are considered biomarkers of exposure, whereas gene mutations and chromosomal alterations are often biomarkers of early biological effects and also can be bioindicators of the carcinogenic process.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19743944 DOI: 10.1080/10408440903164155
Source DB: PubMed Journal: Crit Rev Toxicol ISSN: 1040-8444 Impact factor: 5.635