Creating context for the use of DNA adduct data in cancer risk assessment: I. Data organization

被引:75
作者
Jarabek, Annie M. [2 ]
Pottenger, Lynn H. [3 ]
Andrews, Larry S. [4 ]
Casciano, Daniel [5 ]
Embry, Michelle R. [1 ]
Kim, James H. [1 ]
Preston, R. Julian [2 ]
Reddy, M. Vijayaraj [6 ]
Schoeny, Rita [7 ]
Shuker, David [8 ]
Skare, Julie [9 ]
Swenberg, James [10 ]
Williams, Gary M. [11 ]
Zeiger, Errol [12 ]
机构
[1] ILSI Hlth & Environm Sci Inst, Washington, DC 20005 USA
[2] US EPA, Natl Hlth & Environm Effects Res Lab, Natl Ctr Environm Assessment, Res Triangle Pk, NC 27711 USA
[3] Dow Chem Co USA, Midland, MI 48674 USA
[4] Rohm & Haas Co, Spring House, PA 19477 USA
[5] Dan Casciano & Associates, Little Rock, AR USA
[6] Merck Res Labs, West Point, PA USA
[7] US EPA, Off Water, Washington, DC 20460 USA
[8] Open Univ, Milton Keynes MK7 6AA, Bucks, England
[9] Procter & Gamble Co, Cent Prod Safety, Cincinnati, OH USA
[10] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC USA
[11] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
[12] Errol Zeiger Consulting, Chapel Hill, NC USA
关键词
Biomarkers; cancer; DNA adducts; mode of action; risk assessment; DOSE-DEPENDENT TRANSITIONS; RAT-LIVER CARCINOGENESIS; SURROGATE END-POINTS; VINYL-CHLORIDE; ETHYLENE-OXIDE; SEQUENCE CONTEXT; HUMAN RELEVANCE; REACTIVE CARCINOGENS; LUNG TUMORIGENESIS; OXIDATIVE STRESS;
D O I
10.1080/10408440903164155
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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.
引用
收藏
页码:659 / 678
页数:20
相关论文
共 133 条
[1]   The use of non-tumor data in cancer risk assessment: reflections on butadiene, vinyl chloride, and benzene [J].
Albertini, R ;
Clewell, H ;
Himmelstein, MW ;
Morinello, E ;
Olin, S ;
Preston, J ;
Scarano, L ;
Smith, MT ;
Swenberg, J ;
Tice, R ;
Travis, C .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2003, 37 (01) :105-132
[2]   Propylene oxide: Genotoxicity profile of a rodent nasal carcinogen [J].
Albertini, Richard J. ;
Sweeney, Lisa A. .
CRITICAL REVIEWS IN TOXICOLOGY, 2007, 37 (06) :489-520
[3]  
[Anonymous], CONCEPTS INHALATION
[4]  
[Anonymous], EPA600890066F OFF RE
[5]  
[Anonymous], 2005, DNA Repair and Mutagenesis
[6]  
[Anonymous], 2006, Agency for Toxic Substances and Disease Registry, P1
[7]  
[Anonymous], 2002, The Genetic Basis of Human Cancer
[8]  
Barbin A, 1997, CANCER RES, V57, P1695
[9]   ANALYSIS OF BUTADIENE, BUTADIENE MONOXIDE, AND BUTADIENE DIOXIDE IN BLOOD BY GAS-CHROMATOGRAPHY GAS-CHROMATOGRAPHY MASS-SPECTROSCOPY [J].
BECHTOLD, WE ;
STRUNK, MR ;
THORNTONMANNING, JR ;
HENDERSON, RF .
CHEMICAL RESEARCH IN TOXICOLOGY, 1995, 8 (02) :182-187
[10]   Genetic instability in cancer: Theory and experiment [J].
Beckman, RA ;
Loeb, LA .
SEMINARS IN CANCER BIOLOGY, 2005, 15 (06) :423-435