Future of toxicology - Mechanisms of toxicity and drug safety: Where do we go from here?

被引:53
作者
Stevens, James L. [1 ]
机构
[1] Lilly Res Labs, Greenfield, IN 46140 USA
关键词
D O I
10.1021/tx060213n
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recent high-profile drug withdrawals increase the pressure on regulators and the pharmaceutical industry to improve preclinical safety testing. Understanding mechanisms of drug toxicity is an essential step toward improving drug safety testing by providing the basis for mechanism-based risk assessments. Nonetheless, despite several decades of research on mechanisms of drug-induced toxicity and the application of various new technologies to preclinical safety assessment, the overall impact on preclinical safety testing has been modest. Assessing the risk of exposing humans to new drug candidates still depends on preclinical testing in animals, which in many, but not all cases, predicts outcomes in humans accurately. The following offers a perspective on the challenges and opportunities facing efforts to improve preclinical safety testing and outlines gaps and needs that must be addressed. A case is built for focusing solutions on defined problems within the current safety testing paradigm rather than imposing wholesale change. Targets for application of new technologies, including in silico screening, biomarkers, surrogate assays and 'omic technologies, are outlined. Improving drug safety testing will depend on improving the application of mechanism-based risk assessment but will also require improving public and private collaborations in order to focus research regarding the mechanism of drug-induced toxicity on the most important problems.
引用
收藏
页码:1393 / 1401
页数:9
相关论文
共 58 条
  • [11] Dying for a cause: Invertebrate genetics takes on human neurodegeneration
    Driscoll, M
    Gerstbrein, B
    [J]. NATURE REVIEWS GENETICS, 2003, 4 (03) : 181 - 194
  • [12] What is Bayesian statistics?
    Eddy, SR
    [J]. NATURE BIOTECHNOLOGY, 2004, 22 (09) : 1177 - 1178
  • [13] Techniques: Application of systems biology to absorption, distribution, metabolism, excretion and toxicity
    Ekins, S
    Nikolsky, Y
    Nikolskaya, T
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2005, 26 (04) : 202 - 209
  • [14] ELHAGE J, 2004, PRECLINICAL CLIN SAF
  • [15] FDA, 2004, INN STAGN CHALL OPP
  • [16] Fielden MR, 2006, CURR OPIN DRUG DISC, V9, P84
  • [17] Challenges and limitations of gene expression profiling in mechanistic and predictive toxicology
    Fielden, MR
    Zacharewski, TR
    [J]. TOXICOLOGICAL SCIENCES, 2001, 60 (01) : 6 - 10
  • [18] An extracellular matrix microarray for probing cellular differentiation
    Flaim, CJ
    Chien, S
    Bhatia, SN
    [J]. NATURE METHODS, 2005, 2 (02) : 119 - 125
  • [19] Food and Drug Administration Center for Drug Evaluation and Research, 2005, EST MAX SAF START DO, P130
  • [20] Chemical Effects in Biological Systems-Data Dictionary (CEBS-DD): A compendium of terms for the capture and integration of biological study design description, conventional phenotypes, and 'omics data
    Fostel, J
    Choi, D
    Zwickl, C
    Morrison, N
    Rashid, A
    Hasan, A
    Bao, WJ
    Richard, A
    Tong, WD
    Bushel, PR
    Brown, R
    Bruno, M
    Cunningham, ML
    Dix, D
    Eastin, W
    Frade, C
    Garcia, A
    Heinloth, A
    Irwin, R
    Madenspacher, J
    Merrick, BA
    Papoian, T
    Paules, R
    Rocca-Serra, P
    Sansone, AS
    Stevens, J
    Tomer, K
    Yang, CH
    Waters, M
    [J]. TOXICOLOGICAL SCIENCES, 2005, 88 (02) : 585 - 601