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Anane Aidoo, Ph.D., Research Biologist, Division of Genetic & Reproductive Toxicology, FDA, National Center for Toxicological Research

Georgia State University, B.S., 1975, Biology, Atlanta, Georgia
Clark Atlanta University, M.S. 1979, Microbiology
Clark Atlanta University, Ph.D., 1986, Cell Biology

Experience:

  • 1977-1978: Graduate Research Training, Centers for Disease Control and Prevention, Atlanta, GA
  • 1978-1980 Laboratory Scientist, Georgia State Department of Health, Atlanta, GA
  • 1980-1981 Laboratory Instructor, GA
  • 1981-1982 Technician/Curator, Biology Department, Clark Atlanta University, Atlanta, GA
  • 1984-1985 Teaching Assistant, Atlanta Junior College, Atlanta, GA
  • 1986 Laboratory Instructor, Spelman College, Atlanta, GA
  • 1986-1987 Research Associate, Endocrinology Laboratory, Clark Atlanta University, Atlanta, GA
  • 1987-1990 Oak Ridge Institute of Science and Engineering (ORISE) Post Doctoral Research Fellow, Division of Genetic Toxicology, National Center for Toxicological Research, Jefferson, AR
  • 1989-present Adjunct Professor, University of Arkansas, Pine Bluff, AR
  • 1990-1992 Senior Staff Fellow, Division of Genetic Toxicology, National Center for Toxicological Research, Jefferson, AR
  • 1992-1994 Research Biologist, Division of Genetic Toxicology, National Center for Toxicological Research. Jefferson AR
  • 1994-present Research Biologist (GS-13), Division of Genetic Toxicology, National Center for Toxicological Research, Jefferson, AR

Honors:

  • FDA Commendable Service Award, 2000
  • Cash Award for Special Act of Service, 2000
  • FDA Incentive Cash Awards, 1994-1999
  • FDA Equal Opportunity Achievement Award, 1997
  • NCTR EEO Outstanding Service Award, 1995
  • Clark Atlanta University Best Research Award, 1989
  • National Science Foundation Award, 1985-1986
  • National Research Council Service Award. 1982-1985
  • National Deans List, 1982

Current Primary Research Interests: Genetic & Reproductive Toxicology.

  • The use of rat lymphocyte Hprt assay as a biomarker to investigate the mechanisms of age-associated spontaneous and chemically induced mutations
  • Influence of dietary supplements on the mutagenicity/carcinogenicity of environmental genotoxicants, including food-borne carcinogens
  • Mitochondrial DNA mutation
  • Influence of dietary restriction on spontaneous mutation occurring in rodents and humans

Representative publications:

  • Aidoo, A., Lyn-Cook, L.E., Mittlestaedt, R.A. Heflich, R.H., and Casciano, D.A. "Induction of 6-thioguanine-resistant lymphocytes in Fischer 344 rats following in vivo exposure to N-ethyl-N-nitrosourea and cyclophosphamide." Environ Mol Mutagen, 17:141-151 (1991).

  • Aidoo, A., Lyn-Cook, L.E., Heflich, R.H., George, E.O., and Casciano, D.A. "The effect of treatment time, treatment schedule and animal age on the frequency of 6-thioguanine resistant T-lymphocytes induced in Fischer 344 rats by N-ethyl-N-nitrosourea." Mutation Res., 298:169-178 (1993).

  • Smith, A., Fullerton, N.F., Aidoo, A., Heflich, R.H., and Beland, F.A. "DNA adduct formation in relation to lymphocyte mutations and lung tumor induction in F344 rats treated with the environmental pollutant 1,6-dinitropyrene, Environ Health Perspect., 99:277-280 (1993).
  • Aidoo, A., Lyn-Cook, L.E., Lensing, S., and Wamer, W. "Ascorbic acid (vitamin C) modulates the mutagenic effects produced by an alkylating agent in vivo." Environ Mol Mutagen., 24:220-228 (1994).

  • Aidoo, A., Lyn-Cook, L.E., Lensing, S., Bishop, M.E., Wamer, W. "In vivo mutagenic activity of beta-carotene in rat spleen lymphocytes." Carcinogenesis, 6:2237-2241 (1995).

  • Casciano D.A., Chou, M., Lyn-Cook, L.E., and Aidoo, A. "Calorie restriction modulates chemically induced in vivo somatic mutation frequency." Environ Mol Mutagen., 27:162-164 (1996).
  • Heflich, R.H., Mittelstaedt, R.A., Manjanatha, M.G., Lyn-Cook, L.E., and Aidoo, A. "DNA sequence analysis of Hprt mutations in lymphocytes from Sprague-Dawley rats treated with 7,12-dimethylbenz[a]anthracene." Environ Mol Mutagen., 28:5-12 (1996).

  • Manjanatha, M.G., Lyn-Cook, L.E., Culp, S.J., Beland, F.A., Heflich, R.H., and Aidoo, A. "Lymphocyte mutant frequency in relation to DNA adduct formation in rats treated with tumorigenic doses of mammary carcinogen 7,12-dimethylbenz[a]anthracene." Mutations Res., 357:89-96 (1996).

  • Desai, V.G., Lyn-Cook, L.E., Aidoo, A., Casciano. D.A., and Feuers, R.J. "Modulation of antioxidant enzymes in bleomycin-treated rats by vitamin C and b -carotene." Nutr Cancer, 29:127-132 (1997).

  • Aidoo, A., Morris, S.M., and Casciano, D.A. "Development and utilization of the rat lymphocyte Hprt mutation assay." Mutation Res., 387:69-88 (1997).

  • Manjanatha, M.G., Shelton, S.D., Aidoo, A., Lyn-Cook, L.E., and Casciano, D.A. "Comparison of in vivo mutagenesis in the endogenous Hprt gene and the lacI transgene of Big Blue rats treated with DMBA." Mutation Res., 401:165-178 (1998).

  • Chen, T.A., Aidoo, A., Manjanatha, M.G., Mittelstaedt, R.A. Shelton, S.D., Lyn-Cook, L.E., Casciano, D.A., and Heflich, R.H. "Comparison of mutant frequency and types of mutations induced by thiotepa in the endogenous Hprt gene and transgenic lacI gene of Big Blue rats." Mutation Res., 403:199-214 (1998).

  • Aidoo, A., Desai, V.G., Lyn-Cook, L.E., Chen, J.J., Feuers, R.J., and Casciano, D.A. "Attenuation of bleomycin-induced Hprt mutant frequency in female and male rats by calorie restriction." Mutation Res., 430:155-163 (1999).

  • Casciano, D.A., Aidoo, A., Chen, T., Mittestaedt, R.A., Manjanatha, M.G., and Heflich, R.H. "Hprt mutant frequency and molecular analysis of Hprt mutations in rats treated with mutagenic carcinogens." Mutation Res., 431:389-395 (1999).

  • Desai, V.G., Aidoo, A., Li, J., Lyn-Cook, L.E., Casciano, D.A., and Feuers, R.J. "Effects of bleomycin on liver antioxidant enzymes and the electron transport system from ad libitum-fed and dietary-restricted female and male Fischer 344 rats." Nutr Cancer, 36:42-51 (2000).

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