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Investigators and Program Directors

Xinxin Ding

Xinxin Ding

Research Scientist, Wadsworth Center, Molecular Toxicology
Professor, School of Public Health, Biomedical Sciences and Environmental Health Sciences

Ph.D., Biological Chemistry, University of Michigan (1988)
Postdoctoral training: Biological Chemistry, University of Michigan

E-mail: dingx@wadsworth.org

<< Research Interests

Select Publications

  • Zhou, X., Zhang, X., Weng, Y., Fang, C., Kaminsky, L., and Ding, X.: High abundance of testosterone and salivary androgen-binding protein in the lateral nasal gland of male mice. J. Steroid Biochem. Mol. Biol. In press.
  • D’Agostino, J., Zhuo, X., Shadid, M., Morgan, D. G., Zhang, X., Shu, Y.-Z., Humphreys, W. G., Yost, G. S., and Ding, X.: The pneumotoxin 3-methylindole is a substrate as well as a mechanism-based inactivator of CYP2A13, a human cytochrome P450 enzyme preferentially expressed in the respiratory tract. Drug Metab. Dispos. In press.
  • Wu, H., Zhang, X., Ling, G., D’Agostino, J., and Ding, X.: mechanisms of differential expression of the CYP2A13 7520C and 7520G alleles in human lung: allelic expression analysis for CYP2A13 heterogeneous nuclear RNA, and evidence for the involvement of multiple cis-regulatory single nucleotide polymorphisms. Pharmacogenetics Genomics. In press.
  • Sneitz, N., Court, M. H., Zhang, X., Laajanen, K., Yee, K., Dalton, P., Ding, X., and Finel M.: Human UDP-glucuronosyltransferase UGT2A2: cDNA construction, expression, and functional characterization in comparison with UGT2A1 and UGT2A3. Pharmacogenetics Genomics. In press.
  • Sim, S. C., Miller, W. L., Zhong, X., Arlt, W., Ogata, T., Ding, X., Wolf, C. R., Fluck, C. E., Pandey, A. V., Henderson, C. J., Porter, T. D., Daly, A. K., Nebert, D. W., and Ingelman-Sundberg, M.: Nomenclature for alleles of the cytochrome P450 oxidoreductase gene. Pharmacogenetics Genomics 19, 565–566
  • Zhang, Q.-Y., Fang, C., Dunbar, D., Zhang, J., Kaminsky, L.S., and Ding, X. An intestinal epithelium-specific cytochrome P450 reductase-knockout mouse model: direct evidence for a role of intestinal cytochromes P450 in first-pass clearance of oral nifedipine. Drug Metab. Dispos. 37, 651–657, 2009. NIHMSID #82117
  • Zhang, Q.-Y. and Ding, X. The CYP2F, CYP2G and CYP2J Subfamilies. In Cytochrome P450: Role in the Metabolism and Toxicity of Drugs and Other Xenobiotics. (Ioannides C, Ed), Chapter 10, RSC Publishing, Cambridge, UK, pp. 309-353, 2008.
  • Brusick, D., Small, M. S., Cavalieri, E. L., Chakravarti, D., Ding, X., Longfellow, D. G., Nakamura, G., Rogan, E. C., Swenberg, J. A.: Possible genotoxic modes of action for naphthalene. Regul. Toxicol. Pharmacol. 51, S43–S50, 2008.
  • D’Agostino, J., Zhang, X., Wu, H., Ling, G., Zhang, Q-Y., and Ding, X.: Characterization of CYP2A13*2, a variant cytochrome P450 allele previously found to be associated with decreased incidence of lung adenocarcinoma in smokers. Drug Metab. Dispos. 36, 2316–2323, 2008. NIHMSID #60659
  • Fang, C., Gu, J., Xie, F., Behr, M., Yang, W., Abel, E. D., and Ding, X.: Deletion of the NADPH-cytochrome P450 reductase gene in cardiomyocytes does not protect mice against doxorubicin-mediated cardiac toxicity. Drug Metab. Dispos., 36, 1722-1828, 2008. NIHMSID #49730
  • Dostalek, M., Hardy, K. D., Milne, G. L., Morrow, J. D., Chen, C., Gonzalez, F. J., Gu, J., Ding, X., Martin, M. V., and Guengerich, F. P.: Development of oxidative stress by cytochrome P450 induction in rodents is selective for barbiturates and related to loss of pyridine nucleotide-dependent protective systems. J. Biol. Chem., 283, 17147–17157, 2008.
  • Fang, C., Behr, M., Xie, F., Lu, S., Doret, M., Luo, H., Yang, W., Aldous, K., Ding, X., and Gu, J.: Mechanism of chloroform-induced renal toxicity: non-involvement of hepatic cytochrome P450-dependent metabolism. Toxicol. Appl. Pharmacol. 227, 48–55, 2008.
  • Zhang, X., D’Agostino, J., Wu, H., Zhang, Q-Y., von Weymarn, L., Murphy, S. E., and Ding, X.: CYP2A13: Variable expression and role in human lung microsomal metabolic activation of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1- butanone. J. Pharmacol. Expt. Ther. 323, 570-578, 2007.
  • Zhang, Q-Y., Kaminsky, L. S., Dunbar, D., and Ding, X.: Role of small intestinal cytochrome P450 in the bioavailability of oral nifedipine. Drug Metab. Dispos. 35, 1617–1623, 2007.
  • Weng, Y., Fang, C., Turesky, R. J., Behr, B., Kaminsky, L. S., and Ding, X.: Determination of the role of target tissue metabolism in lung carcinogenesis using conditional cytochrome P450 reductase-null mice. Cancer Res. 67, 7825-7832, 2007.
  • Gu, J., Chen, C-S., Wei, Y., Fang, C., Xie, F., Kannan, K., Yang, W., Waxman, D. J., and Ding, X.: A mouse model with liver-specific deletion and global suppression of the NADPH-cytochrome P450 reductase gene: characterization and utility for in vivo studies of cyclophosphamide disposition. J. Pharmacol. Expt. Ther. 321, 9-17, 2007.
  • Ling, G., Wei, Y., and Ding, X.: Transcriptional regulation of human CYP2A13 expression in the respiratory tract by C/EBP and epigenetic modulation. Mol. Pharmacol. 71, 807-816, 2007.

Contact Information

Phone: (518) 486-2585
Fax: (518)-473-8722
E-mail: dingx@wadsworth.org