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Issam Makhoul, MD
Kelly Mercer, PhD
Postdoctoral Fellow

                                                                                  Doctoral Degree                                                            Department of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences

Postdoctoral Training                                                     Postdoctoral Fellowship, Department of Pharmaceutical Sciences,St. Jude Children's Research Hospital, Memphis, TN

Postdoctoral Fellowship, College of Medicine, Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR.

Postdoctoral Fellowship, College of Public Health, Department of Environmental and Occupational Health, University of Arkansas for Medical Sciences, Little Rock, AR.

Research Interests                                                 Identifying tumor characteristics in breast cancer that influence patient response to therapy.  Genetic variants of mitochondrial uncoupling protein-2 (UCP2) alter mRNA and protein levels.  Given that UCP2 is involved in neutralizing reactive oxygen species, and that many chemotherapeutic agents used to treat breast tumors generate reactive oxygen species, UCP2 expression in breast tumors may be important for therapeutic efficacy.

E-mail: kmercer@uams.edu

 
 

 

Selected Publications::

Zharov, P., Mercer, K.E., Glitovskaya, E.N., and Smeltzer, M.S. (2006) Photothermal nanotherapeutics and nanodiagnostics for selective killing of bacteria targeted with gold nanoparticles.  Biophysical Journal, 90(2):  619-627

Leggas, M., Adachi, M. Scheffer, G.L., Sun, D., Wielinga, P., Du, G., Mercer, K.E., Shuang, Y., Panetta, J.C., Jonhston, B., Scheper, R.J., Stewart, C., and Schuetz, J.D. (2004) MRP4 confers resistance to topotecan and acts as a double agent in protecting the brain from chemotherapy.  Molecular Cell Biology, 24(17):  7612-7621.

Krishnamurthy P., Ross, D.D., Nakanishi, T., Bailey-Dell, K., Zhou, S., Mercer, K.E., Sarkadi, B., Sorrentino, B.P., and Schuetz, J.D. (2004) The stem cell marker Bcrp/ABCG2 enhances hypoxic cell survival through interactions with heme.  Journal of Biological Chemistry, 279(23):  24218-24225.

Mercer, K.E., Ahn, C., Compadre, C.M., and Drake, R.R. (2002) Mutation of herpesvirus thymidine kinase to generate ganciclovir-specific kinases for use in cancer gene therapy.  Protein Engineering, 15(11):  903-911.

Drake, R.R., Pitlyk, K., McMasters, R.A., Mercer, K.E., Young, H., and Moyer, M.P. (2000) Connexin-independent conference of ganciclovir-mediated killing to bystander effect resistant cell lines by a herpes simplex virus thymidine kinase expressing colon cell line.  Molecular Therapy, 2(5):  515-523.

McMasters, R., Wilbert, T.N., Jones, K.E., Pitlyk, K., Saylors, R.L., Moyer, M.P., Chambers, T.C., and Drake, R.R. (2000) Evaluation of two-drug combinations that increase apoptosis and modulate Bak and Bcl-XL expression in human colon tumor cell lines transduced with HSV thymidine kinase.  Cancer Gene Therapy, 7(4):  563-573.

McMasters, R., Jones, K.E., Saylors, R.L., Hendrix, E.M. Moyer, M.P., and Drake, R.R. (1998) Lack of baystander killing in HSV-TK transduced colon cell lines due to deficient connexin 43 gap junction formation.  Human Gene Therapy, 9(15):  2253-2261.








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