Biomedical Research Education & Training
Faculty Member

Ho, Richard Hsinshin, M.D.
Associate Professor of Pediatrics

Lab Url: N/A

Phone Number: 615-936-2802

Email Address: richard.ho@vanderbilt.edu

Ho, Richard's picture
Academic history
M.S.C.I., Vanderbilt University School of Medicine
M.D., Vanderbilt University
B.S., Duke University

Office Address   Mailing Address

338 PRB

397 PRB Vanderbilt University Medical Center 37232


Research Keywords
Drug uptake transporters Pharmacogenetics of drug transport,Cancer,DRUG metabolism,Genetics,Molecular medicine,Pharmacokinetics,Pharmacology,Polymorphism

Patient Care Specialty
Pediatric Hematology/Oncology

Research Specialty
Drug Uptake Transporters and Chemotherapy Disposition

Research Description
Our research program focuses on the molecular mechanisms by which drug transporters contribute to overall chemotherapy disposition and interindividual response to drug therapy in cancer therapy. Drug transport proteins have important roles in modulating the absorption, distribution, and excretion of many drugs and drug metabolites as well as endogenous substances. They tend to be highly expressed in tissues of importance to drug disposition, including the liver, intestine, kidney and at the blood:brain barrier. To this extent, a major focus in my lab centers on the contribution of specific drug uptake transporters, in particular the organic anion transporting polypeptide (OATP) family and bile acid uptake transporters, to the disposition of pediatric chemotherapeutic agents. In addition, another area of major focus is cancer pharmacogenetics, the study of the role of inheritance in the individual variation in chemotherapy response. Projects are primarily laboratory based with translational promise and rely on background knowledge in the fields of molecular biology and clinical pharmacology. We utilize a number of in vitro techniques to study these transporter proteins, including vaccinia-based expression systems for functional transport studies, drug screening, and drug inhibition studies, protein expression studies utilizing western analysis, immunohistochemistry and immunofluorescent confocal microscopy, and generation of polarized stable cell lines for directional transport studies and comprehensive kinetic analysis. We have also integrated animal models utilizing recently generated knockout mice for various transporter genes into our research program for in vitro:in vivo correlative data in our drug disposition studies.

Moreover, our research has important implications for drug discovery and experimental therapeutics. ADME (absorption, distribution, metabolism and excretion) deficiency is one of the major causes of failure during drug development. In vitro ADME screening of potential lead compounds and drug candidates in the early discovery phase has been employed as a more cost-effective approach to identify compounds that have unfavorable drug-like characteristics. Many compounds with promising pharmacological characteristics never become drugs because they have poor solubility, quickly degrade in biological fluids and tissues or rapidly metabolized in the liver. Utilizing our in vitro screening transport and detailed studies of kinetic analysis, we are able to identify potential drug compounds as substrates for a complement of drug uptake and efflux transporters, which may have important implications not only for drug disposition in vivo, but also for drug toxicity, efficacy and tissue targeting. Furthermore, as many of the transporters we study are known to be polymorphic, we have the ability to assess transporter polymorphisms for differential transport of drugs and/or drug metabolites, which may have significant consequences for determining the interindividual response to anticancer agents.
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Clinical Interests
Clinical pharmacology
Drug disposition and toxicity
Pharmacogenetics and pharmacokinetics
Oncology

Publications
Frangoul, H, Min, E, Wang, W, Chandrasekhar, R, Calder, C, Evans, M, Manes, B, Bruce, K, Brown, V, Ho, R, Domm, J. Incidence and risk factors for hypogammaglobulinemia in pediatric patients following allo-SCT. Bone Marrow Transplant, 48(11), 1456-9, 2013

Lavoie Smith, EM, Li, L, Hutchinson, RJ, Ho, R, Burnette, WB, Wells, E, Bridges, C, Renbarger, J. Measuring vincristine-induced peripheral neuropathy in children with acute lymphoblastic leukemia. Cancer Nurs, 36(5), E49-60, 2013

Minson, KA, Prasad, P, Vear, S, Borinstein, S, Ho, R, Domm, J, Frangoul, H. t(17;19) in Children with Acute Lymphocytic Leukemia: A Report of 3 Cases and a Review of the Literature. Case Rep Hematol, 2013, 563291, 2013

Vear, SI, Stein, CM, Ho, RH. Warfarin pharmacogenomics in children. Pediatr Blood Cancer, 60(9), 1402-7, 2013

Degorter, MK, Ho, RH, Leake, BF, Tirona, RG, Kim, RB. Interaction of Three Regiospecific Amino Acid Residues Is Required for OATP1B1 Gain of OATP1B3 Substrate Specificity. Mol Pharm, 9(4), 986-95, 2012

Korhonen, K, Lovvorn, HN, Koyama, T, Koehler, E, Calder, C, Manes, B, Evans, M, Bruce, K, Ho, RH, Domm, J, Frangoul, H. Incidence, risk factors, and outcome of pneumatosis intestinalis in pediatric stem cell transplant recipients. Pediatr Blood Cancer, 58(4), 616-20, 2012

McManus, MP, Wang, L, Calder, C, Manes, B, Evans, M, Bruce, K, Ho, RH, Domm, J, Frangoul, H. Comparison of pre-cryopreserved and post-thaw-and-wash-nucleated cell count on major outcomes following unrelated cord blood transplant in children. Pediatr Transplant, 2012

Eckrich, MJ, Yang, E, Domm, J, Ho, R, Calder, C, Manes, B, Bleesing, J, Frangoul, H. A unique clinical presentation of X-linked lymphoproliferative syndrome with a novel mutation in SH2D1A and review of the literature. J Pediatr Hematol Oncol, 33(1), e39-42, 2011

Esbenshade, AJ, Ho, RH, Shintani, A, Zhao, Z, Smith, LA, Friedman, DL. Dapsone-induced methemoglobinemia: a dose-related occurrence. Cancer, 117(15), 3485-92, 2011 PMCID:3044558

Ho, RH, Leake, BF, Urquhart, BL, Gregor, JC, Dawson, PA, Kim, RB. Functional characterization of genetic variants in the apical sodium-dependent bile acid transporter (ASBT; SLC10A2). J Gastroenterol Hepatol, 26(12), 1740-8, 2011

Schwarz, UI, Meyer zu Schwabedissen, HE, Tirona, RG, Suzuki, A, Leake, BF, Mokrab, Y, Mizuguchi, K, Ho, RH, Kim, RB. Identification of novel functional organic anion-transporting polypeptide 1B3 polymorphisms and assessment of substrate specificity. Pharmacogenet Genomics, 21(3), 103-14, 2011 PMCID:3044558

Ho, RH, Leake, BF, Kilkenny, DM, Meyer Zu Schwabedissen, HE, Glaeser, H, Kroetz, DL, Kim, RB. Polymorphic variants in the human bile salt export pump (BSEP; ABCB11): functional characterization and interindividual variability. Pharmacogenet Genomics, 20(1), 45-57, 2010 PMCID:2883163

Eckrich, MJ, Domm, J, Ho, R, Whitlock, JA, Frangoul, H. Autologous stem cell transplant in a patient with Down syndrome and relapsed Hodgkin lymphoma. Pediatr Blood Cancer, 53(7), 1327-8, 2009

Frangoul, H, Wang, L, Harrell, FE, Ho, R, Domm, J. Preengraftment syndrome after unrelated cord blood transplant is a strong predictor of acute and chronic graft-versus-host disease. Biol Blood Marrow Transplant, 15(11), 1485-8, 2009

Piro, CC, Crossno, CL, Collier, A, Ho, R, Koyama, T, Frangoul, H. Initial vancomycin dosing in pediatric oncology and stem cell transplant patients. J Pediatr Hematol Oncol, 31(1), 3-7, 2009

Lavin, VA, Hamid, R, Patterson, J, Alford, C, Ho, R, Yang, E. Use of human androgen receptor gene analysis to aid the diagnosis of JMML in female noonan syndrome patients. Pediatr Blood Cancer, 51(2), 298-302, 2008

Meyer zu Schwabedissen, HE, Tirona, RG, Yip, CS, Ho, RH, Kim, RB. Interplay between the nuclear receptor pregnane X receptor and the uptake transporter organic anion transporter polypeptide 1A2 selectively enhances estrogen effects in breast cancer. Cancer Res, 68(22), 9338-47, 2008 PMCID:2597047

Urquhart, BL, Ware, JA, Tirona, RG, Ho, RH, Leake, BF, Schwarz, UI, Zaher, H, Palandra, J, Gregor, JC, Dresser, GK, Kim, RB. Breast cancer resistance protein (ABCG2) and drug disposition: intestinal expression, polymorphisms and sulfasalazine as an in vivo probe. Pharmacogenet Genomics, 18(5), 439-48, 2008 PMCID:2597047

Bagatell, R, Gore, L, Egorin, MJ, Ho, R, Heller, G, Boucher, N, Zuhowski, EG, Whitlock, JA, Hunger, SP, Narendran, A, Katzenstein, HM, Arceci, RJ, Boklan, J, Herzog, CE, Whitesell, L, Ivy, SP, Trippett, TM. Phase I pharmacokinetic and pharmacodynamic study of 17-N-allylamino-17-demethoxygeldanamycin in pediatric patients with recurrent or refractory solid tumors: a pediatric oncology experimental therapeutics investigators consortium study. Clin Cancer Res, 13(6), 1783-8, 2007

Ho, RH, Choi, L, Lee, W, Mayo, G, Schwarz, UI, Tirona, RG, Bailey, DG, Michael Stein, C, Kim, RB. Effect of drug transporter genotypes on pravastatin disposition in European- and African-American participants. Pharmacogenet Genomics, 17(8), 647-56, 2007 PMCID:2597047

Ho, RH, Tirona, RG, Leake, BF, Glaeser, H, Lee, W, Lemke, CJ, Wang, Y, Kim, RB. Drug and bile acid transporters in rosuvastatin hepatic uptake: function, expression, and pharmacogenetics. Gastroenterology, 130(6), 1793-806, 2006

McRae, MP, Lowe, CM, Tian, X, Bourdet, DL, Ho, RH, Leake, BF, Kim, RB, Brouwer, KL, Kashuba, AD. Ritonavir, saquinavir, and efavirenz, but not nevirapine, inhibit bile acid transport in human and rat hepatocytes. J Pharmacol Exp Ther, 318(3), 1068-75, 2006

Calder, C, Hays, SR, Manes, B, Lavin, VA, Ho, RH, Frangoul, H. Successful bone marrow harvest during pregnancy. Bone Marrow Transplant, 35(6), 631-2, 2005

Ho, RH, Kim, RB. Transporters and drug therapy: implications for drug disposition and disease. Clin Pharmacol Ther, 78(3), 260-77, 2005

Jones, E, Koyama, T, Ho, RH, Kuttesch, J, Shankar, S, Whitlock, JA, Cartwright, J, Frangoul, H. Safety and efficacy of a continuous infusion, patient-controlled antiemetic pump for children receiving emetogenic chemotherapy. Pediatr Blood Cancer, 48(3), 330-332, 2005

Ho, RH, Johnson, J, Dev, VG, Whitlock, JA. A novel t(2;20)(q35;p12) in embryonal rhabdomyosarcoma. Cancer Genet Cytogenet, 151(1), 73-7, 2004

Ho, RH, Leake, BF, Roberts, RL, Lee, W, Kim, RB. Ethnicity-dependent polymorphism in Na+-taurocholate cotransporting polypeptide (SLC10A1) reveals a domain critical for bile acid substrate recognition. J Biol Chem, 279(8), 7213-22, 2004


Postdoctoral Position Available
No

Postdoctoral Position Details
N/A

Updated Date
11/14/2013