Wataru Yamamoto

ORCID: 0000-0003-0574-014X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cardiac electrophysiology and arrhythmias
  • Cancer therapeutics and mechanisms
  • Neuroscience and Neural Engineering
  • Drug Transport and Resistance Mechanisms
  • Colorectal Cancer Treatments and Studies
  • Ion channel regulation and function
  • Genomics, phytochemicals, and oxidative stress
  • Cancer Treatment and Pharmacology
  • Cellular transport and secretion
  • Cardiac Arrhythmias and Treatments
  • Lung Cancer Research Studies
  • Bioactive Compounds and Antitumor Agents
  • Gastric Cancer Management and Outcomes
  • Exercise and Physiological Responses
  • Atrial Fibrillation Management and Outcomes
  • Chemical Reactions and Isotopes
  • Cancer Mechanisms and Therapy
  • Lung Cancer Treatments and Mutations
  • Pain Mechanisms and Treatments
  • Receptor Mechanisms and Signaling
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Pancreatic function and diabetes
  • Ion Channels and Receptors
  • Calcium signaling and nucleotide metabolism
  • Renal and Vascular Pathologies

Saitama Medical University
2006-2025

Social Insurance Saitama Chuo Hospital
2025

Teijin (Japan)
2010-2017

Japan Medical Association
2017

Tokyo University of Science
2014-2015

Yokohama City University Medical Center
2015

Yokohama City University
2015

Kanagawa Cancer Center
2013

Kanagawa Prefectural Hospital Organization
2013

New York Blood Center
2011

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) are anticipated to be a useful tool for conducting proarrhythmia risk assessments of drug candidates. However, torsadogenic prediction paradigm using hiPSC-CMs has not yet been fully established.Extracellular field potentials (FPs) were recorded from the multi-electrode array (MEA) system. The effects on FPs evaluated with 60 drugs, including 57 various clinical risks. Actual concentrations in medium measured equilibrium...

10.1016/j.vascn.2016.12.003 article EN cc-by-nc-nd Journal of Pharmacological and Toxicological Methods 2016-12-10

The aims of this study were to (1) characterize basic electrophysiological elements human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) that correspond clinical properties such as QT-RR relationship, (2) determine the applicability QT correction and analysis methods, (3) if how these in-vitro parameters could be used in risk assessment for adverse drug-induced effects Torsades de pointes (TdP). Field potential recordings obtained from commercially available hiPSC-CMs using...

10.1371/journal.pone.0167348 article EN cc-by PLoS ONE 2016-12-06

The acetylcholine-activated K(+) current (I(K,ACh)) is a novel candidate for atrial-specific antiarrhythmic therapy. present study investigates the involvement of I(K,ACh) in atrial fibrillation (AF) using NTC-801, potent and selective blocker.The effects substituted 4-(aralkylamino)-2,2-dimethyl-3,4-dihydro-2H-benzopyran-3-ol, on other cardiac ionic currents (I(Na), I(CaL), I(to), I(Kur), I(Kr), I(Ks), I(Kl), I(KATP), I(f)) ventricular action potentials were examined vitro. NTC-801 potently...

10.1161/circep.110.951608 article EN Circulation Arrhythmia and Electrophysiology 2010-12-15

S‐1 is an oral anticancer agent composed of tegafur (FT), 5‐chloro‐2,4‐dihydroxypyridine (CDHP), and potassium oxonate. CDHP added to prevent degradation 5‐fluorouracil (5‐FU) by inhibiting dihydropyrimidine dehydrogenase. CYP2A6 involved in the biotransformation FT 5‐FU. Thus, we prospectively analyzed effects genotype, plasma level CDHP, patient characteristics on pharmacokinetic (PK) variability Fifty‐four Japanese patients with metastatic or recurrent cancers who received were enrolled....

10.1111/j.1349-7006.2008.00773.x article EN other-oa Cancer Science 2008-04-01

ATP-binding cassette, sub-family C, number 2 (ABCC2) is involved in the biliary excretion of irinotecan and its metabolites, SN-38 glucuronide. Effects ABCC2 genotype on pharmacokinetics (PK) metabolites were examined Japanese patients with metastatic colorectal cancer receiving plus infusional 5-fluorouracil/leucovorin (FOLFIRI). genotypes (−1549G>A, −1023G>A, −1019A>G, −24C>T, 1249G>A 3972C>T) haplotypes analyzed for 67 cancer. PK was also a subset 31 FOLFIRI. Relationship between or...

10.1248/bpb.31.2137 article EN Biological and Pharmaceutical Bulletin 2008-01-01

Mechanical allodynia, such as static and dynamic is a prominent feature of neuropathic pain syndromes. The aim this study to characterize primary sensory neurons mediating the mechanical allodynia in rat chronic constriction injury (CCI) model with combination pharmacological histological investigations. N-(4-Tertiarybutylphenyl)-4-(3-chloropyridin-2-yl) tetrahydropyrazine-1(2H)-carbox-amide (BCTC), selective competitive antagonist vanilloid receptor 1 (TRPV1), resiniferatoxin, which causes...

10.1211/jpp.60.6.0006 article EN Journal of Pharmacy and Pharmacology 2008-05-13

Irinotecan (CPT-11) is a camptothecin analog with low (about 10-20%) and variable oral bioavailability in animal models. Here, Caco-2 cells were used to evaluate the transepithelial transport of CPT-11 its metabolites. demonstrated significant expression P-glycoprotein (P-gp), multidrug resistance-associated protein canalicular multispecific organic anion transporter. Both lactone carboxylate forms SN-38 actively transported across cell monolayers, mainly by apical-localized P-gp pump....

10.1097/00001813-200106000-00003 article EN Anti-Cancer Drugs 2001-06-01

The present study examines the effects of NTC-801, a highly selective acetylcholine (ACh) receptor-activated potassium (KACh) channel blocker, on atrial fibrillation (AF) in canine model with electrical remodeling. An experimental substrate for AF was created dogs via left (LA) tachypacing (400 bpm, 3-5 weeks). dofetilide, and flecainide were intravenously infused 15 minutes, inducibility, effective refractory period (ERP), conduction velocity examined. effect NTC-801 termination also...

10.1097/fjc.0000000000000065 article EN Journal of Cardiovascular Pharmacology 2013-12-17

We attempted to determine a target of chemotherapy specific glioblastoma cells ensure favorable response anticancer drugs, through comparison in biologic nature related drug resistance with other types cancer cells. Using 13 human cell lines including 3 lines, gene expression analysis and biochemical quantitative assay were performed for total 12 properties, which have been linked action. Although most genes resistance, such as MDR1, MRP, MGMT GSTpi, overexpressed T98G, U-373MG, U-251MG...

10.3892/ijo.16.2.295 article EN International Journal of Oncology 2000-02-01

The precise mechanisms of resistance to camptothecin (CPT)-derived DNA topoisomerase (topo I) inhibitors and the determinants remain unclear. We found that a repair protein, O(6)-methylguanine-DNA methyltransferase (MGMT), participated in irinotecan hydrochloride (CPT-11), its active metabolite SN-38, novel CPT derivative, DX-8951f. In 17 human cancer cell lines, MGMT gene expression level closely correlated with sensitivity derivatives, inhibition activity by nontoxic 5 microM...

10.1111/j.1349-7006.2002.tb01205.x article EN other-oa Japanese Journal of Cancer Research 2002-01-01

The dynamic assembly and disassembly of actin filaments is essential for the formation transport vesicles during endocytosis. In yeast, two types structures, namely cortical patches cytoplasmic cables, play a direct role in endocytosis, but how their interaction regulated remains unclear. Here we show that Srv2/CAP, an evolutionally conserved regulator, required efficient endocytosis due to its aid initial vesicle invagination cables these move along. Deletion SRV2 gene results appearance...

10.1242/jcs.176651 article EN Journal of Cell Science 2015-01-01

β-tubulin (β-TUB), Bcl-XL, and additionally glutathione S-transferase π (GSTπ) were found to participate in sensitivity docetaxel (TXT) 7 human gastrointestinal cancer cell lines. The gene expression level of β-TUB, GSTπ was closely correlated with the IC50 for TXT. β-TUB amount related TXT resistance, GST activity 30-min treatment setting. Bcl-XL transfection increased resistance COLO201 cells, whereas inhibition by ethacrynic acid enhanced cytotoxicity. Continuous expression, but mRNA...

10.3892/ijo.20.2.333 article EN International Journal of Oncology 2002-02-01

Gefitinib (Iressa) is an anticancer drug that selectively inhibits tyrosine kinases of epidermal growth factor receptor. might affect CYP3A4-mediated metabolism, since the a substrate human CYP3A. In this study, we evaluated effects gefitinib on metabolism catalyzed by CYP3A4. The formation NPC (7-ethyl-10-(4-amino-1-piperidino)carbonyloxycamptothecin) and APC (7-ethyl-10-[4-<i>N</i>-(5-aminopentanoic acid)-1-piperidino]carbonyloxycamptothecin) from irinotecan were examined with use liver...

10.1124/dmd.105.006205 article EN Drug Metabolism and Disposition 2005-08-24

ObjectiveThis phase I/II study determined the recommended dose of FOLFIRI (irinotecan, infusional 5-fluorouracil and leucovorin) for Japanese patients with advanced colorectal cancer, evaluated safety at in without UDP-glucuronosyltransferase 1A1*28 allele which caused reduced enzyme expression.

10.1093/jjco/hyq197 article EN Japanese Journal of Clinical Oncology 2010-10-21

"Musculoskeletal pain may be associated with imatinib withdrawal syndrome in chronic myeloid leukemia patients." Leukemia & Lymphoma, 57(2), pp. 496–497

10.3109/10428194.2015.1064531 article EN Leukemia & lymphoma/Leukemia and lymphoma 2015-06-22

The author presents a statistical analysis of foreign bodies in the air and food passages based on data obtained from 37 medical school hospitals throughout Japan.Of 7371 total number cases 1571 (20.3%) were respiratory tract 5800 (79.7%) passage; latter constitutes 3.6 times former.Sex: Of number, 4365 (59.3%) males 3006 (40.7%) females: ratio between two sexes is 3 to 2. In passage accounted 891 females 650, 3444 2356 respectively.Age: my experience youngest patient was one month old...

10.2468/jbes.10.91 article EN Nihon Kikan Shokudoka Gakkai Kaiho 1959-01-01

A network composed of activation and inactivation pathways to regulate mitomycin C (MMC) action is suggested exist in human cancer cells. COLO201 colon cells were stably transfected with NQO1 cDNA that encodes NAD(P)H:quinone oxidoreductase (DT-diaphorase, DTD), a clonal cell line about 57-fold elevated DTD activity was obtained. Northern analysis revealed expression the NADPH:cytochrome P450 reductase (P450 reductase) gene decreased transfectant, COLO201/NQO1, associated increase...

10.1111/j.1349-7006.1999.tb00785.x article EN other-oa Japanese Journal of Cancer Research 1999-05-01
Coming Soon ...