نتایج جستجو برای: oct1

تعداد نتایج: 439  

Journal: :British Journal of Pharmacology 2021

Background and Purpose The metabolic activity of cytochrome P450 (CYP) 2D6 is highly variable CYP2D6 genotypes insufficiently explain the extensive intermediate phenotypes, limiting prediction drug response plus adverse reactions. Since prototypic substrates are positively charged, aim this study was to evaluate organic cation transporters (OCTs) multidrug toxin extrusion proteins (MATEs) as po...

2011
Jinsuk Kang Ben Goodman Yixian Zheng Dean Tantin

BACKGROUND Transcription factor Oct1 regulates multiple cellular processes. It is known to be phosphorylated during the cell cycle and by stress, however the upstream kinases and downstream consequences are not well understood. One of these modified forms, phosphorylated at S335, lacks the ability to bind DNA. Other modification states besides phosphorylation have not been described. METHODOL...

2017
Marleen Julia Meyer Tina Seitz Jürgen Brockmöller Mladen Vassilev Tzvetkov

BACKGROUND Ranitidine (Zantac®) is a H2-receptor antagonist commonly used for the treatment of acid-related gastrointestinal diseases. Ranitidine was reported to be a substrate of the organic cation transporters OCT1 and OCT2. The hepatic transporter OCT1 is highly genetically variable. Twelve major alleles confer partial or complete loss of OCT1 activity. The effects of these polymorphisms are...

2015
Jin Qian Xuan Kong Niantao Deng Patrick Tan Haoyan Chen Jilin Wang Zhaoli Li Ye Hu Weiping Zou Jie Xu Jing-Yuan Fang

OBJECTIVE Octamer transcription factor 1 (OCT1) was found to be expressed in intestinal metaplasia and gastric cancer (GC), but the exact roles of OCT1 in GC remain unclear. The objective of this study was to determine the functional and prognostic implications of OCT1 in GC. DESIGN Expression of OCT1 was examined in paired normal and cancerous gastric tissues and the prognostic significance ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2014
Anne T Nies Elke Schaeffeler Heiko van der Kuip Ingolf Cascorbi Oliver Bruhn Michael Kneba Christiane Pott Ute Hofmann Christopher Volk Shuiying Hu Sharyn D Baker Alex Sparreboom Peter Ruth Hermann Koepsell Matthias Schwab

PURPOSE In addition to mutated BCR-ABL1 kinase, the organic cation transporter 1 (OCT1, encoded by SLC22A1) has been considered to contribute to imatinib resistance in patients with chronic myeloid leukemia (CML). As data are conflicting as to whether OCT1 transports imatinib and may serve as a clinical biomarker, we used a combination of different approaches including animal experiments to elu...

2017
Zuolian Shen Jinsuk Kang Arvind Shakya Marcin Tabaka Elke A Jarboe Aviv Regev Dean Tantin

Embryonic stem cells co-express Oct4 and Oct1, a related protein with similar DNA-binding specificity. To study the role of Oct1 in ESC pluripotency and transcriptional control, we constructed germline and inducible-conditional Oct1-deficient ESC lines. ESCs lacking Oct1 show normal appearance, self-renewal and growth but manifest defects upon differentiation. They fail to form beating cardiomy...

Journal: :Genes & development 2009
Jinsuk Kang Matthew Gemberling Mitsuhiro Nakamura Frank G Whitby Hiroshi Handa William G Fairbrother Dean Tantin

Oct1 and Oct4 are homologous transcription factors with similar DNA-binding specificities. Here we show that Oct1 is dynamically phosphorylated in vivo following exposure of cells to oxidative and genotoxic stress. We further show that stress regulates the selectivity of both proteins for specific DNA sequences. Mutation of conserved phosphorylation target DNA-binding domain residues in Oct1, a...

Journal: :Blood 2013
Austen J J Worth Olga Nikolajeva Robert Chiesa Kanchan Rao Paul Veys Persis J Amrolia

not rely on OCT1 transporter activity. Functional OCT1 activity was determined by subtracting the uptake in the presence of amantadine, a specific OCT1 inhibitor according to the authors, from the uptake observed in unmanipulated cells. Examination of the data presented in their Figure 2 suggest that the IUR of imatinib in the absence of 500 mM of amantadine was increased by;50% in OCT1-transfe...

Journal: :The Journal of pharmacology and experimental therapeutics 1998
Y Urakami M Okuda S Masuda H Saito K I Inui

We have isolated a kidney-specific organic cation transporter, rat OCT2, which is distinct from rat OCT1 (Okuda M, Saito H, Urakami Y, Takano M and Inui K (1996) Biochem Biophys Res Commun 224:500-507). In our study, the functional characteristics and membrane localization of OCT1 and OCT2 were investigated by uptake studies using MDCK cells transfected with rat OCT1 or OCT2 cDNA (MDCK-OCT1 or ...

Journal: :The Journal of clinical investigation 2007
Yan Shu Steven A Sheardown Chaline Brown Ryan P Owen Shuzhong Zhang Richard A Castro Alexandra G Ianculescu Lin Yue Joan C Lo Esteban G Burchard Claire M Brett Kathleen M Giacomini

Metformin is among the most widely prescribed drugs for the treatment of type 2 diabetes. Organic cation transporter 1 (OCT1) plays a role in the hepatic uptake of metformin, but its role in the therapeutic effects of the drug, which involve activation of AMP-activated protein kinase (AMPK), is unknown. Recent studies have shown that human OCT1 is highly polymorphic. We investigated whether OCT...

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