نتایج جستجو برای: as3mt gene

تعداد نتایج: 1141406  

2008
Sujata De Chaudhuri Pritha Ghosh Nilendu Sarma Papiya Majumdar Tanmoy Jyoti Sau Santanu Basu Susanta Roychoudhury Kunal Ray Ashok K. Giri

BACKGROUND Individual variability in arsenic metabolism may underlie individual susceptibility toward arsenic-induced skin lesions and skin cancer. Metabolism of arsenic proceeds through sequential reduction and oxidative methylation being mediated by the following genes: purine nucleoside phosphorylase (PNP), arsenic (+3) methyltransferase (As3MT), glutathione S-transferase omega 1 (GSTO1), an...

2011
Xuefeng Ren Maria Aleshin William J. Jo Russel Dills David A. Kalman Christopher D. Vulpe Martyn T. Smith Luoping Zhang

BACKGROUND In humans, inorganic arsenic (iAs) is metabolized to methylated arsenical species in a multistep process mainly mediated by arsenic (+3 oxidation state) methyltransferase (AS3MT). Among these metabolites is monomethylarsonous acid (MMAIII), the most toxic arsenic species. A recent study in As3mt-knockout mice suggests that unidentified methyltransferases could be involved in alternat...

Journal: :Toxicology and applied pharmacology 2009
Ya-Tang Liao Wan-Fen Li Chien-Jen Chen Ronald J Prineas Wei J Chen Zhu-Ming Zhang Chien-Wen Sun Shu-Li Wang

Arsenic has been linked to increased prevalence of cancer and cardiovascular disease (CVD), but the long-term impact of arsenic exposure remains unclear. Human paraoxonase (PON1) is a high-density lipoprotein-associated antioxidant enzyme which hydrolyzes oxidized lipids and is thought to be protective against atherosclerosis, but evidence remains limited to case-control studies. Only recently ...

2012
Brandon L. Pierce Muhammad G. Kibriya Lin Tong Farzana Jasmine Maria Argos Shantanu Roy Rachelle Paul-Brutus Ronald Rahaman Muhammad Rakibuz-Zaman Faruque Parvez Alauddin Ahmed Iftekhar Quasem Samar K. Hore Shafiul Alam Tariqul Islam Vesna Slavkovich Mary V. Gamble Md Yunus Mahfuzar Rahman John A. Baron Joseph H. Graziano Habibul Ahsan

Arsenic contamination of drinking water is a major public health issue in many countries, increasing risk for a wide array of diseases, including cancer. There is inter-individual variation in arsenic metabolism efficiency and susceptibility to arsenic toxicity; however, the basis of this variation is not well understood. Here, we have performed the first genome-wide association study (GWAS) of...

Journal: :Chemical Research in Toxicology 2014

2015
Andrea M. Allan Alexander K. Hafez Matthew T. Labrecque Elizabeth R. Solomon M. Nabil Shaikh Xianyun Zheng Abdulmehdi Ali

Previously we have shown that prenatal moderate arsenic exposure (50 ppb) disrupts glucocorticoid receptor (GR) programming and that these changes continue into adolescence in males. However, it was not clear what the molecular mechanisms were promoting these GR programming changes or if these changes occurred in arsenic-exposed females. In the present studies, we assessed the effects of arseni...

2017
Fatemeh Farhid Fatemeh Nadali Bahram Chahardouli Saeed Mohammadi Shahrbano Rostami Kamran Alimoghaddam Ardeshir Ghavamzadeh

Background: To determine the frequency of the single nucleotide polymorphism M287T in exon 9 of the AS3MT gene in Iranian population and to assess the difference in allele frequencies with other ethnicities. Subjects and Methods: Genotyping analysis was performed on 150 healthy subjects using the PCR-RFLP assay. We used chi-square analysis to check the deviation from Hardy-Weinberg equilibrium ...

2012
Huiqi Li Karin Engström Marie Vahter Karin Broberg

Inorganic arsenic is a strong carcinogen, possibly by interaction with the telomere length. The aim of the study was to evaluate how chronic arsenic exposure from drinking water as well as the arsenic metabolism efficiency affect the individual telomere length and the expression of telomere-related genes. Two hundred two women with a wide range in exposure to arsenic via drinking water (3.5-200...

2017
Poojitha Balakrishnan Dhananjay Vaidya Nora Franceschini V. Saroja Voruganti Matthew O. Gribble Karin Haack Sandra Laston Jason G. Umans Kevin A. Francesconi Walter Goessler Kari E. North Elisa Lee Joseph Yracheta Lyle G. Best Jean W. MacCluer Jack Kent Shelley A. Cole Ana Navas-Acien

BACKGROUND Metabolism of inorganic arsenic (iAs) is subject to inter-individual variability, which is explained partly by genetic determinants. OBJECTIVES We investigated the association of genetic variants with arsenic species and principal components of arsenic species in the Strong Heart Family Study (SHFS). METHODS We examined variants previously associated with cardiometabolic traits (...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2014
Puttappa R Dodmane Lora L Arnold David E Muirhead Shugo Suzuki Masanao Yokohira Karen L Pennington Bhavana J Dave Xiufen Lu X Chris Le Samuel M Cohen

Inorganic arsenic (iAs) is a known human carcinogen at high exposures, increasing the incidences of urinary bladder, skin, and lung cancers. In most mammalian species, ingested iAs is excreted mainly through urine primarily as dimethylarsinic acid (DMA(V)). In wild-type (WT) mice, iAs, DMA(V), and dimethylarsinous acid (DMA(III)) exposures induce formation of intramitochondrial urothelial inclu...

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