HUGO ID Detailed Result 6664


HUGO ID 6664
Symbol LOX
Name lysyl oxidase
#Occurrence 73
#Paper 2

 


PMID Match String Actual String Score Flanking text Edited by Edit
16647138LOXLOX3.3Thus cyclooxygenases (COX), COX lipoxygenases (LOX), LOX and epoxygenases (EPOX) EPOX metabolize AA to prostaglandins thromboxanes leukotrienes 
16647138LOXLOX3.3In contrast COX and LOX metabolize DHA to resolvins docosatrienes and neuroprotectins 
16647138LOXLOX3.3tissues express several different isoforms of PLA 2 COX and LOX under normal or stimulated situations ( Kis et al. 2003 
16647138LOXLOX3.3How the isoforms of PLA 2 COX and LOX enzymes interact with each other remains to be elucidated 
16647138LOXLOX3.3Eicosanoid synthesis through COX and LOX enzymes may involve different AA substrate pools and may be 
16647138LOXLOX3.3In addition to the abovementioned lipid mediators COX LOX and EPOX-catalyzed reactions also produce reactive oxygen species (ROS) ROS 
16647138LOXLOX3.3studies on the multiplicity properties regulation and roles of COX LOX and EPOX in brain tissue 
16647138LOXLOX3.3discussion would initiate more studies on the importance of COX LOX EPOX and their lipid mediators in neurological disorders 
16647138LOXLOX3.3The inhibition of COX LOX and EPOX activities may provide an attractive approach for designing 
16647138LOXLOX3.3Lipoxygenases (LOX) LOX 
16647138LOXLOX3.3at which they oxidize arachidonic acid characterizes the lipoxygenases (LOX) LOX 
16647138LOXLOX3.35-hydroxyeicosatetraenoic acid (5-HETE), 5-HETE involves 5-LOX 12-LOX the most common LOX in the brain ( Hambrecht et al. 1987 with its 
16647138LOXLOX3.3LOX are non-heme iron-containing dioxygenases that insert molecular oxygen into arachidonic 
16647138LOXLOX3.3LOX have a molecular mass of 75 to 78 kDa 
16647138LOXLOX3.3Like non-neural tissues three forms of LOX are present in the brain 
16647138LOXLOX3.3LOX also catalyze a dehydration reaction generating an unstable epoxide intermediate 
16647138LOXLOX3.3In addition to the COX and LOX pathways the cytochrome P450 (CYP450) CYP450 pathways also catalyze arachidonic 
16647138LOXLOX3.3Roles of COX LOX and EPOX in brain tissue 
16647138LOXLOX3.3COX LOX and EPOX are important enzymes involved in the generation of 
16647138LOXLOX3.3enzymes catalyze the conversion of AA into prostaglandins and thromboxanes LOX generates leukotrienes and lipoxins and EPOX activity produces epoxyeicosatrienoic acids 
16647138LOXLOX3.3release AA metabolites by reactions catalyzed by PLA 2 COX LOX and EPOX depends upon not only on neural cell type 
16647138LOXLOX3.3generation of PGE 2 LTB 4 and PAF through COX-2 LOX and acetyl-CoA acetyltransferase reactions respectively 
16647138LOXLOX3.3PLA 2 COX-2 and LOX inhibitors have been used to treat acute inflammation and pain 
16647138LOXLOX3.3Involvement of COX and LOX in neurodegeneration 
16647138LOXLOX3.3degeneration by the activation of caspases PLA 2 COX and LOX resulting in apoptotic cell death 
16647138LOXLOX3.3the observation that inhibitors of caspases PLA 2 COX and LOX block apoptosis ( Farooqui et al. 2004 Farooqui and Horrocks 
16647138LOXLOX3.3evidence suggests that all isoforms of PLA 2 COX and LOX along with caspases are involved in apoptotic cell death 
16647138LOXLOX3.3The stimulation of COX and LOX isoforms and oxidation of arachidonic acid is harmful to neurons 
16647138LOXLOX3.3Involvement of COX and LOX in pain state 
16647138LOXLOX3.3Involvement of COX and LOX in synaptic plasticity 
16647138LOXLOX-generated0.1In brain tissue COX- and LOX-generated metabolites of AA may modulate synaptic plasticity not only through 
16647138LOXLOX3.3effects of arachidonic acid were antagonized by nordihydroguaiaretic acid a LOX inhibitor indicating that its metabolites were responsible for these effects 
16647138LOXLOX3.3Gene deletion studies_amp_#x2014 COX and LOX 
16647138LOXLOX3.3Early indications of an involvement of COX and LOX in traumatic brain injury arose from studies on feline cerebral 
16647138LOXLOX3.3inhibitors of PLA 2 as well as inhibitors of COX LOX and cytochrome P450 isozymes to reverse the depolarization 
16647138LOXLOX3.3of CA1 pyramidal cells following the application of two non-selective LOX inhibitors nordihydroguaiaretic acid and esculentin a selective 5-LOX inhibitor AA861 
16647138LOXLOX3.3cultured neurons to arachidonic acid caused apoptotic neuronal death which LOX and CY450 inhibitors greatly reduced with COX inhibitors having less 
16647138LOXLOX3.3Role of COX LOX and EPOX in excitotoxic injury 
16647138LOXLOX3.3These enzymes include PLA 2 COX-2 LOX and EPOX 
16647138LOXLOX3.3and Bazan 1987 indicating the stimulation of both COX and LOX activity 
16647138LOXLOX3.3The involvement of COX and LOX pathways in AD has been extensively studied in brain tissue 
16647138LOXLOX3.3indicate that arachidonic-acid-mediated neuronal death can be prevented by the LOX inhibitors nordihydroguaiaretic acid AA861 and baicalein and the EPOX inhibitors 
16647138LOXLOX3.3This suggests that LOX and EPOX pathways may also be involved in LOX- and 
16647138LOXLOX-0.1that LOX and EPOX pathways may also be involved in LOX- and EPOX-generated metabolite-induced neurodegeneration ( Kwon et al. 2005 
16647138LOXLOX3.3The neuroprotective effects of LOX and EPOX inhibitors may relate to downregulation of free radical 
16647138LOXLOX3.3At present information on LOX and EPOX expression and their activities is not available for 
16647138LOXLOX3.3No information is available on LOX and EPOX expression and activities in PD brains 
16647138LOXLOX3.3The involvement of LOX and EPOX in the pathogenesis of PD has been studied 
16647138LOXLOX3.3This suggests that a LOX pathway is associated with neuronal degeneration in PD 
16647138LOXLOX3.3Collective evidence suggests that changes in COX LOX and EPOX activities may not be the primary effect but 
16647138LOXLOX3.3Future perspectives interactions among multiple forms of COX LOX and EPOX and their relationship to upstream PLA 2 isoforms 
16647138LOXLOX3.3Although transcripts activities and immunoreactive proteins for COX LOX and EPOX are widely expressed throughout the brain very little 
16647138LOXLOX3.3The occurrence of isoforms of COX LOX and EPOX enzymes in cytoplasm and other subcellular organelles (plasma 
16647138LOXLOX3.3The multiplicity of COX LOX and EPOX enzymes in brain tissue provides diversity in their 
16647138LOXLOX3.3This behavior complicates the analysis of COX LOX and EPOX function at cellular and subcellular levels 
16647138LOXLOX3.3one considers the coupling mechanisms of various isoforms of COX LOX and EPOX with different receptors at cellular and subcellular levels 
16647138LOXLOX3.3Some isoforms of COX LOX and EPOX are constitutively expressed while others are inducible in 
16647138LOXLOX3.3The isoforms of COX LOX and EPOX may not function interchangeably but act in parallel 
16647138LOXLOX3.3It is likely that various isoforms of COX LOX and EPOX act on different cellular pools of arachidonic acid 
16647138LOXLOX3.3Thus the interactions among COX LOX and EPOX-generated metabolites at plasma membrane cytoplasmic and nuclear membrane 
16647138LOXLOX3.3to speculate that coordinated cross talk not only among COX LOX and EPOX isozymes but also with upstream PLA 2 isozymes 
16647138LOXLOX3.3In the nuclear membrane and nucleus COX LOX and EPOX-mediated signaling has the advantage over plasma membrane signaling 
16647138LOXLOX3.3In brain tissue the activities of COX LOX and EPOX isoforms may depend not only on the structural 
16647138LOXLOX3.3The ability of COX LOX and EPOX isoforms to orchestrate complex prostaglandin leukotriene HETE and 
16647138LOXLOX3.3The activation of COX LOX and EPOX isoforms at a subcellular level in neural cells 
16647138LOXLOX3.3Therefore a strict regulation of COX LOX and EPOX isozymes is very important for normal brain function 
16647138LOXLOX3.3As stated above the regulation of COX LOX and EPOX activities is complex and mediated by several factors 
16647138LOXLOX3.3To understand the contribution of isoforms of COX LOX and EPOX in physiological and disease processes a systematic approach 
16647138LOXLOX3.3enzymic mechanisms include three systems COX isozymes which synthesize prostaglandins LOX isozymes which generate hydroxyl derivatives and leukotrienes and EPOX isozymes 
16647138LOXLOX3.3AD PD ALS and CJD stimulation and upregulation of COX LOX and EPOX isozyme activities and the generation of excessive amounts 
16647138LOXLOX3.3These metabolites not only antagonize the effect of COX LOX and EPOX-generated products but also counteract leukocyte infiltration and proinflammatory 
16647138LOXLOX3.3Elevated activities of isoforms of COX LOX and EPOX at cellular and subcellular levels in ischemia and 
15210305lysyl oxidaselysyl oxidase1.0these _amp_#x201c;inducible_amp_#x201d; elements by virtue of their responsiveness to a wide range of cell _amp_#x201c;injury_amp_#x201d; events include thioredoxin lysyl oxidase lo flavin containing monooxygenase fmo1 interleukin i receptor accessory protein il 1racp and a transcript representing a possible 14 3 3 spinal cord isoform [ 59 and 60 ].