Document Information


PMID 19118282  (  )
Title A new look at the eye: aldosterone and mineralocorticoid receptors as novel targets in retinal vasculopathy.
Abstract

NOTE: Color highlight is limited to the abstract and SciMiner text-mining mode. If you see much more identified targets below from "Targets by SciMiner Summary" and "Targets by SciMiner Full list", they may have been identified from the full text.



Targets by SciMiner Summary

HUGO ID Symbol Target Name #Occur ActualStr
12680VEGFAvascular endothelial growth factor A10VEGF | vascular endothelial growth factor |
4057G6PDglucose-6-phosphate dehydrogenase8glucose 6 phosphate dehydrogenase g6pd | G6PD |
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)8angiotensinogen | ang ii | Ang |
14874NOX5NADPH oxidase, EF-hand calcium binding domain 57nadph oxidase |
7891NOX4NADPH oxidase 45Nox4 |
9958RENrenin4renin |
2578CYBBcytochrome b-245, beta polypeptide (chronic granulomatous disease)3Nox2 |
7660NCF1neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1)2p47phox |
2707ACEangiotensin I converting enzyme (peptidyl-dipeptidase A) 12angiotensin converting enzyme |
2577CYBAcytochrome b-245, alpha polypeptide2p22phox |
7661NCF2neutrophil cytosolic factor 2 (65kDa, chronic granulomatous disease, autosomal 2)1p67phox |
10618CCL2chemokine (C-C motif) ligand 21monocyte chemoattractant protein 1 |
2592CYP11B2cytochrome P450, family 11, subfamily B, polypeptide 21aldosterone synthase |
5464IGF1insulin-like growth factor 1 (somatomedin C)1insulin like growth factor 1 |
5208HSD11B1hydroxysteroid (11-beta) dehydrogenase 11hsd1 |
18305ATP6AP2ATPase, H+ transporting, lysosomal accessory protein 21renin receptor |
9393PRKCAprotein kinase C, alpha1protein kinase c |
6018IL6interleukin 6 (interferon, beta 2)1interleukin 6 |
7662NCF4neutrophil cytosolic factor 4, 40kDa1p40phox |
7979NR3C2nuclear receptor subfamily 3, group C, member 21mineralocorticoid receptor |
11765TGFAtransforming growth factor, alpha1transforming growth factor |

 


Targets by SciMiner Full list

HUGO ID Symbol Name ActualStr Score FlankingText
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4Activated MR inhibits G6PD and increases Nox4-based NADPH oxidase localized in the plasma membrane
12680VEGFAvascular endothelial growth factor AVEGF3.5of ROS (oxidative oxidative stress stimulates redox-sensitive pathways possibly involving VEGF to promote angiogenesis inflammation and fibrosis which underlie retinal vasculopathy
7891NOX4NADPH oxidase 4Nox41.2Key Words Nox4 _amp_#149 G6PD _amp_#149 angiogenesis _amp_#149 spironolactone
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4Key Words Nox4 _amp_#149 G6PD _amp_#149 angiogenesis _amp_#149 spironolactone
12680VEGFAvascular endothelial growth factor AVEGF3.5vascular permeability and angiogenesis is vascular endothelial growth factor (VEGF), VEGF which signals through protein kinase C mitogen-activated protein kinases and
12680VEGFAvascular endothelial growth factor AVEGF3.5mitogen-activated protein kinases and reactive oxygen species (ROS) ROS through VEGF receptor 1 (fms-like fms-like tyrosine kinase-1 and VEGF receptor 2
12680VEGFAvascular endothelial growth factor AVEGF3.5ROS through VEGF receptor 1 (fms-like fms-like tyrosine kinase-1 and VEGF receptor 2 (fetal fetal liver kinase-1
12680VEGFAvascular endothelial growth factor AVEGF3.5VEGF expression is increased by glucose advanced glycation end products transforming
12680VEGFAvascular endothelial growth factor AVEGF3.5Blocking effects of VEGF with intravitreal anti-VEGF drugs such as pegaptanib ranibizumab and bevacizumab
12680VEGFAvascular endothelial growth factor AVEGF3.5Moreover VEGF is pleiotropic affecting a broad spectrum of endothelial neuronal and
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)Ang2.0more effective in treating retinal vasculopathy especially because angiotensin (Ang) Ang II and aldosterone are proinflammatory fibrogenic and angiogenic and because
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)Ang2.0Renin angiotensin-converting enzyme angiotensinogen Ang II and Ang II receptors have been shown at the
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)Ang2.0Renin angiotensin-converting enzyme angiotensinogen Ang II and Ang II receptors have been shown at the mRNA and protein
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)Ang2.0that interruption of the RAS with angiotensin-converting enzyme inhibitors or Ang II type 1 (AT AT 1 receptor (AT AT 1
12680VEGFAvascular endothelial growth factor AVEGF3.5aldosterone increases proliferation and tubulogenesis to a similar magnitude as VEGF and that this is associated with activation of the MR
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4aldosterone influences redox state are downregulation of glucose-6-phosphate dehydrogenase (G6PD), G6PD which is a major source of reduced NAD(P)H, NAD P
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4Wilkinson-Berka et al demonstrated that aldosterone decreases G6PD mRNA expression in retinal endothelial cells and that retinal nicotinamide
2578CYBBcytochrome b-245, beta polypeptide (chronic granulomatous disease)Nox20.0phosphate reduced oxidase 4 (NADPH NADPH oxidase Nox 4 a Nox2 homolog is upregulated in oxygen-induced retinopathy ( Figure
7891NOX4NADPH oxidase 4Nox41.2In oxygen-induced retinopathy Nox4 expression was increased especially in the presence of aldosterone and
7891NOX4NADPH oxidase 4Nox41.2Nox4 is expressed in nonphagocytic cells including vascular endothelium is localized
2578CYBBcytochrome b-245, beta polypeptide (chronic granulomatous disease)Nox20.0vascular endothelium is localized to the endoplasmic reticulum and unlike Nox2 it only requires p22phox and not p47phox p40phox or p67phox
2577CYBAcytochrome b-245, alpha polypeptidep22phox0.0to the endoplasmic reticulum and unlike Nox2 it only requires p22phox and not p47phox p40phox or p67phox for its activation
7660NCF1neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1)p47phox0.0reticulum and unlike Nox2 it only requires p22phox and not p47phox p40phox or p67phox for its activation
7662NCF4neutrophil cytosolic factor 4, 40kDap40phox0.0and unlike Nox2 it only requires p22phox and not p47phox p40phox or p67phox for its activation
7661NCF2neutrophil cytosolic factor 2 (65kDa, chronic granulomatous disease, autosomal 2)p67phox0.0Nox2 it only requires p22phox and not p47phox p40phox or p67phox for its activation
7891NOX4NADPH oxidase 4Nox41.2Of the Nox proteins Nox4 has been shown to be strongly proangiogenic possibly through upregulation
12680VEGFAvascular endothelial growth factor AVEGF3.5been shown to be strongly proangiogenic possibly through upregulation of VEGF signaling
2578CYBBcytochrome b-245, beta polypeptide (chronic granulomatous disease)Nox20.0Nox2 p22phox and p47phox classic subunits of NADPH oxidase have also
2577CYBAcytochrome b-245, alpha polypeptidep22phox0.0Nox2 p22phox and p47phox classic subunits of NADPH oxidase have also been
7660NCF1neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1)p47phox0.0Nox2 p22phox and p47phox classic subunits of NADPH oxidase have also been implicated in
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4Moreover the fact that retinal gene expression of G6PD is reduced and that of Nox4 is increased does not
7891NOX4NADPH oxidase 4Nox41.2retinal gene expression of G6PD is reduced and that of Nox4 is increased does not necessarily mean that protein levels are
4057G6PDglucose-6-phosphate dehydrogenaseG6PD3.4mean that protein levels are changed nor that activity of G6PD or NADPH oxidase is altered
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0activated mr inhibits g6pd and increases nox4 based nadph oxidase localized in the plasma membrane and endoplasmic reticulum er to generate the ros superoxide o[ 2] and h 2 o 2 .
7979NR3C2nuclear receptor subfamily 3, group C, member 2mineralocorticoid receptor1.0here we learn that similar to what has been suggested in the heart brain and vasculature the eye has a dynamic aldosterone mineralocorticoid receptor mr system that plays an important pathophysiological role in the development of retinal vasculopathy.
9393PRKCAprotein kinase C, alphaprotein kinase c1.0among the many factors that have been implicated in vascular permeability and angiogenesis is vascular endothelial growth factor vegf which signals through protein kinase c mitogen activated protein kinases and reactive oxygen species ros through vegf receptor 1 fms like tyrosine kinase 1 and vegf receptor 2 fetal liver kinase 1 .
12680VEGFAvascular endothelial growth factor Avascular endothelial growth factor1.0among the many factors that have been implicated in vascular permeability and angiogenesis is vascular endothelial growth factor vegf which signals through protein kinase c mitogen activated protein kinases and reactive oxygen species ros through vegf receptor 1 fms like tyrosine kinase 1 and vegf receptor 2 fetal liver kinase
5464IGF1insulin-like growth factor 1 (somatomedin C)insulin like growth factor 11.0vegf expression is increased by glucose advanced glycation end products transforming growth factor b and insulin like growth factor 1 all of which are modulated by the renin angiotensin aldosterone system.
9958RENreninrenin1.0vegf expression is increased by glucose advanced glycation end products transforming growth factor b and insulin like growth factor 1 all of which are modulated by the renin angiotensin aldosterone system.
11765TGFAtransforming growth factor, alphatransforming growth factor1.0vegf expression is increased by glucose advanced glycation end products transforming growth factor b and insulin like growth factor 1 all of which are modulated by the renin angiotensin aldosterone system.
9958RENreninrenin1.0this raises the possibility that targeting upstream regulatory systems such as the renin angiotensin aldosterone system may be more effective in treating retinal vasculopathy especially because angiotensin ang ii and aldosterone are proinflammatory fibrogenic and angiogenic and because t
9958RENreninrenin1.0 treating retinal vasculopathy especially because angiotensin ang ii and aldosterone are proinflammatory fibrogenic and angiogenic and because the eye possesses a functionally active local intracrine renin angiotensin system ras .
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)ang ii1.0aises the possibility that targeting upstream regulatory systems such as the renin angiotensin aldosterone system may be more effective in treating retinal vasculopathy especially because angiotensin ang ii and aldosterone are proinflammatory fibrogenic and angiogenic and because the eye possesses a functionally active local intracrine renin angiotensin system ras .
9958RENreninrenin1.0renin angiotensin converting enzyme angiotensinogen ang ii and ang ii receptors have been shown at the mrna and protein levels in humans rats and rabbits in the vasculature neurons and glia.
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)ang ii1.0renin angiotensin converting enzyme angiotensinogen ang ii and ang ii receptors have been shown at the mrna and protein levels in humans rats and rabbits in the vasculature neurons and glia.
2707ACEangiotensin I converting enzyme (peptidyl-dipeptidase A) 1angiotensin converting enzyme1.0renin angiotensin converting enzyme angiotensinogen ang ii and ang ii receptors have been shown at the mrna and protein levels in humans rats and rabbits in the vasculature neurons and glia.
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)angiotensinogen1.0renin angiotensin converting enzyme angiotensinogen ang ii and ang ii receptors have been shown at the mrna and protein levels in humans rats and rabbits in the vasculature neurons and glia.
333AGTangiotensinogen (serpin peptidase inhibitor, clade A, member 8)ang ii1.0experimental studies and clinical observations demonstrated that interruption of the ras with angiotensin converting enzyme inhibitors or ang ii type 1 at 1 receptor at 1 r blockers ameliorating many of the vascular abnormalities that develop in diabetic retinopathy and retinopathy of prematurity.
2707ACEangiotensin I converting enzyme (peptidyl-dipeptidase A) 1angiotensin converting enzyme1.0experimental studies and clinical observations demonstrated that interruption of the ras with angiotensin converting enzyme inhibitors or ang ii type 1 at 1 receptor at 1 r blockers ameliorating many of the vascular abnormalities that develop in diabetic retinopathy and retinopathy of prematurity.
18305ATP6AP2ATPase, H+ transporting, lysosomal accessory protein 2renin receptor1.0prorenin has also been implicated in retinal vascular injury because handle region peptide which binds to pro renin receptor as a decoy peptide and inhibits the nonproteolytic activation of prorenin inhibited retinal neovascularization in mice with oxygen induced retinopathy.
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0licated in volume homeostasis and na balance is now recognized to be a potent profibrotic and proinflammatory mediator in the heart vasculature and kidneys with effects mediated through activation of nadph oxidase and increased generation of ros oxidative stress .
6018IL6interleukin 6 (interferon, beta 2)interleukin 61.0ltiple signaling molecules including mitogen activated protein kinases protein tyrosine phosphatases tyrosine kinases ion channels and proinflammatory genes such as monocyte chemoattractant protein 1 interleukin 6 and nuclear factor kappab.
10618CCL2chemokine (C-C motif) ligand 2monocyte chemoattractant protein 11.0gh redox sensitive regulation of multiple signaling molecules including mitogen activated protein kinases protein tyrosine phosphatases tyrosine kinases ion channels and proinflammatory genes such as monocyte chemoattractant protein 1 interleukin 6 and nuclear factor kappab.
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0ong the various mechanisms through which aldosterone influences redox state are downregulation of glucose 6 phosphate dehydrogenase g6pd which is a major source of reduced nad p h and upregulation of nadph oxidase a key enzyme involved in vascular ros generation.
4057G6PDglucose-6-phosphate dehydrogenaseglucose 6 phosphate dehydrogenase1.0among the various mechanisms through which aldosterone influences redox state are downregulation of glucose 6 phosphate dehydrogenase g6pd which is a major source of reduced nad p h and upregulation of nadph oxidase a key enzyme involved in vascular ros generation.
4057G6PDglucose-6-phosphate dehydrogenaseglucose 6 phosphate dehydrogenase g6pd1.0among the various mechanisms through which aldosterone influences redox state are downregulation of glucose 6 phosphate dehydrogenase g6pd which is a major source of reduced nad p h and upregulation of nadph oxidase a key enzyme involved in vascular ros generation.
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0wilkinson berka et al demonstrated that aldosterone decreases g6pd mrna expression in retinal endothelial cells and that retinal nicotinamide adenine dinucleotide phosphate reduced oxidase 4 nadph oxidase [nox]4 a nox2 homolog is upregulated in oxygen induced retinopathy figure .
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0growing evidence indicates an important role for nadph oxidase in retinal vascular inflammation.
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0nox2 p22phox and p47phox classic subunits of nadph oxidase have also been implicated in nadph oxidase derived ros in vascular retinopathy.
14874NOX5NADPH oxidase, EF-hand calcium binding domain 5nadph oxidase1.0moreover the fact that retinal gene expression of g6pd is reduced and that of nox4 is increased does not necessarily mean that protein levels are changed nor that activity of g6pd or nadph oxidase is altered.
2592CYP11B2cytochrome P450, family 11, subfamily B, polypeptide 2aldosterone synthase1.0wilkinson berka et al suggest that this may be so because genes for the enzymes responsible for aldosterone synthesis namely 11b hydroxysteroid dehydrogenase type 1 11b hsd1 11b hsd2 and aldosterone synthase are expressed in retina.
5208HSD11B1hydroxysteroid (11-beta) dehydrogenase 1hsd11.0wilkinson berka et al suggest that this may be so because genes for the enzymes responsible for aldosterone synthesis namely 11b hydroxysteroid dehydrogenase type 1 11b hsd1 11b hsd2 and aldosterone synthase are expressed in retina.