keyword
https://read.qxmd.com/read/36543799/the-ufm1-system-regulates-er-phagy-through-the-ufmylation-of-cyb5r3
#21
JOURNAL ARTICLE
Ryosuke Ishimura, Afnan H El-Gowily, Daisuke Noshiro, Satoko Komatsu-Hirota, Yasuko Ono, Mayumi Shindo, Tomohisa Hatta, Manabu Abe, Takefumi Uemura, Hyeon-Cheol Lee-Okada, Tarek M Mohamed, Takehiko Yokomizo, Takashi Ueno, Kenji Sakimura, Tohru Natsume, Hiroyuki Sorimachi, Toshifumi Inada, Satoshi Waguri, Nobuo N Noda, Masaaki Komatsu
Protein modification by ubiquitin-like proteins (UBLs) amplifies limited genome information and regulates diverse cellular processes, including translation, autophagy and antiviral pathways. Ubiquitin-fold modifier 1 (UFM1) is a UBL covalently conjugated with intracellular proteins through ufmylation, a reaction analogous to ubiquitylation. Ufmylation is involved in processes such as endoplasmic reticulum (ER)-associated protein degradation, ribosome-associated protein quality control at the ER and ER-phagy...
December 21, 2022: Nature Communications
https://read.qxmd.com/read/36479222/revealing-oxidative-stress-related-genes-in-osteoporosis-and-advanced-structural-biological-study-for-novel-natural-material-discovery-regarding-mapkapk2
#22
JOURNAL ARTICLE
Yingjing Zhao, Weihang Li, Kuo Zhang, Meng Xu, Yujia Zou, Xiaotong Qiu, Tianxing Lu, Bo Gao
OBJECTIVES: This study aimed to find novel oxidative stress (OS)-related biomarkers of osteoporosis (OP), together with targeting the macromolecule Mitogen-activated protein kinase-activated protein kinase 2 ( MAPKAPK2 ) protein to further discover potential novel materials based on an advanced structural biology approach. METHODS: Gene expression profiles of GSE35958 were obtained from the Gene Expression Omnibus (GEO) database, which were included for weighted gene co-expression network analysis (WGCNA) and differential analysis to identify the most correlated module, to identify OS-related hub genes in the progression of OP...
2022: Frontiers in Endocrinology
https://read.qxmd.com/read/36441026/cytochrome-b5-reductases-redox-regulators-of-cell-homeostasis
#23
REVIEW
Robert Hall, Shuai Yuan, Katherine Wood, Mate Katona, Adam C Straub
The cytochrome-b5 reductase (CYB5R) family of flavoproteins is known to regulate reduction-oxidation (redox) balance in cells. The five enzyme members are highly compartmentalized at the subcellular level and function as "redox switches" enabling the reduction of several substrates, such as heme and coenzyme Q. Critical insight into the physiological and pathophysiological significance of CYB5R enzymes has been gleaned from several human genetic variants that cause congenital disease and a broad spectrum of chronic human diseases...
October 29, 2022: Journal of Biological Chemistry
https://read.qxmd.com/read/36174878/cigarette-smoke-induces-pulmonary-arterial-dysfunction-through-an-imbalance-in-the-redox-status-of-the-soluble-guanylyl-cyclase
#24
JOURNAL ARTICLE
J Sevilla-Montero, O Munar-Rubert, J Pino-Fadón, C Aguilar-Latorre, M Villegas-Esguevillas, B Climent, M Agrò, C Choya-Foces, A Martínez-Ruiz, E Balsa, C Muñoz-Calleja, R M Gómez-Punter, E Vázquez-Espinosa, A Cogolludo, M J Calzada
Chronic obstructive pulmonary disease (COPD), whose main risk factor is cigarette smoking (CS), is one of the most common diseases globally. Some COPD patients also develop pulmonary hypertension (PH), a severe complication that leads to premature death. Evidence suggests reactive oxygen species (ROS) involvement in COPD and PH, especially regarding pulmonary artery smooth muscle cells (PASMC) dysfunction. However, the effects of CS-driven oxidative stress on the pulmonary vasculature are not completely understood...
September 26, 2022: Free Radical Biology & Medicine
https://read.qxmd.com/read/36164636/isolated-diaphorase-from-bovine-erythrocyte-cannot-reduce-oxidized-cytoglobin-metcygb
#25
JOURNAL ARTICLE
Gissi Novientri, Mohamad Sadikin, Sri Widia Jusman
Background: Cytoglobin (Cygb) is a relatively newly identified globin protein that acts as an oxygen transporter in tissues like hemoglobin (Hb) in erythrocytes and myoglobin (Mb) in muscles. The natural oxidation of the Fe2+ ion in its heme group into metglobin (globin-Fe3+ ) made the loses of oxygen binding functions. It is known metHb and metMb can be reduced enzymatically using diaphorase or cyb5r3. However, metCygb reductase had not been previously identified. This study aims to analyze the reducing activity of bovine diaphorase on metCygb...
July 2022: Reports of Biochemistry & Molecular Biology
https://read.qxmd.com/read/36106636/loss-of-cardiomyocyte-cyb5r3-impairs-redox-equilibrium-and-causes-sudden-cardiac-death
#26
JOURNAL ARTICLE
Nolan T Carew, Heidi M Schmidt, Shuai Yuan, Joseph C Galley, Robert Hall, Helene M Altmann, Scott A Hahn, Megan P Miller, Katherine C Wood, Bethann Gabris, Margaret C Stapleton, Sean Hartwick, Marco Fazzari, Yijen L Wu, Mohamed Trebak, Brett A Kaufman, Charles F McTiernan, Francisco J Schopfer, Placido Navas, Patrick H Thibodeau, Dennis M McNamara, Guy Salama, Adam C Straub
Sudden cardiac death (SCD) in patients with heart failure (HF) is allied with an imbalance in reduction and oxidation (redox) signaling in cardiomyocytes; however, the basic pathways and mechanisms governing redox homeostasis in cardiomyocytes are not fully understood. Here, we show that cytochrome b5 reductase 3 (CYB5R3), an enzyme known to regulate redox signaling in erythrocytes and vascular cells, is essential for cardiomyocyte function. Using a conditional cardiomyocyte-specific CYB5R3-knockout mouse, we discovered that deletion of CYB5R3 in male, but not female, adult cardiomyocytes causes cardiac hypertrophy, bradycardia, and SCD...
September 15, 2022: Journal of Clinical Investigation
https://read.qxmd.com/read/36029161/soluble-guanylate-cyclase-activator-bay-54-6544-improves-vasomotor-function-and-survival-in-an-accelerated-ageing-mouse-model
#27
JOURNAL ARTICLE
Ehsan Ataei Ataabadi, Keivan Golshiri, Annika A Jüttner, René de Vries, Ingrid Van den Berg-Garrelds, Nicole M A Nagtzaam, Hina N Khan, Frank P J Leijten, Renata M C Brandt, Willem A Dik, Ingrid van der Pluijm, A H Jan Danser, Peter Sandner, Anton J M Roks
DNA damage is a causative factor in ageing of the vasculature and other organs. One of the most important vascular ageing features is reduced nitric oxide (NO)soluble guanylate cyclase (sGC)-cyclic guanosine monophosphate (cGMP) signaling. We hypothesized that the restoration of NO-sGC-cGMP signaling with an sGC activator (BAY 54-6544) may have beneficial effects on vascular ageing and premature death in DNA repair-defective mice undergoing accelerated ageing. Eight weeks of treatment with a non-pressor dosage of BAY 54-6544 restored the decreased in vivo microvascular cutaneous perfusion in progeroid Ercc1∆/- mice to the level of wild-type mice...
August 27, 2022: Aging Cell
https://read.qxmd.com/read/35906899/quantification-of-spatial-pharmacogene-expression-heterogeneity-in-breast-tumors
#28
JOURNAL ARTICLE
Nicholas R Powell, Rebecca M Silvola, John S Howard, Sunil Badve, Todd C Skaar, Joseph Ipe
BACKGROUND: Chemotherapeutic drug concentrations vary across different regions of tumors and this is thought to be involved in development of chemotherapy resistance. Insufficient drug delivery to some regions of the tumor may be due to spatial differences in expression of genes involved in the disposition, transport, and detoxification of drugs (pharmacogenes). Therefore, in this study, we analyzed the spatial expression of 286 pharmacogenes in six breast cancer tissues using the recently developed Visium spatial transcriptomics platform to (1) determine if these pharmacogenes are expressed heterogeneously across tumor tissue and (2) to determine which pharmacogenes have the most spatial expression heterogeneity...
July 30, 2022: Cancer reports
https://read.qxmd.com/read/35794887/transcriptional-profiles-analysis-of-covid-19-and-malaria-patients-reveals-potential-biomarkers-in-children
#29
Nzungize Lambert, Jonas A Kengne-Ouafo, WesongaMakokha Rissy, Umuhoza Diane, Ken Murithi, Peter Kimani, Olaitan I Awe, Allissa Dillman
The clinical presentation overlap between malaria and COVID-19 poses special challenges for rapid diagnosis in febrile children. In this study, we collected RNA-seq data of children with malaria and COVID-19 infection from the public databases as raw data in fastq format paired end files. A group of six, five and two biological replicates of malaria, COVID-19 and healthy donors respectively were used for the study. We conducted differential gene expression analysis to visualize differences in the expression profiles...
July 1, 2022: bioRxiv
https://read.qxmd.com/read/35527283/cyb5r3-overexpression-preserves-skeletal-muscle-mitochondria-and-autophagic-signaling-in-aged-transgenic-mice
#30
JOURNAL ARTICLE
Sara López-Bellón, Sandra Rodríguez-López, José A González-Reyes, M Isabel Burón, Rafael de Cabo, José M Villalba
Cytochrome b5 reductase 3 (CYB5R3) overexpression activates respiratory metabolism and exerts prolongevity effects in transgenic mice, mimicking some of the salutary effects of calorie restriction. The aim of our study was to understand how CYB5R3 overexpression targets key pathways that modulate the rate of aging in skeletal muscle, a postmitotic tissue with a greater contribution to resting energy expenditure. Mitochondrial function, autophagy and mitophagy markers were evaluated in mouse hind limb skeletal muscles from young-adult (7 months old) and old (24 months old) males of wild-type and CYB5R3-overexpressing genotypes...
May 9, 2022: GeroScience
https://read.qxmd.com/read/35104462/cyb5r3-homozygous-pathogenic-variant-as-a-rare-cause-of-cyanosis-in-the-newborn
#31
D Molina Herranz, C García Escudero, S Rite Gracia, Y Aguilar de la Red, J Martínez Nieto, S Izquierdo Álvarez, M A Montañés Gracia, V Recasens, C F Hernández Mata
Detailed below is a very illustrative case of a rare pathology of recessive congenital methemoglobinemia. The patient, a newborn female, was homozygous for c.535G>A, p.(Ala179Thr) a pathogenic variant in the CYB5R3 gene. The reported population frequency of the allele is 0.853%, demonstrating why it is remarkable to find both parents are heterozygous carriers without consanguinity. A brief review of previously published cases is also presented.
January 29, 2022: Clinical Biochemistry
https://read.qxmd.com/read/35064402/three-novel-mutations-in-cyb5r3-gene-causing-nadh-cytochrome-b5-reductase-enzyme-deficiency-leads-to-recessive-congenital-methaemoglobinemia
#32
JOURNAL ARTICLE
Anuradha Deorukhkar, Anuja Kulkarni, Prabhakar Kedar
BACKGROUND: Methemoglobin is the reduced form of haemoglobin that is normally found in the blood in levels < 1%. Methemoglobinemia can occur as a congenital or acquired disease. Two types of recessive congenital methaemoglobinemia (RCM) are caused by the NADH-dependent cytochrome b5 reductase enzyme deficiency of the CYB5R3 gene. RCM-I is characterized by higher methaemoglobin levels (> 2 g/dL), causing only cyanosis, whereas RCM-II is associated with cyanosis with neurological impairment...
March 2022: Molecular Biology Reports
https://read.qxmd.com/read/35052663/redox-regulation-of-%C3%AE-globin-in-vascular-physiology
#33
JOURNAL ARTICLE
Laurent Kiger, Julia Keith, Abdullah Freiwan, Alfonso G Fernandez, Heather Tillman, Brant E Isakson, Mitchell J Weiss, Christophe Lechauve
Interest in the structure, function, and evolutionary relations of circulating and intracellular globins dates back more than 60 years to the first determination of the three-dimensional structure of these proteins. Non-erythrocytic globins have been implicated in circulatory control through reactions that couple nitric oxide (NO) signaling with cellular oxygen availability and redox status. Small artery endothelial cells (ECs) express free α-globin, which causes vasoconstriction by degrading NO. This reaction converts reduced (Fe2+ ) α-globin to the oxidized (Fe3+ ) form, which is unstable, cytotoxic, and unable to degrade NO...
January 14, 2022: Antioxidants (Basel, Switzerland)
https://read.qxmd.com/read/34936088/benign-prostatic-hyperplasia-obstruction-ameliorated-using-a-soluble-guanylate-cyclase-activator
#34
JOURNAL ARTICLE
Irina V Zabbarova, Youko Ikeda, Mark G Kozlowski, Pradeep Tyagi, Lori A Birder, Basu Chakrabarty, Subashan Kpg Perera, Rajiv Dhir, Adam C Straub, Peter Sandner, Karl-Erik Andersson, Marcus J Drake, Christopher H Fry, Anthony J Kanai
Benign prostatic hyperplasia (BPH) is a feature of ageing males. Up to half demonstrate bladder outlet obstruction (BOO) with associated lower urinary tract symptoms (LUTS) including bladder overactivity. Current therapies to reduce obstruction, such as α1-adrenoceptor antagonists and 5α-reductase inhibitors, are not effective in all patients. The phosphodiesterase-5 inhibitor (PDE5I) tadalafil is also approved to treat BPH and LUTS, suggesting a role for nitric oxide (NO• ), soluble guanylate cyclase (sGC), and cGMP signalling pathways...
April 2022: Journal of Pathology
https://read.qxmd.com/read/34785403/proteome-dynamics-and-bioinformatics-reveal-major-alterations-in-the-turnover-rate-of-functionally-related-cardiac-and-plasma-proteins-in-a-dog-model-of-congestive-heart-failure
#35
JOURNAL ARTICLE
Khatia Gabisonia, Gia Burjanadze, Felix Woitek, Ayse Keles, Mitsuru Seki, Nikoloz Gorgodze, Lucia Carlucci, Serguei Ilchenko, Clara Kurishima, Kenneth Walsh, Helen Piontkivska, Fabio A Recchia, Takhar Kasumov
Protein pool turnover is a critically important cellular homeostatic component, yet it has been little explored in the context of heart failure (HF) pathophysiology. We used in vivo 2 H labeling/proteome dynamics for the nonbiased discovery of turnover alterations involving functionally linked cardiac and plasma proteins in canine tachypacing-induced HF, an established preclinical model of dilated cardiomyopathy. Compared with controls, dogs with congestive HF displayed bidirectional turnover changes of 28 cardiac proteins, that is, a reduced half-life of several key enzymes involved in glycolysis, homocysteine metabolism and glycogenesis, and increased half-life of proteins involved in proteolysis...
April 2022: Journal of Cardiac Failure
https://read.qxmd.com/read/34660776/identification-of-specific-cell-subpopulations-and-marker-genes-in-ovarian-cancer-using-single-cell-rna-sequencing
#36
JOURNAL ARTICLE
Yan Li, Juan Wang, Fang Wang, Chengzhen Gao, Yuanyuan Cao, Jianhua Wang
Objective: Ovarian cancer is the deadliest gynaecological cancer globally. In our study, we aimed to analyze specific cell subpopulations and marker genes among ovarian cancer cells by single-cell RNA sequencing (RNA-seq). Methods: Single-cell RNA-seq data of 66 high-grade serous ovarian cancer cells were employed from the Gene Expression Omnibus (GEO). Using the Seurat package, we performed quality control to remove cells with low quality. After normalization, we detected highly variable genes across the single cells...
2021: BioMed Research International
https://read.qxmd.com/read/34656824/cooperation-between-cyb5r3-and-nox4-via-coenzyme-q-mitigates-endothelial-inflammation
#37
JOURNAL ARTICLE
Shuai Yuan, Scott A Hahn, Megan P Miller, Subramaniam Sanker, Michael J Calderon, Mara Sullivan, Atinuke M Dosunmu-Ogunbi, Marco Fazzari, Yao Li, Michael Reynolds, Katherine C Wood, Claudette M St Croix, Donna Stolz, Eugenia Cifuentes-Pagano, Placido Navas, Sruti Shiva, Francisco J Schopfer, Patrick J Pagano, Adam C Straub
NADPH oxidase 4 (NOX4) regulates endothelial inflammation by producing hydrogen peroxide (H2 O2 ) and to a lesser extent O2 •- . The ratio of NOX4-derived H2 O2 and O2 •- can be altered by coenzyme Q (CoQ) mimics. Therefore, we hypothesize that cytochrome b5 reductase 3 (CYB5R3), a CoQ reductase abundant in vascular endothelial cells, regulates inflammatory activation. To examine endothelial CYB5R3 in vivo, we created tamoxifen-inducible endothelium-specific Cyb5r3 knockout mice (R3 KO). Radiotelemetry measurements of systolic blood pressure showed systemic hypotension in lipopolysaccharides (LPS) challenged mice, which was exacerbated in R3 KO mice...
October 14, 2021: Redox Biology
https://read.qxmd.com/read/34557495/identification-and-validation-of-a-nine-gene-amino-acid-metabolism-related-risk-signature-in-hcc
#38
JOURNAL ARTICLE
Yajuan Zhao, Junli Zhang, Shuhan Wang, Qianqian Jiang, Keshu Xu
Background: Hepatocellular carcinoma (HCC) is the world's second most deadly cancer, and metabolic reprogramming is its distinguishing feature. Among metabolite profiling, variation in amino acid metabolism supports tumor proliferation and metastasis to the most extent, yet a systematic study on the role of amino acid metabolism-related genes in HCC is still lacking. An effective amino acid metabolism-related prediction signature is urgently needed to assess the prognosis of HCC patients for individualized treatment...
2021: Frontiers in Cell and Developmental Biology
https://read.qxmd.com/read/34536439/smooth-muscle-cell-cyb5r3-preserves-cardiac-and-vascular-function-under-chronic-hypoxic-stress
#39
JOURNAL ARTICLE
Brittany G Durgin, Katherine C Wood, Scott A Hahn, Brenda McMahon, Jeffrey J Baust, Adam C Straub
Chronic hypoxia is a major driver of cardiovascular complications, including heart failure. The nitric oxide (NO) - soluble guanylyl cyclase (sGC) - cyclic guanosine monophosphate (cGMP) pathway is integral to vascular tone maintenance. Specifically, NO binds its receptor sGC within vascular smooth muscle cells (SMC) in its reduced heme (Fe2+ ) form to increase intracellular cGMP production, activate protein kinase G (PKG) signaling, and induce vessel relaxation. Under chronic hypoxia, oxidative stress drives oxidation of sGC heme (Fe2+ →Fe3+ ), rendering it NO-insensitive...
January 2022: Journal of Molecular and Cellular Cardiology
https://read.qxmd.com/read/34467556/recommendations-for-diagnosis-and-treatment-of-methemoglobinemia
#40
REVIEW
Achille Iolascon, Paola Bianchi, Immacolata Andolfo, Roberta Russo, Wilma Barcellini, Elisa Fermo, Gergely Toldi, Stefano Ghirardello, Davis Rees, Richard Van Wijk, Antonis Kattamis, Patrick G Gallagher, Noemi Roy, Ali Taher, Razan Mohty, Andreas Kulozik, Lucia De Franceschi, Antonella Gambale, Mariane De Montalembert, Gian Luca Forni, Cornelis L Harteveld, Josef Prchal
Methemoglobinemia is a rare disorder associated with oxidization of divalent ferro-iron of hemoglobin (Hb) to ferri-iron of methemoglobin (MetHb). Methemoglobinemia can result from either inherited or acquired processes. Acquired forms are the most common, mainly due to the exposure to substances that cause oxidation of the Hb both directly or indirectly. Inherited forms are due either to autosomal recessive variants in the CYB5R3 gene or to autosomal dominant variants in the globin genes, collectively known as HbM disease...
December 1, 2021: American Journal of Hematology
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