Extracellular NAD


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
20 01 2020
Historique:
received: 14 08 2019
accepted: 29 12 2019
entrez: 22 1 2020
pubmed: 22 1 2020
medline: 1 12 2020
Statut: epublish

Résumé

Changes in nicotinamide adenine dinucleotide (NAD

Identifiants

pubmed: 31959836
doi: 10.1038/s41598-020-57506-9
pii: 10.1038/s41598-020-57506-9
pmc: PMC6971268
doi:

Substances chimiques

Reactive Oxygen Species 0
X-ray Repair Cross Complementing Protein 1 0
XRCC1 protein, human 0
NAD 0U46U6E8UK
Poly(ADP-ribose) Polymerases EC 2.4.2.30
5'-Nucleotidase EC 3.1.3.5
Sirtuins EC 3.5.1.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

651

Subventions

Organisme : NIEHS NIH HHS
ID : U01 ES029518
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES014811
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA148629
Pays : United States

Références

Kepp, O., Loos, F., Liu, P. & Kroemer, G. Extracellular nucleosides and nucleotides as immunomodulators. Immunol. Rev. 280, 83–92, https://doi.org/10.1111/imr.12571 (2017).
doi: 10.1111/imr.12571 pubmed: 29027229
Wilde, L. et al. Metabolic coupling and the R everse Warburg Effect in cancer: Implications for novel biomarker and anticancer agent development. Semin. Oncol. 44, 198–203, https://doi.org/10.1053/j.seminoncol.2017.10.004 (2017).
doi: 10.1053/j.seminoncol.2017.10.004 pubmed: 29248131 pmcid: 5737780
Otto, A. M., Hintermair, J. & Janzon, C. NADH-linked metabolic plasticity of MCF-7 breast cancer cells surviving in a nutrient-deprived microenvironment. J. Cell Biochem. 116, 822–835, https://doi.org/10.1002/jcb.25038 (2015).
doi: 10.1002/jcb.25038 pubmed: 25530451
Thongon, N. et al. Cancer cell metabolic plasticity allows resistance to NAMPT inhibition but invariably induces dependence on LDHA. Cancer Metab. 6, 1, https://doi.org/10.1186/s40170-018-0174-7 (2018).
doi: 10.1186/s40170-018-0174-7 pubmed: 29541451 pmcid: 5844108
Bogan, K. L. & Brenner, C. Nicotinic acid, nicotinamide, and nicotinamide riboside: a molecular evaluation of NAD+ precursor vitamins in human nutrition. Annu. Rev. Nutr. 28, 115–130, https://doi.org/10.1146/annurev.nutr.28.061807.155443 (2008).
doi: 10.1146/annurev.nutr.28.061807.155443 pubmed: 18429699
Imai, S. & Guarente, L. NAD+ and sirtuins in aging and disease. Trends Cell Biol. 24, 464–471, https://doi.org/10.1016/j.tcb.2014.04.002 (2014).
doi: 10.1016/j.tcb.2014.04.002 pubmed: 24786309 pmcid: 4112140
Verdin, E. NAD(+) in aging, metabolism, and neurodegeneration. Science 350, 1208–1213, https://doi.org/10.1126/science.aac4854 (2015).
doi: 10.1126/science.aac4854 pubmed: 26785480 pmcid: 26785480
Sauve, A. A. NAD+ and vitamin B3: from metabolism to therapies. J. Pharmacol. Exp. Ther. 324, 883–893, https://doi.org/10.1124/jpet.107.120758 (2008).
doi: 10.1124/jpet.107.120758 pubmed: 18165311
Kennedy, B. E. et al. NAD(+) salvage pathway in cancer metabolism and therapy. Pharmacol. Res. 114, 274–283, https://doi.org/10.1016/j.phrs.2016.10.027 (2016).
doi: 10.1016/j.phrs.2016.10.027 pubmed: 27816507
Belenky, P., Bogan, K. L. & Brenner, C. NAD+ metabolism in health and disease. Trends Biochem. Sci. 32, 12–19, https://doi.org/10.1016/j.tibs.2006.11.006 (2007).
doi: 10.1016/j.tibs.2006.11.006 pubmed: 17161604
Bruzzone, S. et al. A self-restricted CD38-connexin 43 cross-talk affects NAD+ and cyclic ADP-ribose metabolism and regulates intracellular calcium in 3T3 fibroblasts. J. Biol. Chem. 276, 48300–48308, https://doi.org/10.1074/jbc.M107308200 (2001).
doi: 10.1074/jbc.M107308200 pubmed: 11602597
Gorelik, A., Randriamihaja, A., Illes, K. & Nagar, B. A key tyrosine substitution restricts nucleotide hydrolysis by the ectoenzyme NPP5. FEBS J. 284, 3718–3726, https://doi.org/10.1111/febs.14266 (2017).
doi: 10.1111/febs.14266 pubmed: 28898552
Hottiger, M. O. SnapShot: ADP-Ribosylation Signaling. Mol. Cell 62, 472, https://doi.org/10.1016/j.molcel.2016.04.019 (2016).
doi: 10.1016/j.molcel.2016.04.019 pubmed: 27153542
Chalkiadaki, A. & Guarente, L. The multifaceted functions of sirtuins in cancer. Nat. Rev. Cancer 15, 608–624, https://doi.org/10.1038/nrc3985 (2015).
doi: 10.1038/nrc3985 pubmed: 26383140
Fouquerel, E. & Sobol, R. W. ARTD1 (PARP1) activation and NAD(+) in DNA repair and cell death. DNA Repair. (Amst.) 23, 27–32, https://doi.org/10.1016/j.dnarep.2014.09.004 (2014).
doi: 10.1016/j.dnarep.2014.09.004
Fouquerel, E. et al. ARTD1/PARP1 negatively regulates glycolysis by inhibiting hexokinase 1 independent of NAD+ depletion. Cell Rep. 8, 1819–1831, https://doi.org/10.1016/j.celrep.2014.08.036 (2014).
doi: 10.1016/j.celrep.2014.08.036 pubmed: 25220464 pmcid: 4177344
Goellner, E. M. et al. Overcoming temozolomide resistance in glioblastoma via dual inhibition of NAD+ biosynthesis and base excision repair. Cancer Res. 71, 2308–2317, https://doi.org/10.1158/0008-5472.CAN-10-3213 (2011).
doi: 10.1158/0008-5472.CAN-10-3213 pubmed: 21406402 pmcid: 3077901
van der Veer, E. et al. Extension of human cell lifespan by nicotinamide phosphoribosyltransferase. J. Biol. Chem. 282, 10841–10845, https://doi.org/10.1074/jbc.C700018200 (2007).
doi: 10.1074/jbc.C700018200 pubmed: 17307730
Gong, B. et al. Nicotinamide riboside restores cognition through an upregulation of proliferator-activated receptor-gamma coactivator 1alpha regulated beta-secretase 1 degradation and mitochondrial gene expression in Alzheimer’s mouse models. Neurobiol. Aging 34, 1581–1588, https://doi.org/10.1016/j.neurobiolaging.2012.12.005 (2013).
doi: 10.1016/j.neurobiolaging.2012.12.005 pubmed: 23312803 pmcid: 3632303
Brown, K. D. et al. Activation of SIRT3 by the NAD(+) precursor nicotinamide riboside protects from noise-induced hearing loss. Cell Metab. 20, 1059–1068, https://doi.org/10.1016/j.cmet.2014.11.003 (2014).
doi: 10.1016/j.cmet.2014.11.003 pubmed: 25470550 pmcid: 4940130
Gujar, A. D. et al. An NAD+-dependent transcriptional program governs self-renewal and radiation resistance in glioblastoma. Proc. Natl Acad. Sci. USA 113, E8247–E8256, https://doi.org/10.1073/pnas.1610921114 (2016).
doi: 10.1073/pnas.1610921114 pubmed: 27930300
Surjana, D., Halliday, G. M. & Damian, D. L. Role of nicotinamide in DNA damage, mutagenesis, and DNA repair. J Nucleic Acids 2010, https://doi.org/10.4061/2010/157591 (2010).
doi: 10.4061/2010/157591
Almeida, G. S. et al. PARP inhibitor rucaparib induces changes in NAD levels in cells and liver tissues as assessed by MRS. NMR Biomed 30, https://doi.org/10.1002/nbm.3736 (2017).
doi: 10.1002/nbm.3736
Clement, J., Wong, M., Poljak, A., Sachdev, P. & Braidy, N. The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging. Rejuvenation Res. 22, 121–130, https://doi.org/10.1089/rej.2018.2077 (2019).
doi: 10.1089/rej.2018.2077 pubmed: 30124109 pmcid: 6482912
Hassa, P. O. & Hottiger, M. O. The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADP-ribose polymerases. Front. Biosci. 13, 3046–3082 (2008).
doi: 10.2741/2909
Ray Chaudhuri, A. & Nussenzweig, A. The multifaceted roles of PARP1 in DNA repair and chromatin remodelling. Nat. Rev. Mol. Cell Biol. 18, 610–621, https://doi.org/10.1038/nrm.2017.53 (2017).
doi: 10.1038/nrm.2017.53 pubmed: 28676700 pmcid: 6591728
Posavec Marjanovic, M., Crawford, K. & Ahel, I. PARP, transcription and chromatin modeling. Semin. Cell & developmental Biol. 63, 102–113, https://doi.org/10.1016/j.semcdb.2016.09.014 (2017).
doi: 10.1016/j.semcdb.2016.09.014
Hottiger, M. O. Nuclear ADP-Ribosylation and Its Role in Chromatin Plasticity, Cell Differentiation, and Epigenetics. Annu. Rev. Biochem. 84, 227–263, https://doi.org/10.1146/annurev-biochem-060614-034506 (2015).
doi: 10.1146/annurev-biochem-060614-034506 pubmed: 25747399
Kim, M. Y., Mauro, S., Gevry, N., Lis, J. T. & Kraus, W. L. NAD+-dependent modulation of chromatin structure and transcription by nucleosome binding properties of PARP-1. Cell 119, 803–814, https://doi.org/10.1016/j.cell.2004.11.002 (2004).
doi: 10.1016/j.cell.2004.11.002 pubmed: 15607977
Doksani, Y. & de Lange, T. Telomere-Internal Double-Strand Breaks Are Repaired by Homologous Recombination and PARP1/Lig3-Dependent End-Joining. Cell Rep. 17, 1646–1656, https://doi.org/10.1016/j.celrep.2016.10.008 (2016).
doi: 10.1016/j.celrep.2016.10.008 pubmed: 27806302 pmcid: 5125555
Fang, E. F. et al. Defective mitophagy in XPA via PARP-1 hyperactivation and NAD(+)/SIRT1 reduction. Cell 157, 882–896, https://doi.org/10.1016/j.cell.2014.03.026 (2014).
doi: 10.1016/j.cell.2014.03.026 pubmed: 24813611 pmcid: 4625837
Scheibye-Knudsen, M. et al. A high-fat diet and NAD(+) activate Sirt1 to rescue premature aging in cockayne syndrome. Cell Metab. 20, 840–855, https://doi.org/10.1016/j.cmet.2014.10.005 (2014).
doi: 10.1016/j.cmet.2014.10.005 pubmed: 25440059 pmcid: 4261735
Fang, E. F. et al. NAD(+) Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair. Cell Metab. 24, 566–581, https://doi.org/10.1016/j.cmet.2016.09.004 (2016).
doi: 10.1016/j.cmet.2016.09.004 pubmed: 27732836 pmcid: 5777858
Braidy, N. et al. Role of Nicotinamide Adenine Dinucleotide and Related Precursors as Therapeutic Targets for Age-Related Degenerative Diseases: Rationale, Biochemistry, Pharmacokinetics, and Outcomes. Antioxid. Redox Signal. 30, 251–294, https://doi.org/10.1089/ars.2017.7269 (2019).
doi: 10.1089/ars.2017.7269 pubmed: 29634344
Hou, Y. et al. NAD(+) supplementation normalizes key Alzheimer’s features and DNA damage responses in a new AD mouse model with introduced DNA repair deficiency. Proc. Natl Acad. Sci. USA 115, E1876–E1885, https://doi.org/10.1073/pnas.1718819115 (2018).
doi: 10.1073/pnas.1718819115 pubmed: 29432159
Garten, A., Petzold, S., Korner, A., Imai, S. & Kiess, W. Nampt: linking NAD biology, metabolism and cancer. Trends Endocrinol. Metab. 20, 130–138, https://doi.org/10.1016/j.tem.2008.10.004 (2009).
doi: 10.1016/j.tem.2008.10.004 pubmed: 19109034
Drevs, J., Loser, R., Rattel, B. & Esser, N. Antiangiogenic potency of FK866/K22.175, a new inhibitor of intracellular NAD biosynthesis, in murine renal cell carcinoma. Anticancer. Res. 23, 4853–4858 (2003).
pubmed: 14981935
Maldi, E. et al. Nicotinamide phosphoribosyltransferase (NAMPT) is over-expressed in melanoma lesions. Pigment. Cell & melanoma Res. 26, 144–146, https://doi.org/10.1111/pcmr.12037 (2013).
doi: 10.1111/pcmr.12037
Garten, A. et al. Physiological and pathophysiological roles of NAMPT and NAD metabolism. Nat. reviews. Endocrinol. 11, 535–546, https://doi.org/10.1038/nrendo.2015.117 (2015).
doi: 10.1038/nrendo.2015.117
Wang, P. & Miao, C. Y. NAMPT as a Therapeutic Target against Stroke. Trends Pharmacol. Sci. 36, 891–905, https://doi.org/10.1016/j.tips.2015.08.012 (2015).
doi: 10.1016/j.tips.2015.08.012 pubmed: 26538317
Hasmann, M. & Schemainda, I. FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis. Cancer Res. 63, 7436–7442 (2003).
pubmed: 14612543
Watson, M. et al. The small molecule GMX1778 is a potent inhibitor of NAD+ biosynthesis: strategy for enhanced therapy in nicotinic acid phosphoribosyltransferase 1-deficient tumors. Mol. Cell Biol. 29, 5872–5888, https://doi.org/10.1128/MCB.00112-09 (2009).
doi: 10.1128/MCB.00112-09 pubmed: 19703994 pmcid: 2772749
Khan, J. A., Tao, X. & Tong, L. Molecular basis for the inhibition of human NMPRTase, a novel target for anticancer agents. Nat. Struct. Mol. Biol. 13, 582–588, https://doi.org/10.1038/nsmb1105 (2006).
doi: 10.1038/nsmb1105 pubmed: 16783377
Galli, U. et al. Medicinal chemistry of nicotinamide phosphoribosyltransferase (NAMPT) inhibitors. J. medicinal Chem. 56, 6279–6296, https://doi.org/10.1021/jm4001049 (2013).
doi: 10.1021/jm4001049
Holen, K., Saltz, L. B., Hollywood, E., Burk, K. & Hanauske, A. R. The pharmacokinetics, toxicities, and biologic effects of FK866, a nicotinamide adenine dinucleotide biosynthesis inhibitor. Invest. N. Drugs 26, 45–51, https://doi.org/10.1007/s10637-007-9083-2 (2008).
doi: 10.1007/s10637-007-9083-2
von Heideman, A., Berglund, A., Larsson, R. & Nygren, P. Safety and efficacy of NAD depleting cancer drugs: results of a phase I clinical trial of CHS 828 and overview of published data. Cancer Chemother. Pharmacol. 65, 1165–1172, https://doi.org/10.1007/s00280-009-1125-3 (2010).
doi: 10.1007/s00280-009-1125-3
Grozio, A. et al. CD73 protein as a source of extracellular precursors for sustained NAD+ biosynthesis in FK866-treated tumor cells. J. Biol. Chem. 288, 25938–25949, https://doi.org/10.1074/jbc.M113.470435 (2013).
doi: 10.1074/jbc.M113.470435 pubmed: 23880765 pmcid: 3764798
Billington, R. A. et al. Emerging functions of extracellular pyridine nucleotides. Mol. Med. 12, 324–327, https://doi.org/10.2119/2006-00075.Billington (2006).
doi: 10.2119/2006-00075.Billington pubmed: 17380199 pmcid: 1829198
Yoshino, J., Mills, K. F., Yoon, M. J. & Imai, S. Nicotinamide mononucleotide, a key NAD(+) intermediate, treats the pathophysiology of diet- and age-induced diabetes in mice. Cell Metab. 14, 528–536, https://doi.org/10.1016/j.cmet.2011.08.014 (2011).
doi: 10.1016/j.cmet.2011.08.014 pubmed: 21982712 pmcid: 3204926
Bieganowski, P. & Brenner, C. Discoveries of nicotinamide riboside as a nutrient and conserved NRK genes establish a Preiss-Handler independent route to NAD+ in fungi and humans. Cell 117, 495–502, https://doi.org/10.1016/s0092-8674(04)00416-7 (2004).
doi: 10.1016/s0092-8674(04)00416-7 pubmed: 15137942
Trammell, S. A., Yu, L., Redpath, P., Migaud, M. E. & Brenner, C. Nicotinamide Riboside Is a Major NAD+ Precursor Vitamin in Cow Milk. J. Nutr. 146, 957–963, https://doi.org/10.3945/jn.116.230078 (2016).
doi: 10.3945/jn.116.230078 pubmed: 27052539 pmcid: 6879052
Bruzzone, S., Guida, L., Zocchi, E., Franco, L. & De Flora, A. Connexin 43 hemi channels mediate Ca2+-regulated transmembrane NAD+ fluxes in intact cells. FASEB J. 15, 10–12, https://doi.org/10.1096/fj.00-0566fje (2001).
doi: 10.1096/fj.00-0566fje pubmed: 11099492
Sociali, G. et al. Antitumor effect of combined NAMPT and CD73 inhibition in an ovarian cancer model. Oncotarget 7, 2968–2984, https://doi.org/10.18632/oncotarget.6502 (2016).
doi: 10.18632/oncotarget.6502 pubmed: 26658104
Garavaglia, S. et al. The high-resolution crystal structure of periplasmic Haemophilus influenzae NAD nucleotidase reveals a novel enzymatic function of human CD73 related to NAD metabolism. Biochem. J. 441, 131–141, https://doi.org/10.1042/BJ20111263 (2012).
doi: 10.1042/BJ20111263 pubmed: 21933152
Jin, D. et al. CD73 on tumor cells impairs antitumor T-cell responses: a novel mechanism of tumor-induced immune suppression. Cancer Res. 70, 2245–2255, https://doi.org/10.1158/0008-5472.CAN-09-3109 (2010).
doi: 10.1158/0008-5472.CAN-09-3109 pubmed: 20179192 pmcid: 2883609
Beavis, P. A., Stagg, J., Darcy, P. K. & Smyth, M. J. CD73: a potent suppressor of antitumor immune responses. Trends immunology 33, 231–237, https://doi.org/10.1016/j.it.2012.02.009 (2012).
doi: 10.1016/j.it.2012.02.009
Allard, B., Turcotte, M. & Stagg, J. Targeting CD73 and downstream adenosine receptor signaling in triple-negative breast cancer. Expert. Opin. therapeutic targets 18, 863–881, https://doi.org/10.1517/14728222.2014.915315 (2014).
doi: 10.1517/14728222.2014.915315
Koszalka, P. et al. CD73 on B16F10 melanoma cells in CD73-deficient mice promotes tumor growth, angiogenesis, neovascularization, macrophage infiltration and metastasis. Int. J. Biochem. Cell Biol. 69, 1–10, https://doi.org/10.1016/j.biocel.2015.10.003 (2015).
doi: 10.1016/j.biocel.2015.10.003 pubmed: 26545615
Ratajczak, J. et al. NRK1 controls nicotinamide mononucleotide and nicotinamide riboside metabolism in mammalian cells. Nat. Commun. 7, 13103, https://doi.org/10.1038/ncomms13103 (2016).
doi: 10.1038/ncomms13103 pubmed: 27725675 pmcid: 5476803
Morandi, F. et al. Microvesicles released from multiple myeloma cells are equipped with ectoenzymes belonging to canonical and non-canonical adenosinergic pathways and produce adenosine from ATP and NAD. Oncoimmunology 7, e1458809, https://doi.org/10.1080/2162402X.2018.1458809 (2018).
doi: 10.1080/2162402X.2018.1458809 pubmed: 30221054 pmcid: 6136872
Canto, C., Sauve, A. A. & Bai, P. Crosstalk between poly(ADP-ribose) polymerase and sirtuin enzymes. Mol. Asp. Med. 34, 1168–1201, https://doi.org/10.1016/j.mam.2013.01.004 (2013).
doi: 10.1016/j.mam.2013.01.004
Sykora, P. et al. Next generation high throughput DNA damage detection platform for genotoxic compound screening. Sci. Rep. 8, 2771, https://doi.org/10.1038/s41598-018-20995-w (2018).
doi: 10.1038/s41598-018-20995-w pubmed: 29426857 pmcid: 5807538
Singh, N. P. The comet assay: Reflections on its development, evolution and applications. Mutat. Res. Rev. Mutat Res 767, 23–30, https://doi.org/10.1016/j.mrrev.2015.05.004 (2016).
doi: 10.1016/j.mrrev.2015.05.004 pubmed: 27036063
Pu, X., Wang, Z. & Klaunig, J. E. Alkaline Comet Assay for Assessing DNA Damage in Individual Cells. Curr. Protoc. Toxicol. 65(3 12), 11–11, https://doi.org/10.1002/0471140856.tx0312s65 (2015).
doi: 10.1002/0471140856.tx0312s65
Almeida, K. H. & Sobol, R. W. A unified view of base excision repair: lesion-dependent protein complexes regulated by post-translational modification. DNA Repair. (Amst.) 6, 695–711, https://doi.org/10.1016/j.dnarep.2007.01.009 (2007).
doi: 10.1016/j.dnarep.2007.01.009
Roberts, E. L., Newton, R. P. & Axford, A. T. Plasma purine nucleoside phosphorylase in cancer patients. Clinica Chim. acta; Int. J. Clin. Chem. 344, 109–114, https://doi.org/10.1016/j.cccn.2004.02.008 (2004).
doi: 10.1016/j.cccn.2004.02.008
Ulanovskaya, O. A., Zuhl, A. M. & Cravatt, B. F. NNMT promotes epigenetic remodeling in cancer by creating a metabolic methylation sink. Nat Chem Biol, https://doi.org/10.1038/nchembio.1204 (2013).
doi: 10.1038/nchembio.1204
Eckert, M. A. et al. Proteomics reveals NNMT as a master metabolic regulator of cancer-associated fibroblasts. Nature 569, 723–728, https://doi.org/10.1038/s41586-019-1173-8 (2019).
doi: 10.1038/s41586-019-1173-8 pubmed: 31043742 pmcid: 6690743
Gao, J. et al. Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. Sci. Signal. 6, pl1, https://doi.org/10.1126/scisignal.2004088 (2013).
doi: 10.1126/scisignal.2004088 pubmed: 23550210 pmcid: 4160307
Cerami, E. et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer discovery 2, 401–404, https://doi.org/10.1158/2159-8290.CD-12-0095 (2012).
doi: 10.1158/2159-8290.CD-12-0095 pubmed: 22588877
Spychala, J. et al. Role of estrogen receptor in the regulation of ecto-5′-nucleotidase and adenosine in breast cancer. Clin. Cancer Res. 10, 708–717 (2004).
doi: 10.1158/1078-0432.CCR-0811-03
Chmielewski, J. P. et al. CD38 Inhibits Prostate Cancer Metabolism and Proliferation by Reducing Cellular NAD(+) Pools. Mol. Cancer Res. 16, 1687–1700, https://doi.org/10.1158/1541-7786.MCR-17-0526 (2018).
doi: 10.1158/1541-7786.MCR-17-0526 pubmed: 30076241 pmcid: 6214722
Yamamoto-Katayama, S. et al. Crystallographic studies on human BST-1/CD157 with ADP-ribosyl cyclase and NAD glycohydrolase activities. J. Mol. Biol. 316, 711–723, https://doi.org/10.1006/jmbi.2001.5386 (2002).
doi: 10.1006/jmbi.2001.5386 pubmed: 11866528
Schmidt-Brauns, J. et al. Is a NAD pyrophosphatase activity necessary for Haemophilus influenzae type b multiplication in the blood stream? Int. J. Med. Microbiol. 291, 219–225, https://doi.org/10.1078/1438-4221-00122 (2001).
doi: 10.1078/1438-4221-00122 pubmed: 11554562
Kemmer, G. et al. NadN and e (P4) are essential for utilization of NAD and nicotinamide mononucleotide but not nicotinamide riboside in Haemophilus influenzae. J. Bacteriol. 183, 3974–3981, https://doi.org/10.1128/JB.183.13.3974-3981.2001 (2001).
doi: 10.1128/JB.183.13.3974-3981.2001 pubmed: 11395461 pmcid: 95280
Reidl, J. et al. NADP and NAD utilization in Haemophilus influenzae. Mol. Microbiol. 35, 1573–1581 (2000).
doi: 10.1046/j.1365-2958.2000.01829.x
Yang, Y., Mohammed, F. S., Zhang, N. & Sauve, A. A. Dihydronicotinamide riboside is a potent NAD(+) concentration enhancer in vitro and in vivo. J. Biol. Chem. 294, 9295–9307, https://doi.org/10.1074/jbc.RA118.005772 (2019).
doi: 10.1074/jbc.RA118.005772 pubmed: 30948509
Rahimova, R. et al. Identification of allosteric inhibitors of the ecto-5′-nucleotidase (CD73) targeting the dimer interface. PLoS Comput. Biol. 14, e1005943, https://doi.org/10.1371/journal.pcbi.1005943 (2018).
doi: 10.1371/journal.pcbi.1005943 pubmed: 29377887 pmcid: 5805337
Liu, L. et al. Quantitative Analysis of NAD Synthesis-Breakdown Fluxes. Cell Metab. 27, 1067–1080 e1065, https://doi.org/10.1016/j.cmet.2018.03.018 (2018).
doi: 10.1016/j.cmet.2018.03.018 pubmed: 29685734 pmcid: 5932087
Fletcher, R. S. et al. Nicotinamide riboside kinases display redundancy in mediating nicotinamide mononucleotide and nicotinamide riboside metabolism in skeletal muscle cells. Mol. Metab. 6, 819–832, https://doi.org/10.1016/j.molmet.2017.05.011 (2017).
doi: 10.1016/j.molmet.2017.05.011 pubmed: 28752046 pmcid: 5518663
Sanjana, N. E., Shalem, O. & Zhang, F. Improved vectors and genome-wide libraries for CRISPR screening. Nat. Methods 11, 783–784, https://doi.org/10.1038/nmeth.3047 (2014).
doi: 10.1038/nmeth.3047 pubmed: 25075903 pmcid: 4486245
Shalem, O. et al. Genome-scale CRISPR-Cas9 knockout screening in human cells. Science 343, 84–87, https://doi.org/10.1126/science.1247005 (2014).
doi: 10.1126/science.1247005 pubmed: 24336571 pmcid: 24336571
Nikiforov, A., Kulikova, V. & Ziegler, M. The human NAD metabolome: Functions, metabolism and compartmentalization. Crit. Rev. Biochem. Mol. Biol. 50, 284–297, https://doi.org/10.3109/10409238.2015.1028612 (2015).
doi: 10.3109/10409238.2015.1028612 pubmed: 25837229 pmcid: 4673589
Grozio, A. et al. Slc12a8 is a nicotinamide mononucleotide transporter. Nat. Metab. 1, 47–57, https://doi.org/10.1038/s42255-018-0009-4 (2019).
doi: 10.1038/s42255-018-0009-4 pubmed: 31131364 pmcid: 6530925
Hanzlikova, H., Gittens, W., Krejcikova, K., Zeng, Z. & Caldecott, K. W. Overlapping roles for PARP1 and PARP2 in the recruitment of endogenous XRCC1 and PNKP into oxidized chromatin. Nucleic Acids Res. 45, 2546–2557, https://doi.org/10.1093/nar/gkw1246 (2017).
doi: 10.1093/nar/gkw1246 pubmed: 27965414
Gassman, N. R. & Wilson, S. H. Micro-irradiation tools to visualize base excision repair and single-strand break repair. DNA Repair. (Amst.) 31, 52–63, https://doi.org/10.1016/j.dnarep.2015.05.001 (2015).
doi: 10.1016/j.dnarep.2015.05.001 pmcid: 4458156
Holton, N. W., Andrews, J. F. & Gassman, N. R. Application of Laser Micro-irradiation for Examination of Single and Double Strand Break Repair in Mammalian Cells. Journal of visualized experiments: JoVE, https://doi.org/10.3791/56265 (2017).
Kulikova, V. A., Gromyko, D. V. & Nikiforov, A. A. The Regulatory Role of NAD in Human and Animal Cells. Biochem. (Mosc.) 83, 800–812, https://doi.org/10.1134/S0006297918070040 (2018).
doi: 10.1134/S0006297918070040
Zhang, N. & Sauve, A. A. Regulatory Effects of NAD(+) Metabolic Pathways on Sirtuin Activity. Prog. Mol. Biol. Transl. Sci. 154, 71–104, https://doi.org/10.1016/bs.pmbts.2017.11.012 (2018).
doi: 10.1016/bs.pmbts.2017.11.012 pubmed: 29413178
Sharif, T. et al. Regulation of Cancer and Cancer-Related Genes via NAD(). Antioxid. Redox Signal. 30, 906–923, https://doi.org/10.1089/ars.2017.7478 (2019).
doi: 10.1089/ars.2017.7478 pubmed: 29334761
Fessel, J. P. & Oldham, W. M. Nicotine Adenine Dinucleotides: The Redox Currency of the Cell. Antioxid. Redox Signal. 28, 165–166, https://doi.org/10.1089/ars.2017.7439 (2018).
doi: 10.1089/ars.2017.7439 pubmed: 29113451 pmcid: 5911702
Ostapkowicz, A., Inai, K., Smith, L., Kreda, S. & Spychala, J. Lipid rafts remodeling in estrogen receptor-negative breast cancer is reversed by histone deacetylase inhibitor. Mol. Cancer Ther. 5, 238–245, https://doi.org/10.1158/1535-7163.MCT-05-0226 (2006).
doi: 10.1158/1535-7163.MCT-05-0226 pubmed: 16505096
Turcotte, M. et al. CD73 is associated with poor prognosis in high-grade serous ovarian cancer. Cancer Res. 75, 4494–4503, https://doi.org/10.1158/0008-5472.CAN-14-3569 (2015).
doi: 10.1158/0008-5472.CAN-14-3569 pubmed: 26363007
VanLinden, M. R. et al. Subcellular Distribution of NAD+ between Cytosol and Mitochondria Determines the Metabolic Profile of Human Cells. J. Biol. Chem. 290, 27644–27659, https://doi.org/10.1074/jbc.M115.654129 (2015).
doi: 10.1074/jbc.M115.654129 pubmed: 26432643 pmcid: 4646015
Svilar, D., Goellner, E. M., Almeida, K. H. & Sobol, R. W. Base excision repair and lesion-dependent subpathways for repair of oxidative DNA damage. Antioxid. Redox Signal. 14, 2491–2507, https://doi.org/10.1089/ars.2010.3466 (2011).
doi: 10.1089/ars.2010.3466 pubmed: 20649466 pmcid: 3096496
Masson, M. et al. XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol. Cell Biol. 18, 3563–3571, https://doi.org/10.1128/mcb.18.6.3563 (1998).
doi: 10.1128/mcb.18.6.3563 pubmed: 9584196 pmcid: 108937
Breslin, C. et al. The XRCC1 phosphate-binding pocket binds poly (ADP-ribose) and is required for XRCC1 function. Nucleic Acids Res. 43, 6934–6944, https://doi.org/10.1093/nar/gkv623 (2015).
doi: 10.1093/nar/gkv623 pubmed: 26130715 pmcid: 4538820
Okano, S., Lan, L., Caldecott, K. W., Mori, T. & Yasui, A. Spatial and temporal cellular responses to single-strand breaks in human cells. Mol. Cell Biol. 23, 3974–3981, https://doi.org/10.1128/mcb.23.11.3974-3981.2003 (2003).
doi: 10.1128/mcb.23.11.3974-3981.2003 pubmed: 12748298 pmcid: 155230
Fang, Q. et al. HSP90 regulates DNA repair via the interaction between XRCC1 and DNA polymerase beta. Nat. Commun. 5, 5513, https://doi.org/10.1038/ncomms6513 (2014).
doi: 10.1038/ncomms6513 pubmed: 25423885 pmcid: 4246423
Park, M. J. et al. PTEN suppresses hyaluronic acid-induced matrix metalloproteinase-9 expression in U87MG glioblastoma cells through focal adhesion kinase dephosphorylation. Cancer Res. 62, 6318–6322 (2002).
pubmed: 12414663
Ishii, N. et al. Frequent co-alterations of TP53, p16/CDKN2A, p14ARF, PTEN tumor suppressor genes in human glioma cell lines. Brain Pathol. 9, 469–479 (1999).
doi: 10.1111/j.1750-3639.1999.tb00536.x
Stein, G. H. T98G: an anchorage-independent human tumor cell line that exhibits stationary phase G1 arrest in vitro. J. Cell. Physiol. 99, 43–54, https://doi.org/10.1002/jcp.1040990107 (1979).
doi: 10.1002/jcp.1040990107 pubmed: 222778
Tang, J. B. et al. Bioenergetic metabolites regulate base excision repair-dependent cell death in response to DNA damage. Mol. Cancer Res. 8, 67–79, https://doi.org/10.1158/1541-7786.MCR-09-0411 (2010).
doi: 10.1158/1541-7786.MCR-09-0411 pubmed: 20068071 pmcid: 2808464
Svilar, D. et al. Alkylation sensitivity screens reveal a conserved cross-species functionome. Mol. Cancer Res. 10, 1580–1596, https://doi.org/10.1158/1541-7786.MCR-12-0168 (2012).
doi: 10.1158/1541-7786.MCR-12-0168 pubmed: 23038810

Auteurs

Anna Wilk (A)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Faisal Hayat (F)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Richard Cunningham (R)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Jianfeng Li (J)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Silvia Garavaglia (S)

Department of Pharmaceutical Sciences, University of Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy.

Leila Zamani (L)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.

Davide M Ferraris (DM)

Department of Pharmaceutical Sciences, University of Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy.

Peter Sykora (P)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Amelia Technologies, 14676 Rothgeb Drive, Rockville, MD, 20850, USA.

Joel Andrews (J)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.

Jennifer Clark (J)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Amanda Davis (A)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.

Laurent Chaloin (L)

Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier, CNRS, 34293, Montpellier, France.

Menico Rizzi (M)

Department of Pharmaceutical Sciences, University of Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy.

Marie Migaud (M)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA.

Robert W Sobol (RW)

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA. rwsobol@health.southalabama.edu.
Department of Pharmacology, College of Medicine, University of South Alabama, Mobile, AL, 36604, USA. rwsobol@health.southalabama.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH