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1Academic Journal
المؤلفون: E. V. Slukhanchuk, V. O. Bitsadze, A. G. Solopova, J. Kh. Khizroeva, N. D. Degtyareva, D. V. Shcherbakov, J.-C. Gris, I. Elalamy, A. D. Makatsariya, Е. В. Слуханчук, В. О. Бицадзе, А. Г. Солопова, Д. Х. Хизроева, Н. Д. Дегтярева, Д. В. Щербаков, Ж.-К. Гри, И. Элалами, А. Д. Макацария
المصدر: Obstetrics, Gynecology and Reproduction; Vol 17, No 1 (2023); 53-64 ; Акушерство, Гинекология и Репродукция; Vol 17, No 1 (2023); 53-64 ; 2500-3194 ; 2313-7347
مصطلحات موضوعية: рак, neutrophil extracellular traps, NETs, myeloperoxidase, MPO, D-dimer, citrullinated histone H3, citH3, cancer, внеклеточные ловушки нейтрофилов, миелопероксидаза, МПО, D-димер, цитруллинированный гистон Н3
وصف الملف: application/pdf
Relation: https://www.gynecology.su/jour/article/view/1566/1091; https://www.gynecology.su/jour/article/view/1566/1096; Timp J.F., Braekkan S.K., Versteeg H.H., Cannegieter S.C. Epidemiology of cancer-associated venous thrombosis. Blood. 2013;122(10):1712–23. https://doi.org/10.1182/blood-2013-04-460121.; Klerk C.P., Smorenburg S.M., Otten H.-M. et al. The effect of low molecular weight heparin on survival in patients with advanced malignancy. J Clin Oncol. 2005;23(10):2130–5. https://doi.org/10.1200/JCO.2005.03.134.; Akl E.A., Schünemann H.J. Routine heparin for patients with cancer? One answer, more questions. N Engl J Med. 2012;366(7):661–2. https://doi.org/10.1056/NEJMe1113672.; Stakos D.A., Kambas K., Konstantinidis T. et al. Expression of functional tissue factor by neutrophil extracellular traps in culprit artery of acute myocardial infarction. Eur Heart J. 2015;36(22):1405–14. https://doi.org/10.1093/eurheartj/ehv007.; Gould T.J., Vu T.T., Swystun L.L. et al. Neutrophil extracellular traps promote thrombin generation through platelet-dependent and plateletindependent mechanisms. Arterioscler Thromb Vasc Biol. 2014;34(9):1977–84. https://doi.org/10.1161/ATVBAHA.114.304114.; Hanahan D., Weinberg R.A. Hallmarks of cancer: the next generation. Cell. 2011;144(5):646–74. https://doi.org/10.1016/j.cell.2011.02.013.; Demers M., Krause D.S., Schatzberg D. et al. Cancers predispose neutrophils to release extracellular DNA traps that contribute to cancerassociated thrombosis. Proc Natl Acad Sci U S A. 2012;109(32):13076– 81. https://doi.org/10.1073/pnas.1200419109.; Cedervall J., Zhang Y., Huang H. et al. Neutrophil extracellular traps accumulate in peripheral blood vessels and compromise organ function in tumor-bearing animals. Cancer Res. 2015;75(13):2653–62. https://doi.org/10.1158/0008-5472.CAN-14-3299.; Nierodzik M.L., Karpatkin S. Thrombin induces tumor growth, metastasis, and angiogenesis: Evidence for a thrombin-regulated dormant tumor phenotype. Cancer Cell. 2006;10(5):355–62. https://doi.org/10.1016/j.ccr.2006.10.002.; Brinkmann V., Reichard U., Goosmann C. et al. Neutrophil extracellular traps kill bacteria. Science. 2004;303(5663):1532–5. https://doi.org/10.1126/science.1092385.; Papayannopoulos V. Neutrophil extracellular traps in immunity and disease. Nat Rev Immunol. 2018;18(2):134–47. https://doi.org/10.1038/nri.2017.105.; Wong S.L., Demers M., Martinod K. et al. Diabetes primes neutrophils to undergo NETosis, which impairs wound healing. Nat Med. 2015;21(7):815–9. https://doi.org/10.1038/nm.3887.; Schauer C., Janko C., Munoz L.E. et al. Aggregated neutrophil extracellular traps limit inflammation by degrading cytokines and chemokines. Nat Med. 2014;20(5):511–7. https://doi.org/10.1038/nm.3547.; El-Shebini E.M., Shoeib S.A., Elghotmy A.H. Neutrophil extracellular traps in systemic lupus erythematosus. Menoufia Med J. 2020;33(3):729–32. https://doi.org/10.4103/mmj.mmj_431_18.; Manneras-Holm L., Baghaei F., Holm G. et al. Coagulation and fibrinolytic disturbances in women with polycystic ovary syndrome. J Clin Endocrinol Metab. 2011;96(4):1068–76. https://doi.org/10.1210/jc.2010-2279.; Gray R.D., Hardisty G., Regan K.H. et al. Delayed neutrophil apoptosis enhances NET formation in cystic fibrosis. Thorax. 2018;73(2):134–44. https://doi.org/10.1136/thoraxjnl-2017-210134.; Fuchs T.A., Brill A., Duerschmied D. et al. Extracellular DNA traps promote thrombosis. Proc Natl Acad Sci U S A. 2010;107(36):15880–5. https://doi.org/10.1073/pnas.1005743107.; Wang L., Zhou X., Yin Y. et al. Hyperglycemia induces neutrophil extracellular traps formation through an NADPH oxidase-dependent pathway in diabetic retinopathy. Front Immunol. 2019;9:3076. https://doi.org/10.3389/fimmu.2018.03076.; Warnatsch A., Ioannou M., Wang Q., Papayannopoulos V. Inflammation. Neutrophil extracellular traps license macrophages for cytokine production in atherosclerosis. Science. 2015;349(6245):316–20. https://doi.org/10.1126/science.aaa8064.; Gould T., Lysov Z., Liaw P. Extracellular DNA and histones: double-edged swords in immunothrombosis. J Thromb Haemost. 2015;13 Suppl 1:S82– S91. https://doi.org/10.1111/jth.12977.; Demers M., Wagner D.D. Neutrophil extracellular traps: A new link to cancer-associated thrombosis and potential implications for tumor progression. Oncoimmunology. 2013;2(2):e22946. https://doi.org/10.4161/onci.22946.; Delabranche X., Helms J., Meziani F. Immunohaemostasis: a new view on haemostasis during sepsis. Ann Intensive Care. 2017;7():117. https://doi.org/10.1186/s13613-017-0339-5.; Naudin C., Burillo E., Blankenberg S. et al. Factor XII contact activation. Semin Thromb Hemost. 2017;43(8):814–26. https://doi.org/10.1055/s-0036-1598003.; Vu T.T., Leslie B.A., Stafford A.R. et al. Histidine-rich glycoprotein binds DNA and RNA and attenuates their capacity to activate the intrinsic coagulation pathway. Thromb Haemost. 2016;115(1):89–98. https://doi.org/10.1160/TH15-04-0336.; Noubouossie D.F., Whelihan M.F., Yu Y.-B. et al. In vitro activation of coagulation by human neutrophil DNA and histone proteins but not neutrophil extracellular traps. Blood. 2017;129(8):1021–9. https://doi.org/10.1182/blood-2016-06-722298.; Komissarov A.A., Florova G., Idell S. Effects of extracellular DNA on plasminogen activation and fibrinolysis. J Biol Chem. 2011;286(49):41949–62. https://doi.org/10.1074/jbc.M111.301218.; Varjú I., Longstaff C., Szabó L. et al. DNA, histones and neutrophil extracellular traps exert anti-fibrinolytic effects in a plasma environment. Thromb Haemost. 2015;113(6):1289–98. https://doi.org/10.1160/TH14-08-0669.; Longstaff C., Varjú I., Sótonyi P. et al. Mechanical stability and fibrinolytic resistance of clots containing fibrin, DNA, and histones. J Biol Chem. 2013;288(10):6946–56. https://doi.org/10.1074/jbc.M112.404301.; Qi H., Yang S., Zhang L. Neutrophil extracellular traps and endothelial dysfunction in atherosclerosis and thrombosis. Front Immunol. 2017;8:928. https://doi.org/10.3389/fimmu.2017.00928.; Xu J., Zhang X., Pelayo R. et al. Extracellular histones are major mediators of death in sepsis. Nat Med. 2009;15(11):1318–21. https://doi.org/10.1038/nm.2053.; Saffarzadeh M., Juenemann C., Queisser M.A. et al. Neutrophil extracellular traps directly induce epithelial and endothelial cell death: a predominant role of histones. PLoS One. 2012;7(2):e32366. https://doi.org/10.1371/journal.pone.0032366.; Fuchs T.A., Abed U., Goosmann C. et al. Novel cell death program leads to neutrophil extracellular traps. J Cell Biol. 2007;176(2):231–41. https://doi.org/10.1083/jcb.200606027.; Barranco-Medina S., Pozzi N., Vogt A.D., Di Cera E. Histone H4 promotes prothrombin autoactivation. J Biol Chem. 2013;288(50):35749–57. https://doi.org/10.1074/jbc.M113.509786.; Ammollo C.T., Semeraro F., Xu J. et al. Extracellular histones increase plasma thrombin generation by impairing thrombomodulin-dependent protein C activation. J Thromb Haemost. 2011;9(9):1795–803. https://doi.org/10.1111/j.1538-7836.2011.04422.x.; Gould T.J., Vu T.T., Stafford A.R. et al. Cell-free DNA modulates clot structure and impairs fibrinolysis in sepsis. Arterioscler Thromb Vasc Biol. 2015;35(12):2544–53. https://doi.org/10.1161/ATVBAHA.115.306035.; Mantovani A., Allavena P., Sica A., Balkwill F. Cancer-related inflammation. Nature. 2008;454(7203):436–44. https://doi.org/10.1038/nature07205.; Metzler K.D., Fuchs T.A., Nauseef W.M. et al. Myeloperoxidase is required for neutrophil extracellular trap formation: implications for innate immunity. Blood. 2011;117(3):953–9. https://doi.org/10.1182/blood2010-06-290171.; Al-Benna S., Shai Y., Jacobsen F., Steinstraesser L. Oncolytic activities of host defense peptides. Int J Mol Sci. 2011;12(11):8027–51. https://doi.org/10.3390/ijms12118027.; Acuff H.B., Carter K.J., Fingleton B. et al. Matrix metalloproteinase-9 from bone marrow–derived cells contributes to survival but not growth of tumor cells in the lung microenvironment. Cancer Res. 2006;66(1):259– 66. https://doi.org/10.1158/0008-5472.CAN-05-2502.; Masson V., De La Ballina L.R., Munaut C. et al. Contribution of host MMP-2 and MMP-9 to promote tumor vascularization and invasion of malignant keratinocytes. FASEB J. 2005;19(2):234–6. https://doi.org/10.1096/fj.04-2140fje.; Pahler J.C., Tazzyman S., Erez N. et al. Plasticity in tumor-promoting inflammation: impairment of macrophage recruitment evokes a compensatory neutrophil response. Neoplasia. 2008;10(4):329–40. https://doi.org/10.1593/neo.07871.; Berger-Achituv S., Brinkmann V., Abu-Abed U. et al. A proposed role for neutrophil extracellular traps in cancer immunoediting. Front Iimmunol. 2013;4:48. https://doi.org/10.3389/fimmu.2013.00048.; Cools-Lartigue J., Spicer J., McDonald B. et al. Neutrophil extracellular traps sequester circulating tumor cells and promote metastasis. J Clin Invest. 2013;123(8):3446–58. https://doi.org/10.1172/JCI67484.; Gregory A.D., Houghton A.M. Tumor-associated neutrophils: new targets for cancer therapy. Cancer Res. 2011;71()7:2411–6. https://doi.org/10.1158/0008-5472.CAN-10-2583.; https://www.gynecology.su/jour/article/view/1566
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2Academic Journal
المؤلفون: K. S. Nurbaeva, T. M. Reshetnyak, M. V. Cherkasova, A. M. Lila, К. С. Нурбаева, Т. М. Решетняк, М. В. Черкасова, А. М. Лила
المساهمون: The article has been conducted within basic scientific topic № 122040400024-7., Статья подготовлена в рамках фундаментальной научной темы № 122040400024-7.
المصدر: Modern Rheumatology Journal; Том 17, № 4 (2023); 19-27 ; Современная ревматология; Том 17, № 4 (2023); 19-27 ; 2310-158X ; 1996-7012
مصطلحات موضوعية: системная красная волчанка, citrullinated histone H3, systemic lupus erythematosus, цитруллинированный гистон Н3
وصف الملف: application/pdf
Relation: https://mrj.ima-press.net/mrj/article/view/1455/1380; Насонов ЕЛ, Соловьев СК, Аршинов АВ. Системная красная волчанка: история и современность. Научно-практическая ревматология. 2022;60(4):397-412.; Pan L, Lu MP, Wang JH, et al. Immunological pathogenesis and treatment of systemic lupus erythematosus. World J Pediatr. 2020 Feb;16(1):19-30. doi:10.1007/s12519-019-00229-3.; Wirestam L, Arve S, Linge P, Bengtsson AA. Neutrophils-Important Communicators in Systemic Lupus Erythematosus and Anti-phospholipid Syndrome. Front Immunol. 2019 Nov 22;10:2734. doi:10.3389/fimmu.2019.02734.; Mayadas TN, Cullere X, Lowell CA. The multifaceted functions of neutrophils. Annu Rev Pathol. 2014; 9:181-218. doi:10.1146/annurev-pathol-020712-164023.; Brinkmann V, Reichard U, Goosmann C, et al. Neutrophil extracellular traps kill bacteria. Science. 2004 Mar 5;303(5663):1532-5. doi:10.1126/science.1092385.; Fousert E, Toes R, Desai J. Neutrophil Extracellular Traps (NETs) Take the Central Stage in Driving Autoimmune Responses. Cells. 2020 Apr 8;9(4):915. doi:10.3390/cells9040915.; Salemme R, Peralta LN, Meka SH, et al. The Role of NETosis in Systemic Lupus Erythematosus. J Cell Immunol. 2019;1(2):33-42. doi:10.33696/immunology.1.008.; Sørensen OE, Borregaard N. Neutrophil extracellular traps — the dark side of neutrophils. J Clin Invest. 2016 May 2; 126(5): 1612-20. doi:10.1172/JCI84538.; Thalin C, Lundstrom S, Seignez C, et al. Citrullinated histone H3 as a novel prognostic blood marker in patients with advanced cancer. PLoS One. 2018 Jan 11;13(1):e0191231. doi:10.1371/journal.pone.0191231.; Paues Goranson S, Thalin C, Lundstrom A, et al. Circulating H3Cit is elevated in a human model of endotoxemia and can be detected bound to microvesicles. Sci Rep. 2018 Aug 23;8(1):12641. doi:10.1038/s41598-018-31013-4.; Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997 Sep;40(9):1725. doi:10.1002/art.1780400928.; Miyakis S, Lockshin MD, Atsumi T, et al. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thromb Haemost. 2006 Feb;4(2):295-306. doi:10.1111/j.1538-7836.2006.01753.x.; Touma Z, Urowitz MB, Ibanez D, et al. SLEDAI-2k 10 days versus SLEDAI-2k 30 days in a longitudinal evaluation. Lupus. 2011 Jan; 20(1):67-70. doi:10.1177/0961203310385163.; Gladman DD, Goldsmith CH, Urowitz MB, et al. The Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index for Systemic Lupus Erythematosus International Comparison. J Rheumatol. 2000 Feb;27(2):373-6.; Александрова ЕН, Новиков АА, Решетняк ТМ и др. Антитела к 2-гликопротеину 1 и антитела к кардиолипину при антифосфолипидном синдроме: анализ чувствительности и специфичности. Клиническая медицина. 2003;(9):25-31.; Bolouri N, Akhtari M, Farhadi E, et al. Role of the innate and adaptive immune responses in the pathogenesis of systemic lupus erythematosus. Inflamm Res. 2022 Jun; 71 (5-6):537-554. doi:10.1007/s00011-022-01554-6; Hakkim A, Furnrohr BG, Amann K, et al. Impairment of neutrophil extracellular trap degradation is associated with lupus nephritis. Proc Natl Acad Sci U S A. 2010 May 25; 107(21):9813-8. doi:10.1073/pnas.0909927107. Epub 2010 May 3.; Villanueva E, Yalavarthi S, Berthier CC, et al. Netting neutrophils induce endothelial damage, infiltrate tissues, and expose immunostimulatory molecules in systemic lupus erythematosus. J Immunol. 2011 Jul 1;187(1): 538-52. doi:10.4049/jimmunol.1100450. Epub 2011 May 25.; Leffler J, Martin M, Gullstrand B, et al. Neutrophil extracellular traps that are not degraded in systemic lupus erythematosus activate complement exacerbating the disease. J Immunol. 2012 Apr 1;188(7):3522-31. doi:10.4049/jimmunol.1102404. Epub 2012 Feb 17.; Carmona-Rivera C, Zhao W, Yalavarthi S, et al. Neutrophil extracellular traps induce endothelial dysfunction in systemic lupus erythematosus through the activation of matrix metalloproteinase-2. Ann Rheum Dis. 2015 Jul;74(7):1417-24. doi:10.1136/annrheumdis-2013-204837. Epub 2014 Feb 25.; Zhang S, Lu X, Shu X, et al. Elevated plasma cfDNA may be associated with active lupus nephritis and partially attributed to ab-normal regulation of neutrophil extracellular traps (NETs) in patients with systemic lupus erythematosus. Intern Med. 2014;53(24): 2763-71. doi:10.2169/internalmedicine.53.2570; Van der Linden M, van den Hoogen LL, Westerlaken GHA, et al. Neutrophil extracellular trap release is associated with antinuclear antibodies in systemic lupus erythematosus and anti-phospholipid syndrome. Rheumatology (Oxford). 2018 Jul 1;57(7):1228-1234. doi:10.1093/rheumatology/key067; Jeremic I, Djuric O, Nikolic M, et al. Neutrophil extracellular traps-associated markers are elevated in patients with systemic lupus erythematosus. Rheumatol Int. 2019 Nov; 39(11):1849-1857. doi:10.1007/s00296-019-04426-1. Epub 2019 Aug 23.; El-Ghoneimy DH, Hesham M, Hasan R, et al. The behavior of neutrophil extracellular traps and NADPH oxidative activity in pediatric systemic lupus erythematosus: relation to disease activity and lupus nephritis. Clin Rheumatol. 2019 Sep;38(9):2585-2593. doi:10.1007/s10067-019-04547-9; Bruschi M, Bonanni A, Petretto A, et al. Neutrophil Extracellular Traps Profiles in Patients with Incident Systemic Lupus Erythematosus and Lupus Nephritis. J Rheumatol. 2020 Mar;47(3):377-386. doi:10.3899/jrheum.181232; Moore S, Juo HH, Nielsen CT, et al. Role of Neutrophil Extracellular Traps Regarding Patients at Risk of Increased Disease Activity and Cardiovascular Comorbidity in Systemic Lupus Erythematosus. J Rheumatol. 2020 Nov 1;47(11):1652-1660. doi:10.3899/jrheum.190875. Epub 2019 Dec 15.; Hanata N, Ota M, Tsuchida Y, et al. Serum extracellular traps associate with the activation of myeloid cells in SLE patients with the low level of anti-DNA antibodies. Sci Rep. 2022 Nov 1;12(1):18397. doi:10.1038/s41598-022-23076-1.; Reshetnyak T, Nurbaeva K, Ptashnik I, Kudriaeva A, Belogurov A, Lila A, Nasonov E. Markers of NETosis in Patients with Systemic Lupus Erythematosus and Anti-phospholipid Syndrome. Int J Mol Sci. 2023 May 24;24(11):9210. doi:10.3390/ijms24119210.; Mutua V, Gershwin LJ. A Review of Neutrophil Extracellular Traps (NETs) in Disease: Potential Anti-NETs Therapeutics. Clin Rev Allergy Immunol. 2021 Oct;61(2):194-211. doi:10.1007/s12016-020-08804-7.; Peng W, Wu S, Wang W. Correlation of serum citrullinated histone H3 levels with disease activity in patients with rheumatoid arthritis. Clin Exp Rheumatol. 2023 Feb 23. doi:10.55563/clinexprheumatol/i3bcss. Online ahead of print.; Parackova Z, Zentsova I, Malcova H, et al. Increased histone citrullination in juvenile idiopathic arthritis. Front Med (Lausanne). 2022 Aug 19;9:971121. doi:10.3389/fmed.2022.971121.; Kuczia P, Zuk J, Iwaniec T, et al. Citrullinated histone H3, a marker of extracellular trap formation, is increased in blood of stable asthma patients. Clin Transl Allergy. 2020 Jul 13;10:31. doi:10.1186/s13601-020-00337-8.; Ronchetti L, Terrenato I, Ferretti M, et al. Circulating cell free DNA and citrullinated histone H3 as useful biomarkers of NETosis in endometrial cancer. J Exp Clin Cancer Res. 2022 Apr 21;41(1):151. doi:10.1186/s13046-022-02359-5; Zuo Y, Yalavarthi S, Shi H, et al. Neutrophil extracellular traps in COVID-19. JCI Insight. 2020 Jun 4;5(11):e138999. doi:10.1172/jci.insight.138999.; Ng H, Havervall S, Rosell A, et al. Circulating Markers of Neutrophil Extracellular Traps Are of Prognostic Value in Patients With COVID-19. Arterioscler Thromb Vasc Biol. 2021 Feb;41(2):988-994. doi:10.1161/ATVBAHA.120.315267.; Tian Y, Russo RM, Li Y, et al. Serum citrullinated histone H3 concentrations differentiate patients with septic verses non-septic shock and correlate with disease severity. Infection. 2021 Feb;49(1):83-93. doi:10.1007/s15010-020-01528-y.; Pan B, Li Y, Liu Y, et al. Circulating CitH3 Is a Reliable Diagnostic and Prognostic Biomarker of Septic Patients in Acute Pancreatitis. Front Immunol. 2021 Nov 17;12: 766391. doi:10.3389/fimmu.2021.766391.; https://mrj.ima-press.net/mrj/article/view/1455