Перспективы использования miRNA-378 в качестве сердечно-сосудистого биологического маркера: обзор литературы

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19. Yuan W., Liang X., Liu Y., et al. Mechanism of miR-378a-3p enriched in M2 macrophage-derived extracellular vesicles in cardiomyocyte pyroptosis after MI // Hypertens Res. 2022. Vol. 45, N. 4. P. 650–664. doi: 10.1038/s41440-022-00851-1
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21. Yan T., Li X., Nian T., et al. Salidroside inhibits ischemia/reperfusion-induced myocardial apoptosis by targeting mir-378a-3p via the IGF1R/PI3K/AKT signaling pathway // Transplant Proc. 2022. Vol. 54, N. 7. P. 1970–1983. doi: 10.1016/j.transproceed.2022.05.017
22. Ganesan J., Ramanujam D., Sassi Y., et al. MiR-378 controls cardiac hypertrophy by combined repression of mitogen-activated protein kinase pathway factors // Circulation. 2013. Vol. 127, N. 21. P. 2097–2106. doi: 10.1161/CIRCULATIONAHA.112.000882
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doi: 10.1515/med-2023-0831
26. Florczyk-Soluch U., Polak K., Sabo R., et al. Compromised diabetic heart function is not affected by miR-378a upregulation upon hyperglycemia // Pharmacol Rep. 2023. Vol. 75, N. 6. P. 1556–1570. doi: 10.1007/s43440-023-00535-8 
27. Li X. lncRNA MALAT1 promotes diabetic retinopathy by upregulating PDE6G via miR-378a-3p // Arch Physiol Biochem. 2021. Vol. 21. P. 1–9. doi: 10.1080/13813455.2021.1985144
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31. Chaulin A.M. The essential strategies to mitigate cardiotoxicity caused by doxorubicin // Life (Basel). 2023. Vol. 13, N. 11. P. 2148. doi: 10.3390/life13112148 
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doi: 10.1002/jcp.26615
35. Zhang H., Hao J., Sun X., et al. Circulating pro-angiogenic micro-ribonucleic acid in patients with coronary heart disease // Interact Cardiovasc Thorac Surg. 2018. Vol. 27, N. 3.
P. 336–342. doi: 10.1093/icvts/ivy058 
36. Li H., Gao F., Wang X., et al. Circulating microRNA-378 levels serve as a novel biomarker for assessing the severity of coronary stenosis in patients with coronary artery disease // Biosci Rep. 2019. Vol. 39, N. 5. P. BSR20182016. doi: 10.1042/BSR20182016
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40. Беграмбекова Ю.Л., Каранадзе Н.А., Плисюк А.Г., и др. Комплексная физическая реабилитация пациентов с хронической сердечной недостаточностью: влияние на клинико-функциональные показатели и анализ проблем, связанных с набором в исследование // Российский кардиологический журнал. 2022. Т. 27, № 2. С. 4814.
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41. Pala M. Exercise and microrna // Georgian Med News. 2023. N. 345. P. 146–153. 
42. Xu T., Zhou Q., Che L., et al. Circulating miR-21, miR-378, and miR-940 increase in response to an acute exhaustive exercise in chronic heart failure patients // Oncotarget. 2016. Vol. 7, N. 11. P. 12414–12425. doi: 10.18632/oncotarget.6966 

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1. Alieva AM, Teplova NV, Kislyakov VA, et al. Biomarkers in cardiology: microrna and heart failure. Terapija. 2022;(1):60–70. doi: 10.18565/therapy.2022.1.60-70
2. Li X, Han Y, Meng Y, et al. Small RNA-big impact: exosomal miRNAs in mitochondrial dysfunction in various diseases. RNA Biol. 2024;21(1):1–20.
doi: 10.1080/15476286.2023.2293343
3. Searles CD. MicroRNAs and Cardiovascular Disease Risk. Curr Cardiol Rep. 2024;26(2):51–60. doi: 10.1007/s11886-023-02014-1 
4. Yan J, Zhong X, Zhao Y, et al. Role and mechanism of miRNA in cardiac microvascular endothelial cells in cardiovascular diseases. Front Cardiovasc Med. 2024;11:1356152.
doi: 10.3389/fcvm.2024.1356152
5. Cao Y, Zheng M, Sewani MA, et al. The miR-17-92 cluster in cardiac health and disease. Birth Defects Res. 2024;116(1):e2273. doi: 10.1002/bdr2.2273 
6. Alieva AM, Reznik EV, Teplova NV, et al. MicroRNA-34a in cardiovascular disease: a glimpse into the future. Russian Cardiology Bulletin. 2023;18(1):14–22.
doi: 10.17116/Cardiobulletin20231801114
7. Wang H, Shi J, Wang J, et al. MicroRNA‑378: An important player in cardiovascular diseases (Review). Mol Med Rep. 2023;28(3):172. doi: 10.3892/mmr.2023.13059 
8. Alieva AM, Teplova NV, Reznik EV, et al. miRNA-122 as a new player in cardiovascular disease. Rossiiskii meditsinskii zhurnal. 2022;28(4):451–463. doi: 10.17816/medjrf111180
9. Krist B, Florczyk U, Pietraszek-Gremplewicz K, et al. The Role of miR-378a in Metabolism, Angiogenesis, and Muscle Biology. Int J Endocrinol. 2015;2015:281756.
doi: 10.1155/2015/281756
10. Kuang Z, Wu J, Tan Y, et al. MicroRNA in the Diagnosis and Treatment of Doxorubicin-Induced Cardiotoxicity. Biomolecules. 2023;13(3):568. doi: 10.3390/biom13030568 
11. Li Y, Jiang J, Liu W, et al. microRNA-378 promotes autophagy and inhibits apoptosis in skeletal muscle. Proc Natl Acad Sci U S A. 2018;115(46):E10849–E10858.
doi: 10.1073/pnas.1803377115
12. Camps C, Saini HK, Mole DR, et al. Integrated analysis of microRNA and mRNA expression and association with HIF binding reveals the complexity of microRNA expression regulation under hypoxia. Mol Cancer. 2014;13:28. doi: 10.1186/1476-4598-13-28
13. Zhang J, Ma J, Long K, et al. Overexpression of exosomal cardioprotective miRNAs mitigates hypoxia-induced H9c2 cells apoptosis. Int J Mol Sci. 2017;18(4):711.
doi: 10.3390/ijms18040711
14. Xing Y, Hou J, Guo T, et al. microRNA-378 promotes mesenchymal stem cell survival and vascularization under hypoxic-ischemic conditions in vitro. Stem Cell Res Ther. 2014;5(6):130. doi: 10.1186/scrt520 
15. Zhang H, Hao J, Sun X, et al. Circulating pro-angiogenic micro-ribonucleic acid in patients with coronary heart disease. Interact Cardiovasc Thorac Surg. 2018;27(3):336–342.
doi: 10.1093/icvts/ivy058 
16. Templin C, Volkmann J, Emmert MY, et al. Increased proangiogenic activity of mobilized CD34+ progenitor cells of patients with acute ST-segment-elevation myocardial infarction: Role of differential microRNA-378 expression. Arterioscler Thromb Vasc Biol. 2017;37(2):341–349. doi: 10.1161/ATVBAHA.116.308695
17. Chong H, Wei Z, Na M, et al. The PGC-1α/NRF1/miR-378a axis protects vascular smooth muscle cells from FFA-induced proliferation, migration and inflammation in atherosclerosis. Atherosclerosis. 2020;297:136–145. doi: 10.1016/j.atherosclerosis.2020.02.001
18. Chen W, Li X, Wang J, et al. miR-378a modulates macrophage phagocytosis and differentiation through targeting CD47-SIRPα axis in atherosclerosis. Scand J Immunol. 2019;90(1):e12766. doi: 10.1111/sji.12766 
19. Yuan W, Liang X, Liu Y, et al. Mechanism of miR-378a-3p enriched in M2 macrophage-derived extracellular vesicles in cardiomyocyte pyroptosis after MI. Hypertens Res. 2022;45(4):650–664. doi: 10.1038/s41440-022-00851-1
20. Zhou R, Jia Y, Wang Y, et al. Elevating miR-378 strengthens the isoflurane-mediated effects on myocardial ischemia-reperfusion injury in mice via suppression of MAPK1. Am J Transl Res. 2021;13(4):2350–2364. 
21. Yan T, Li X, Nian T, et al. Salidroside inhibits ischemia/reperfusion-induced myocardial apoptosis by targeting mir-378a-3p via the IGF1R/PI3K/AKT signaling pathway. Transplant Proc. 2022;54(7):1970–1983. doi: 10.1016/j.transproceed.2022.05.017
22. Ganesan J, Ramanujam D, Sassi Y, et al. MiR-378 controls cardiac hypertrophy by combined repression of mitogen-activated protein kinase pathway factors. Circulation. 2013;127(21):2097–2106. doi: 10.1161/CIRCULATIONAHA.112.000882
23. Chen YH, Zhong LF, Hong X, et al. Integrated Analysis of circRNA-miRNA-mRNA ceRNA Network in Cardiac Hypertrophy. Front Genet. 2022;13:781676.
doi: 10.3389/fgene.2022.781676
24. Sun F, Zhuang Y, Zhu H, et al. LncRNA PCFL promotes cardiac fibrosis via miR-378/GRB2 pathway following myocardial infarction. J Mol Cell Cardiol. 2019;133:188–198.
doi: 10.1016/j.yjmcc.2019.06.011
25. Wu L, Gao B, Shen M, et al. lncRNA LENGA sponges miR-378 to promote myocardial fibrosis in atrial fibrillation. Open Med (Wars). 2023;18(1):20230831.
doi: 10.1515/med-2023-0831
26. Florczyk-Soluch U, Polak K, Sabo R, et al. Compromised diabetic heart function is not affected by miR-378a upregulation upon hyperglycemia. Pharmacol Rep.
2023;75(6):1556–1570. doi: 10.1007/s43440-023-00535-8
27. Li X. lncRNA MALAT1 promotes diabetic retinopathy by upregulating PDE6G via miR-378a-3p. Arch Physiol Biochem. 2021;21:1–9. doi: 10.1080/13813455.2021.1985144
28. Froldi G. View on metformin: Antidiabetic and pleiotropic effects, pharmacokinetics, side effects, and sex-related differences. Pharmaceuticals (Basel). 2024;17(4):478.
doi: 10.3390/ph17040478 
29. Khokhar M, Roy D, Bajpai NK, et al. Metformin mediates microRNA-21 regulated circulating matrix metalloproteinase-9 in diabetic nephropathy: an in-silico and clinical study. Arch Physiol Biochem. 2023;129(6):1200–1210. doi: 10.1080/13813455.2021.1922457
30. Machado IF, Teodoro JS, Castela AC, et al. miR-378a-3p participates in metformin's mechanism of action on C2C12 cells under hyperglycemia. Int J Mol Sci. 2021;22(2):541.
doi: 10.3390/ijms22020541
31. Chaulin AM. The essential strategies to mitigate cardiotoxicity caused by Doxorubicin. Life (Basel). 2023;13(11):2148. doi: 10.3390/life13112148
32. Mattioli R, Ilari A, Colotti B, et al. Doxorubicin and other anthracyclines in cancers: Activity, chemoresistance and its overcoming. Mol Aspects Med. 2023;93:101205.
doi: 10.1016/j.mam.2023.101205
33. Wang Y, Zhang Q, Wei C, et al. MiR-378 modulates energy imbalance and apoptosis of mitochondria induced by doxorubicin. Am J Transl Res. 2018;10(11):3600–3609.
34. Wang Y, Cui X, Wang Y, et al. Protective effect of miR378* on doxorubicin-induced cardiomyocyte injury via calumenin. J Cell Physiol. 2018;233(10):6344–6351.
doi: 10.1002/jcp.26615
35. Zhang H, Hao J, Sun X, et al. Circulating pro-angiogenic micro-ribonucleic acid in patients with coronary heart disease. Interact Cardiovasc Thorac Surg. 2018;27(3):336–342.
doi: 10.1093/icvts/ivy058
36. Li H, Gao F, Wang X, et al. Circulating microRNA-378 levels serve as a novel biomarker for assessing the severity of coronary stenosis in patients with coronary artery disease. Biosci Rep. 2019;39(5):BSR20182016. doi: 10.1042/BSR20182016
37. Shen J, Chang C, Ma J, et al. Potential of circulating proangiogenic microRNAs for predicting major adverse cardiac and cerebrovascular events in unprotected left main coronary artery disease patients who underwent coronary artery bypass grafting. Cardiology. 2021;146(3):400–408. doi: 10.1159/000509275
38. Dai R, Liu Y, Zhou Y, et al. Potential of circulating pro-angiogenic microRNA expressions as biomarkers for rapid angiographic stenotic progression and restenosis risks in coronary artery disease patients underwent percutaneous coronary intervention. J Clin Lab Anal. 2020;34(1):e23013. doi: 10.1002/jcla.23013
39. Chen Z, Li C, Xu Y, et al. Circulating level of miR-378 predicts left ventricular hypertrophy in patients with aortic stenosis. PLoS One. 2014;9(8):e105702.
doi: 10.1371/journal.pone.0105702
40. Begrambekova YuL, Karanadze NA, Plisyuk AG, et al. Comprehensive physical rehabilitation of patients with heart failure: impact on clinical and functional status and analysis of problems related to the enrollment. Russian Journal of Cardiology. 2022;27(2):4814. doi: 10.15829/1560-4071-2022-4814
41. Pala M. Exercise and microrna. Georgian Med News. 2023;(345):146–153. 
42. Xu T, Zhou Q, Che L, et al. Circulating miR-21, miR-378, and miR-940 increase in response to an acute exhaustive exercise in chronic heart failure patients. Oncotarget. 2016;7(11):12414–12425. doi: 10.18632/oncotarget.6966 

А.М. Алиева*¹, Н.Х. Хаджиева², И.Е. Байкова¹, А.М. Рахаев³, И.А. Котикова¹, И.Г. Никитин<sup>1

1</sup>Российский национальный исследовательский медицинский университет им. Н.И. Пирогова, Москва, Россия;
²Клиника генетики ДНК «МедЭстет», Москва, Россия;
³Кабардино-Балкарский государственный университет им. Х.М. Бербекова, Нальчик, Россия
*amisha_alieva@mail.ru

________________________________________________

Amina M. Alieva*¹, Nyurzhanna Kh. Khadzhieva², Irina E. Baykova¹, Alik M. Rakhaev³, Irina A. Kotikova¹, Igor G. Nikitin<sup>1

1</sup>Pirogov Russian National Research Medical University, Moscow, Russia;
²Clinic of DNA Genetics “MedEstet”, Moscow, Russia;
³Kabardino-Balkarian State University named after H.M. Berbekov, Nalchik, Russia
*amisha_alieva@mail.ru