Cited by 88MicroRNA in disease regulationPlant Molecular Biology ResearchNeuroinflammation and Neurodegeneration Mechanisms

let-7 microRNAs: Their Role in Cerebral and Cardiovascular Diseases, Inflammation, Cancer, and Their Regulation

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Bernstein, David L., Jiang, Xinpei, Rom, Slava·2021·Biomedicines

Abstract

The let-7 family is among the first microRNAs found. Recent investigations have indicated that it is highly expressed in many systems, including cerebral and cardiovascular systems. Numerous studies have implicated the aberrant expression of let-7 members in cardiovascular diseases, such as stroke, myocardial infarction (MI), cardiac fibrosis, and atherosclerosis as well as in the inflammation related to these diseases. Furthermore, the let-7 microRNAs are involved in development and differentiation of embryonic stem cells in the cardiovascular system. Numerous genes have been identified as target genes of let-7, as well as a number of the let-7’ regulators. Further studies are necessary to identify the gene targets and signaling pathways of let-7 in cardiovascular diseases and inflammatory processes. The bulk of the let-7’ regulatory proteins are well studied in development, proliferation, differentiation, and cancer, but their roles in inflammation, cardiovascular diseases, and/or stroke are not well understood. Further knowledge on the regulation of let-7 is crucial for therapeutic advances. This review focuses on research progress regarding the roles of let-7 and their regulation in cerebral and cardiovascular diseases and associated inflammation.

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  • let-7a-5p inhibits EMT and reduces fibrosis.

    “It has been reported to inhibit EMT and reduce fibrosis, both of which are crucial factors in the progression of AMD.”

    From rAAV-mediated Multi-miRNA Delivery Targeting MAPK Pathway Suppresses Laser-induced Choroidal Neovascularization in Mice (2026) · cites this paper as [27]

    Section 1, “The let-7 Family and Inflammation” (page unavailable), links the let-7 family to FGF/TGF-β signaling in endothelial cells, and the References list studies concerning let-7 and endothelial-to-mesenchymal transition and let-7i and vascular fibrosis. The copy does not say that let-7a-5p specifically inhibits EMT or reduces fibrosis; its mention of let-7a-5p explains miRNA naming, not those effects. (LLM, conf=0.76)

    Experimental — accuracy not yet measured
  • The three selected miRNAs-hsa-miR-122-5p, hsa-let-7a-5p, and hsa-miR-26a-5p-provide complementary and comprehensive coverage of almost all critical genes associated with the MAPK signaling pathway.

    “From this analysis, we selected the three abundant miRNAs-hsa-miR-122-5p, hsa-let-7a-5p, and hsa-miR26a-5p-based on their complementary and comprehensive coverage of almost all the critical genes associated with the MAPK signaling pathway 27-33 as analyzed using miRTarBase version 8.0 and TarBase v8.0 integrated within miRNet (Figure S1).”

    From rAAV-mediated Multi-miRNA Delivery Targeting MAPK Pathway Suppresses Laser-induced Choroidal Neovascularization in Mice (2026) · cites this paper as [27]

    Section 1 discusses let-7 targets involved in cell signaling, and the References list a study of miR-98 targeting MAPK6, but neither passage addresses the claimed coverage of MAPK-pathway genes by the three selected miRNAs. Searches for MAPK coverage, the three miRNA names, and the named target databases found no passage assessing that combination. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

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  1. [1]Reinhart B.J. Slack F.J. Basson M. Pasquinelli A.E. Bettinger J.C. Rougvie A.E. Horvitz H.R. Ruvkun G. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans Nat. Cell Biol. 2000 403 901 906 10.1038/35002607 10706289 · DOI
  2. [2]Ali A. Bouma G.J. Anthony R.V. Winger Q.A. The Role of LIN28-let-7-ARID3B Pathway in Placental Development Int. J. Mol. Sci. 2020 21 3637 10.3390/ijms21103637 PMC7279312 32455665 · DOI
  3. [3]Roush S. Slack F.J. The let-7 family of microRNAs Trends Cell Biol. 2008 18 505 516 10.1016/j.tcb.2008.07.007 18774294 · DOI
  4. [4]Hertel J. Bartschat S. Wintsche A. Otto C. The Students of the Bioinformatics Computer Lab Stadler P.F. Evolution of the let-7 microRNA Family RNA Biol. 2012 9 231 241 10.4161/rna.18974 22617875 PMC3384580 · DOI
  5. [5]Wu Y.-C. Chen C.-H. Mercer A. Sokol N.S. let-7-Complex MicroRNAs Regulate the Temporal Identity of Drosophila Mushroom Body Neurons via chinmo Dev. Cell 2012 23 202 209 10.1016/j.devcel.2012.05.013 22814608 PMC3401410 · DOI
  6. [6]Lee H. Han S. Kwon C.S. Lee D. Biogenesis and regulation of the let-7 miRNAs and their functional implications Protein Cell 2016 7 100 113 10.1007/s13238-015-0212-y 26399619 PMC4742387 · DOI
  7. [7]Bartel D.P. MicroRNAs: Genomics, Biogenesis, Mechanism, and Function Cell 2004 116 281 297 10.1016/S0092-8674(04)00045-5 14744438 · DOI
  8. [8]Eder P.S. Devine R.J. Dagle J. Walder J.A. Substrate Specificity and Kinetics of Degradation of Antisense Oligonucleotides by a 3′ Exonuclease in Plasma Antisense Res. Dev. 1991 1 141 151 10.1089/ard.1991.1.141 1841656 · DOI
  9. [9]Li S. Wang X. Gu Y. Chen C. Wang Y. Liu J. Hu W. Yu B. Wang Y. Ding F. Let-7 microRNAs Regenerate Peripheral Nerve Regeneration by Targeting Nerve Growth Factor Mol. Ther. 2015 23 423 433 10.1038/mt.2014.220 25394845 PMC4351454 · DOI
  10. [10]Gérard C. Lemaigre F. Gonze D. Modeling the Dynamics of Let-7-Coupled Gene Regulatory Networks Linking Cell Proliferation to Malignant Transformation Front. Physiol. 2019 10 848 10.3389/fphys.2019.00848 31354514 PMC6637753 · DOI
  11. [11]Wei J. Li H. Wang S. Li T. Fan J. Liang X. Li J. Han Q. Zhu L. Fan L. let-7 Enhances Osteogenesis and Bone Formation While Repressing Adipogenesis of Human Stromal/Mesenchymal Stem Cells by Regulating HMGA2 Stem Cells Dev. 2014 23 1452 1463 10.1089/scd.2013.0600 24617339 PMC4066225 · DOI
  12. [12]Tolonen A. Magga J. Szabó Z. Viitala P. Gao E. Moilanen A. Ohukainen P. Vainio L. Koch W.J. Kerkelä R. Inhibition of Let-7 micro RNA attenuates myocardial remodeling and improves cardiac function postinfarction in mice Pharmacol. Res. Perspect. 2014 2 e00056 10.1002/prp2.56 25505600 PMC4186442 · DOI
  13. [13]Jiang X.-M. Yu X.-F. Wang Z.-K. Liu F.-F. Wang Y. Let-7a gene knockdown protects against cerebral ischemia/reperfusion injury Neural Regen. Res. 2016 11 262 269 10.4103/1673-5374.177734 27073379 PMC4810990 · DOI
  14. [14]Na H.S.T. Nuo M. Meng Q.-T. Xia Z.-Y. The Pathway of Let-7a-1/2-3p and HMGB1 Mediated Dexmedetomidine Inhibiting Microglia Activation in Spinal Cord Ischemia-Reperfusion Injury Mice J. Mol. Neurosci. 2019 69 106 114 10.1007/s12031-019-01338-4 31190218 · DOI
  15. [15]Cho K.J. Song J. Oh Y. Lee J.E. MicroRNA-Let-7a regulates the function of microglia in inflammation Mol. Cell. Neurosci. 2015 68 167 176 10.1016/j.mcn.2015.07.004 26221772 · DOI
  16. [16]Wang S. Zhou H. Wu D. Ni H. Chen Z. Chen C. Xiang Y. Dai K. Chen X. Li X. MicroRNA let-7a regulates angiogenesis by targetingTGFBR3mRNA J. Cell. Mol. Med. 2019 23 556 567 10.1111/jcmm.13960 30467960 PMC6307798 · DOI
  17. [17]Ham O. Lee S.-Y. Lee C.Y. Park J.-H. Lee J. Seo H.-H. Cha M.-J. Choi E. Kim S. Hwang K.-C. let-7b suppresses apoptosis and autophagy of human mesenchymal stem cells transplanted into ischemia/reperfusion injured heart 7by targeting caspase-3 Stem Cell Res. Ther. 2015 6 147 10.1186/s13287-015-0134-x 26296645 PMC4546263 · DOI
  18. [18]Long G. Wang F. Li H. Yin Z. Sandip C. Lou Y. Wang Y. Chen C. Wang D.W. Circulating miR-30a, miR-126 and let-7b as biomarker for ischemic stroke in humans BMC Neurol. 2013 13 178 10.1186/1471-2377-13-178 24237608 PMC3840584 · DOI
  19. [19]Chi N. Chiou H. Chou S. Hu C. Chen K. Chang C. Hsieh Y. Hyperglycemia-related FAS gene and hsa-let-7b-5p as markers of poor outcomes for ischaemic stroke Eur. J. Neurol. 2020 27 1647 1655 10.1111/ene.14288 32352616 · DOI
  20. [20]Li S. Chen L. Zhou X. Li J. Liu J. miRNA-223-3p and let-7b-3p as potential blood biomarkers associated with the ischemic penumbra in rats Acta Neurobiol. Exp. 2019 79 205 216 10.21307/ane-2019-018 31342956 · DOI
  21. [21]Bernstein D.L. Zuluaga-Ramirez V. Gajghate S. Reichenbach N.L. Polyak B. Persidsky Y. Rom S. miR-98 reduces endothelial dysfunction by protecting blood–brain barrier (BBB) and improves neurological outcomes in mouse ischemia/reperfusion stroke model Br. J. Pharmacol. 2019 40 1953 1965 10.1177/0271678X19882264 PMC7786850 31601141 · DOI · Paper page
  22. [22]Li H.-W. Meng Y. Xie Q. Yi W.-J. Lai X.-L. Bian Q. Wang J. Wang J.-F. Yu G. miR-98 protects endothelial cells against hypoxia/reoxygenation induced-apoptosis by targeting caspase-3 Biochem. Biophys. Res. Commun. 2015 467 595 601 10.1016/j.bbrc.2015.09.058 26367177 · DOI
  23. [23]Rom S. Dykstra H. Zuluaga-Ramirez V. Reichenbach N.L. Persidsky Y. miR-98 and let-7g* Protect the Blood-Brain Barrier Under Neuroinflammatory Conditions Br. J. Pharmacol. 2015 35 1957 1965 10.1038/jcbfm.2015.154 PMC4671116 26126865 · DOI · Paper page
  24. [24]Bernstein D.L. Rom S. Let-7g* and miR-98 Reduce Stroke-Induced Production of Proinflammatory Cytokines in Mouse Brain Front. Cell Dev. Biol. 2020 8 632 10.3389/fcell.2020.00632 32766248 PMC7379105 · DOI
  25. [25]Bernstein D.L. Gajghate S. Reichenbach N.L. Winfield M. Persidsky Y. Heldt N.A. Rom S. let-7g counteracts endothelial dysfunction and ameliorating neurological functions in mouse ischemia/reperfusion stroke model Brain Behav. Immun. 2020 87 543 555 10.1016/j.bbi.2020.01.026 32017988 PMC7316629 · DOI
  26. [26]Xiang W. Tian C. Peng S. Zhou L. Pan S. Deng Z. Let-7i attenuates human brain microvascular endothelial cell damage in oxygen glucose deprivation model by decreasing toll-like receptor 4 expression Biochem. Biophys. Res. Commun. 2017 493 788 793 10.1016/j.bbrc.2017.08.093 28844675 · DOI
  27. [27]Jickling G.C. Ander B.P. Shroff N. Orantia M. Stamova B. Dykstra-Aiello C. Hull H. Zhan X. Liu D. Sharp F.R. Leukocyte response is regulated by microRNA let7i in patients with acute ischemic stroke Neurology 2016 87 2198 2205 10.1212/WNL.0000000000003354 27784773 PMC5123554 · DOI
  28. [28]Chen D. Li L. Wang Y. Xu R. Peng S. Zhou L. Deng Z. Ischemia-reperfusion injury of brain induces endothelial-mesenchymal transition and vascular fibrosis via activating let-7i/TGF-βR1 double-negative feedback loop FASEB J. 2020 34 7178 7191 10.1096/fj.202000201R 32274860 · DOI
  29. [29]Lin Z. Ge J. Wang Z. Ren J. Wang X. Xiong H. Gao J. Zhang Y. Zhang Q. Let-7e modulates the inflammatory response in vascular endothelial cells through ceRNA crosstalk Sci. Rep. 2017 7 42498 10.1038/srep42498 28195197 PMC5307339 · DOI
  30. [30]Huang S. Lv Z. Guo Y. Li L. Zhang Y. Zhou L. Yang B. Wu S. Zhang Y. Xie C. Identification of Blood Let-7e-5p as a Biomarker for Ischemic Stroke PLoS ONE 2016 11 e0163951 10.1371/journal.pone.0163951 27776139 PMC5077157 · DOI
  31. [31]Nguyen T. Su C. Singh M. Let-7i inhibition enhances progesterone-induced functional recovery in a mouse model of ischemia Proc. Natl. Acad. Sci. USA 2018 115 E9668 E9677 10.1073/pnas.1803384115 30237284 PMC6187141 · DOI
  32. [32]Yuan H. Zhang H. Hong L. Zhao H. Wang J. Li H. Che H. Zhang Z. MicroRNA let-7c-5p Suppressed Lipopolysaccharide-Induced Dental Pulp Inflammation by Inhibiting Dentin Matrix Protein-1-Mediated Nuclear Factor kappa B (NF-κB) Pathway In Vitro and In Vivo Med Sci. Monit. 2018 24 6656 6665 10.12659/MSM.909093 30238933 PMC6162970 · DOI
  33. [33]Wong L.L. Saw E.L. Lim J.Y. Zhou Y. Richards A.M. Wang P. MicroRNA Let-7d-3p Contributes to Cardiac Protection via Targeting HMGA2 Int. J. Mol. Sci. 2019 20 1522 10.3390/ijms20071522 PMC6480063 30934671 · DOI
  34. [34]Hsu P.-Y. Hsi E. Wang T.-M. Lin R.-T. Liao Y.-C. Juo S.-H.H. MicroRNA let-7g possesses a therapeutic potential for peripheral artery disease J. Cell. Mol. Med. 2016 21 519 529 10.1111/jcmm.12997 27696675 PMC5323674 · DOI
  35. [35]Zhuang Y. Peng H. Mastej V. Chen W. MicroRNA Regulation of Endothelial Junction Proteins and Clinical Consequence Mediat. Inflamm. 2016 2016 1 6 10.1155/2016/5078627 PMC5143735 27999452 · DOI
  36. [36]Bao M.-H. Feng X. Zhang Y.-W. Lou X.-Y. Cheng Y. Zhou H.-H. Let-7 in Cardiovascular Diseases, Heart Development and Cardiovascular Differentiation from Stem Cells Int. J. Mol. Sci. 2013 14 23086 23102 10.3390/ijms141123086 24284400 PMC3856107 · DOI
  37. [37]Joshi S. Wei J. Bishopric N.H. A cardiac myocyte-restricted Lin28/let-7 regulatory axis promotes hypoxia-mediated apoptosis by inducing the AKT signaling suppressor PIK3IP1 Biochim. Biophys. Acta (BBA) Mol. Basis Dis. 2016 1862 240 251 10.1016/j.bbadis.2015.12.004 PMC4732518 26655604 · DOI
  38. [38]Hennchen M. Stubbusch J. Makhfi I.A.-E. Kramer M. Deller T. Pierre-Eugene C. Janoueix-Lerosey I. Delattre O. Ernsberger U. Schulte J.H. Lin28B and Let-7 in the Control of Sympathetic Neurogenesis and Neuroblastoma Development J. Neurosci. 2015 35 16531 16544 10.1523/JNEUROSCI.2560-15.2015 26674877 PMC6605513 · DOI
  39. [39]Gulman N.K. Armon L. Shalit T. Urbach A. Heterochronic regulation of lung development via the Lin28-Let-7 pathway FASEB J. 2019 33 12008 12018 10.1096/fj.201802702R 31373834 PMC6902705 · DOI
  40. [40]Fairchild C.L.A. Cheema S.K. Wong J. Hino K. Simó S. La Torre A. Let-7 regulates cell cycle dynamics in the developing cerebral cortex and retina Sci. Rep. 2019 9 15336 10.1038/s41598-019-51703-x 31653921 PMC6814839 · DOI
  41. [41]Morgado A.L. Rodrigues C.M.P. Solá S. MicroRNA-145 Regulates Neural Stem Cell Differentiation Through the Sox2-Lin28/let-7 Signaling Pathway STEM CELLS 2016 34 1386 1395 10.1002/stem.2309 26849971 · DOI
  42. [42]Deng Z. Wei Y. Yao Y. Gao S. Wang X. Let-7f promotes the differentiation of neural stem cells in rats Am. J. Transl. Res. 2020 12 5752 5761 33042454 PMC7540113
  43. [43]Chen P.-Y. Qin L. Barnes C. Charisse K. Yi T. Zhang X. Ali R. Medina P.P. Yu J. Slack F.J. FGF Regulates TGF-β Signaling and Endothelial-to-Mesenchymal Transition via Control of let-7 miRNA Expression Cell Rep. 2012 2 1684 1696 10.1016/j.celrep.2012.10.021 23200853 PMC3534912 · DOI · Paper page
  44. [44]Kalomoiris S. Cicchetto A.C. Lakatos K. Nolta J.A. Fierro F.A. Fibroblast Growth Factor 2 Regulates High Mobility Group A2 Expression in Human Bone Marrow-Derived Mesenchymal Stem Cells J. Cell. Biochem. 2016 117 2128 2137 10.1002/jcb.25519 26888666 PMC5497688 · DOI
  45. [45]Liao Y.-C. Wang Y.-S. Guo Y.-C. Lin W.-L. Chang M.-H. Juo S.-H.H. Let-7g Improves Multiple Endothelial Functions Through Targeting Transforming Growth Factor-Beta and SIRT-1 Signaling J. Am. Coll. Cardiol. 2014 63 1685 1694 10.1016/j.jacc.2013.09.069 24291274 · DOI
  46. [46]Mozos I. Malainer C. Horbańczuk J. Gug C. Stoian D. Luca C.T. Atanasov A.G. Inflammatory Markers for Arterial Stiffness in Cardiovascular Diseases Front. Immunol. 2017 8 1058 10.3389/fimmu.2017.01058 28912780 PMC5583158 · DOI
  47. [47]Tonini T. Rossi F. Claudio P.P. Molecular basis of angiogenesis and cancer Oncogene 2003 22 6549 6556 10.1038/sj.onc.1206816 14528279 · DOI
  48. [48]Isanejad A. Alizadeh A.M. Shalamzari S.A. Khodayari H. Khodayari S. Khori V. Khojastehnjad N. MicroRNA-206, let-7a and microRNA-21 pathways involved in the anti-angiogenesis effects of the interval exercise training and hormone therapy in breast cancer Life Sci. 2016 151 30 40 10.1016/j.lfs.2016.02.090 26924493 · DOI
  49. [49]Wang T. Wang G. Hao D. Liu X. Wang D. Ning N. Li X. Aberrant regulation of the LIN28A/LIN28B and let-7 loop in human malignant tumors and its effects on the hallmarks of cancer Mol. Cancer 2015 14 1 13 10.1186/s12943-015-0402-5 26123544 PMC4512107 · DOI
  50. [50]Buonfiglioli A. Efe I.E. Guneykaya D. Ivanov A. Huang Y. Orlowski E. Krüger C. Deisz R.A. Markovic D. Flüh C. let-7 MicroRNAs Regulate Microglial Function and Suppress Glioma Growth through Toll-Like Receptor 7 Cell Rep. 2019 29 3460 3471.e7 10.1016/j.celrep.2019.11.029 31825829 · DOI
  51. [51]Wu T. Jia J. Xiong X. He H. Bu L. Zhao Z. Huang C. Zhang W. Increased Expression of Lin28B Associates with Poor Prognosis in Patients with Oral Squamous Cell Carcinoma PLoS ONE 2013 8 e83869 10.1371/journal.pone.0083869 24386298 PMC3875533 · DOI
  52. [52]Tristán-Ramos P. Rubio-Roldan A. Peris G. Sánchez L. Amador-Cubero S. Viollet S. Cristofari G. Heras S.R. The tumor suppressor microRNA let-7 inhibits human LINE-1 retrotransposition Nat. Commun. 2020 11 1 14 10.1038/s41467-020-19430-4 33177501 PMC7658363 · DOI
  53. [53]Chen Y. Xie C. Zheng X. Nie X. Wang Z. Liu H. Zhao Y. LIN28/let-7/PD-L1 Pathway as a Target for Cancer Immunotherapy Cancer Immunol. Res. 2019 7 487 497 10.1158/2326-6066.CIR-18-0331 30651289 · DOI
  54. [54]Mardani R. Abadi M.H.J.N. Motieian M. Taghizadeh-Boroujeni S. Bayat A. Farsinezhad A. Gheibi-Hayat S.M. Motieian M. Pourghadamyari H. MicroRNA in leukemia: Tumor suppressors and oncogenes with prognostic potential J. Cell. Physiol. 2019 234 8465 8486 10.1002/jcp.27776 30515779 · DOI
  55. [55]Brennan E. Wang B. McClelland A. Mohan M. Marai M. Beuscart O. Derouiche S. Gray S. Pickering R. Tikellis C. Protective Effect of let-7 miRNA Family in Regulating Inflammation in Diabetes-Associated Atherosclerosis Diabetes 2017 66 2266 2277 10.2337/db16-1405 28487436 · DOI
  56. [57]Li X.-X. Di X. Cong S. Wang Y. Wang K. The role of let-7 and HMGA2 in the occurrence and development of lung cancer: A systematic review and meta-analysis Eur. Rev. Med. Pharmacol. Sci. 2018 22 8353 8366 30556876
  57. [58]Tsang W.P. Kwok T.T. Let-7a microRNA suppresses therapeutics-induced cancer cell death by targeting caspase-3 Apoptosis 2008 13 1215 1222 10.1007/s10495-008-0256-z 18758960 · DOI
  58. [59]Zha W. Guan S. Liu N. Li Y. Tian Y. Chen Y. Wang Y. Wu F. Let-7a inhibits Bcl-xl and YAP1 expression to induce apoptosis of trophoblast cells in early-onset severe preeclampsia Sci. Total Environ. 2020 745 139919 10.1016/j.scitotenv.2020.139919 32721616 · DOI
  59. [60]Zhang H. Xiong X. Gu L. Xie W. Zhao H. CD4 T cell deficiency attenuates ischemic stroke, inhibits oxidative stress, and enhances Akt/mTOR survival signaling pathways in mice Chin. Neurosurg. J. 2018 4 1 7 10.1186/s41016-018-0140-9 32832192 PMC7398241 · DOI
  60. [61]Wang G. Zhang Z. Ayala C. Dunet D.O. Fang J. George M.G. Costs of Hospitalization for Stroke Patients Aged 18-64 Years in the United States J. Stroke Cerebrovasc. Dis. 2014 23 861 868 10.1016/j.jstrokecerebrovasdis.2013.07.017 23954598 PMC4544732 · DOI
  61. [62]Shi X.-Y. Wang H. Wang W. Gu Y.-H. MiR-98-5p regulates proliferation and metastasis of MCF-7 breast cancer cells by targeting Gab2 Eur. Rev. Med. Pharmacol. Sci. 2020 24 10914 33215398
  62. [63]Chen Y.-L. Qiao Y.-C. Xu Y. Ling W. Pan Y.-H. Huang Y.-C. Geng L.-J. Zhao H.-L. Zhang X.-X. Serum TNF-α concentrations in type 2 diabetes mellitus patients and diabetic nephropathy patients: A systematic review and meta-analysis Immunol. Lett. 2017 186 52 58 10.1016/j.imlet.2017.04.003 28414180 · DOI
  63. [64]Hu C. Huang S. Wu F. Ding H. miR-98 inhibits cell proliferation and induces cell apoptosis by targeting MAPK6 in HUVECs Exp. Ther. Med. 2018 15 2755 2760 10.3892/etm.2018.5735 29456679 PMC5795499 · DOI
  64. [65]Zhao C. Popel A.S. Computational Model of MicroRNA Control of HIF-VEGF Pathway: Insights into the Pathophysiology of Ischemic Vascular Disease and Cancer PLoS Comput. Biol. 2015 11 e1004612 10.1371/journal.pcbi.1004612 26588727 PMC4654485 · DOI
  65. [66]Wang L. Lin Z.Q. Wong A. COVID-Net: A tailored deep convolutional neural network design for detection of COVID-19 cases from chest X-ray images Sci. Rep. 2020 10 1 12 10.1038/s41598-020-76550-z 33177550 PMC7658227 · DOI
  66. [67]Chirshev E. Oberg K. Ioffe Y.J. Unternaehrer J.J. Let-7as biomarker, prognostic indicator, and therapy for precision medicine in cancer Clin. Transl. Med. 2019 8 24 10.1186/s40169-019-0240-y 31468250 PMC6715759 · DOI
  67. [68]Hammell C.M. Karp X. Ambros V. A feedback circuit involving let-7-family miRNAs and DAF-12 integrates environmental signals and developmental timing in Caenorhabditis elegans Proc. Natl. Acad. Sci. USA 2009 106 18668 18673 10.1073/pnas.0908131106 19828440 PMC2774035 · DOI
  68. [69]Bethke A. Fielenbach N. Wang Z. Mangelsdorf D.J. Antebi A. Nuclear Hormone Receptor Regulation of MicroRNAs Controls Developmental Progression Science 2009 324 95 98 10.1126/science.1164899 19342589 PMC2757405 · DOI
  69. [70]Chang T.-C. Yu D. Lee Y.-S. Wentzel E.A. Arking D.E. West K.M. Dang C.V. Thomas-Tikhonenko A. Mendell J.T. Widespread microRNA repression by Myc contributes to tumorigenesis Nat. Genet. 2007 40 43 50 10.1038/ng.2007.30 18066065 PMC2628762 · DOI
  70. [71]Wang Z. Lin S. Li J.J. Xu Z. Yao H. Zhu X. Xie D. Shen Z. Sze J. Li K. MYC Protein Inhibits Transcription of the MicroRNA Cluster MC-let-7a-1∼let-7d via Noncanonical E-box* J. Biol. Chem. 2011 286 39703 39714 10.1074/jbc.M111.293126 21903590 PMC3220549 · DOI
  71. [72]Van Wynsberghe P.M. Finnegan E.F. Stark T. Angelus E.P. Homan K.E. Yeo E. Pasquinelli A.E. The Period protein homolog LIN-42 negatively regulates microRNA biogenesis in C. elegans Dev. Biol. 2014 390 126 135 10.1016/j.ydbio.2014.03.017 24699545 PMC4077587 · DOI
  72. [73]McCulloch K.A. Rougvie A.E. Caenorhabditis elegans period homolog lin-42 regulates the timing of heterochronic miRNA expression Proc. Natl. Acad. Sci. USA 2014 111 15450 15455 10.1073/pnas.1414856111 25319259 PMC4217435 · DOI
  73. [74]Heo I. Joo C. Cho J. Ha M. Han J. Kim V.N. Lin28 Mediates the Terminal Uridylation of let-7 Precursor MicroRNA Mol. Cell 2008 32 276 284 10.1016/j.molcel.2008.09.014 18951094 · DOI
  74. [75]Rybak A. Fuchs H. Smirnova L. Brandt C. Pohl E.E. Nitsch R. Wulczyn F.G. A feedback loop comprising lin-28 and let-7 controls pre-let-7 maturation during neural stem-cell commitment Nat. Cell Biol. 2008 10 987 993 10.1038/ncb1759 18604195 · DOI
  75. [76]Viswanathan S. Daley G.Q. Gregory R.I. Selective Blockade of MicroRNA Processing by Lin28 Science 2008 320 97 100 10.1126/science.1154040 18292307 PMC3368499 · DOI
  76. [77]Hagan J.P. Piskounova E. Gregory R.I. Lin28 recruits the TUTase Zcchc11 to inhibit let-7 maturation in mouse embryonic stem cells Nat. Struct. Mol. Biol. 2009 16 1021 1025 10.1038/nsmb.1676 19713958 PMC2758923 · DOI · Paper page
  77. [78]Heo I. Joo C. Kim Y.-K. Ha M. Yoon M.-J. Cho J. Yeom K.-H. Han J. Kim V.N. TUT4 in Concert with Lin28 Suppresses MicroRNA Biogenesis through Pre-MicroRNA Uridylation Cell 2009 138 696 708 10.1016/j.cell.2009.08.002 19703396 · DOI · Paper page
  78. [79]Piskounova E. Polytarchou C. Thornton J.E. Lapierre R.J. Pothoulakis C. Hagan J.P. Iliopoulos D. Gregory R.I. Lin28A and lin28B Inhibit let-7 microRNA biogenesis by distinct mechanisms Cell 2011 147 1066 1079 10.1016/j.cell.2011.10.039 22118463 PMC3227872 · DOI
  79. [80]Thornton J.E. Chang H.-M. Piskounova E. Gregory R.I. Lin28-mediated control of let-7 microRNA expression by alternative TUTases Zcchc11 (TUT4) and Zcchc6 (TUT7) RNA 2012 18 1875 1885 10.1261/rna.034538.112 22898984 PMC3446710 · DOI
  80. [81]Newman M.A. Thomson J.M. Hammond S.M. Lin-28 interaction with the Let-7 precursor loop mediates regulated microRNA processing RNA 2008 14 1539 1549 10.1261/rna.1155108 18566191 PMC2491462 · DOI
  81. [82]Heo I. Ha M. Lim J. Yoon M.-J. Park J.-E. Kwon S.C. Chang H. Kim V.N. Mono-Uridylation of Pre-MicroRNA as a Key Step in the Biogenesis of Group II let-7 MicroRNAs Cell 2012 151 521 532 10.1016/j.cell.2012.09.022 23063654 · DOI
  82. [83]Barnes L.D. Garrison P.N. Siprashvili Z. Guranowski A. Robinson A.K. Ingram S.W. Croce C.M. Ohta M. Huebner K. Fhit, a Putative Tumor Suppressor in Humans, Is a Dinucleoside 5‘,5‘ ‘‘-P1,P3-Triphosphate Hydrolase† Biochemistry 1996 35 11529 11535 10.1021/bi961415t 8794732 · DOI
  83. [84]Chae H.-J. Seo J.B. Kim S.-H. Jeon Y.-J. Suh S.-S. Fhit induces the reciprocal suppressions between Lin28/Let-7 and miR-17/92miR Int. J. Med Sci. 2021 18 706 714 10.7150/ijms.51429 33437205 PMC7797533 · DOI
  84. [85]Kufe D.W. Mucins in cancer: Function, prognosis and therapy Nat. Rev. Cancer 2009 9 874 885 10.1038/nrc2761 19935676 PMC2951677 · DOI
  85. [86]Alam M. Ahmad R. Rajabi H. Kufe D. MUC1-C Induces the LIN28B→LET-7→HMGA2 Axis to Regulate Self-Renewal in NSCLC Mol. Cancer Res. 2015 13 449 460 10.1158/1541-7786.MCR-14-0363 25368430 PMC4369171 · DOI
  86. [87]Kufe D.W. MUC1-C oncoprotein as a target in breast cancer: Activation of signaling pathways and therapeutic approaches Oncogene 2012 32 1073 1081 10.1038/onc.2012.158 22580612 PMC3621754 · DOI
  87. [88]Kawahara H. Okada Y. Imai T. Iwanami A. Mischel P.S. Okano H. Musashi1 Cooperates in Abnormal Cell Lineage Protein 28 (Lin28)-mediated Let-7 Family MicroRNA Biogenesis in Early Neural Differentiation J. Biol. Chem. 2011 286 16121 16130 10.1074/jbc.M110.199166 21378162 PMC3091221 · DOI
  88. [89]Kim S.H. Park B.-O. Kim K. Park B.C. Park S.G. Kim J.-H. Kim S. Sjögren Syndrome antigen B regulates LIN28-let-7 axis in Caenorhabditis elegans and human Biochim. Biophys. Acta (BBA) Bioenerg. 2021 1864 194684 10.1016/j.bbagrm.2021.194684 33484878 · DOI
  89. [90]Teplova M. Yuan Y.-R. Phan A.T. Malinina L. Ilin S. Teplov A. Patel D.J. Structural Basis for Recognition and Sequestration of UUUOH 3′ Temini of Nascent RNA Polymerase III Transcripts by La, a Rheumatic Disease Autoantigen Mol. Cell 2006 21 75 85 10.1016/j.molcel.2005.10.027 16387655 PMC4689297 · DOI
  90. [91]Stefano J.E. Purified lupus antigen la recognizes an oligouridylate stretch common to the 3′ termini of RNA polymerase III transcripts Cell 1984 36 145 154 10.1016/0092-8674(84)90083-7 6607117 · DOI
  91. [92]Choudhury N.R. Nowak J.S. Zuo J. Rappsilber J. Spoel S.H. Michlewski G. Trim25 Is an RNA-Specific Activator of Lin28a/TuT4-Mediated Uridylation Cell Rep. 2014 9 1265 1272 10.1016/j.celrep.2014.10.017 25457611 PMC4542301 · DOI
  92. [93]Lee S.H. Cho S. Kim M.S. Choi K. Cho J.Y. Gwak H.-S. Kim Y.-J. Yoo H. Lee S.-H. Park J.B. The ubiquitin ligase human TRIM71 regulates let-7 microRNA biogenesis via modulation of Lin28B protein Biochim. Biophys. Acta (BBA) Bioenerg. 2014 1839 374 386 10.1016/j.bbagrm.2014.02.017 24602972 · DOI
  93. [94]Chang H.-M. Martinez N.J. Thornton J.E. Hagan J.P. Nguyen K.D. Gregory R.I. Trim71 cooperates with microRNAs to repress Cdkn1a expression and promote embryonic stem cell proliferation Nat. Commun. 2012 3 923 10.1038/ncomms1909 22735451 PMC3518406 · DOI
  94. [95]Rybak A. Fuchs H. Hadian K. Smirnova L. Wulczyn E.A. Michel G. Nitsch R. Krappmann D. Wulczyn F.G. The let-7 target gene mouse lin-41 is a stem cell specific E3 ubiquitin ligase for the miRNA pathway protein Ago2 Nat. Cell Biol. 2009 11 1411 1420 10.1038/ncb1987 19898466 · DOI
  95. [96]Liu Q. Chen X. Novak M.K. Zhang S. Hu W. Repressing Ago2 mRNA translation by Trim71 maintains pluripotency through inhibiting let-7 microRNAs eLife 2021 10 10 10.7554/eLife.66288 33599613 PMC7906602 · DOI
  96. [97]Kim C.W. Vo M.-T. Kim H.K. Lee H.H. Yoon N.A. Lee B.J. Min Y.J. Joo W.D. Cha H.J. Park J.W. Ectopic over-expression of tristetraprolin in human cancer cells promotes biogenesis of let-7 by down-regulation of Lin28 Nucleic Acids Res. 2011 40 3856 3869 10.1093/nar/gkr1302 22210895 PMC3351177 · DOI
  97. [98]Shaw G. Kamen R. A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradation Cell 1986 46 659 667 10.1016/0092-8674(86)90341-7 3488815 · DOI
  98. [100]Chaulk S.G. Lattanzi V.J. Hiemer S.E. Fahlman R.P. Varelas X. The Hippo Pathway Effectors TAZ/YAP Regulate Dicer Expression and MicroRNA Biogenesis through Let-7 J. Biol. Chem. 2014 289 1886 1891 10.1074/jbc.C113.529362 24324261 PMC3900939 · DOI · Paper page
  99. [101]Chawla G. Sokol N.S. ADAR mediates differential expression of polycistronic microRNAs Nucleic Acids Res. 2014 42 5245 5255 10.1093/nar/gku145 24561617 PMC4005697 · DOI
  100. [102]Bahn J.H. Ahn J. Lin X. Zhang Q. Lee J.-H. Civelek M. Xiao X. Genomic analysis of ADAR1 binding and its involvement in multiple RNA processing pathways Nat. Commun. 2015 6 1 13 10.1038/ncomms7355 25751603 PMC4355961 · DOI
  101. [103]Nemlich Y. Greenberg E. Ortenberg R. Besser M.J. Barshack I. Jacob-Hirsch J. Jacoby E. Eyal E. Rivkin L. Prieto V.G. MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growth J. Clin. Investig. 2013 123 2703 2718 10.1172/JCI62980 23728176 PMC3668823 · DOI
  102. [104]Zipeto M.A. Court A.C. Sadarangani A. Santos N.P.D. Balaian L. Chun H.-J. Pineda G. Morris S.R. Mason C.N. Geron I. ADAR1 Activation Drives Leukemia Stem Cell Self-Renewal by Impairing Let-7 Biogenesis Cell Stem Cell 2016 19 177 191 10.1016/j.stem.2016.05.004 27292188 PMC4975616 · DOI
  103. [105]Ota H. Sakurai M. Gupta R. Valente L. Wulff B.-E. Ariyoshi K. Iizasa H. Davuluri R.V. Nishikura K. ADAR1 Forms a Complex with Dicer to Promote MicroRNA Processing and RNA-Induced Gene Silencing Cell 2013 153 575 589 10.1016/j.cell.2013.03.024 23622242 PMC3651894 · DOI
  104. [106]Germanguz I. Lowry W.E. RNA editing as an activator of self-renewal in cancer Stem Cell Investig. 2016 3 68 10.21037/sci.2016.10.01 PMC5104573 27868050 · DOI
  105. [107]Michlewski G. Guil S. Semple C. Cáceres J.F. Posttranscriptional Regulation of miRNAs Harboring Conserved Terminal Loops Mol. Cell 2008 32 383 393 10.1016/j.molcel.2008.10.013 18995836 PMC2631628 · DOI
  106. [108]Jain N. Lin H.-C. Morgan C.E. Harris M.E. Tolbert B.S. Rules of RNA specificity of hnRNP A1 revealed by global and quantitative analysis of its affinity distribution Proc. Natl. Acad. Sci. USA 2017 114 2206 2211 10.1073/pnas.1616371114 28193894 PMC5338530 · DOI
  107. [109]Michlewski G. Cáceres J.F. Antagonistic role of hnRNP A1 and KSRP in the regulation of let-7a biogenesis Nat. Struct. Mol. Biol. 2010 17 1011 1018 10.1038/nsmb.1874 20639884 PMC2923024 · DOI
  108. [110]Burd C. Dreyfuss G. RNA binding specificity of hnRNP A1: Significance of hnRNP A1 high-affinity binding sites in pre-mRNA splicing EMBO J. 1994 13 1197 1204 10.1002/j.1460-2075.1994.tb06369.x 7510636 PMC394929 · DOI · Paper page
  109. [111]Trabucchi M. Briata P. Garcia-Mayoral M. Haase A.D. Filipowicz W. Ramos A. Gherzi R. Rosenfeld M.G. The RNA-binding protein KSRP promotes the biogenesis of a subset of microRNAs Nat. Cell Biol. 2009 459 1010 1014 10.1038/nature08025 PMC2768332 19458619 · DOI
  110. [112]Gherzi R. Chen C.-Y. Ramos A. Briata P. KSRP Controls Pleiotropic Cellular Functions Semin. Cell Dev. Biol. 2014 34 2 8 10.1016/j.semcdb.2014.05.004 24845017 · DOI
  111. [114]Buratti E. Baralle F.E. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease Front. Biosci. 2008 13 867 878 10.2741/2727 17981595 · DOI
  112. [115]Buratti E. De Conti L. Stuani C. Romano M. Baralle M. Baralle F. Nuclear factor TDP-43 can affect selected microRNA levels FEBS J. 2010 277 2268 2281 10.1111/j.1742-4658.2010.07643.x 20423455 · DOI
  113. [116]Kawahara Y. Mieda-Sato A. TDP-43 promotes microRNA biogenesis as a component of the Drosha and Dicer complexes Proc. Natl. Acad. Sci. USA 2012 109 3347 3352 10.1073/pnas.1112427109 22323604 PMC3295278 · DOI
  114. [117]Haselmann V. Kurz A. Bertsch U. Hübner S. Olempska–Müller M. Fritsch J. Häsler R. Pickl A. Fritsche H. Annewanter F. Nuclear Death Receptor TRAIL-R2 Inhibits Maturation of Let-7 and Promotes Proliferation of Pancreatic and Other Tumor Cells Gastroenterology 2014 146 278 290 10.1053/j.gastro.2013.10.009 24120475 · DOI
  115. [118]Boyerinas B. Park S.-M. Hau A. Murmann A.E. Peter M.E. The role of let-7 in cell differentiation and cancer Endocr.-Relat. Cancer 2010 17 F19 F36 10.1677/ERC-09-0184 19779035 · DOI
  116. [119]Salzman D.W. Shubert-Coleman J. Furneaux H. P68 RNA Helicase Unwinds the Human let-7 MicroRNA Precursor Duplex and Is Required for let-7-directed Silencing of Gene Expression J. Biol. Chem. 2007 282 32773 32779 10.1074/jbc.M705054200 17724023 · DOI
  117. [120]Sakamoto S. Aoki K. Higuchi T. Todaka H. Morisawa K. Tamaki N. Hatano E. Fukushima A. Taniguchi T. Agata Y. The NF90-NF45 Complex Functions as a Negative Regulator in the MicroRNA Processing Pathway Mol. Cell. Biol. 2009 29 3754 3769 10.1128/MCB.01836-08 19398578 PMC2698745 · DOI
  118. [121]Kawai S. Amano A. BRCA1 regulates microRNA biogenesis via the DROSHA microprocessor complex J. Cell Biol. 2012 197 201 208 10.1083/jcb.201110008 22492723 PMC3328391 · DOI
  119. [122]Anderson S.F. Schlegel B.P. Nakajima T. Wolpin E.S. Parvin J.D. BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A Nat. Genet. 1998 19 254 256 10.1038/930 9662397 · DOI
  120. [123]Wilson B.J. Giguère V. Identification of novel pathway partners of p68 and p72 RNA helicases through Oncomine meta-analysis BMC Genom. 2007 8 419 10.1186/1471-2164-8-419 18005418 PMC3225811 · DOI
  121. [124]Fuller-Pace F.V. DExD/H box RNA helicases: Multifunctional proteins with important roles in transcriptional regulation Nucleic Acids Res. 2006 34 4206 4215 10.1093/nar/gkl460 16935882 PMC1616952 · DOI
  122. [125]Davis B.N. Hilyard A.C. Lagna G. Hata A. SMAD proteins control DROSHA-mediated microRNA maturation Nat. Cell Biol. 2008 454 56 61 10.1038/nature07086 18548003 PMC2653422 · DOI
  123. [126]Dubrovska A. Kanamoto T. Lomnytska M. Heldin C.-H. Volodko N. Souchelnytskyi S. TGFβ1/Smad3 counteracts BRCA1-dependent repair of DNA damage Oncogene 2005 24 2289 2297 10.1038/sj.onc.1208443 15735739 · DOI
  124. [127]Yu B. Bi L. Zheng B. Ji L. Chevalier D. Agarwal M. Ramachandran V. Li W. Lagrange T. Walker J.C. The FHA domain proteins DAWDLE in Arabidopsis and SNIP1 in humans act in small RNA biogenesis Proc. Natl. Acad. Sci. USA 2008 105 10073 10078 10.1073/pnas.0804218105 18632581 PMC2481372 · DOI
  125. [128]Li P. Yang X. Wasser M. Cai Y. Chia W. Inscuteable and Staufen Mediate Asymmetric Localization and Segregation of prospero RNA during Drosophila Neuroblast Cell Divisions Cell 1997 90 437 447 10.1016/S0092-8674(00)80504-8 9267024 · DOI
  126. [129]Ren Z. Veksler-Lublinsky I. Morrissey D. Ambros V. Staufen Negatively Modulates MicroRNA Activity in Caenorhabditis elegans G3 Genes|Genomes|Genet. 2016 6 1227 1237 10.1534/g3.116.027300 26921297 PMC4856075 · DOI
  127. [130]Reinsborough C.W. Ipas H. Abell N.S. Gouws E.B. Williams J.P. Mercado M. Berg C.V.D. Xhemalçe B. BCDIN3D RNA methyltransferase stimulates Aldolase C expression and glycolysis through let-7 microRNA in breast cancer cells Oncogene 2021 40 2395 2406 10.1038/s41388-021-01702-y 33664453 PMC8026734 · DOI
  128. [131]Xhemalce B. Robson S.C. Kouzarides T. Human RNA Methyltransferase BCDIN3D Regulates MicroRNA Processing Cell 2012 151 278 288 10.1016/j.cell.2012.08.041 23063121 PMC3640255 · DOI
  129. [132]Suzuki H. Arase M. Matsuyama H. Choi Y.L. Ueno T. Mano H. Sugimoto K. Miyazono K. MCPIP1 Ribonuclease Antagonizes Dicer and Terminates MicroRNA Biogenesis through Precursor MicroRNA Degradation Mol. Cell 2011 44 424 436 10.1016/j.molcel.2011.09.012 22055188 · DOI
  130. [133]Pilotte J. Dupont-Versteegden E.E. Vanderklish P.W. Widespread Regulation of miRNA Biogenesis at the Dicer Step by the Cold-Inducible RNA-Binding Protein, RBM3 PLoS ONE 2011 6 e28446 10.1371/journal.pone.0028446 22145045 PMC3228759 · DOI
  131. [134]Dannoab S. Nishiyamaa H. Higashitsujia H. Yokoia H. Xuea J.-H. Itoha K. Matsudab T. Fujita J. Increased Transcript Level of RBM3, a Member of the Glycine-Rich RNA-Binding Protein Family, in Human Cells in Response to Cold Stress Biochem. Biophys. Res. Commun. 1997 236 804 807 10.1006/bbrc.1997.7059 9245737 · DOI
  132. [135]Großhans H. Johnson T. Reinert K.L. Gerstein M. Slack F.J. The Temporal Patterning MicroRNA let-7 Regulates Several Transcription Factors at the Larval to Adult Transition in C. elegans Dev. Cell 2005 8 321 330 10.1016/j.devcel.2004.12.019 15737928 · DOI
  133. [136]Kumar M.S. Lu J. Mercer K.L. Golub T.R. Jacks T. Impaired microRNA processing enhances cellular transformation and tumorigenesis Nat. Genet. 2007 39 673 677 10.1038/ng2003 17401365 · DOI
  134. [137]Nguyen D.T.T. Richter D. Michel G. Mitschka S. Kolanus W. Cuevas E. Wulczyn F.G. The ubiquitin ligase LIN41/TRIM71 targets p53 to antagonize cell death and differentiation pathways during stem cell differentiation Cell Death Differ. 2017 24 1063 1078 10.1038/cdd.2017.54 28430184 PMC5442473 · DOI
  135. [138]Mooijaart S. Brandt B. Baldal E. Pijpe J. Kuningas M. Beekman M. Zwaan B. Slagboom P. Westendorp R. Van Heemst D. C. elegans DAF-12, Nuclear Hormone Receptors and human longevity and disease at old age Ageing Res. Rev. 2005 4 351 371 10.1016/j.arr.2005.03.006 16051528 · DOI
  136. [139]Balzer E. Moss E.G. Localization of the Developmental Timing Regulator Lin28 to mRNP Complexes, P-bodies and Stress Granules RNA Biol. 2007 4 16 25 10.4161/rna.4.1.4364 17617744 · DOI
  137. [140]Carballo E. Lai W.S. Blackshear P.J. Feedback Inhibition of Macrophage Tumor Necrosis Factor-α Production by Tristetraprolin Science 1998 281 1001 1005 10.1126/science.281.5379.1001 9703499 · DOI
  138. [141]Lykke-Andersen J. Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1 Genes Dev. 2005 19 351 361 10.1101/gad.1282305 15687258 PMC546513 · DOI
  139. [142]Yang W. Chendrimada T.P. Wang Q. Higuchi M. Seeburg P.H. Shiekhattar R. Nishikura K. Modulation of microRNA processing and expression through RNA editing by ADAR deaminases Nat. Struct. Mol. Biol. 2005 13 13 21 10.1038/nsmb1041 16369484 PMC2950615 · DOI
  140. [143]Suzuki H. Yamagata K. Sugimoto K. Iwamoto T. Kato S. Miyazono K. Modulation of microRNA processing by p53 Nat. Cell Biol. 2009 460 529 533 10.1038/nature08199 19626115 · DOI
  141. [144]Chen Y. Chan J. Chen W. Li J. Sun M. Kannan G.S. Mok Y.-K. Yuan Y.A. Jobichen C. SYNCRIP, a new player in pri-let-7a processing RNA 2020 26 290 305 10.1261/rna.072959.119 31907208 PMC7025501 · DOI
  142. [145]Kim I.-M. Wang Y. Park K.-M. Tang Y. Teoh J.-P. Vinson J. Traynham C.J. Pironti G. Mao L. Su H. β-Arrestin1–Biased β 1 -Adrenergic Receptor Signaling Regulates MicroRNA Processing Circ. Res. 2014 114 833 844 10.1161/CIRCRESAHA.114.302766 24334028 PMC3955054 · DOI
  143. [146]Li X. Lin W.-J. Chen C.-Y. Si Y. Zhang X. Lu L. Suswam E. Zheng L. King P.H. KSRP: A checkpoint for inflammatory cytokine production in astrocytes Glia 2012 60 1773 1784 10.1002/glia.22396 22847996 PMC3629690 · DOI
  144. [147]Winzen R. Thakur B.K. Dittrich-Breiholz O. Shah M. Redich N. Dhamija S. Kracht M. Holtmann H. Functional Analysis of KSRP Interaction with the AU-Rich Element of Interleukin-8 and Identification of Inflammatory mRNA Targets Mol. Cell. Biol. 2007 27 8388 8400 10.1128/MCB.01493-07 17908789 PMC2169186 · DOI
  145. [148]Zhu H. Gui Q. Hui X. Wang X. Jiang J. Ding L. Sun X. Wang Y. Chen H. TGF-β1/Smad3 Signaling Pathway Suppresses Cell Apoptosis in Cerebral Ischemic Stroke Rats Med. Sci. Monit. 2017 23 366 376 10.12659/MSM.899195 28110342 PMC5282965 · DOI
  146. [149]Chen C.-Y. Choong O.K. Liu L.-W. Cheng Y.-C. Li S.-C. Yen C.Y. Wu M.-R. Chiang M.-H. Tsang T.-J. Wu Y.-W. MicroRNA let-7-TGFBR3 signalling regulates cardiomyocyte apoptosis after infarction EBioMedicine 2019 46 236 247 10.1016/j.ebiom.2019.08.001 31401194 PMC6712055 · DOI
  147. [150]Cao L. Kong L.-P. Yu Z.-B. Han S.-P. Bai Y.-F. Zhu J. Hu X. Zhu C. Zhu S. Guo X.-R. microRNA expression profiling of the developing mouse heart Int. J. Mol. Med. 2012 30 1095 1104 10.3892/ijmm.2012.1092 22895573 · DOI
  148. [151]Kahl A. Blanco I. Jackman K. Baskar J. Milaganur Mohan H. Rodney-Sandy R. Zhang S. Iadecola C. Hochrainer K. Cerebral ischemia induces the aggregation of proteins linked to neurodegenerative diseases Sci. Rep. 2018 8 2701 10.1038/s41598-018-21063-z 29426953 PMC5807442 · DOI
  149. [152]Thammisetty S.S. Pedragosa J. Weng Y.C. Calon F. Planas A. Kriz J. Age-related deregulation of TDP-43 after stroke enhances NF-κB-mediated inflammation and neuronal damage J. Neuroinflammation 2018 15 1 15 10.1186/s12974-018-1350-y 30413172 PMC6230239 · DOI
  150. [153]Skau E. Henriksen E. Wagner P. Hedberg P. Siegbahn A. Leppert J. GDF-15 and TRAIL-R2 are powerful predictors of long-term mortality in patients with acute myocardial infarction Eur. J. Prev. Cardiol. 2017 24 1576 1583 10.1177/2047487317725017 28762762 · DOI
  151. [154]Jin Z. Liang J. Li J. Kolattukudy P.E. Absence of MCP-induced Protein 1 Enhances Blood–Brain Barrier Breakdown after Experimental Stroke in Mice Int. J. Mol. Sci. 2019 20 3214 10.3390/ijms20133214 31261992 PMC6651107 · DOI
  152. [155]Ávila-Gómez P. Vieites-Prado A. Dopico-López A. Bashir S. Fernández-Susavila H. Gubern C. Pérez-Mato M. Correa-Paz C. Iglesias-Rey R. Sobrino T. Cold stress protein RBM3 responds to hypothermia and is associated with good stroke outcome Brain Commun. 2020 2 fcaa078 10.1093/braincomms/fcaa078 33585816 PMC7869850 · DOI

Authors
Bernstein, D. L., Jiang, X., & Rom, S.
Affiliations
Temple University (US)
Corresponding author
Rom, Slava
Venue
Biomedicines
Publisher
MDPI AG
Published
2021-05-26
Volume
9
Issue
6
Pages
606
ISSN
2227-9059 (ISSN-L)
OpenAlex
W3165282034
Cited by
88
References
165
Citations by year
2026: 15 · 2025: 13 · 2024: 22 · 2023: 17 · 2022: 16 · 2021: 5
FWCI
1.81
Type
journal article
Language
en
Open access
Locations
  • Biomedicines (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • TUScholarShare (Temple University) (submittedVersion, cc-by)
Funders
National Institute of Neurological Disorders and Stroke (R01NS101135)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
let-7 microRNA, microRNA regulation, cardiovascular disease, cerebrovascular disease, stroke, myocardial infarction, myocardial fibrosis, atherosclerosis, inflammation, embryonic stem cell differentiation, cancer, miRNA target genes

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