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MicroRNA-378 Suppressed Osteogenesis of MSCs and Impaired Bone Formation via Inactivating Wnt/β-Catenin Signaling

Feng, Lu, Zhang, Jin-fang, Shi, Liu, Yang, Zheng-meng, Wu, Tian-yi, Wang, Hai-xing, Lin, Wei-ping, Lu, Ying-fei, Lo, Jessica Hiu Tung, Zhu, Da-hai, Li, Gang·2020·Molecular Therapy Nucleic Acids
DOI 10.1016/j.omtn.2020.07.018PMC PMC7452050

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Research works printed but not linked: 30

  1. Carrer, 2012, Control of mitochondrial metabolism and systemic energy homeostasis by microRNAs 378 and 378∗, Proc. Natl. Acad. Sci. USA, 109, 15330, 10.1073/pnas.1207605109 · DOI
  2. Huang, 2014, MicroRNA-125b regulates osteogenic differentiation of mesenchymal stem cells by targeting Cbfβ in vitro, Biochimie, 102, 47, 10.1016/j.biochi.2014.02.005 · DOI
  3. Xie, 2016, The role of miR-135-modified adipose-derived mesenchymal stem cells in bone regeneration, Biomaterials, 75, 279, 10.1016/j.biomaterials.2015.10.042 · DOI
  4. Li, 2008, A microRNA signature for a BMP2-induced osteoblast lineage commitment program, Proc. Natl. Acad. Sci. USA, 105, 13906, 10.1073/pnas.0804438105 · DOI
  5. Kim, 2009, miR-196a regulates proliferation and osteogenic differentiation in mesenchymal stem cells derived from human adipose tissue, J. Bone Miner. Res., 24, 816, 10.1359/jbmr.081230 · DOI
  6. Zhang, 2011, MiRNA-20a promotes osteogenic differentiation of human mesenchymal stem cells by co-regulating BMP signaling, RNA Biol., 8, 829, 10.4161/rna.8.5.16043 · DOI
  7. Zhang, 2011, MiR-637 maintains the balance between adipocytes and osteoblasts by directly targeting Osterix, Mol. Biol. Cell, 22, 3955, 10.1091/mbc.e11-04-0356 · DOI
  8. Hupkes, 2014, MicroRNA miR-378 promotes BMP2-induced osteogenic differentiation of mesenchymal progenitor cells, BMC Mol. Biol., 15, 1, 10.1186/1471-2199-15-1 · DOI
  9. You, 2014, MiR-378 overexpression attenuates high glucose-suppressed osteogenic differentiation through targeting CASP3 and activating PI3K/Akt signaling pathway, Int. J. Clin. Exp. Pathol., 7, 7249
  10. Kahai, 2009, MicroRNA miR-378 regulates nephronectin expression modulating osteoblast differentiation by targeting GalNT-7, PLoS ONE, 4, e7535, 10.1371/journal.pone.0007535 · DOI
  11. Cawthorn, 2012, Wnt6, Wnt10a and Wnt10b inhibit adipogenesis and stimulate osteoblastogenesis through a β-catenin-dependent mechanism, Bone, 50, 477, 10.1016/j.bone.2011.08.010 · DOI
  12. Yu, 2014, Expression profiling of PPARγ-regulated microRNAs in human subcutaneous and visceral adipogenesis in both genders, Endocrinology, 155, 2155, 10.1210/en.2013-2105 · DOI
  13. Yu, 2014, MicroRNA-378 functions as an onco-miR in nasopharyngeal carcinoma by repressing TOB2 expression, Int. J. Oncol., 44, 1215, 10.3892/ijo.2014.2283 · DOI
  14. Chen, 2012, MicroRNA-378 is associated with non-small cell lung cancer brain metastasis by promoting cell migration, invasion and tumor angiogenesis, Med. Oncol., 29, 1673, 10.1007/s12032-011-0083-x · DOI
  15. Ma, 2014, MiR-378 promotes the migration of liver cancer cells by down-regulating Fus expression, Cell. Physiol. Biochem., 34, 2266, 10.1159/000369669 · DOI
  16. Xu, 2014, TNF-α, IL-6, and leptin increase the expression of miR-378, an adipogenesis-related microRNA in human adipocytes, Cell Biochem. Biophys., 70, 771, 10.1007/s12013-014-9980-x · DOI
  17. Huang, 2015, MiR-378a-3p enhances adipogenesis by targeting mitogen-activated protein kinase 1, Biochem. Biophys. Res. Commun., 457, 37, 10.1016/j.bbrc.2014.12.055 · DOI
  18. Liu, 2015, MiR-378 Plays an Important Role in the Differentiation of Bovine Preadipocytes, Cell. Physiol. Biochem., 36, 1552, 10.1159/000430318 · DOI
  19. Zhang, 2016, miR-378 Activates the Pyruvate-PEP Futile Cycle and Enhances Lipolysis to Ameliorate Obesity in Mice, EBioMedicine, 5, 93, 10.1016/j.ebiom.2016.01.035 · DOI
  20. Duan, 2016, The role of the wnt/β-catenin signaling pathway in formation and maintenance of bone and teeth, Int. J. Biochem. Cell Biol., 77, 23, 10.1016/j.biocel.2016.05.015 · DOI
  21. Huang, 2015, MicroRNA-378 regulates neural stem cell proliferation and differentiation in vitro by modulating Tailless expression, Biochem. Biophys. Res. Commun., 466, 214, 10.1016/j.bbrc.2015.09.011 · DOI
  22. Zeng, 2017, miR-378 suppresses the proliferation, migration and invasion of colon cancer cells by inhibiting SDAD1, Cell. Mol. Biol. Lett., 22, 12, 10.1186/s11658-017-0041-5 · DOI
  23. Yu, 2016, Activation of Hepatic Stellate Cells is Inhibited by microRNA-378a-3p via Wnt10a, Cell. Physiol. Biochem., 39, 2409, 10.1159/000452509 · DOI
  24. Tang, 2009, BMP-9-induced osteogenic differentiation of mesenchymal progenitors requires functional canonical Wnt/beta-catenin signalling, J. Cell. Mol. Med., 13, 2448, 10.1111/j.1582-4934.2008.00569.x · DOI
  25. Semenov, 2006, LRP5 mutations linked to high bone mass diseases cause reduced LRP5 binding and inhibition by SOST, J. Biol. Chem., 281, 38276, 10.1074/jbc.M609509200 · DOI
  26. James, 2006, Different roles of Runx2 during early neural crest-derived bone and tooth development, J. Bone Miner. Res., 21, 1034, 10.1359/jbmr.060413 · DOI
  27. Jing, 2016, Suppression of EZH2 Prevents the Shift of Osteoporotic MSC Fate to Adipocyte and Enhances Bone Formation During Osteoporosis, Mol. Ther., 24, 217, 10.1038/mt.2015.152 · DOI
  28. Sun, 2015, mir-21 overexpressing mesenchymal stem cells accelerate fracture healing in a rat closed femur fracture model, BioMed Res. Int., 2015, 412327, 10.1155/2015/412327 · DOI
  29. Hauser, 2012, Analysis of serum microRNAs (miR-26a-2∗, miR-191, miR-337-3p and miR-378) as potential biomarkers in renal cell carcinoma, Cancer Epidemiol., 36, 391, 10.1016/j.canep.2012.04.001 · DOI
  30. Xu, 2016, Human fetal mesenchymal stem cell secretome enhances bone consolidation in distraction osteogenesis, Stem Cell Res. Ther., 7, 134, 10.1186/s13287-016-0392-2 · DOI

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Metadata

Authors
Feng, L., Zhang, J.-F., Shi, L., Yang, Z.-M., Wu, T.-Y., Wang, H.-X., Lin, W.-P., Lu, Y.-F., Lo, J. H. T., Zhu, D.-H., & Li, G.
Venue
Molecular Therapy Nucleic Acids
Publisher
Elsevier BV
Published
2020-09
Volume
21
Pages
1017-1028
ISSN
2162-2531
DOI
10.1016/j.omtn.2020.07.018
PMC
PMC7452050
Cited by
46
References
2
Language
en
Licence
Funders
  • National Natural Science Foundation of China (81772322)
  • Chinese University of Hong Kong
  • Innovation and Technology Commission - Hong Kong (ITS/448/18)
  • General Research Fund of Shanghai Normal University (14120118, 14160917, 9054014 N_CityU102/15, C7030-18G, T13-402/17-N)

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