References
- Aguero, J., Hadri, L., Hammoudi, N., Leonardson, L., Hajjar, R.J., and Ishikawa, K. (2017). Inhaled gene transfer for pulmonary circulation. Methods Mol. Biol. 1521, 339-349.
- Berenbaum, F. (2013). Osteoarthritis as an inflammatory disease (osteoarthritis is not osteoarthrosis!). Osteoarthritis Cartilage 21, 16-21. https://doi.org/10.1016/j.joca.2012.11.012
- Cruz, C.M., Rinna, A., Forman, H.J., Ventura, A.L., Persechini, P.M., and Ojcius, D.M. (2007). ATP activates a reactive oxygen speciesdependent oxidative stress response and secretion of proinflammatory cytokines in macrophages. J. Biol. Chem. 282, 2871-9. https://doi.org/10.1074/jbc.M608083200
- Dave, M. and Amin, A.R. (2013). Yin-Yang regulation of prostaglandins and nitric oxide by PGD2 in human arthritis: reversal by celecoxib. Immunol. Lett. 152, 47-54. https://doi.org/10.1016/j.imlet.2013.04.002
- Dinarello, C.A. (2009). Immunological and inflammatory functions of the interleukin-1 family. Annu. Rev. Immunol. 27, 519-550. https://doi.org/10.1146/annurev.immunol.021908.132612
- Eichelser, C., Stuckrath, I., Muller, V., Milde-Langosch, K., Wikman, H., Pantel, K., and Schwarzenbach, H. (2014). Increased serum levels of circulating exosomal microRNA-373 in receptor-negative breast cancer patients. Oncotarget 5, 9650-9563. https://doi.org/10.18632/oncotarget.2520
- Fechner, H., Vetter, R., Kurreck, J., and Poller, W. (2017). Silencing genes in the heart. Methods Mol. Biol. 1521, 17-39.
- Fu, Y., Lei, J., Zhuang, Y., Zhang, K., and Lu, D. (2016). Overexpression of HMGB1 A-box reduced IL-1beta-induced MMP expression and the production of inflammatory mediators in human chondrocytes. Exp. Cell Res. 349, 184-190. https://doi.org/10.1016/j.yexcr.2016.10.014
- Jiang, L.B., Lee, S., Wang, Y., Xu, Q.T., Meng, D.H., and Zhang, J. (2016). Adipose-derived stem cells induce autophagic activation and inhibit catabolic response to pro-inflammatory cytokines in rat chondrocytes. Osteoarthritis Cartilage 24, 1071-1081. https://doi.org/10.1016/j.joca.2015.12.021
- Johnson, V.L., and Hunter, D.J. (2014). The epidemiology of osteoarthritis. Best Pract. Res. Clin. Rheumatol. 28, 5-15. https://doi.org/10.1016/j.berh.2014.01.004
- Karlsen, T.A., de Sourza, G.A., Odegaard, B., Engebretsen, L., and Brinchmann, J.E. (2016). microRNA-140 inhibits inflammation and stimulates chondrogenesis in a model of interleukin 1beta-induced osteoarthritis. Mol. Ther. Nucleic. Acids 5, e373. https://doi.org/10.1038/mtna.2016.64
- Kim, E.H., and Heo, C.Y. (2014). Current applications of adiposederived stem cells and their future perspectives. World J. Stem Cells 6, 65-68. https://doi.org/10.4252/wjsc.v6.i1.65
- Lai, J.H., Kajiyama, G., Smith, R.L., Maloney, W., and Yang, F. (2013). Stem cells catalyze cartilage formation by neonatal articular chondrocytes in 3D biomimetic hydrogels. Sci. Rep. 3, 3553. https://doi.org/10.1038/srep03553
- Lambert, C., Dubuc, J.E., Montell, E., Verges, J., Munaut, C., Noel, A., and Henrotin, Y. (2014). Gene expression pattern of cells from inflamed and normal areas of osteoarthritis synovial membrane. Arthritis Rheumatol. 66, 960-968. https://doi.org/10.1002/art.38315
- Le Feuvre, R.A., Brough, D., Iwakura, Y., Takeda, K., and Rothwell, N. J. (2002). Priming of macrophages with lipopolysaccharide potentiates P2X7-mediated cell death via a caspase-1-dependent mechanism, independently of cytokine production. J. Biol. Chem. 277, 3210-3218. https://doi.org/10.1074/jbc.M104388200
- Lee, K.H., Goan, Y.G., Hsiao, M., Lee, C.H., Jian, S.H., Lin, J.T., Chen, Y.L., and Lu, P.J. (2009). MicroRNA-373 (miR-373) posttranscriptionally regulates large tumor suppressor, homolog 2 (LATS2) and stimulates proliferation in human esophageal cancer. Exp. Cell Res. 315, 2529-2538. https://doi.org/10.1016/j.yexcr.2009.06.001
- Lohse, R., Krebs, W., Kunz, B., Mau, S., Raatzsch, H., Rothkope, M., and Vogler, H. (1975). [The complex documentation of bladder neoplasms by means of electronic data processing]. Z. Urol. Nephrol. 68, 241-250.
- MakkiI, M.S., and Haqqi, T.M. (2016). Histone deacetylase inhibitor vorinostat (SAHA) suppresses IL-1beta-induced matrix metallopeptidase-13 expression by inhibiting IL-6 in osteoarthritis chondrocyte. Am. J. Pathol. 186, 2701-2708. https://doi.org/10.1016/j.ajpath.2016.06.010
- Meng, X., Muller, V., Milde-langosch, K., Trillsch, F., Pantel, K., and Schwarzenbach, H. (2016). Circulating cell-free miR-373, miR-200a, miR-200b and miR-200c in patients with epithelial ovarian cancer. Adv. Exp. Med. Biol. 924, 3-8.
- Papanagnou, P., Stivarou, T., and Tsironi, M. (2016). The role of miRNAs in common inflammatory arthropathies: osteoarthritis and gouty arthritis. Biomolecules 6, pii: E44. https://doi.org/10.3390/biom6040044
- Place, R.F., Li, L.C., Pookot, D., Noonan, E.J., and Dahiya, R. (2008). MicroRNA-373 induces expression of genes with complementary promoter sequences. Proc. Natl. Acad. Sci. USA 105, 1608-1613. https://doi.org/10.1073/pnas.0707594105
- Shi, L.B., Cai, H.X., Chen, L.K., Wu, Y., Zhu, S.A., Gong, X.N., Xia, Y.X., Ouyang, H.W., and Zou, X.H. (2014). Tissue engineered bulking agent with adipose-derived stem cells and silk fibroin microspheres for the treatment of intrinsic urethral sphincter deficiency. Biomaterials 35, 1519-1530. https://doi.org/10.1016/j.biomaterials.2013.11.025
- Song, J., Kim, D., Chun, C.H., and Jin, E.J. (2015). miR-370 and miR- 373 regulate the pathogenesis of osteoarthritis by modulating onecarbon metabolism via SHMT-2 and MECP-2, respectively. Aging Cell 14, 826-837. https://doi.org/10.1111/acel.12363
- Stone, A.V., Loeser, R.F., Vanderman, K.S., Long, D.L., Clark, S.C., and Ferguson, C.M. (2014). Pro-inflammatory stimulation of meniscus cells increases production of matrix metalloproteinases and additional catabolic factors involved in osteoarthritis pathogenesis. Osteoarthritis Cartilage 22, 264-274. https://doi.org/10.1016/j.joca.2013.11.002
- Takahashi, K., Goomer, R.S., Harwood, F., Kubo, T., Hirasawa, Y., and Amiel, D. (1999). The effects of hyaluronan on matrix metalloproteinase-3 (MMP-3), interleukin-1beta(IL-1beta), and tissue inhibitor of metalloproteinase-1 (TIMP-1) gene expression during the development of osteoarthritis. Osteoarthritis Cartilage 7, 182-190. https://doi.org/10.1053/joca.1998.0207
- Tsezou, A. (2014). Osteoarthritis year in review (2014: genetics and genomics. Osteoarthritis Cartilage 22, 2017-2024. https://doi.org/10.1016/j.joca.2014.07.024
- Van Lent, P.L., and Van den Berg, W.B. (2013). Mesenchymal stem cell therapy in osteoarthritis: advanced tissue repair or intervention with smouldering synovial activation? Arthritis. Res. Ther. 15, 112. https://doi.org/10.1186/ar4190
- Yu, X., Su, B., Ge, P., Wang, Z., Li, S., Huang, B., Gong, Y., and Lin, J. (2015). Human adipose derived stem cells induced cell apoptosis and s phase arrest in bladder tumor. Stem Cells Int. 2015, 619290.
- Yudoh, K., Nguyen, v.T., Nakamura, H., Hongo-Masuko, K., Kato, T., and Nishioka, K. (2005). Potential involvement of oxidative stress in cartilage senescence and development of osteoarthritis: oxidative stress induces chondrocyte telomere instability and downregulation of chondrocyte function. Arthritis Res. Ther. 7, R380-391. https://doi.org/10.1186/ar1499
Cited by
- Can photobiomodulation associated with implantation of mesenchymal adipose-derived stem cells attenuate the expression of MMPs and decrease degradation of type II collagen in an experimental model of osteoarthritis? vol.33, pp.5, 2018, https://doi.org/10.1007/s10103-018-2466-0
- Epigallocatechin-3-gallate enhances the osteoblastogenic differentiation of human adipose-derived stem cells vol.13, pp.None, 2017, https://doi.org/10.2147/dddt.s192683
- Conditioned Serum Enhances the Chondrogenic and Immunomodulatory Behavior of Mesenchymal Stem Cells vol.10, pp.None, 2019, https://doi.org/10.3389/fphar.2019.00699
- The Concentration of Plasma Provides Additional Bioactive Proteins in Platelet and Autologous Protein Solutions vol.47, pp.8, 2019, https://doi.org/10.1177/0363546519849671
- Experimental Study on the Correlation between miRNA-373 and HIF-1α, MMP-9, and VEGF in the Development of HIE vol.2021, pp.None, 2021, https://doi.org/10.1155/2021/5553486