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Effect of lncRNA SNHG3 on the proliferation, apoptosis, migration and invasion of osteosarcoma cells by targeting miR-514a-5p |
TAN Xiaoqian MEI Haibo WU Jiangyan YAN An |
Department of Orthopaedics, Hu’nan Children’s Hospital, Hu’nan Province, Changsha 410007, China |
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Abstract Objective To explore the effect of long non-coding RNA small nucleolar RNA host gene 3 (SNHG3) on the proliferation, apoptosis, migration and invasion of osteosarcoma cells and its mechanism. Methods The expression of SNHG3 and miR-514a-5p in osteoblasts hFOB1.19 and osteosarcoma cells SW-1353, HOS, U-2OS, and Saos-2 were detected by qRT-PCR. U-2OS cells in logarithmic growth phase were transfected. They were divided into si-NC group (transfected si-NC), si-SNHG3 group (transfected si-SNHG3), miR-NC group (transfected miR-NC), miR-514a-5p group (transfected miR-514a-5p), si-SNHG3+anti-miR-NC group (co-transfected si-SNHG3 and anti-miR-NC) and si-SNHG3 +anti-miR-514a-5p group (co-transfected with si-SNHG3 and anti-miR-514a-5p). CCK-8 assay and flow cytometry were used to check cell viability and apoptosis. The expression of c-Myc, Bax, and MMP-2 protein were detected by Western blot. Cell migration and invasion were tested by Transwell chamber experiment. The target relationship between SNHG3 and miR-514a-5p was analyzed by dual luciferase experiment. Results The expression of SNHG3 in osteosarcoma cells SW-1353, HOS, U-2OS, and Saos-2 were higher than those of osteoblasts hFOB1.19, and the expression of miR-514a-5p were lower than that of osteoblasts hFOB1.19, and the differences were statistically significant (P < 0.05). The SNHG3, cell viability, migrating cells, invasive cells, and the expression of c-Myc, MMP-2 protein in si-SNHG3 group were lower than those in si-NC group; while the apoptosis rate and the expression of Bax protein were higher than those in si-NC group, and the differences were statistically significant (P < 0.05). The miR-514a-5p expression, apoptosis rate, and the expression of Bax protein in miR-514a-5p group were higher than those in miR-NC group; while cell viability, migrating cells, invasive cells, the expression of c-Myc, MMP-2 protein were lower than those of miR-NC group, and the differences were statistically significant (P < 0.05). SNHG3 wild type luciferase activity of miR-514a-5p group was lower than that of miR-NC group, and the difference was statistically significant (P < 0.05), while SNHG3 mutant luciferase activity in miR-514a-5p group and miR-NC group showed no statistical significance (P > 0.05). The miR-514a-5p expression, apoptosis rate, and the expression of Bax protein in si-SNHG3+anti-miR-514a-5p group were lower than those in si-SNHG3+anti-miR-NC group, while cell viability, migrating cells, invaded cells, the expression of c-Myc and MMP-2 protein were higher than those in si-SNHG3+anti-miR-NC group, and the differences were statistically significant (P < 0.05). Conclusion Knockdown of SNHG3 can significantly inhibit the proliferation, invasion and migration of osteosarcoma cells, and also promote the apoptosis of osteosarcoma cells, the mechanism of which may be related to miR-514a-5p.
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[1] Brown HK,Tellez-Gabriel M,Heymann D. Cancer stem cells in osteosarcoma [J]. Cancer Lett,2017,386:189-195.
[2] Sadykova LR,Ntekim AI,Muyangwa-Semenova M,et al. Epidemiology and risk Factors of osteosarcoma [J]. Cancer Invest,2020,38(5):259-269.
[3] Zhou Y,Yang D,Yang QC,et al. Single-cell RNA landscape of intratumoral heterogeneity and immunosuppressive microenvironment in advanced osteosarcoma [J]. Nat Commun,2020,11(1):6322.
[4] Harrison DJ,Geller DS,Gill JD,et al. Current and future therapeutic approaches for osteosarcoma [J]. Expert Rev Anticancer Ther,2018,18(1):39-50.
[5] Lilienthal I,Herold N. Targeting molecular mechanisms underlying treatment efficacy and resistance in osteosarcoma:A review of current and future strategies [J]. Int J Mol Sci,2020,21(18):6885.
[6] Wang XS,Peng L,Gong XJ,et al. LncRNA HIF1A-AS2 promotes osteosarcoma progression by acting as a sponge of miR-129-5p [J]. Aging(Albany NY),2019,11(24):11803-11813.
[7] Liu SW,Li JC,Kang L,et al. Degradation of long non-coding RNA-CIR decelerates proliferation,invasion and migration,but promotes apoptosis of osteosarcoma cells [J]. Cancer Cell Int,2019,19(1):349.
[8] Huang Y,Xu YQ,Feng SY,et al. LncRNA TDRG1 promotes proliferation,invasion and epithelial-mesenchymal transformation of osteosarcoma through PI3K/AKT signal pathway [J]. Cancer Manag Res,2020,12:4531-4540.
[9] Zheng SN,Jiang F,Ge DW,et al. LncRNA SNHG3/miRNA-151a-3p/RAB22A axis regulates invasion and migration of osteosarcoma [J]. Biomed Pharmacother,2019,112:108695.
[10] Li W,Yang FQ,Sun CM,et al. circPRRC2A promotes angiogenesis and metastasis through epithelial-mesenchymal transition and upregulates TRPM3 in renal cell carcinoma [J]. Theranostics,2020,10(10):4395-4409.
[11] Verma AH,Kumar TS,Madhumathi K,et al. Curcumin releasing eggshell derived carbonated apatite nanocarriers for combined anti-cancer,anti-inflammatory and bone regenerative therapy [J]. J Nanosci Nanotechnol,2019,19(11):6872-6880
[12] Yang CF,Tian Y,Zhao F,et al. Bone Microenvironment and osteosarcoma metastasis [J]. Int J Mol Sci,2020,21(19):6985.
[13] Moreno F,Cacciavillano W,Cipolla M,et al. Childhood osteosarcoma:Incidence and survival in Argentina. Report from the National Pediatric Cancer Registry,ROHA Network 2000-2013 [J]. Pediatr Blood Cancer,2017,64(10):e26533.
[14] Sanchez Calle A,Kawamura Y,Yamamoto Y,et al. Emerging roles of long non-coding RNA in cancer [J]. Cancer Sci,2018,109(7):2093-2100.
[15] Ju C,Zhou R,Sun J,et al. LncRNA SNHG5 promotes the progression of osteosarcoma by sponging the miR-212-3p/SGK3 axis [J]. Cancer Cell Int,2018,18(1):141.
[16] Xu RD,Feng F,Yu XS,et al. LncRNA SNHG4 promotes tumour growth by sponging miR-224-3p and predicts poor survival and recurrence in human osteosarcoma [J]. Cell Prolif,2018,51(6):e12515.
[17] Chen J,Wu Z,Zhang Y. LncRNA SNHG3 promotes cell growth by sponging miR-196a-5p and indicates the poor survival in osteosarcoma [J]. Int J Immunopathol Pharmacol,2019,33:2058738418820743.
[18] 王倩倩,任传利.miR-486-5p在肿瘤发生与发展及其他疾病中的最新研究进展[J].国际检验医学杂志,2020, 41(22):2801-2804,2816.
[19] Wang JC,Liu SZ,Shi JY,et al. The Role of miRNA in the diagnosis,prognosis,and treatment of osteosarcoma [J]. Cancer Biother Radiopharm,2019,34(10):605-613.
[20] Cai WT,Guan P,Lin MX,et al. MiRNA-206 suppresses the metastasis of osteosarcoma via targeting Notch3 [J]. J Biol Regul Homeost Agents,2020,34(3):775-783.
[21] Huang CW,Wang QJ,Ma SS,et al. A four serum-miRNA panel serves as a potential diagnostic biomarker of osteosarcoma [J]. Int J Clin Oncol,2019,24(8):976-982.
[22] Chen G,Zhou H. MiRNA-708/CUL4B axis contributes into cell proliferation and apoptosis of osteosarcoma [J]. Eur Rev Med Pharmacol Sci,2018,22(17):5452-5459.
[23] Wang XS,Peng L,Gong XJ,et al. miR-423-5p inhibits osteosarcoma proliferation and invasion through directly targeting STMN1 [J]. Cell Physiol Biochem,2018,50(6):2249-2259.
[24] Wu DJ,Zhang H,Ji F,et al. MicroRNA-17 promotes osteosarcoma cells proliferation and migration and inhibits apoptosis by regulating SASH1 expression [J]. Pathol Res Pract,2019,215(1):115-120.
[25] Hu WQ,Li HL,Wang SZ. LncRNA SNHG7 promotes the proliferation of nasopharyngeal carcinoma by miR-514a-5p/ELAVL1 axis [J]. BMC Cancer,2020,20(1):376. |
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