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lncRNA FLVCR-AS1 promotes osteosarcoma growth by targeting miR381-3p/CCND1

PURPOSE: This article reports on FLVCR-AS1 effects on osteosarcoma (OS) growth. METHODS: Tumor tissue and adjacent normal tissue of 48 OS patients were collected. HOS and 143B cells were transfected. Gene expression was examined with qRT-PCR and Western blot. CCK8 assays and cell cloning was perform...

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Detalles Bibliográficos
Autores principales: Yang, Guang, He, Fei, Duan, Hao, Shen, Jianlin, Dong, Qirong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966140/
https://www.ncbi.nlm.nih.gov/pubmed/32021264
http://dx.doi.org/10.2147/OTT.S214813
Descripción
Sumario:PURPOSE: This article reports on FLVCR-AS1 effects on osteosarcoma (OS) growth. METHODS: Tumor tissue and adjacent normal tissue of 48 OS patients were collected. HOS and 143B cells were transfected. Gene expression was examined with qRT-PCR and Western blot. CCK8 assays and cell cloning was performed to measure cell proliferation. Cell cycle and apoptosis were assessed. Luciferase-reporter gene assays and RNA pull-down tests were used to detect targeting relationships between genes. RESULTS: Prominently higher FLVCR-AS1 expression was found in OS tissue and cells, and was associated with poor prognosis (P<0.05, P<0.01, or P<0.001). Compared with the siCtrl group, 143B and HOS cells of the siFLVCR-AS1 group had significantly lower OD(450) values and clone numbers and obviously higher percentages of cells in the G(1) phase and apoptosis (P<0.01 or P<0.001). miR381-3p expression was directly inhibited by FLVCR-AS1, and CCND1 expression was directly suppressed by miR381-3p. Compared with the FLVCR-AS1 group, 143B cells of the FLVCR-AS1(+) miR381-3p mimic group and FLVCR-AS1(+) siCCND1 group showed remarkably lower OD(450) values and clone numbers obviously higher apoptosis and percentage of cells in the G(1) phase (P<0.05, P<0.01, or P<0.001). CONCLUSION: FLVCR-AS1 promoted OS growth by upregulating CCND1 expression via downregulation of miR381-3p.