2018Zhonghua xiaoerwaike zazhiRequires access

Effect of LncRNA CRNDE on the proliferation, apoptosis and migration of brain glioma cells

Wenyue Deng, Shiyuan Jing, Qing-Li Suo, Ruilong Gong, Yingying Lu

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Abstract

Objective To explore the effect of LncRNA CRNDE on the proliferation, apoptosis and migration of brain glioma cells. Methods LncRNA CRNDE was interfered by SiRNA in U251 cells.PE Annexin V-FITC staining and CCK-8 assay were employed for observing the effect of interfering LncRNA CRNDE on cell proliferation and apoptosis.And the capacity of cell migration was detected by scratch test. Results After 12 h transfection, statistically significant difference existed between control and SiRNA (si783, si809) groups.However, there was no statistically significant difference between SiRNA (si783, si809) and non-transfected groups.After 24 h, 48 h transfection, statistically significant difference existed between SiRNA (si783, si809) group and control and non-transfected groups (P 0.05). Cell migration experiment indicated that cell count of transfected group (287.2±28.6) was lower than non-transfected group (518.2±29.9) and control group (471.6±29.4) (P 0.05). Conclusions CRNDE can effectively enhance cell proliferation and migration of glioma cells and decrease the rate of cell apoptosis. Key words: Glioma; Cell proliferation; Apoptosis; Cell migration assay; LncRNA CRNDE

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What this paper is about

Objective To explore the effect of LncRNA CRNDE on the proliferation, apoptosis and migration of brain glioma cells. Methods LncRNA CRNDE was interfered by SiRNA in U251 cells.PE Annexin V-FITC staining and CCK-8 assay were employed for observing the effect of interfering LncRNA CRNDE on cell proliferation and apoptosis.And the capacity of cell migration was detected by scratch test. Results After 12 h transfection, statistically significant difference existed between control and SiRNA (si783, si809) groups.However, there was no statistically significant difference between SiRNA (si783, si809) and non-transfected groups.After 24 h, 48 h transfection, statistically significant difference existed between SiRNA (si783, si809) group and control and non-transfected groups (P 0.05). Cell migration experiment indicated that cell count of transfected group (287.2±28.6) was lower than non-transfected group (518.2±29.9) and control group (471.6±29.4) (P 0.05). Conclusions CRNDE can effectively enhance cell proliferation and migration of glioma cells and decrease the rate of cell apoptosis. Key words: Glioma; Cell proliferation; Apoptosis; Cell migration assay; LncRNA CRNDE

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Available abstract

Objective To explore the effect of LncRNA CRNDE on the proliferation, apoptosis and migration of brain glioma cells. Methods LncRNA CRNDE was interfered by SiRNA in U251 cells.PE Annexin V-FITC staining and CCK-8 assay were employed for observing the effect of interfering LncRNA CRNDE on cell proliferation and apoptosis.And the capacity of cell migration was detected by scratch test. Results After 12 h transfection, statistically significant difference existed between control and SiRNA (si783, si809) groups.However, there was no statistically significant difference between SiRNA (si783, si809) and non-transfected groups.After 24 h, 48 h transfection, statistically significant difference existed between SiRNA (si783, si809) group and control and non-transfected groups (P 0.05). Cell migration experiment indicated that cell count of transfected group (287.2±28.6) was lower than non-transfected group (518.2±29.9) and control group (471.6±29.4) (P 0.05). Conclusions CRNDE can effectively enhance cell proliferation and migration of glioma cells and decrease the rate of cell apoptosis. Key words: Glioma; Cell proliferation; Apoptosis; Cell migration assay; LncRNA CRNDE

Key concepts: Transfection, Apoptosis, Glioma, Cell growth, Annexin, Medicine, Cell, Cell migration

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Effect of LncRNA CRNDE on the proliferation, apoptosis and migration of brain glioma cells — Research Paper | ScholarLens