摘要
目的探讨长链非编码RNA GAS5(lnc RNA GAS5)对喉癌Hep2细胞增殖和凋亡的影响及可能机制。方法采用实时荧光定量PCR(QPCR)检测喉癌和癌旁正常组织中GAS5的表达,分析其表达与喉癌临床病理特征的关系。Hep2细胞中分别转染pc DNA3. 1-GAS5或si GAS5,另分别转染pc DNA3. 1-NC或si NC作对照。MTT法检测转染后Hep2细胞增殖活性,流式细胞术检测Hep2细胞周期和凋亡,QPCR法和Western blotting法检测E2F1、BTF3 m RNA和蛋白的表达。结果喉癌组织和癌旁正常组织中GAS5表达水平分别为0. 56±0. 10和0. 98±0. 11,差异有统计学意义(P<0. 05)。GAS5表达与分化程度、TNM分期有关。pc DNA3. 1-GAS5组24、48、72、96 h Hep2细胞存活率明显低于pc DNA3. 1-NC组,差异有统计学意义(P<0. 05); si GAS5组细胞存活率明显高于si NC组,差异有统计学意义(P <0. 05)。pc DNA3. 1-GAS5组细胞G1期细胞比例为(68. 14±4. 33)%,高于pc DNA3. 1-NC组,差异有统计学意义(P<0. 05)。pc DNA3. 1-GAS组凋亡率高于pc DNA3. 1-NC组,差异有统计学意义(P<0. 05)。pc DNA3. 1-GAS5组细胞E2F1、BTF3 m RNA和蛋白的水平均低于pc DNA3. 1-NC组,差异具有统计学意义(P<0. 05); si GAS5组细胞E2F1、BTF3 m RNA和蛋白的水平均高于si NC组,差异具有统计学意义(P<0. 05)。结论GAS5可负性调控E2F1和BTF3表达,从而参与调控喉癌细胞的增殖和凋亡。
Objective To investigate the effect of long non-coding RNA GAS5 （lncRNA GAS5） on proliferation and apoptosis of laryngeal carcinoma Hep2 cells and its possible mechanism.Methods Real-time fluorescence quantitative PCR （QPCR） was used to detect the expression of GAS5 in laryngeal carcinoma and adjacent normal tissues. The relationship between the expression of GAS5 and the clinicopathological features of laryngeal carcinoma was analyzed. Hep2 cells were transfected with pcDNA3.1-GAS5 or siGAS5, and pcDNA3.1-NC or siNC respectively as control. MTT assay was used to detect the proliferation activity of Hep2 cells after transfection, and Hep2 cell cycle and apoptosis were detected by flow cytometry. QPCR and Western blotting were used to detect the expression of E2F1 and BTF3 mRNA and protein.Results The expression levels of GAS5 in laryngeal carcinoma and adjacent normal tissues were 0.56±0.10 and 0.98±0.11 respectively, and the difference was statistically significant（ P 〈0.05）. The expression of GAS5 was related to the degree of differentiation and TNM stage. The survival rate of Hep2 cells in pcDNA3.1-GAS5 group at 24, 48, 72 and 96 hours was significantly lower than that in pcDNA3.1-NC group （ P 〈0.05）, and that in siGAS5 group was significantly higher than that in siNC group （ P 〈0.05）. The proportion of G 1 phase cells transfected with pcDNA3.1-GAS5 was（68.14±4.33）% higher than that of pcDNA3.1-NC group（ P 〈0.05）. The apoptotic rate in group pcDNA3.1-GAS5 was higher than that in group pcDNA3.1-NC, and the difference was statistically significant （ P 〈0.05）. The mRNA and protein levels of E2F1 and BTF3 in pcDNA3.1-GAS5 transfection group were significantly lower than those in pcDNA3.1-NC group （ P 〈0.05）; the mRNA and protein levels of E2F1 and BTF3 in siGAS5 transfection group were significantly higher than those in siNC group （ P 〈0.05）.Conclusion GAS5 can negatively regulate the expression of E2F1 and BTF3, and thus participate in the regulation of
作者
贺松坡
曹银生
张晓静
HE Songpo;CAO Yinsheng;ZHANG Xiaojing(Department of ENT,Xuchang Central Hospital,Xuchang 461000,China)
出处
《临床肿瘤学杂志》
CAS
北大核心
2018年第9期811-816,共6页
Chinese Clinical Oncology
关键词
喉癌
GAS5
转录因子E2F1
通用转录因子3
增殖
凋亡
Laryngeal carcinoma
GAS5
Transcription factor E2F1
Basic transcription factor 3
Proliferation
Prognosis
