基础医学与临床 ›› 2017, Vol. 37 ›› Issue (12): 1712-1719.

• 研究论文 • 上一篇    下一篇

硒化合物诱导高危型HPV亚型宫颈癌细胞凋亡

熊洁琦1,郭玲1,陈夏2,娄远蕾3,刘丝荪2,郭菲4   

  1. 1. 江西省妇幼保健院
    2. 南昌大学第一附属医院
    3. 南昌大学第一附属医院泌尿外科研究所
    4. 南昌大学第一附属医院烧伤中心
  • 收稿日期:2016-12-13 修回日期:2017-03-15 出版日期:2017-12-05 发布日期:2017-11-29
  • 通讯作者: 郭菲 E-mail:guofei2005@126.com
  • 基金资助:
    江西省自然科学基金

Selenium compound induces apoptosis of cervical carcinoma cells of high risk HPV subtypes

  • Received:2016-12-13 Revised:2017-03-15 Online:2017-12-05 Published:2017-11-29

摘要: 目的 探讨二氧化硒(SeO2)对高危型HPV亚型宫颈癌细胞凋亡的诱导作用及其分子途径。方法 不同浓度SeO2分别作用于高危型HPV亚型宫颈癌细胞HeLa(HPV18+)和Caski(HPV16+)24 h,光学显微镜下观察细胞形态;四甲基偶氮唑蓝(MTT)比色法检测细胞增殖及活力;流式细胞计量术(FCM)检测细胞凋亡率;Western blot测定细胞内caspase-3和p53蛋白表达;Stem-loop实时定量PCR检测凋亡相关miRNA LET-7a表达。结果 SeO2作用后宫颈癌细胞变圆、皱缩;SeO2呈量效依赖关系抑制宫颈癌细胞增殖,其中HeLa细胞在7.5~30 μmol/L组抑制作用显著;Caski细胞在SeO2低浓度组即有显著抑制作用(P<0.05)。宫颈癌细胞凋亡率亦随SeO2浓度升高而升高,在Caski细胞上升更加明显。SeO2可明显上调宫颈癌细胞系中caspase-3与p53蛋白水平,在HeLa细胞中二者均于7.5 μmol/L处达到峰值。Caski细胞从7.5 μmol/L组开始凋亡蛋白表达量显著性升高(P<0.05)。SeO2还可显著上调两细胞系实验组细胞LET-7a表达水平,且均在7.5 μmol/L处出现峰值。结论 SeO2通过上调高危型HPV亚型宫颈癌细胞中凋亡相关蛋白p53蛋白及miRNA LET-7a的表达,经caspase-3途径诱导细胞凋亡。对于SeO2诱导宫颈癌细胞凋亡,HPV16+型较HPV18+型宫颈癌细胞更为敏感。

关键词: 二氧化硒(SeO2), 高危HPV亚型, 凋亡, miRNA, LET-7a

Abstract: Objective To investigate the inducing effects and related pathways of selenium dioxide (SeO2) on the apoptosis in 2 human cervical carcinoma cell lines of high risk of HPV subtypes. Methods HeLa (HPV-18-positive) and Caski (HPV-16-positive) cells were treated with different concentrations of SeO2 for 24 h respectively. Morphological changes of HeLa and Caski cells were observed under inverted optical microscope; cell proliferation and activity were examined by MTT assay; flow cytometry was employed to detect the cell apoptosis; the expressions of apoptosis-related proteins caspase-3 and p53 in cervical carcinoma cell lines were determined by Western blot analysis; the effects of SeO2 on apoptosis-related miRNA LET-7a expression was detected by Stem-loop reverse transcription-polymerase chain reaction (RT-PCR). Results Cell morphology was changed obviously in vitro. Cells became rounded and shrunken. SeO2 markedly inhibited cell proliferation and viability in a dose-dependent manner in both cell lines; In HeLa cells the inhibitory effects induced by 7.5~30 μmol/L of SeO2 were significant(P<0.05); The inhibitory effects on Caski were statistical significant(P<0.05) even in low concentrations of SeO2. The apoptosis rates induced by SeO2 increased dose-dependently in cervical carcinoma cell lines, which were higher in Caski. SeO2 could up-regulate the apoptosis-related proteins levels in cervical carcinoma cell lines. The expressions of caspase-3 and p53 in HeLa cells both significantly increased compared with control group (P<0.05), and peaked at the concentration of 7.5 μmol/L. Treated with higher concentrations(7.5~30 μmol/L) of SeO2, the expression on Caski cells increased significantly (P<0.05). SeO2 could induce the expression of apoptosis-related miRNA LET-7a both in HeLa cells and Caski cells with statistical meanings (P<0.05); the induction effects reached its climax at the concentration of 7.5 μmol/L bothly. Conclusions SeO2 shows anti-tumor properties via apoptosis pathway by up-regulating the expressions of apoptosis-related proteins caspase-3,the mechanisms involve inducing effects of p53 and LET-7a in cervical cancer cell lines. The apoptosis-inducing effect of SeO2 is more sensitive in HPV16+ cell line compared with HPV18+ cell line.

Key words: Selenium Dioxide (SeO2), High Risk of HPV Subtypes, Apoptosis, miRNA, LET-7a

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