[1]沈惠群,沈松菲.5-Aza-CdR对胃癌中SOX17基因表达的影响[J].福建医药杂志,2024,46(01):24-29.[doi:10.20148/j.fmj.2024.01.007]
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5-Aza-CdR对胃癌中SOX17基因表达的影响()
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《福建医药杂志》[ISSN:1002-2600/CN:35-1071/R]

卷:
46
期数:
2024年01期
页码:
24-29
栏目:
临床研究
出版日期:
2024-02-15

文章信息/Info

文章编号:
1002-2600(2024)01-0024-06
作者:
沈惠群1沈松菲2
1 福建医科大学附属漳州市医院肿瘤内科,漳州363000;2 福建医科大学附属协和医院肿瘤内科,福州350001
关键词:
胃癌SOX17基因甲基化
分类号:
R735.2
DOI:
10.20148/j.fmj.2024.01.007
文献标志码:
A
摘要:
目的检测胃癌中SOX17的表达情况,探讨5-Aza-CdR对胃癌细胞SOX17表达的影响。方法采用免疫组织化学染色(immunohistochmeistry,IHC)法检测胃癌组织及癌旁组织中SOX17蛋白的表达情况,分析其表达与患者临床病理参数的关系。实时定量聚合酶链式反应(real-time polymerase chain reaction,Real-time PCR)和蛋白质印迹(Western blot)法检测胃癌细胞株MGC-803、MKN-45、AGS及正常胃黏膜细胞株GES-1中SOX17基因 mRNA和蛋白的表达情况。甲基化特异性PCR(methylation specific PCR,MSP)法检测胃癌细胞系SOX17基因启动子区甲基化情况。CCK-8法和流式细胞仪分别检测5-Aza-CdR对AGS细胞增殖和细胞周期的影响。结果与癌旁组织相比,胃癌组织SOX17蛋白阳性表达率明显降低(癌旁组织80.48% vs.胃癌组织19.51%,P<0.001),与胃癌患者性别、年龄、临床分期、分化程度、是否伴脉管癌栓无关。SOX17基因mRNA和蛋白在各胃癌细胞系表达明显降低(P<0.05),且在AGS细胞中表达最低。SOX17基因启动子区在AGS和MKN45细胞中均完全甲基化,MGC-803细胞部分甲基化,GES-1细胞完全非甲基化。去甲基化药物5-Aza-CdR可下调甲基转移酶的表达,逆转SOX17基因甲基化,使其mRNA和蛋白表达上调。5-Aza-CdR还可抑制AGS细胞的增殖并使细胞阻滞于G0/G1期。结论5-Aza-CdR可逆转胃癌细胞SOX17基因甲基化,上调其mRNA和蛋白表达,从而抑制胃癌的发生发展。

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备注/Memo

备注/Memo:
基金项目:福建医科大学启航基金(2022QH1276)
通信作者:沈松菲,Email:shensongfei@163.com
更新日期/Last Update: 2024-02-15