沉默中期因子对肝癌细胞恶性生物学行为的影响  

Effect of midkine knockdown for malignant biological feature in human hepatocellular carcinoma

作　　者：刘晶华[1] 邹玉[2] 吴钧[3] 常巍[1] 

机构地区：[1]云南省第二人民医院消化内科,云南昆明650001 [2]昆明医科大学统计教研室,云南昆明650000 [3]云南省昆明市第一人民医院神经外科,云南昆明650031

出　　处：《中国现代医学杂志》2017年第11期36-40,共5页China Journal of Modern Medicine

摘　　要：目的探讨中期因子(MDK)在肝细胞肝癌(HCC)中的表达及对肿瘤细胞增殖、凋亡及侵袭能力的影响。方法选取2015年1月-2016年10月该院收治的50例肝癌患者组织标本,免疫组织化学染色分析组织中MDK的表达。利用沉默核糖核酸(si RNA)沉默人肝细胞癌HepG2细胞内MDK表达,分别采用CCK-8、流式细胞仪及插入式细胞培养皿、穿透小室(Transwell)检测沉默MDK后HepG2细胞增殖、凋亡及侵袭能力变化。结果肝癌组织中MDK蛋白的表达水平较癌旁组织提高(χ~2=19.643,P=0.000);在HepG2细胞中,沉默MDK的表达可抑制HepG2细胞增殖(F=22.204,P=0.037)和侵袭(t=5.611,P=0.008)能力,并提高HepG2细胞的凋亡比例(t=5.702,P=0.006)。结论 MDK在肝癌中表达升高,沉默肝癌HepG2细胞内MDK表达能够抑制肝癌细胞生长和侵袭。Objective To study the expression and roles of midkine （MDK） in human hepatocellular carcinoma （HCC）. Methods A total of 50 HCC tissues and tumor adjacent tissues were collected to detect the expression of MDK by immunohistochemieal staining. The expression of MDK in HepG2 cells was silenced by siRNA. Cell proliferation, apoptosis and invasion were detected by CCK-8, flow cytometry and Transwell, respectively. Results MDK expression was up-regulated in HCC tissues （P〈 0.05）. Knockdown MDK in HCC cells was significantly down-regulated cell proliferation, invasion and induced apoptosis. Conclusions MDK is over-expressed in HCC tissues. Knockdown MDK can inhibit growth and invasion on HepG2 cells.

关 键 词：中期因子 肝细胞癌 增殖 凋亡 侵袭 

分 类 号：R735.7[医药卫生—肿瘤]