lncRNA HAGLR促卵巢癌细胞生长和上皮-间充质转化的机制研究  被引量:1

Mechanism of lncRNA HAGLR promoting ovarian cancer cell growth and epithelial-mesenchymal transition

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作  者:李俊[1] 王晓黎 俞岩 周俏苗 LI Jun;WANG Xiao-li;YU Yan;ZHOU Qiao-miao(Department of Gynecology,Affiliated Children´s Hospital of Hainan Medical University,Haikou Hainan 571100,China)

机构地区:[1]海南医学院附属儿童医院妇科,海南海口571100

出  处:《局解手术学杂志》2024年第6期491-496,共6页Journal of Regional Anatomy and Operative Surgery

基  金:海南省卫生健康行业科研项目(21A200465)。

摘  要:目的研究长链非编码RNA同源盒D基因簇反义生长相关长链非编码RNA(lncRNA HAGLR)通过调控核苷酸结合寡聚化结构域样受体家族pyrin结构域蛋白3(NLRP3)炎症小体对卵巢癌细胞生长和上皮-间充质转化(EMT)的调控作用。方法培养卵巢正常细胞IOSE-80(IOSE-80组)以及卵巢癌细胞A2780(A2780组)。然后将A2780随机分为lncRNA HAGLR沉默组(siHAGLR组)、沉默阴性对照组(siNC组)、siHAGLR联合NLRP3抑制剂MCC950处理组(siHAGLR+MCC950组)。qRT-PCR法检测lncRNA HAGLR的表达。Western blot检测NLRP3炎症小体相关蛋白NLRP3、caspase-1、ASC和EMT相关蛋白Vimentin、Snail1、α-SMA、Twist1的表达。CCK-8法检测A2780细胞的增殖活性。Transwell法检测A2780细胞的迁移和侵袭能力。细胞克隆形成实验检测A2780细胞的生长能力。TUNEL染色检测A2780细胞的凋亡。结果与IOSE-80组相比,A2780组lncRNA HAGLR、Vimentin、Snail1、α-SMA、Twist1表达均上调(P<0.05),但NLRP3、caspase-1、ASC的表达均下调(P<0.05)。与siNC组相比,siHAGLR组的lncRNA HAGLR、Vimentin、Snail1、α-SMA、Twist1表达均下调(P<0.05),但NLRP3、caspase-1、ASC的表达均上调(P<0.05),细胞增殖率、细胞克隆数以及迁移和侵袭数均明显减少(P<0.05),细胞凋亡数则增加(P<0.05)。与siHAGLR组相比,siHAGLR+MCC950组的lncRNA HAGLR表达无明显变化(P>0.05),而Vimentin、Snail1、α-SMA、Twist1表达均上调(P<0.05),但NLRP3、caspase-1、ASC的表达均下调(P<0.05),细胞增殖率、细胞克隆数以及迁移和侵袭数均显著增加(P<0.05),细胞凋亡数则减少(P<0.05)。结论lncRNA HAGLR通过抑制NLRP3炎症小体促进卵巢癌细胞的生长和EMT。Objective To investigate the effect of long noncoding RNA Homeobox D gene cluster antisense growth-associated long noncoding RNA(lncRNA HAGLR)on ovarian cancer cell growth and epithelial-mesenchymal transition(EMT)by regulating nucleotidebinding oligomerization domain-like receptor family pyrin domain-containing protein 3(NLRP3)inflammasome.Methods The normal ovarian cell IOSE-80(IOSE-80 group)and the ovarian cancer cell A2780(A2780 group)were cultured.Then A2780 cells were randomly divided into the lncRNA HAGLR silencing group(siHAGLR group),silencing negative control group(siNC group),and siHAGLR combined with NLRP3 inhibitor MCC950 treatment group(siHAGLR+MCC950 group).The expression of lncRNA HAGLR was detected by qRT-PCR.The expressions of NLRP3 inflammasome-related proteins NLRP3,caspase-1,ASC and EMT-related proteins Vimentin,Snail1,α-SMA,Twist1 were detected by Western blot.CCK-8 assay was used to detect the proliferation activity of A2780 cells;Transwell assay was used to detect cell migration and invasion ability of A2780 cells.Cell clone formation assay was used to detect the growth ability of A2780 cells.TUNEL staining was used to detect the apoptosis of A2780 cells.Results Compared with the IOSE-80 group,the expressions of lncRNA HAGLR,Vimentin,Snail1,α-SMA,Twist1 in the A2780 group were all up-regulated(P<0.05),while the expressions of NLRP3,caspase-1,and ASC were all down-regulated(P<0.05).Compared with the siNC group,the expressions of lncRNA HAGLR,Vimentin,Snail1,α-SMA,Twist1 in the siHAGLR group were all down-regulated(P<0.05),while the expressions of NLRP3,caspase-1,and ASC were all up-regulated(P<0.05),the cell proliferation rate,number of cell clones,migration and invasion were significantly reduced(P<0.05),while the cell apoptosis number was increased(P<0.05).Compared with the siHAGLR group,there was no significant change in the expression of lncRNA HAGLR in the siHAGLR+MCC950 group(P>0.05),while the expressions of Vimentin,Snail1,α-SMA,Twist1 were all up-regulated(P<0.05),while the expr

关 键 词:长链非编码RNA同源盒D基因簇反义生长相关长链非编码RNA 核苷酸结合寡聚化结构域样受体家族pyrin结构域蛋白3 炎症小体 卵巢癌细胞 上皮-间充质转化 

分 类 号:R737.31[医药卫生—肿瘤]

 

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