首页|TP53INP1介导TGF-β1对膀胱癌细胞增殖、迁移的影响

TP53INP1介导TGF-β1对膀胱癌细胞增殖、迁移的影响

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目的 分析肿瘤蛋白 53 诱导的核蛋白 1(TP53INP1)介导转化生长因子-β1(TGF-β1)对膀胱癌细胞增殖、迁移的影响.方法 选取 2019 年 3 月至 2022 年 3 月膀胱癌切除术的患者癌组织、癌旁组织标本 40 例,检测TP53INP1、TGF-β1 表达量.膀胱癌细胞传代培养后分为TP53INP1-NC组、TP53INP1 组、TGF-β1-NC组、TGF-β1 组、TP53INP1+anti-TGF-β1-NC组、TP53INP1+anti-TGF-β1 组.分析各组细胞增殖、凋亡、迁移情况.结果 与癌组织比较,癌旁组织TP53INP1、TGF-β1 表达量较低(P<0.05).与TP53INP1-NC组比较,TP53INP1 组TP53INP1、B淋巴细胞瘤-2相关X蛋白(Bax)、天冬氨酸特异性半胱氨酸蛋白酶 3(Caspase-3)、上皮性钙黏附素(E-cadherin)表达量、凋亡率水平较高,增殖率、细胞迁移数水平、B淋巴细胞瘤 2 基因(Bcl-2)、基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶-9(MMP-9)表达量较低(P<0.05).与TGF-β1-NC组比较,TGF-β1 组TGF-β1、Bax、Caspase-3、E-cadherin表达量、凋亡率水平较高,增殖率、细胞迁移数水平、Bcl-2、MMP-2、MMP-9 表达量较低(P<0.05).双荧光素酶报告试验显示,与TGF-β1-NC组比较,TGF-β1 组WT-TP53INP1 荧光素酶活性降低(P<0.05),对MUT-TP53INP1 荧光素酶活性影响较小(P>0.05).与TP53INP1+anti-TGF-β1-NC组比较,TP53INP1+anti-TGF-β1 组TGF-β1、Bax、Caspase-3、E-cadherin表达量、凋亡率水平较低(P<0.05),增殖率、细胞迁移数水平、Bcl-2、MMP-2、MMP-9 表达量较高(P<0.05).结论 TP53INP1 可能通过靶向作用于TGF-β1 而参与膀胱癌细胞增殖、凋亡、迁移,为膀胱癌诊治提供了新方向.
Effect of TP53INP1-mediated TGF-β1 on the proliferation and migration of bladder cancer cells
Objective To analyze the effect of tumor protein 53 induced nuclear protein 1(TP53INP1)-mediated transformation growth factor-β1(TGF-β1)on the proliferation and migration of bladder cancer cells.Methods The expression levels of TP53INP1 and TGF-β1 were detected in 40 bladder cancer tissues and paracancerous tissues in patients undergoing bladder cancer resection in our hospital from March 2019 to March 2022.Bladder cancer cells were cultured and passaged in vitro.They were divided into TP53inp1-NC group,TP53INP1 group,TGF-β1-NC group,TGF-β1 group,TP53INP1 group +anti-TGF-β1-NC group,and TP53INP1 group +anti-TGF-β1 group based on the specific cell transfection.Cell proliferation,apoptosis and migration were analyzed.Results The expressions of TP53INP1 and TGF-β1 in paracancerous tissues were significantly lower than those of breast cancer carcinoma tissues(P<0.05).Compared with those of TP53inp1-NC group,the expression levels of TP53INP1,B-lymphocytoma-2-associated X protein(Bax),aspartate-specific cysteine protease 3(Caspase-3),and epithelial cadherin(E-cadherin)and apoptotic rate in TP53INP1 group were significantly higher,while the proliferative rate,number of migratory cells and the expression levels of B lymphoblastoma 2 gene(Bcl-2),matrix metalloproteinase-2(MMP-2)and matrix metalloproteinase-9(MMP-9)were significantly lower(P<0.05).Compared with those of TGF-β1-NC group,the expression levels of TGF-β1,Bax,Caspase-3 and E-cadherin and apoptotic rate were significantly higher in TGF-β1 group,while the proliferative rate,number of migratory cells,and expression levels of Bcl-2,MMP-2,and MMP-9 were significantly lower(P<0.05).Dual-luciferase reporter assay showed that compared with that of TGF-β1-NC group,the luciferase activity of WT-TP53INP1 in TGF-β1 group was significantly lower(P<0.05),and that of MUT-TP53INP1 was not significantly changed(P>0.05).Compared with those of TP53INP1 group +anti-TGF-β1-NC group,TP53INP1 group +anti-TGF-β1 group had lower expression levels of TGF-β1,Bax,Caspase-3,and E-cadherin and apoptotic rate,but higher proliferative rate,number of migratory cells,and expression levels of Bcl-2,MMP-2 and MMP-9(P<0.05).Conclusion TP53INP1 may participate in the proliferation,apoptosis and migration of bladder cancer cells by targeting TGF-β1,providing a new direction for the diagnosis and treatment of bladder cancer.

tumor protein 53 induced nucleoprotein 1transforming growth factor-β1bladder cancerproliferatemigration

广雨龙、杨扬

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563000 贵州省遵义市,贵州航天医院泌尿外科

肿瘤蛋白53诱导的核蛋白1 转化生长因子-β1 膀胱癌 增殖 迁移

遵义市科技计划项目

遵市科合HZ字[2020]165号

2024

河北医药
河北省医学情报研究所

河北医药

CSTPCD
影响因子:1.075
ISSN:1002-7386
年,卷(期):2024.46(1)
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