首页|幽门螺杆菌上调ADAMTS14激活Hippo信号通路对胃癌进展的影响及其机制

幽门螺杆菌上调ADAMTS14激活Hippo信号通路对胃癌进展的影响及其机制

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目的 研究Ⅰ型血小板结合蛋白基序的解聚蛋白样金属蛋白酶14基因(ADAMTS14)对幽门螺杆菌(Hp)感染相关胃癌进展的影响及其机制,探讨ADAMTS14作为胃癌生物治疗新靶点的可能性。方法 利用癌症基因组图谱(TCGA)及高通量基因表达数据库(GEO)分析胃癌组织及Hp阳性胃黏膜中差异表达的基因,筛选可能的靶点;对于选定的靶点ADAMTS14,分析其在胃癌及Hp阳性胃黏膜中的表达模式;对胃癌中与ADAMTS14共表达的基因进行京都基因与基因组百科全书(KEGG)数据库分析;利用Kaplan-Meier Plotter数据库分析ADAMTS14高低表达与胃癌患者预后的相关性;利用实时荧光定量PCR(RT-qPCR)和免疫组化方法分析30例胃癌患者的ADAMTS14表达水平,采用χ2检验分析ADAMTS14蛋白表达与临床病理特征之间的关系;利用GEO数据库分析Hp感染与ADAMTS14表达的关系,并通过细胞系感染实验验证;利用小干扰RNA沉默胃癌细胞系NCI-N87中ADAMTS14的表达,分析其对胃癌细胞功能的影响;利用RT-qPCR和Western blotting分析敲低ADAMTS14对Hippo信号通路下游靶基因表达的影响。结果 通过分析TCGA和GEO数据库,共得到16个与Hp感染及胃癌密切相关的基因;在TCGA数据库中,ADAMTS14在胃癌组织中的表达水平高于健康人胃黏膜(P<0。001);RT-qPCR及免疫组化结果也显示,ADAMTS14在胃癌组织中的表达水平高于癌旁组织(P<0。01);生存分析显示ADAMTS14高表达患者的预后不良(P<0。001);GSE60427的数据显示ADAMTS14在Hp感染的胃黏膜及细胞系中表达上调(P<0。001);Hp P12菌株感染NCI-N87细胞后ADAMTS14表达高于未感染组(P<0。0001);敲低胃癌细胞系NCI-N87中ADAMTS14明显抑制了胃癌细胞的增殖及迁移(P<0。05),以及Hippo信号通路靶基因BMP7、BMPR2、FZD4、PARD3、SAV1的表达(P<0。05)。结论 ADAMTS14在Hp感染的胃黏膜及胃癌组织中高表达,可能通过调控Hippo信号通路促进胃癌进展,有望作为Hp感染相关胃癌的新标志物及治疗靶点。
Effects of Helicobacter pylori on gastric cancer progression by upregulating ADAMTS14 and activating Hippo signaling pathway and its underlying mechanisms
Objective To analyze the effects and mechanisms of a disintegrin and metalloproteinase with thrombospondin motifs 14(ADAMTS14)gene in gastric cancer associated with Helicobacter pylori(Hp)infection and explore the potential of ADAMTS14 as a novel target for biological therapy of gastric cancer.Methods The Caner Genome Atlas(TCGA)and Gene Expression Omnibus(GEO)databases were utilized to analyze differentially expressed genes in gastric cancer tissues and Hp-positive gastric mucosa,and to screen potential targets.For the selected target ADAMTS14,its expression pattern in gastric cancer and Hp-positive gastric mucosa was analyzed.Kyoto Encyclopedia of Genes and Genomes(KEGG)analysis was performed on the genes co-expressed with ADAMTS14 in gastric cancer.Kaplan-Meier Plotter database was used to analyze the correlation between high-and low-ADAMTS14 expression and prognosis of gastric cancer patients.The expression of ADAMTS14 and its relationship with clinicopathological features in 30 patients with gastric cancer were analyzed using real-time fluorescent quantitative PCR(RT-qPCR)and immunohistochemistry.The relationship between Hp infection and ADAMTS14 expression was analyzed using GEO database,and confirmed by cell line infection experiment.ADAMTS14 expression in gastric cancer cell line NCI-N87 was silenced by small interfering RNA to analyze its effect on the function of gastric cancer cells;The effect of ADAMTS14 knockdown on downstream target genes of Hippo signaling pathway was analyzed by RT-qPCR and Western blotting.Results A total of 16 genes closely related to Hp infection and gastric cancer were identified by analyzing the TCGA and GEO databases.According to TCGA database,the ADAMTS14 expression in gastric cancer tissues was higher than that in healthy gastric mucosa(P<0.0001).RT-qPCR and immunohistochemistry results also showed higher ADAMTS14 expression in gastric cancer tissues compared to adjacent tissues(P<0.01).Survival analysis demonstrated poor prognosis in patients with high ADAMTS14 expression(P<0.001).Data from GSE60427 showed that ADAMTS14 expression was upregulated in Hp-infected gastric mucosa and cell lines(P<0.001).After Hp P12 infection,the ADAMTS14 expression in NCI-N87 cells was higher than that in uninfected group.ADAMTS14 knockdown significantly inhibited the proliferation and migration of NCI-N87 cells(P<0.05),and it also significantly inhibited the expression of Hippo signaling pathway target genes,including BMP7,BMPR2,FZD4,PARD3 and SAV1(P<0.05).Conclusion ADAMTS14 is highly expressed in Hp-positive gastric mucosa and gastric cancer tissues,which may accelerate gastric cancer progression by regulating Hippo signaling pathway,and holds potential as a new marker and therapeutic target for Hp infective gastric cancer.

gastric cancerHelicobacter pyloriADAMTS14Hippo signaling pathway

张博、米阳、刘斌、鲁彦文、郑鹏远

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郑州大学第五附属医院消化内科,河南郑州 450052

郑州大学医学科学院,河南郑州 450052

胃癌 幽门螺杆菌 Ⅰ型血小板结合蛋白基序的解聚蛋白样金属蛋白酶14 Hippo信号通路

国家重点研发计划郑州大学学科建设重点专项

2020YFC2006101XKZDJC202001

2024

解放军医学杂志
人民军医出版社

解放军医学杂志

CSTPCD北大核心
影响因子:1.644
ISSN:0577-7402
年,卷(期):2024.49(9)
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