首页|ODC1基因对前列腺癌细胞PC-3 LncRNA表达影响的初步观察与分析

ODC1基因对前列腺癌细胞PC-3 LncRNA表达影响的初步观察与分析

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目的 探讨鸟氨酸脱羧酶1(ODC1)基因对前列腺癌细胞PC-3 LncRNA表达的影响,为进一步研究其作用及调控机制提供一些实验基础和线索.方法 以前列腺癌细胞PC-3作为研究对象,敲低ODC1基因,经q-PCR检测及 WB检测验证后采用Illumina Novaseq 6000,PE150模式进行高通量测序,测序结果应用编码潜能分析方法(CPC分析、CNCI分析、CPAT分析、LGC分析)进行预测筛选,对筛选出的lncRNAs行差异分析、顺式作用元件分析以及GO和KEGG富集分析.再选择文献报道中与前列腺癌关系密切的几个功能lncRNAs,采用q-PCR进行验证.结果 (1)在ODC1敲低PC-3细胞中筛选到341个lncRNA,差异表达的lncRNA中上调154个,下调128个.符合条件的差异lncRNA与差异表达基因共表达的顺式调控靶标有38个.(2)差异表达lncRNAs行GO和KEGG富集分析显示,lncRNA靶标基因参与体内多种生物学通路,如磷脂酰肌醇3激酶/蛋白激酶B信号通路(PI3K-Akt信号通路)、Ras信号通路等,还与肿瘤血管生成、细胞群增殖、正调控细胞分裂等密切相关.(3)q-PCR法验证结果:LINC00973、TERC表达显著下调、LINC00638表达显著上调,与GO和KEGG富集分析得到的lncRNA差异表达情况一致.结论 敲低ODC1基因可导致PC-3细胞lncRNAs差异表达,ODC1基因有可能通过lncRNAs影响细胞信号通路,促进肿瘤的发生发展.本实验为进一步研究ODC1基因在前列腺癌中的作用提供了一些新的实验基础.
Preliminary observation and analysis of effect of ornithine decarboxylase 1(ODC1)gene on PC-3 LncRNA expression in prostate cancer cells
Objective To explore the effect of ornithine decarboxylase 1(ODC1)gene on PC-3 LncRNA ex-pression in prostate cancer cells,and to provide some experimental basis and clues for further study of its role and regulation mechanism.Methods Prostate cancer cell PC-3 was selected as the research object,ODC1 gene was knocked down,q-PCR detection and WB detection were verified and Illumina Novaseq 6000 and PE150 models were used for high-throughput sequencing.Coding potential analysis method(CPC analysis,CNCI analysis,CPAT analysis and LGC analysis)were used to predict and screen the se-quencing results,and the selected lncRNAs were analyzed by difference analysis,cis-acting element analy-sis and GO and KEGG enrichment analysis.Several functional lncRNAs reported to be closely related to prostate cancer were selected and verified by q-PCR.Results(1)341 lncRNA were selected in ODC1 knockdown PC-3 cells,with 154 upregulated and 128 downregulated in the differentially expressed ln-cRNA.There were 38 cis-regulated targets of eligible differential lncRNA being differentially expressed with differentially expressed genes.(2)GO and KEGG enrichment analysis of differential expressed lncR-NAs showed that lncRNA target genes were involved in various biological pathways in vivo,such as phos-phatidylinositol 3 kinase/protein kinase B signaling pathway(PI3K-Akt signaling pathway),Ras signaling pathway,and were also closely related to tumor angiogenesis,cell population proliferation,and positive regulation of cell division.(3)q-PCR validation results:LINC00973 and TERC was significantly downreg-ulated,and LINC00638 was significantly upregulated,which was consistent with the differential expres-sion of lncRNA obtained by GO and KEGG enrichment analysis.Conclusion Knockdown of ODC1 leads to differential expression of lncRNAs in PC-3 cells,and it is possible that ODC1 gene affects cell signaling pathway through lncRNAs to promote the occurrence and development of tumors.This experiment pro-vides some new experimental basis for further investigating the role of the ODC1 gene in prostate cancer.

prostate cancerODC1 genelncRNAdifferential expression

宋尖卓、马健、陈鹏

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新疆医科大学附属肿瘤医院泌尿科,乌鲁木齐 830011

前列腺癌 ODC1基因 lncRNA 差异表达

新疆维吾尔自治区自然科学基金

2022D01C285

2024

新疆医科大学学报
新疆医科大学

新疆医科大学学报

CSTPCD
影响因子:0.76
ISSN:1009-5551
年,卷(期):2024.47(4)
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