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首页|期刊导航|基础医学与临床|C12ORF66对MYCN扩增的高危神经母细胞瘤细胞的活性调控

C12ORF66对MYCN扩增的高危神经母细胞瘤细胞的活性调控OACSTPCD

Regulatory effect of C12ORF66 on viability of MYCN amplified high-risk neuroblastoma cells

中文摘要英文摘要

目的 探究 12 号染色体开放阅读框 66(C12ORF66)对MYCN扩增神经母细胞瘤(NB)细胞系活性的调控效应.方法 通过 R2 数据库 GSE16476 和 GSE49710 数据集,分析 MYCN 扩增和 MYCN 非扩增 NB 细胞中C12ORF66 表达量,以及C12ORF66 表达量与患儿预后的相关性.RT-qRCR检测正常组织永生化细胞系、MYCN扩增及MYCN非扩增细胞系中C12ORF66 mRNA表达差异.构建瞬时敲低和稳定敲低C12ORF66 的MYCN扩增细胞株,对照组和敲低组细胞进行实时无标记动态细胞分析(RTCA)、集落形成能力检测及Ki67 免疫荧光染色.结果 R2 数据库分析显示MYCN扩增NB患儿样本中C12ORF66 表达显著高于MYCN非扩增NB患儿样本,并且C12ORF66 表达与患儿预后负相关(P<0.05).细胞实验表明,与MYCN非扩增细胞系CHLA-255 和SH-SY5Y相比,C12ORF66 在MYCN扩增细胞系 BE(2)-C和 SK-N-BE(2)中表达显著升高(P<0.001).瞬时或稳定敲低C12ORF66,MYCN扩增NB细胞增殖显著减缓(P<0.001),集落形成能力显著降低(P<0.001),Ki67 阳性细胞比例显著减少(P<0.05).结论 C12ORF66 在MYCN扩增NB患儿样本和细胞系中高表达,且与患儿预后负相关,敲低C12ORF66 显著抑制NB细胞活性.

Objective To explore the effect of open reading frame 66(C12ORF66)located at chromosome 12 on the viability of MYCN amplified NB cell lines.Methods DDatasets GSE16476 and GSE49710 in R2 database were analyzed for expression level of C12ORF66 in MYCN amplified and MYCN non-amplified NB cells and its potential correlation with the prognosis of pediatric patients.C12ORF66 mRNA expression level in normal tissue immortalized cell lines,MYCN amplified and MYCN non-amplified cell lines were detected by RT-qRCR.Transient or stable knockdown of C12ORF66 cell lines were constructed to compare the difference in real time cellular analysis(RTCA),colony formation,Ki67 positive cells between the control group and the C12ORF66 knockdown group.Results By analyzing R2 datasets,C12ORF66 level in MYCN amplified samples was significantly higher than that in MYCN non-amplified samples,and the expression of C12ORF66 was negatively correlated with the prognosis of pediatric patients(P<0.05).C12ORF66 highly expressed in MYCN-amplified BE(2)-C and SK-N-BE(2)cell lines than in MYCN non-amplified CHLA-255 and SH-SY5Y cell lines(P<0.001).Transient or stable knockdown of C12ORF66 resulted in significant slow down of proliferation of MYCN amplified NB cells(P<0.001),the colony formation ability was significantly reduced(P<0.001),and the proportion of Ki67 positive cells was significantly decreased(P<0.05).Conclusions C12ORF66 was highly expressed in MYCN amplified clinical NB samples and cell lines which is believed to be correlated with poor prognosis of pediatric patients.C12ORF66 knockdown signifi-cantly inhibits cell viability of NB cells.

贾安娜;战世佳;张璇;郭金鑫;于永波;郭永丽;常艳

国家儿童医学中心 首都医科大学附属北京儿童医院 儿科重大疾病研究教育部重点实验室 北京市儿科研究所儿童耳鼻咽喉头颈外科疾病北京市重点实验室,北京 100045

临床医学

12号染色体开放阅读框66SK-N-BE(2)细胞MYCN扩增细胞增殖

chromosome 12 open reading frame 66SK-N-BE(2)cellMYCN amplifiedcell proliferation

《基础医学与临床》 2024 (003)

288-294 / 7

国家自然科学基金(82141118,82293660/82293665)

10.16352/j.issn.1001-6325.2024.03.0288

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