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A promoter variant of lncRNA GAS5 is functionally associated with the development of osteosarcoma

机译:LNCRNA气体5的启动子变体在功能上与骨肉瘤的发育有关

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Background Previous studies showed that genetic variant rs145204276 in the promoter region of GAS5 was associated with the development of human cancer including colorectal cancer and hepatocellular cancer. This study aimed to investigate the role of rs145204276 in the development of osteosarcoma (OS). Methods 132 OS patients and 1270 healthy controls were recruited for the genotyping analysis of rs145204276. Promoter methylation level of GAS5 was determined for all patients. The tumor tissues and the adjacent normal tissue were collected from 42 patients during surgery and the relative expression of GAS5 was then quantified by Real-time PCR. The Chi-square test was used to determine the difference of genotype and allele frequency between the patients and the controls. The gene expression and the percentage of methylation alleles were compared among different genotypes of rs145204276 with One-way ANOVA test. Results Compared with the controls, patients were found to have significantly lower rate of genotype del/del (7.6% vs. 8.7%, p?=?0.024). The frequency of allele del was significantly lower in the patients than in the controls (23.5% vs. 30.1%, p?=?0.021). Compared with than patients with genotype ins/ins, those with genotype del/del had remarkably higher expression of GAS5 (0.0033?±?0.0019?vs. 0.0018?±?0.0006, p??0.001). Patients with genotype del/del were found to have obviously hypermethylation at the 7th CpG site as compared with those with genotype ins/ins (38.7%?±?21.1% vs. 20.5%?±?8.2%, p??0.001). Conclusions The genetic variant rs145204276 is functionally associated with the susceptibility of OS, which can function as a protective factor in the incidence of OS possibly through the regulation of GAS5.
机译:背景技术前面的研究表明,Gas5的启动子区域中的遗传变异RS145204276与在内的人类癌症的发育有关,包括结肠直肠癌和肝细胞癌。本研究旨在调查RS145204276在骨肉瘤(OS)发展中的作用。方法招募了132例患者和1270例健康对照,用于对145204276的基因分型分析。为所有患者确定促进剂甲基化水平。在手术期间从42例患者收集肿瘤组织和相邻的正常组织,然后通过实时PCR定量气体5的相对表达。 Chi-Square测试用于确定患者与对照之间的基因型和等位基因频率的差异。在单向ANOVA测试中比较了基因表达和甲基化等位基因的百分比,以145204276的不同基因型比较。结果与对照相比,发现患者的基因型Del / Del率明显较低(7.6%对8.7%,p?= 0.024)。患者的等位基因DEL的频率显着低于对照(23.5%vs.30.1%,p?= 0.021)。与基因型INS / INS的患者相比,那些有基因型DEL / DEL的患者的气体5表达显着(0.0033Ω±0.0019≤0.0018?±0.0018,p?<0.001)。与基因型INS / INS的那些(38.7%?±21.1%vs.21.1%,p?<0.001)相比,患有基因型Del / Del的患者在第7个CPG部位具有明显的高甲基化。 。结论遗传变异RS145204276在功能上与OS的易感性相关,其可以作为可能通过气体5的调节作为OS的发生率的保护因子。

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