翼状胬肉中LncRNAs的差异表达谱。

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY
Jiusheng Zheng, Zhixin Ding, Lixin Mei, Huixiang Jin, Pengfei Zhang, Jinghong Yao, Guangming Liu, Shuting Li, Yinping Liu
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引用次数: 0

摘要

目的:通过基因芯片技术筛选长链非编码rna (lncRNAs)在翼状胬肉中的差异表达,并对差异表达的lncRNAs HOTTIP和RP1-261G23.7进行研究,探讨其在翼状胬肉发病中的可能机制。方法:收集2016年6月至2017年5月在皖南医学院燕鸡山医院眼科行手术的标本40例,其中翼状胬肉组织标本20例(男6例,女14例,年龄47 ~ 84岁,平均68.1岁),斜视患者正常鼻球结膜组织20例(男9例,女11例,年龄41 ~ 88岁,平均61.6岁)。每组随机抽取4个样本,采用高通量基因芯片检测技术检测lncRNA表达;通过定量实时聚合酶链式反应(qRT-PCR)筛选lncRNA HOTTIP、RP1-261G23.7及其对应的靶基因HOXA13、VEGFA,验证两组之间是否存在显著差异,并分析靶基因HOXA13与VEGFA表达的相关性。结果:(1)实验组和对照组采用SPSS17.0软件进行数据处理。性别和年龄采用卡方检验。统计学结果均为P > 0.05,统计学差异无统计学意义。(2)高通量基因芯片检测斜视患者与正常鼻球结膜组织相比,共检测到8271个差异lncrna。其中p值为2的lncrna和Benjamini-Hochberg FDR校正(FDR)结论:(1)lncrna在翼状胬肉中存在差异表达;(2)关键lncRNA HOTTIP、RP1-261G23.7可能是治疗翼状胬肉的新基因靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentially expressed profiles of LncRNAs in pterygium.

Objective: To do the differential expression of long noncoding RNAs (lncRNAs) in pterygium was screened by gene chip technology, and the differentially expressed lncRNAs HOTTIP and RP1-261G23.7 were studied to explore their possible mechanisms in the pathogenesis of pterygium.

Methods: Collected 40 specimens from June 2016 to May 2017 that underwent surgery in the Ophthalmology Department of Yanjishan Hospital of Wannan Medical College, including 20 pterygium tissue specimens (6 males and 14 females, aged 47-84 years, mean age 68.1 years), 20 cases of normal nasal bulbar conjunctival tissue in patients with strabismus (9 males and 11 females, aged 41-88 years, mean age 61.6 years). Four samples from each group were randomly selected to detect lncRNA expression by high-throughput gene chip detection technology; lncRNA HOTTIP, RP1-261G23.7 and corresponding target genes HOXA13, VEGFA were screened by quantitative real time polymerase chain reaction (qRT-PCR) to verify whether there is a significant difference between the two groups, and to analyze the correlation between the expression of the target genes HOXA13 and VEGFA.

Results: (1) SPSS17.0 software was used for data processing in the experimental group and the control group. Gender and age were analyzed by the chi-square test. The statistical results were all P > 0.05, and there was no significant difference in statistics, (2) A total of 8271 differential lncRNAs were detected by high-throughput gene chip detection and compared with normal nasal bulbar conjunctival tissue in patients with strabismus. Among them, lncRNAs with a P-value < 0.05 and log fold change > 2 and Benjamini-Hochberg FDR correction (FDR < 0.05) had 612 upregulated genes and 743 downregulated genes. (3) The two highly differential lncRNAs were selected and verified by qRT-PCR. The results showed that lncRNAs HOTTIP and RP1-261 G23.7 and the corresponding target genes HOXA13 and VEGFA were highly consistent and highly expressed in the control group.

Conclusions: (1) LncRNAs are differentially expressed in pterygium; (2) Key lncRNA HOTTIP, RP1-261G23.7 may be new gene targets for pterygium.

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来源期刊
BMC Ophthalmology
BMC Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
5.00%
发文量
441
审稿时长
6-12 weeks
期刊介绍: BMC Ophthalmology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of eye disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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