Decreased H19, GAS5, and linc0597 Expression and Association Analysis of Related Gene Polymorphisms in Rheumatoid Arthritis
Identifieur interne : 000905 ( Main/Exploration ); précédent : 000904; suivant : 000906Decreased H19, GAS5, and linc0597 Expression and Association Analysis of Related Gene Polymorphisms in Rheumatoid Arthritis
Auteurs : Jun Wu [République populaire de Chine] ; Tian-Ping Zhang [République populaire de Chine] ; Yu-Lan Zhao [République populaire de Chine] ; Bao-Zhu Li [République populaire de Chine] ; Rui-Xue Leng [République populaire de Chine] ; Hai-Feng Pan [République populaire de Chine] ; Dong-Qing Ye [République populaire de Chine]Source :
- Biomolecules [ 2218-273X ] ; 2019.
Abstract
Long noncoding RNAs (lncRNAs) widely participate in human diseases by regulating gene transcription, modulating protein function, or acting as ceRNAs. Yet, their roles in rheumatoid arthritis (RA) remain obscure. In this study, the expression of three lncRNAs (H19, GAS5, and linc0597) in peripheral blood mononuclear cells (PBMCs) were detected in 77 RA patients and 78 controls using quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR). The association of lncRNAs related gene polymorphisms with RA were evaluated in 828 RA patients and 780 controls using TaqMan single nucleotide polymorphism (SNP) genotyping assays. We observed that the expression levels of H19, GAS5 and linc0597 were down-regulated in PBMCs of RA patients, of which GAS5 level decreased in patients with hypocomplementemia, and negatively correlated with C-reactive protein (CRP) level in RA patients. Moreover, we highlighted two related potential functional SNPs, GAS5 rs6790 and linc0597 rs2680700 for associations with RA susceptibility. The precise roles of these lncRNAs in mechanism of RA remain to be further explored.
Url:
DOI: 10.3390/biom10010055
PubMed: 31905737
PubMed Central: 7022387
Affiliations:
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<author><name sortKey="Li, Bao Zhu" sort="Li, Bao Zhu" uniqKey="Li B" first="Bao-Zhu" last="Li">Bao-Zhu Li</name>
<affiliation><nlm:aff id="af1-biomolecules-10-00055">Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 81 Meishan Road, Hefei 230032, China;<email>wj1309230394@126.com</email>
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(J.W.);<email>15715511358@163.com</email>
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(J.W.);<email>15715511358@163.com</email>
(T.-P.Z.);<email>dqjkzhao@126.com</email>
(Y.-L.Z.);<email>libaozhu@ahmu.edu.cn</email>
(B.-Z.L.);<email>lengruixue@ahmu.edu.cn</email>
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<front><div type="abstract" xml:lang="en"><p>Long noncoding RNAs (lncRNAs) widely participate in human diseases by regulating gene transcription, modulating protein function, or acting as ceRNAs. Yet, their roles in rheumatoid arthritis (RA) remain obscure. In this study, the expression of three lncRNAs (H19, GAS5, and linc0597) in peripheral blood mononuclear cells (PBMCs) were detected in 77 RA patients and 78 controls using quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR). The association of lncRNAs related gene polymorphisms with RA were evaluated in 828 RA patients and 780 controls using TaqMan single nucleotide polymorphism (SNP) genotyping assays. We observed that the expression levels of H19, GAS5 and linc0597 were down-regulated in PBMCs of RA patients, of which GAS5 level decreased in patients with hypocomplementemia, and negatively correlated with C-reactive protein (CRP) level in RA patients. Moreover, we highlighted two related potential functional SNPs, GAS5 rs6790 and linc0597 rs2680700 for associations with RA susceptibility. The precise roles of these lncRNAs in mechanism of RA remain to be further explored.</p>
</div>
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<biblStruct><analytic><author><name sortKey="Zhang, T P" uniqKey="Zhang T">T.P. Zhang</name>
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</back>
</TEI>
<affiliations><list><country><li>République populaire de Chine</li>
</country>
<region><li>Anhui</li>
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<settlement><li>Hefei</li>
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</list>
<tree><country name="République populaire de Chine"><region name="Anhui"><name sortKey="Wu, Jun" sort="Wu, Jun" uniqKey="Wu J" first="Jun" last="Wu">Jun Wu</name>
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<name sortKey="Leng, Rui Xue" sort="Leng, Rui Xue" uniqKey="Leng R" first="Rui-Xue" last="Leng">Rui-Xue Leng</name>
<name sortKey="Li, Bao Zhu" sort="Li, Bao Zhu" uniqKey="Li B" first="Bao-Zhu" last="Li">Bao-Zhu Li</name>
<name sortKey="Pan, Hai Feng" sort="Pan, Hai Feng" uniqKey="Pan H" first="Hai-Feng" last="Pan">Hai-Feng Pan</name>
<name sortKey="Ye, Dong Qing" sort="Ye, Dong Qing" uniqKey="Ye D" first="Dong-Qing" last="Ye">Dong-Qing Ye</name>
<name sortKey="Zhang, Tian Ping" sort="Zhang, Tian Ping" uniqKey="Zhang T" first="Tian-Ping" last="Zhang">Tian-Ping Zhang</name>
<name sortKey="Zhao, Yu Lan" sort="Zhao, Yu Lan" uniqKey="Zhao Y" first="Yu-Lan" last="Zhao">Yu-Lan Zhao</name>
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</affiliations>
</record>
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