Association of Long Non-Coding RNAs NEAT1, and MALAT1 expression and pathogenesis of Behçet's disease among Egyptian patients
Behçet's disease (BD)is a chronic inflammatory disease. Immunological defects have been shown to play a significant role in the progression of BD. The expression levels of two long non-coding RNAs (lncRNAs), NEAT1 and MALAT1, were examined in patients with BD to identify their role in the disea...
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Veröffentlicht in: | Saudi journal of biological sciences 2022-08, Vol.29 (8), p.103344-103344, Article 103344 |
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description | Behçet's disease (BD)is a chronic inflammatory disease. Immunological defects have been shown to play a significant role in the progression of BD. The expression levels of two long non-coding RNAs (lncRNAs), NEAT1 and MALAT1, were examined in patients with BD to identify their role in the disease pathogenesis. Both lncRNAs were mentioned as essential regulators of innate immune responses and have a crucial role in inflammatory diseases. Fifty patients with BD and a similar number of control individuals were involved in our study. At enrollment, data was collected from patients and controls, and the disease severity in active cases was determined using the Behçet's Disease Current Activity Form (BDCAF). Levels of the two studied biomarkers in the serum, NEAT1 and MALAT1, were investigated by quantitative RT-PCR (qRT-PCR). NEAT1 levels were significantly turned down in BD patients (fold changes = 0.77,p = 0.0001) and correlated negatively with the BDCAF (r = -0.41;p = 0.003). On the other hand, the MALAT1 levels were significantly up-regulated in BD patients (fold changes = 2.65,p = 0.003). Serum levels of NEAT1 were significantly decreased in patients with active states than in stationary cases (0.387 versus 0.1.99, respectively;p = 0.01) and compared with controls (p = 0.001). Also, NEAT1 levels were significantly increased in patients with stationary states compared to controls (p = 0.03). MALAT1 levels were found to be elevated significantly in the active cases compared with controls. There was a positive association between NEAT1 and MALAT1 levels among BD patients (r = 0.29,p = 0.04).Our findings demonstrate a possible role of NEAT1 and MALAT1 in the pathogenesis of BD. |
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Immunological defects have been shown to play a significant role in the progression of BD. The expression levels of two long non-coding RNAs (lncRNAs), NEAT1 and MALAT1, were examined in patients with BD to identify their role in the disease pathogenesis. Both lncRNAs were mentioned as essential regulators of innate immune responses and have a crucial role in inflammatory diseases. Fifty patients with BD and a similar number of control individuals were involved in our study. At enrollment, data was collected from patients and controls, and the disease severity in active cases was determined using the Behçet's Disease Current Activity Form (BDCAF). Levels of the two studied biomarkers in the serum, NEAT1 and MALAT1, were investigated by quantitative RT-PCR (qRT-PCR). NEAT1 levels were significantly turned down in BD patients (fold changes = 0.77,p = 0.0001) and correlated negatively with the BDCAF (r = -0.41;p = 0.003). On the other hand, the MALAT1 levels were significantly up-regulated in BD patients (fold changes = 2.65,p = 0.003). Serum levels of NEAT1 were significantly decreased in patients with active states than in stationary cases (0.387 versus 0.1.99, respectively;p = 0.01) and compared with controls (p = 0.001). Also, NEAT1 levels were significantly increased in patients with stationary states compared to controls (p = 0.03). MALAT1 levels were found to be elevated significantly in the active cases compared with controls. There was a positive association between NEAT1 and MALAT1 levels among BD patients (r = 0.29,p = 0.04).Our findings demonstrate a possible role of NEAT1 and MALAT1 in the pathogenesis of BD.</description><identifier>ISSN: 1319-562X</identifier><identifier>EISSN: 2213-7106</identifier><identifier>DOI: 10.1016/j.sjbs.2022.103344</identifier><identifier>PMID: 35800145</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Behçet's disease ; Long non-coding RNAs ; MALAT1 ; NEAT1 ; Original</subject><ispartof>Saudi journal of biological sciences, 2022-08, Vol.29 (8), p.103344-103344, Article 103344</ispartof><rights>2022 The Author(s)</rights><rights>2022 The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-db2414be8de8089ed68e91a64e07aea98230e91547e0f1440934a63a21ddcda63</citedby><cites>FETCH-LOGICAL-c432t-db2414be8de8089ed68e91a64e07aea98230e91547e0f1440934a63a21ddcda63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253411/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1319562X22002601$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3536,27903,27904,53769,53771,65309</link.rule.ids></links><search><creatorcontrib>Mohammed, Asmaa</creatorcontrib><creatorcontrib>Shaker, Olfat G.</creatorcontrib><creatorcontrib>Khalil, Mahmoud A.F.</creatorcontrib><creatorcontrib>Elsabagh, Yumn A.</creatorcontrib><creatorcontrib>Gomaa, Mohammed</creatorcontrib><creatorcontrib>Ahmed, Azza M.</creatorcontrib><creatorcontrib>Erfan, Randa</creatorcontrib><title>Association of Long Non-Coding RNAs NEAT1, and MALAT1 expression and pathogenesis of Behçet's disease among Egyptian patients</title><title>Saudi journal of biological sciences</title><description>Behçet's disease (BD)is a chronic inflammatory disease. Immunological defects have been shown to play a significant role in the progression of BD. The expression levels of two long non-coding RNAs (lncRNAs), NEAT1 and MALAT1, were examined in patients with BD to identify their role in the disease pathogenesis. Both lncRNAs were mentioned as essential regulators of innate immune responses and have a crucial role in inflammatory diseases. Fifty patients with BD and a similar number of control individuals were involved in our study. At enrollment, data was collected from patients and controls, and the disease severity in active cases was determined using the Behçet's Disease Current Activity Form (BDCAF). Levels of the two studied biomarkers in the serum, NEAT1 and MALAT1, were investigated by quantitative RT-PCR (qRT-PCR). NEAT1 levels were significantly turned down in BD patients (fold changes = 0.77,p = 0.0001) and correlated negatively with the BDCAF (r = -0.41;p = 0.003). On the other hand, the MALAT1 levels were significantly up-regulated in BD patients (fold changes = 2.65,p = 0.003). Serum levels of NEAT1 were significantly decreased in patients with active states than in stationary cases (0.387 versus 0.1.99, respectively;p = 0.01) and compared with controls (p = 0.001). Also, NEAT1 levels were significantly increased in patients with stationary states compared to controls (p = 0.03). MALAT1 levels were found to be elevated significantly in the active cases compared with controls. There was a positive association between NEAT1 and MALAT1 levels among BD patients (r = 0.29,p = 0.04).Our findings demonstrate a possible role of NEAT1 and MALAT1 in the pathogenesis of BD.</description><subject>Behçet's disease</subject><subject>Long non-coding RNAs</subject><subject>MALAT1</subject><subject>NEAT1</subject><subject>Original</subject><issn>1319-562X</issn><issn>2213-7106</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UU2LE0EUbMTFjat_wNPc9OBk-2tmekCEMWR1IUaQFbw1ne6XpEPSPTtvsriX_Tv-EP_YdpNF8OLpFfVeVcErQt4wOmWU1Ze7Ke5WOOWU80QIIeUzMuGcibJhtH5OJkywtqxq_vOcvETcUVorodgLci4qRSmT1YQ8dIjRejP6GIq4LhYxbIplDOUsOp_g92WHxXLe3bD3hQmu-NotEi7gVz8AYhZltjfjNm4gAHrMLp9g--c3jG-xcB7BIBTmkI3nm_t-9CZkgYcw4itytjZ7hNdP84L8uJrfzL6Ui2-fr2fdorRS8LF0Ky6ZXIFyoKhqwdUKWmZqCbQxYFrFBU1EJRugayYlbYU0tTCcOWddQhfk48m3P64O4GzKHsxe94M_mOFeR-P1v5vgt3oT73TLKyEZSwbvngyGeHsEHPXBo4X93gSIR9S8Vk3DRdPmLH46tUNEHGD9N4ZRnYvTO52L07k4fSouiT6cRJC-cOdh0GjThyw4P4AdtYv-f_JH1GihXA</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Mohammed, Asmaa</creator><creator>Shaker, Olfat G.</creator><creator>Khalil, Mahmoud A.F.</creator><creator>Elsabagh, Yumn A.</creator><creator>Gomaa, Mohammed</creator><creator>Ahmed, Azza M.</creator><creator>Erfan, Randa</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220801</creationdate><title>Association of Long Non-Coding RNAs NEAT1, and MALAT1 expression and pathogenesis of Behçet's disease among Egyptian patients</title><author>Mohammed, Asmaa ; Shaker, Olfat G. ; Khalil, Mahmoud A.F. ; Elsabagh, Yumn A. ; Gomaa, Mohammed ; Ahmed, Azza M. ; Erfan, Randa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-db2414be8de8089ed68e91a64e07aea98230e91547e0f1440934a63a21ddcda63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Behçet's disease</topic><topic>Long non-coding RNAs</topic><topic>MALAT1</topic><topic>NEAT1</topic><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohammed, Asmaa</creatorcontrib><creatorcontrib>Shaker, Olfat G.</creatorcontrib><creatorcontrib>Khalil, Mahmoud A.F.</creatorcontrib><creatorcontrib>Elsabagh, Yumn A.</creatorcontrib><creatorcontrib>Gomaa, Mohammed</creatorcontrib><creatorcontrib>Ahmed, Azza M.</creatorcontrib><creatorcontrib>Erfan, Randa</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Saudi journal of biological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohammed, Asmaa</au><au>Shaker, Olfat G.</au><au>Khalil, Mahmoud A.F.</au><au>Elsabagh, Yumn A.</au><au>Gomaa, Mohammed</au><au>Ahmed, Azza M.</au><au>Erfan, Randa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of Long Non-Coding RNAs NEAT1, and MALAT1 expression and pathogenesis of Behçet's disease among Egyptian patients</atitle><jtitle>Saudi journal of biological sciences</jtitle><date>2022-08-01</date><risdate>2022</risdate><volume>29</volume><issue>8</issue><spage>103344</spage><epage>103344</epage><pages>103344-103344</pages><artnum>103344</artnum><issn>1319-562X</issn><eissn>2213-7106</eissn><abstract>Behçet's disease (BD)is a chronic inflammatory disease. Immunological defects have been shown to play a significant role in the progression of BD. The expression levels of two long non-coding RNAs (lncRNAs), NEAT1 and MALAT1, were examined in patients with BD to identify their role in the disease pathogenesis. Both lncRNAs were mentioned as essential regulators of innate immune responses and have a crucial role in inflammatory diseases. Fifty patients with BD and a similar number of control individuals were involved in our study. At enrollment, data was collected from patients and controls, and the disease severity in active cases was determined using the Behçet's Disease Current Activity Form (BDCAF). Levels of the two studied biomarkers in the serum, NEAT1 and MALAT1, were investigated by quantitative RT-PCR (qRT-PCR). NEAT1 levels were significantly turned down in BD patients (fold changes = 0.77,p = 0.0001) and correlated negatively with the BDCAF (r = -0.41;p = 0.003). On the other hand, the MALAT1 levels were significantly up-regulated in BD patients (fold changes = 2.65,p = 0.003). Serum levels of NEAT1 were significantly decreased in patients with active states than in stationary cases (0.387 versus 0.1.99, respectively;p = 0.01) and compared with controls (p = 0.001). Also, NEAT1 levels were significantly increased in patients with stationary states compared to controls (p = 0.03). MALAT1 levels were found to be elevated significantly in the active cases compared with controls. There was a positive association between NEAT1 and MALAT1 levels among BD patients (r = 0.29,p = 0.04).Our findings demonstrate a possible role of NEAT1 and MALAT1 in the pathogenesis of BD.</abstract><pub>Elsevier B.V</pub><pmid>35800145</pmid><doi>10.1016/j.sjbs.2022.103344</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Behçet's disease Long non-coding RNAs MALAT1 NEAT1 Original |
title | Association of Long Non-Coding RNAs NEAT1, and MALAT1 expression and pathogenesis of Behçet's disease among Egyptian patients |
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