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Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status
Background Long non-coding RNAs (LncRNAs) have recently been considered promising biomarkers for oncogenesis due to their epigenetic regulatory effects. HOTAIR is one of the oncogenic LncRNAs that was previously studied in different non-hematological malignancies. The current study set out to detect...
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Published in: | Egyptian Journal of Medical Human Genetics 2021-06, Vol.22 (1), p.61-9 |
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description | Background Long non-coding RNAs (LncRNAs) have recently been considered promising biomarkers for oncogenesis due to their epigenetic regulatory effects. HOTAIR is one of the oncogenic LncRNAs that was previously studied in different non-hematological malignancies. The current study set out to detect the expression level of HOTAIR LncRNA in AML patients concerning their clinical characteristics, laboratory data, FLT3-ITD, and NPM1 mutations, as well as treatment outcome. This study included quantitative detection of HOTAIR gene expression in 47 cases of AML using quantitative reverse transcription polymerase chain reaction, as well as NPM1 and FLT3-ITD genotyping. Results The HOTAIR expression was significantly higher in AML patients 6.87 (0.001) than in normal controls 1.66 (0.004-6.82) (p 0.007). The HOTAIR expression level was affected by chemotherapy, and it was correlated to hemoglobin level (p 0.001), age, total leukocytic count (p 0.022), and NPM1 mutation (p 0.017). HOTAIR gene expression level showed a correlation to relapse-free survival in the study group (p 0.04). Conclusion HOTAIR is overexpressed in patients with acute myeloid leukemia (AML). HOTAIR pre-treatment and post-chemotherapy gene expression levels can predict chemosensitivity and relapse. |
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HOTAIR is one of the oncogenic LncRNAs that was previously studied in different non-hematological malignancies. The current study set out to detect the expression level of HOTAIR LncRNA in AML patients concerning their clinical characteristics, laboratory data, FLT3-ITD, and NPM1 mutations, as well as treatment outcome. This study included quantitative detection of HOTAIR gene expression in 47 cases of AML using quantitative reverse transcription polymerase chain reaction, as well as NPM1 and FLT3-ITD genotyping. Results The HOTAIR expression was significantly higher in AML patients 6.87 (0.001) than in normal controls 1.66 (0.004-6.82) (p 0.007). The HOTAIR expression level was affected by chemotherapy, and it was correlated to hemoglobin level (p 0.001), age, total leukocytic count (p 0.022), and NPM1 mutation (p 0.017). HOTAIR gene expression level showed a correlation to relapse-free survival in the study group (p 0.04). Conclusion HOTAIR is overexpressed in patients with acute myeloid leukemia (AML). HOTAIR pre-treatment and post-chemotherapy gene expression levels can predict chemosensitivity and relapse.</description><identifier>ISSN: 1110-8630</identifier><identifier>EISSN: 2090-2441</identifier><identifier>DOI: 10.1186/s43042-021-00180-x</identifier><language>eng</language><publisher>Cairo: Springer</publisher><subject>Acute myeloid leukemia ; AML ; Cancer ; Chemotherapy ; Epigenetic inheritance ; Epigenetics ; FLT3-ITD ; Gene expression ; Genes ; Genetic aspects ; Genetic transcription ; Genotyping ; Hemoglobin ; HOTAIR ; LncRNA ; Medical research ; Medicine, Experimental ; Mutation ; Non-coding RNA ; NPM1 ; Patients ; Reverse transcription ; Tumorigenesis</subject><ispartof>Egyptian Journal of Medical Human Genetics, 2021-06, Vol.22 (1), p.61-9</ispartof><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-b5d8af069b8b53ddaa267c69f019c1e2bd355d9107e8e4d362993eb8a62596383</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2670470078/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2670470078?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25733,27903,27904,36991,44569,74872</link.rule.ids></links><search><creatorcontrib>Salah, Mona</creatorcontrib><creatorcontrib>Zawam, Hamdy</creatorcontrib><creatorcontrib>Fouad, Neven Bahaa</creatorcontrib><creatorcontrib>Soliman, Nohair</creatorcontrib><creatorcontrib>Maksoud, Fatma Abdel Wahab Abdel</creatorcontrib><title>Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status</title><title>Egyptian Journal of Medical Human Genetics</title><description>Background Long non-coding RNAs (LncRNAs) have recently been considered promising biomarkers for oncogenesis due to their epigenetic regulatory effects. HOTAIR is one of the oncogenic LncRNAs that was previously studied in different non-hematological malignancies. The current study set out to detect the expression level of HOTAIR LncRNA in AML patients concerning their clinical characteristics, laboratory data, FLT3-ITD, and NPM1 mutations, as well as treatment outcome. This study included quantitative detection of HOTAIR gene expression in 47 cases of AML using quantitative reverse transcription polymerase chain reaction, as well as NPM1 and FLT3-ITD genotyping. Results The HOTAIR expression was significantly higher in AML patients 6.87 (0.001) than in normal controls 1.66 (0.004-6.82) (p 0.007). The HOTAIR expression level was affected by chemotherapy, and it was correlated to hemoglobin level (p 0.001), age, total leukocytic count (p 0.022), and NPM1 mutation (p 0.017). HOTAIR gene expression level showed a correlation to relapse-free survival in the study group (p 0.04). Conclusion HOTAIR is overexpressed in patients with acute myeloid leukemia (AML). HOTAIR pre-treatment and post-chemotherapy gene expression levels can predict chemosensitivity and relapse.</description><subject>Acute myeloid leukemia</subject><subject>AML</subject><subject>Cancer</subject><subject>Chemotherapy</subject><subject>Epigenetic inheritance</subject><subject>Epigenetics</subject><subject>FLT3-ITD</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic transcription</subject><subject>Genotyping</subject><subject>Hemoglobin</subject><subject>HOTAIR</subject><subject>LncRNA</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Mutation</subject><subject>Non-coding RNA</subject><subject>NPM1</subject><subject>Patients</subject><subject>Reverse transcription</subject><subject>Tumorigenesis</subject><issn>1110-8630</issn><issn>2090-2441</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkEtr3DAUhUVoodO0f6ArQdZKrh6WpaXJc8BJSjqlSyPrETRkrIklQ_LvozaBZFHu4j445-NwEfpB4ZhSJU-y4CAYAUYJAFVAng7QioEGwoSgn9CKUgpESQ5f0NectwCy4a1YoT-_yuKecQr46nbTre9wP9m7mw7HCXfXPd6bEv1U8t_dpqn4p4JLwhf9hpP15gybyeGbn9cU75ZSpWnKONdhyd_Q52Aesv_-1g_R74vzzekV6W8v16ddT6zQspCxccoEkHpUY8OdM4bJ1kodgGpLPRsdbxqnKbReeeG4ZFpzPyojWaMlV_wQrV-5LpntsJ_jzszPQzJx-HdI8_1g5hLtgx-Uq35ReZxa0YIxqmYA00prQwjMVdbRK2s_p8fF5zJs0zJPNf5QU0H1QKveVfemQuMUUpmN3cVsh062ur61Zbyqjv-jquX8LtZP-hDr_YPhBVythT8</recordid><startdate>20210625</startdate><enddate>20210625</enddate><creator>Salah, Mona</creator><creator>Zawam, Hamdy</creator><creator>Fouad, Neven Bahaa</creator><creator>Soliman, Nohair</creator><creator>Maksoud, Fatma Abdel Wahab Abdel</creator><general>Springer</general><general>Springer Nature B.V</general><general>SpringerOpen</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope></search><sort><creationdate>20210625</creationdate><title>Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status</title><author>Salah, Mona ; Zawam, Hamdy ; Fouad, Neven Bahaa ; Soliman, Nohair ; Maksoud, Fatma Abdel Wahab Abdel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-b5d8af069b8b53ddaa267c69f019c1e2bd355d9107e8e4d362993eb8a62596383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute myeloid leukemia</topic><topic>AML</topic><topic>Cancer</topic><topic>Chemotherapy</topic><topic>Epigenetic inheritance</topic><topic>Epigenetics</topic><topic>FLT3-ITD</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic transcription</topic><topic>Genotyping</topic><topic>Hemoglobin</topic><topic>HOTAIR</topic><topic>LncRNA</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Mutation</topic><topic>Non-coding RNA</topic><topic>NPM1</topic><topic>Patients</topic><topic>Reverse transcription</topic><topic>Tumorigenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salah, Mona</creatorcontrib><creatorcontrib>Zawam, Hamdy</creatorcontrib><creatorcontrib>Fouad, Neven Bahaa</creatorcontrib><creatorcontrib>Soliman, Nohair</creatorcontrib><creatorcontrib>Maksoud, Fatma Abdel Wahab Abdel</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Egyptian Journal of Medical Human Genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salah, Mona</au><au>Zawam, Hamdy</au><au>Fouad, Neven Bahaa</au><au>Soliman, Nohair</au><au>Maksoud, Fatma Abdel Wahab Abdel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status</atitle><jtitle>Egyptian Journal of Medical Human Genetics</jtitle><date>2021-06-25</date><risdate>2021</risdate><volume>22</volume><issue>1</issue><spage>61</spage><epage>9</epage><pages>61-9</pages><issn>1110-8630</issn><eissn>2090-2441</eissn><abstract>Background Long non-coding RNAs (LncRNAs) have recently been considered promising biomarkers for oncogenesis due to their epigenetic regulatory effects. HOTAIR is one of the oncogenic LncRNAs that was previously studied in different non-hematological malignancies. The current study set out to detect the expression level of HOTAIR LncRNA in AML patients concerning their clinical characteristics, laboratory data, FLT3-ITD, and NPM1 mutations, as well as treatment outcome. This study included quantitative detection of HOTAIR gene expression in 47 cases of AML using quantitative reverse transcription polymerase chain reaction, as well as NPM1 and FLT3-ITD genotyping. Results The HOTAIR expression was significantly higher in AML patients 6.87 (0.001) than in normal controls 1.66 (0.004-6.82) (p 0.007). The HOTAIR expression level was affected by chemotherapy, and it was correlated to hemoglobin level (p 0.001), age, total leukocytic count (p 0.022), and NPM1 mutation (p 0.017). HOTAIR gene expression level showed a correlation to relapse-free survival in the study group (p 0.04). Conclusion HOTAIR is overexpressed in patients with acute myeloid leukemia (AML). HOTAIR pre-treatment and post-chemotherapy gene expression levels can predict chemosensitivity and relapse.</abstract><cop>Cairo</cop><pub>Springer</pub><doi>10.1186/s43042-021-00180-x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute myeloid leukemia AML Cancer Chemotherapy Epigenetic inheritance Epigenetics FLT3-ITD Gene expression Genes Genetic aspects Genetic transcription Genotyping Hemoglobin HOTAIR LncRNA Medical research Medicine, Experimental Mutation Non-coding RNA NPM1 Patients Reverse transcription Tumorigenesis |
title | Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status |
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