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Expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes in peripheral blood mononuclear cells and their correlation with serum levels of oxidative stress and hs‐CRP in the patients with coronary artery disease
Atherosclerosis is a chronic inflammatory disease with high mortality worldwide. The reverse cholesterol transport pathway in macrophage plays an important role in the pathogenesis of coronary artery disease (CAD) and is strongly controlled by regulatory factors. The microRNAs can promote or prevent...
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Published in: | IUBMB life 2021-01, Vol.73 (1), p.223-237 |
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description | Atherosclerosis is a chronic inflammatory disease with high mortality worldwide. The reverse cholesterol transport pathway in macrophage plays an important role in the pathogenesis of coronary artery disease (CAD) and is strongly controlled by regulatory factors. The microRNAs can promote or prevent the formation of atherosclerotic lesions by post‐transcriptional regulation of vital genes in this pathway. Therefore, this study was conducted to investigate the relationship between the expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes and serum levels of hs‐CRP, ox‐LDL, and indices of oxidative stress in the patients with established CAD and controls. A total of 84 subjects (42 patients with CAD and 42 controls) were included in this study. Expression levels of miR‐27a‐3p, miR‐329‐3p, ABCA1, and ABCG1 genes in the peripheral blood mononuclear cells (PBMCs) and serum concentration of hs‐CRP and ox‐LDL were measured by real time‐PCR and ELISA, respectively. Also, oxidative stress parameters in the serum were evaluated by ferric‐reducing antioxidant power (FRAP) and malondialdehyde (MDA) assays. ABCA1 and ABCG1 gene expression in PBMC and serum concentration of FRAP were significantly lower in the CAD group compared to the control group. Expression levels of miR‐27a and miR‐329 and serum levels of hs‐CRP, ox‐LDL, and MDA were significantly higher in the CAD group compared to the control group. Serum levels of hs‐CRP, ox‐LDL, and expression level of miR‐27a have inversely related to ABCA1 and ABCG1 gene expression in all the subjects. An increase in the expression levels of miR‐27a and miR‐329 may lead to the progression of atherosclerosis plaque by downregulating the expression of ABCA1 and ABCG1 genes. |
doi_str_mv | 10.1002/iub.2421 |
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The reverse cholesterol transport pathway in macrophage plays an important role in the pathogenesis of coronary artery disease (CAD) and is strongly controlled by regulatory factors. The microRNAs can promote or prevent the formation of atherosclerotic lesions by post‐transcriptional regulation of vital genes in this pathway. Therefore, this study was conducted to investigate the relationship between the expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes and serum levels of hs‐CRP, ox‐LDL, and indices of oxidative stress in the patients with established CAD and controls. A total of 84 subjects (42 patients with CAD and 42 controls) were included in this study. Expression levels of miR‐27a‐3p, miR‐329‐3p, ABCA1, and ABCG1 genes in the peripheral blood mononuclear cells (PBMCs) and serum concentration of hs‐CRP and ox‐LDL were measured by real time‐PCR and ELISA, respectively. Also, oxidative stress parameters in the serum were evaluated by ferric‐reducing antioxidant power (FRAP) and malondialdehyde (MDA) assays. ABCA1 and ABCG1 gene expression in PBMC and serum concentration of FRAP were significantly lower in the CAD group compared to the control group. Expression levels of miR‐27a and miR‐329 and serum levels of hs‐CRP, ox‐LDL, and MDA were significantly higher in the CAD group compared to the control group. Serum levels of hs‐CRP, ox‐LDL, and expression level of miR‐27a have inversely related to ABCA1 and ABCG1 gene expression in all the subjects. An increase in the expression levels of miR‐27a and miR‐329 may lead to the progression of atherosclerosis plaque by downregulating the expression of ABCA1 and ABCG1 genes.</description><identifier>ISSN: 1521-6543</identifier><identifier>EISSN: 1521-6551</identifier><identifier>DOI: 10.1002/iub.2421</identifier><identifier>PMID: 33263223</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>ABCA1 ; ABCA1 protein ; ABCG1 ; ABCG1 gene ; Adult ; Antioxidants ; Arteriosclerosis ; Atherosclerosis ; Atherosclerosis - blood ; Atherosclerosis - genetics ; Atherosclerosis - metabolism ; Atherosclerosis - pathology ; ATP Binding Cassette Transporter 1 - blood ; ATP Binding Cassette Transporter 1 - genetics ; ATP Binding Cassette Transporter, Subfamily G, Member 1 - blood ; ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics ; ATP-binding protein ; C-Reactive Protein - analysis ; Cardiovascular disease ; Case-Control Studies ; Cholesterol ; Chromosome 3 ; Coronary artery ; Coronary Artery Disease - blood ; Coronary Artery Disease - genetics ; Coronary Artery Disease - metabolism ; Coronary Artery Disease - pathology ; Coronary vessels ; Enzyme-linked immunosorbent assay ; Female ; Gene expression ; Gene Expression Regulation ; Gene regulation ; Heart diseases ; hs‐CRP ; Humans ; Inflammatory diseases ; Leukocytes (mononuclear) ; Leukocytes, Mononuclear - metabolism ; Leukocytes, Mononuclear - pathology ; Low density lipoprotein ; Macrophages ; Male ; Malondialdehyde ; microRNA ; MicroRNAs - blood ; MicroRNAs - genetics ; miRNA ; Oxidative Stress ; Peripheral blood mononuclear cells ; Serum levels ; Transcription</subject><ispartof>IUBMB life, 2021-01, Vol.73 (1), p.223-237</ispartof><rights>2020 International Union of Biochemistry and Molecular Biology</rights><rights>2020 International Union of Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3831-995729f089f3c411db7eb787351ebeeb2a0394a6db370ddf33a48dc408a9ca2a3</citedby><cites>FETCH-LOGICAL-c3831-995729f089f3c411db7eb787351ebeeb2a0394a6db370ddf33a48dc408a9ca2a3</cites><orcidid>0000-0001-5196-5513</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33263223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rafiei, Ali</creatorcontrib><creatorcontrib>Ferns, Gordon A.</creatorcontrib><creatorcontrib>Ahmadi, Reza</creatorcontrib><creatorcontrib>Khaledifar, Arsalan</creatorcontrib><creatorcontrib>Rahimzadeh‐Fallah, Tina</creatorcontrib><creatorcontrib>Mohmmad‐Rezaei, Mina</creatorcontrib><creatorcontrib>Emami, Shohreh</creatorcontrib><creatorcontrib>Bagheri, Nader</creatorcontrib><title>Expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes in peripheral blood mononuclear cells and their correlation with serum levels of oxidative stress and hs‐CRP in the patients with coronary artery disease</title><title>IUBMB life</title><addtitle>IUBMB Life</addtitle><description>Atherosclerosis is a chronic inflammatory disease with high mortality worldwide. The reverse cholesterol transport pathway in macrophage plays an important role in the pathogenesis of coronary artery disease (CAD) and is strongly controlled by regulatory factors. The microRNAs can promote or prevent the formation of atherosclerotic lesions by post‐transcriptional regulation of vital genes in this pathway. Therefore, this study was conducted to investigate the relationship between the expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes and serum levels of hs‐CRP, ox‐LDL, and indices of oxidative stress in the patients with established CAD and controls. A total of 84 subjects (42 patients with CAD and 42 controls) were included in this study. Expression levels of miR‐27a‐3p, miR‐329‐3p, ABCA1, and ABCG1 genes in the peripheral blood mononuclear cells (PBMCs) and serum concentration of hs‐CRP and ox‐LDL were measured by real time‐PCR and ELISA, respectively. Also, oxidative stress parameters in the serum were evaluated by ferric‐reducing antioxidant power (FRAP) and malondialdehyde (MDA) assays. ABCA1 and ABCG1 gene expression in PBMC and serum concentration of FRAP were significantly lower in the CAD group compared to the control group. Expression levels of miR‐27a and miR‐329 and serum levels of hs‐CRP, ox‐LDL, and MDA were significantly higher in the CAD group compared to the control group. Serum levels of hs‐CRP, ox‐LDL, and expression level of miR‐27a have inversely related to ABCA1 and ABCG1 gene expression in all the subjects. An increase in the expression levels of miR‐27a and miR‐329 may lead to the progression of atherosclerosis plaque by downregulating the expression of ABCA1 and ABCG1 genes.</description><subject>ABCA1</subject><subject>ABCA1 protein</subject><subject>ABCG1</subject><subject>ABCG1 gene</subject><subject>Adult</subject><subject>Antioxidants</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - blood</subject><subject>Atherosclerosis - genetics</subject><subject>Atherosclerosis - metabolism</subject><subject>Atherosclerosis - pathology</subject><subject>ATP Binding Cassette Transporter 1 - blood</subject><subject>ATP Binding Cassette Transporter 1 - genetics</subject><subject>ATP Binding Cassette Transporter, Subfamily G, Member 1 - blood</subject><subject>ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics</subject><subject>ATP-binding protein</subject><subject>C-Reactive Protein - analysis</subject><subject>Cardiovascular disease</subject><subject>Case-Control Studies</subject><subject>Cholesterol</subject><subject>Chromosome 3</subject><subject>Coronary artery</subject><subject>Coronary Artery Disease - blood</subject><subject>Coronary Artery Disease - genetics</subject><subject>Coronary Artery Disease - metabolism</subject><subject>Coronary Artery Disease - pathology</subject><subject>Coronary vessels</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Gene regulation</subject><subject>Heart diseases</subject><subject>hs‐CRP</subject><subject>Humans</subject><subject>Inflammatory diseases</subject><subject>Leukocytes (mononuclear)</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Leukocytes, Mononuclear - pathology</subject><subject>Low density lipoprotein</subject><subject>Macrophages</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>microRNA</subject><subject>MicroRNAs - blood</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Oxidative Stress</subject><subject>Peripheral blood mononuclear cells</subject><subject>Serum levels</subject><subject>Transcription</subject><issn>1521-6543</issn><issn>1521-6551</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kctq3DAUhkVpaa7QJyiCbrIYp7r5ouVkyA0CLaFZG9k67ijIkivZuez6CH3BbvokkTPTtBSqzTlCv77zH36E3lFyTAlhH83UHDPB6Cu0S3NGsyLP6euXXvAdtBfjLUmnJPIt2uGcFZwxvot-nj4MAWI03mELd2Aj9h3uzfWv7z9YqRbbljO5wMuT1ZIusHJ6bs8p_goOIjYODxDMsIagLG6s9xr33nk3tRZUwC3YRJ1_jWsw6e5DAKvGeeS9Gdc4Qpj6v6b7B6PT8x3gOM7env-uY7Kxuv48j0scPCQFuDFuEInpnQqPWIURUtEmgopwgN50ykY43NZ9dHN2-mV1kV19Or9cLa-yllecZlLmJZMdqWTHW0GpbkpoyqrkOYUGoGGKcClUoRteEq07zpWodCtIpWSrmOL76GjDHYL_NkEc697EeW_lwE-xZqIomCSkypP0wz_SWz8Fl9wlVXIhqMjJH2AbfIwBunoIpk8L1pTUc-R1iryeI0_S91vg1PSgX4S_M06CbCO4NxYe_wuqL29OnoFPGWu5NA</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Rafiei, Ali</creator><creator>Ferns, Gordon A.</creator><creator>Ahmadi, Reza</creator><creator>Khaledifar, Arsalan</creator><creator>Rahimzadeh‐Fallah, Tina</creator><creator>Mohmmad‐Rezaei, Mina</creator><creator>Emami, Shohreh</creator><creator>Bagheri, Nader</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5196-5513</orcidid></search><sort><creationdate>202101</creationdate><title>Expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes in peripheral blood mononuclear cells and their correlation with serum levels of oxidative stress and hs‐CRP in the patients with coronary artery disease</title><author>Rafiei, Ali ; Ferns, Gordon A. ; Ahmadi, Reza ; Khaledifar, Arsalan ; Rahimzadeh‐Fallah, Tina ; Mohmmad‐Rezaei, Mina ; Emami, Shohreh ; Bagheri, Nader</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3831-995729f089f3c411db7eb787351ebeeb2a0394a6db370ddf33a48dc408a9ca2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ABCA1</topic><topic>ABCA1 protein</topic><topic>ABCG1</topic><topic>ABCG1 gene</topic><topic>Adult</topic><topic>Antioxidants</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - blood</topic><topic>Atherosclerosis - genetics</topic><topic>Atherosclerosis - metabolism</topic><topic>Atherosclerosis - pathology</topic><topic>ATP Binding Cassette Transporter 1 - blood</topic><topic>ATP Binding Cassette Transporter 1 - genetics</topic><topic>ATP Binding Cassette Transporter, Subfamily G, Member 1 - blood</topic><topic>ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics</topic><topic>ATP-binding protein</topic><topic>C-Reactive Protein - analysis</topic><topic>Cardiovascular disease</topic><topic>Case-Control Studies</topic><topic>Cholesterol</topic><topic>Chromosome 3</topic><topic>Coronary artery</topic><topic>Coronary Artery Disease - blood</topic><topic>Coronary Artery Disease - genetics</topic><topic>Coronary Artery Disease - metabolism</topic><topic>Coronary Artery Disease - pathology</topic><topic>Coronary vessels</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Gene regulation</topic><topic>Heart diseases</topic><topic>hs‐CRP</topic><topic>Humans</topic><topic>Inflammatory diseases</topic><topic>Leukocytes (mononuclear)</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Leukocytes, Mononuclear - pathology</topic><topic>Low density lipoprotein</topic><topic>Macrophages</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>microRNA</topic><topic>MicroRNAs - blood</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>Oxidative Stress</topic><topic>Peripheral blood mononuclear cells</topic><topic>Serum levels</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rafiei, Ali</creatorcontrib><creatorcontrib>Ferns, Gordon A.</creatorcontrib><creatorcontrib>Ahmadi, Reza</creatorcontrib><creatorcontrib>Khaledifar, Arsalan</creatorcontrib><creatorcontrib>Rahimzadeh‐Fallah, Tina</creatorcontrib><creatorcontrib>Mohmmad‐Rezaei, Mina</creatorcontrib><creatorcontrib>Emami, Shohreh</creatorcontrib><creatorcontrib>Bagheri, Nader</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>IUBMB life</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rafiei, Ali</au><au>Ferns, Gordon A.</au><au>Ahmadi, Reza</au><au>Khaledifar, Arsalan</au><au>Rahimzadeh‐Fallah, Tina</au><au>Mohmmad‐Rezaei, Mina</au><au>Emami, Shohreh</au><au>Bagheri, Nader</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes in peripheral blood mononuclear cells and their correlation with serum levels of oxidative stress and hs‐CRP in the patients with coronary artery disease</atitle><jtitle>IUBMB life</jtitle><addtitle>IUBMB Life</addtitle><date>2021-01</date><risdate>2021</risdate><volume>73</volume><issue>1</issue><spage>223</spage><epage>237</epage><pages>223-237</pages><issn>1521-6543</issn><eissn>1521-6551</eissn><abstract>Atherosclerosis is a chronic inflammatory disease with high mortality worldwide. The reverse cholesterol transport pathway in macrophage plays an important role in the pathogenesis of coronary artery disease (CAD) and is strongly controlled by regulatory factors. The microRNAs can promote or prevent the formation of atherosclerotic lesions by post‐transcriptional regulation of vital genes in this pathway. Therefore, this study was conducted to investigate the relationship between the expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes and serum levels of hs‐CRP, ox‐LDL, and indices of oxidative stress in the patients with established CAD and controls. A total of 84 subjects (42 patients with CAD and 42 controls) were included in this study. Expression levels of miR‐27a‐3p, miR‐329‐3p, ABCA1, and ABCG1 genes in the peripheral blood mononuclear cells (PBMCs) and serum concentration of hs‐CRP and ox‐LDL were measured by real time‐PCR and ELISA, respectively. Also, oxidative stress parameters in the serum were evaluated by ferric‐reducing antioxidant power (FRAP) and malondialdehyde (MDA) assays. ABCA1 and ABCG1 gene expression in PBMC and serum concentration of FRAP were significantly lower in the CAD group compared to the control group. Expression levels of miR‐27a and miR‐329 and serum levels of hs‐CRP, ox‐LDL, and MDA were significantly higher in the CAD group compared to the control group. Serum levels of hs‐CRP, ox‐LDL, and expression level of miR‐27a have inversely related to ABCA1 and ABCG1 gene expression in all the subjects. An increase in the expression levels of miR‐27a and miR‐329 may lead to the progression of atherosclerosis plaque by downregulating the expression of ABCA1 and ABCG1 genes.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>33263223</pmid><doi>10.1002/iub.2421</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-5196-5513</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ABCA1 ABCA1 protein ABCG1 ABCG1 gene Adult Antioxidants Arteriosclerosis Atherosclerosis Atherosclerosis - blood Atherosclerosis - genetics Atherosclerosis - metabolism Atherosclerosis - pathology ATP Binding Cassette Transporter 1 - blood ATP Binding Cassette Transporter 1 - genetics ATP Binding Cassette Transporter, Subfamily G, Member 1 - blood ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics ATP-binding protein C-Reactive Protein - analysis Cardiovascular disease Case-Control Studies Cholesterol Chromosome 3 Coronary artery Coronary Artery Disease - blood Coronary Artery Disease - genetics Coronary Artery Disease - metabolism Coronary Artery Disease - pathology Coronary vessels Enzyme-linked immunosorbent assay Female Gene expression Gene Expression Regulation Gene regulation Heart diseases hs‐CRP Humans Inflammatory diseases Leukocytes (mononuclear) Leukocytes, Mononuclear - metabolism Leukocytes, Mononuclear - pathology Low density lipoprotein Macrophages Male Malondialdehyde microRNA MicroRNAs - blood MicroRNAs - genetics miRNA Oxidative Stress Peripheral blood mononuclear cells Serum levels Transcription |
title | Expression levels of miR‐27a, miR‐329, ABCA1, and ABCG1 genes in peripheral blood mononuclear cells and their correlation with serum levels of oxidative stress and hs‐CRP in the patients with coronary artery disease |
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