PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34332075-0 2021 Eicosapentaenoic acid membrane incorporation stimulates ABCA1-mediated cholesterol efflux from human THP-1 macrophages. Eicosapentaenoic Acid 0-21 ATP binding cassette subfamily A member 1 Homo sapiens 56-61 26791180-5 2016 RESULTS: On the basis of the meta-analysis of 7 cohorts in the CHARGE consortium, higher plasma HDL cholesterol was associated with fewer C alleles at ATP-binding cassette subfamily A member 1 (ABCA1) rs2246293 (beta = -0.6 mg/dL, P = 0.015) and higher circulating eicosapentaenoic acid (EPA) (beta = 3.87 mg/dL, P = 5.62 x 10(21)). Eicosapentaenoic Acid 265-286 ATP binding cassette subfamily A member 1 Homo sapiens 151-192 26791180-5 2016 RESULTS: On the basis of the meta-analysis of 7 cohorts in the CHARGE consortium, higher plasma HDL cholesterol was associated with fewer C alleles at ATP-binding cassette subfamily A member 1 (ABCA1) rs2246293 (beta = -0.6 mg/dL, P = 0.015) and higher circulating eicosapentaenoic acid (EPA) (beta = 3.87 mg/dL, P = 5.62 x 10(21)). Eicosapentaenoic Acid 265-286 ATP binding cassette subfamily A member 1 Homo sapiens 194-199 26791180-5 2016 RESULTS: On the basis of the meta-analysis of 7 cohorts in the CHARGE consortium, higher plasma HDL cholesterol was associated with fewer C alleles at ATP-binding cassette subfamily A member 1 (ABCA1) rs2246293 (beta = -0.6 mg/dL, P = 0.015) and higher circulating eicosapentaenoic acid (EPA) (beta = 3.87 mg/dL, P = 5.62 x 10(21)). Eicosapentaenoic Acid 288-291 ATP binding cassette subfamily A member 1 Homo sapiens 151-192 26791180-5 2016 RESULTS: On the basis of the meta-analysis of 7 cohorts in the CHARGE consortium, higher plasma HDL cholesterol was associated with fewer C alleles at ATP-binding cassette subfamily A member 1 (ABCA1) rs2246293 (beta = -0.6 mg/dL, P = 0.015) and higher circulating eicosapentaenoic acid (EPA) (beta = 3.87 mg/dL, P = 5.62 x 10(21)). Eicosapentaenoic Acid 288-291 ATP binding cassette subfamily A member 1 Homo sapiens 194-199 19070858-0 2009 Eicosapentaenoic acid reduces ABCA1 serine phosphorylation and impairs ABCA1-dependent cholesterol efflux through cyclic AMP/protein kinase A signaling pathway in THP-1 macrophage-derived foam cells. Eicosapentaenoic Acid 0-21 ATP binding cassette subfamily A member 1 Homo sapiens 30-35 19070858-0 2009 Eicosapentaenoic acid reduces ABCA1 serine phosphorylation and impairs ABCA1-dependent cholesterol efflux through cyclic AMP/protein kinase A signaling pathway in THP-1 macrophage-derived foam cells. Eicosapentaenoic Acid 0-21 ATP binding cassette subfamily A member 1 Homo sapiens 71-76 34332075-5 2021 EPA 70 muM, but not AA 50 muM or DHA 15 muM, increased ABCA1-mediated cholesterol efflux to apolipoprotein (apo) AI by 28% without altering aqueous diffusion. Eicosapentaenoic Acid 0-3 ATP binding cassette subfamily A member 1 Homo sapiens 55-60 34332075-13 2021 In conclusion, EPA membrane incorporation increased ABCA1 functionality in cholesterol-normal human THP-1 macrophages, likely through a combination of different mechanisms. Eicosapentaenoic Acid 15-18 ATP binding cassette subfamily A member 1 Homo sapiens 52-57 29574773-6 2018 While we found no changes in the mRNA expression of ECM components, EPA and DHA treatment reduced levels of ABCG1, ABCA1, and AKAP13 in both cell types. Eicosapentaenoic Acid 68-71 ATP binding cassette subfamily A member 1 Homo sapiens 115-120 28739279-6 2017 EPA 70muM reduced ABCA1-mediated cholesterol efflux to apolipoprotein (apo) AI by 30% without any alteration in ABCA1 expression. Eicosapentaenoic Acid 0-3 ATP binding cassette subfamily A member 1 Homo sapiens 18-23 26776055-0 2016 Eicosapentaenoic acid membrane incorporation impairs ABCA1-dependent cholesterol efflux via a protein kinase A signaling pathway in primary human macrophages. Eicosapentaenoic Acid 0-21 ATP binding cassette subfamily A member 1 Homo sapiens 53-58 26776055-5 2016 Importantly, eicosapentaenoic acid (EPA) (C20:5 n-3) induced a dose-dependent reduction of ABCA1 functionality in both cellular models (-28% for 70muM of EPA in HMDM), without any alterations in ABCA1 expression. Eicosapentaenoic Acid 13-34 ATP binding cassette subfamily A member 1 Homo sapiens 91-96 26776055-5 2016 Importantly, eicosapentaenoic acid (EPA) (C20:5 n-3) induced a dose-dependent reduction of ABCA1 functionality in both cellular models (-28% for 70muM of EPA in HMDM), without any alterations in ABCA1 expression. Eicosapentaenoic Acid 36-39 ATP binding cassette subfamily A member 1 Homo sapiens 91-96 26776055-5 2016 Importantly, eicosapentaenoic acid (EPA) (C20:5 n-3) induced a dose-dependent reduction of ABCA1 functionality in both cellular models (-28% for 70muM of EPA in HMDM), without any alterations in ABCA1 expression. Eicosapentaenoic Acid 36-39 ATP binding cassette subfamily A member 1 Homo sapiens 195-200 26776055-5 2016 Importantly, eicosapentaenoic acid (EPA) (C20:5 n-3) induced a dose-dependent reduction of ABCA1 functionality in both cellular models (-28% for 70muM of EPA in HMDM), without any alterations in ABCA1 expression. Eicosapentaenoic Acid 154-157 ATP binding cassette subfamily A member 1 Homo sapiens 91-96 26776055-9 2016 Moreover, the activation of adenylate cyclase by forskolin and the inhibition of cAMP phosphodiesterase by isobutylmethylxanthine restored ABCA1 cholesterol efflux in EPA-treated human macrophages. Eicosapentaenoic Acid 167-170 ATP binding cassette subfamily A member 1 Homo sapiens 139-144 21151462-2 2010 This study uses a real time RT-PCR technique to investigate the role of conjugated linoleic acid (CLA), alpha-linolenic acid (ALA) and eicosapentaenoic acid (EPA) in the regulation of the ATP-binding cassette A1 (ABCA1) and liver X receptor alpha (LXR) genes, which are involved in cholesterol homeostasis. Eicosapentaenoic Acid 135-156 ATP binding cassette subfamily A member 1 Homo sapiens 188-211 21151462-2 2010 This study uses a real time RT-PCR technique to investigate the role of conjugated linoleic acid (CLA), alpha-linolenic acid (ALA) and eicosapentaenoic acid (EPA) in the regulation of the ATP-binding cassette A1 (ABCA1) and liver X receptor alpha (LXR) genes, which are involved in cholesterol homeostasis. Eicosapentaenoic Acid 135-156 ATP binding cassette subfamily A member 1 Homo sapiens 213-218 21151462-2 2010 This study uses a real time RT-PCR technique to investigate the role of conjugated linoleic acid (CLA), alpha-linolenic acid (ALA) and eicosapentaenoic acid (EPA) in the regulation of the ATP-binding cassette A1 (ABCA1) and liver X receptor alpha (LXR) genes, which are involved in cholesterol homeostasis. Eicosapentaenoic Acid 158-161 ATP binding cassette subfamily A member 1 Homo sapiens 188-211 21151462-2 2010 This study uses a real time RT-PCR technique to investigate the role of conjugated linoleic acid (CLA), alpha-linolenic acid (ALA) and eicosapentaenoic acid (EPA) in the regulation of the ATP-binding cassette A1 (ABCA1) and liver X receptor alpha (LXR) genes, which are involved in cholesterol homeostasis. Eicosapentaenoic Acid 158-161 ATP binding cassette subfamily A member 1 Homo sapiens 213-218 34217521-0 2021 Editorial expression of concern: "Eicosapentaenoic acid reduces ABCA1 serine phosphorylation and impairs ABCA1-dependent cholesterol efflux through cyclic AMP/protein kinase A signaling pathway in THP-1 macrophage-derived foam cells"(Atherosclerosis Volume 204, Issue 2, June 2009, Pages e35-e43). Eicosapentaenoic Acid 34-55 ATP binding cassette subfamily A member 1 Homo sapiens 64-69 34217521-0 2021 Editorial expression of concern: "Eicosapentaenoic acid reduces ABCA1 serine phosphorylation and impairs ABCA1-dependent cholesterol efflux through cyclic AMP/protein kinase A signaling pathway in THP-1 macrophage-derived foam cells"(Atherosclerosis Volume 204, Issue 2, June 2009, Pages e35-e43). Eicosapentaenoic Acid 34-55 ATP binding cassette subfamily A member 1 Homo sapiens 105-110