<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Abdul Manap AS</submitter><funding>Shibaura Institute of Technology, Japan</funding><funding>Taylor’s University, Malaysia</funding><pagination>e10003</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7532763</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>Previously, we reported the synergistic effects of curcumin and piperine in cell cultures as potential anti-cholinesterase and anti-amyloidogenic agents. Due to limited findings on the enrolment of these compounds on epigenetic events in AD, we aimed at elucidating the expression profiles of A&lt;i>β&lt;/i>42-induced SH-SY5Y cells using microarray profiling. In this study, an optimized concentration of 35 µM of curcumin and piperine in combination was used to treat A&lt;i>β&lt;/i>42 fibril and high-throughput microarray profiling was performed on the extracted RNA. This was then compared to curcumin and piperine used singularly at 49.11 µM and 25 µM, respectively. Our results demonstrated that in the curcumin treated group, from the top 10 upregulated and top 10 downregulated significantly differentia</pubmed_abstract><journal>PeerJ</journal><pubmed_title>Explicating anti-amyloidogenic role of curcumin and piperine via amyloid beta (A&lt;i>β&lt;/i>) explicit pathway: recovery and reversal paradigm effects.</pubmed_title><pmcid>PMC7532763</pmcid><funding_grant_id>TUFR/2017/002/04</funding_grant_id><pubmed_authors>Chia A</pubmed_authors><pubmed_authors>Vijayabalan S</pubmed_authors><pubmed_authors>Abdul Manap AS</pubmed_authors><pubmed_authors>Fukui K</pubmed_authors><pubmed_authors>Madhavan P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Explicating anti-amyloidogenic role of curcumin and piperine via amyloid beta (A&lt;i>β&lt;/i>) explicit pathway: recovery and reversal paradigm effects.</name><description>Previously, we reported the synergistic effects of curcumin and piperine in cell cultures as potential anti-cholinesterase and anti-amyloidogenic agents. Due to limited findings on the enrolment of these compounds on epigenetic events in AD, we aimed at elucidating the expression profiles of A&lt;i>β&lt;/i>42-induced SH-SY5Y cells using microarray profiling. In this study, an optimized concentration of 35 µM of curcumin and piperine in combination was used to treat A&lt;i>β&lt;/i>42 fibril and high-throughput microarray profiling was performed on the extracted RNA. This was then compared to curcumin and piperine used singularly at 49.11 µM and 25 µM, respectively. Our results demonstrated that in the curcumin treated group, from the top 10 upregulated and top 10 downregulated significantly differentia</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-04-08T08:20:40.676Z</modification><creation>2020-11-19T16:57:47Z</creation></dates><accession>S-EPMC7532763</accession><cross_references><pubmed>33062432</pubmed><doi>10.7717/peerj.10003</doi></cross_references></HashMap>