<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang SB</submitter><funding>Liaoning Province Natural Science Fund</funding><funding>National Natural Science Fund</funding><pagination>10027-10041</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7520305</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(17)</volume><pubmed_abstract>Both SIRT1 and UVA radiation are involved in cellular damage processes such as apoptosis, senescence and ageing. MicroRNAs (miRNAs) have been reported to be closely related to UV radiation, as well as to SIRT1. In this study, we investigated the connections among SIRT1, UVA and miRNA in human skin primary fibroblasts. Our results showed that UVA altered the protein level of SIRT1 in a time point-dependent manner. Using miRNA microarray, bioinformatics analysis, we found that knocking down SIRT1 could cause up-regulation of miR-27a-5p and the latter could down-regulate SMAD2, and these results were verified by qRT-PCR or Western blot. Furthermore, UVA radiation (5 J/cm&lt;sup>2&lt;/sup> ), knocking down SIRT1 or overexpression of miR-27a-5p led to increased expression of MMP1, and decreased expre</pubmed_abstract><journal>Journal of cellular and molecular medicine</journal><pubmed_title>UVA influenced the SIRT1-miR-27a-5p-SMAD2-MMP1/COL1/BCL2 axis in human skin primary fibroblasts.</pubmed_title><pmcid>PMC7520305</pmcid><funding_grant_id>81972940</funding_grant_id><funding_grant_id>2019-ZD-0763</funding_grant_id><pubmed_authors>Lu YS</pubmed_authors><pubmed_authors>Chen HD</pubmed_authors><pubmed_authors>Gao XH</pubmed_authors><pubmed_authors>Li LM</pubmed_authors><pubmed_authors>Jiang SB</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Wang HX</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>UVA influenced the SIRT1-miR-27a-5p-SMAD2-MMP1/COL1/BCL2 axis in human skin primary fibroblasts.</name><description>Both SIRT1 and UVA radiation are involved in cellular damage processes such as apoptosis, senescence and ageing. MicroRNAs (miRNAs) have been reported to be closely related to UV radiation, as well as to SIRT1. In this study, we investigated the connections among SIRT1, UVA and miRNA in human skin primary fibroblasts. Our results showed that UVA altered the protein level of SIRT1 in a time point-dependent manner. Using miRNA microarray, bioinformatics analysis, we found that knocking down SIRT1 could cause up-regulation of miR-27a-5p and the latter could down-regulate SMAD2, and these results were verified by qRT-PCR or Western blot. Furthermore, UVA radiation (5 J/cm&lt;sup>2&lt;/sup> ), knocking down SIRT1 or overexpression of miR-27a-5p led to increased expression of MMP1, and decreased expre</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2026-05-03T07:14:11.055Z</modification><creation>2020-10-08T07:14:55Z</creation></dates><accession>S-EPMC7520305</accession><cross_references><pubmed>32790210</pubmed><doi>10.1111/jcmm.15610</doi></cross_references></HashMap>