<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2023</volume><submitter>Ling L</submitter><pubmed_abstract>Ginsenoside Rg1 (Rg1) is purified from ginseng with various pharmacological effects, which might facilitate the biological behavior of human amnion-derived mesenchymal stem/stromal cells (hAD-MSCs). This study is aimed at investigating the effects of Rg1 on the biological behavior, such as viability, proliferation, apoptosis, senescence, migration, and paracrine, of hAD-MSCs. hAD-MSCs were isolated from human amnions. The effects of Rg1 on the viability, proliferation, apoptosis, senescence, migration, and paracrine of hAD-MSCs were detected by CCK-8, EdU, flow cytometry, SA-&lt;i>β&lt;/i>-Gal staining, wound healing, and ELISA assays, respectively. The protein expression levels were detected by western blot. Cell cycle distribution was evaluated using flow cytometry. We found that Rg1 promoted </pubmed_abstract><journal>Stem cells international</journal><pagination>7074703</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9946746</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effects of Ginsenoside Rg1 on the Biological Behavior of Human Amnion-Derived Mesenchymal Stem/Stromal Cells (hAD-MSCs).</pubmed_title><pmcid>PMC9946746</pmcid><pubmed_authors>Hua Y</pubmed_authors><pubmed_authors>Hou J</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Ling L</pubmed_authors><pubmed_authors>Shu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effects of Ginsenoside Rg1 on the Biological Behavior of Human Amnion-Derived Mesenchymal Stem/Stromal Cells (hAD-MSCs).</name><description>Ginsenoside Rg1 (Rg1) is purified from ginseng with various pharmacological effects, which might facilitate the biological behavior of human amnion-derived mesenchymal stem/stromal cells (hAD-MSCs). This study is aimed at investigating the effects of Rg1 on the biological behavior, such as viability, proliferation, apoptosis, senescence, migration, and paracrine, of hAD-MSCs. hAD-MSCs were isolated from human amnions. The effects of Rg1 on the viability, proliferation, apoptosis, senescence, migration, and paracrine of hAD-MSCs were detected by CCK-8, EdU, flow cytometry, SA-&lt;i>β&lt;/i>-Gal staining, wound healing, and ELISA assays, respectively. The protein expression levels were detected by western blot. Cell cycle distribution was evaluated using flow cytometry. We found that Rg1 promoted </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T14:17:37.716Z</modification><creation>2025-02-19T02:23:59.776Z</creation></dates><accession>S-EPMC9946746</accession><cross_references><pubmed>36845966</pubmed><doi>10.1155/2023/7074703</doi></cross_references></HashMap>