<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Cho S</submitter><pubmed_abstract>&lt;sub>L&lt;/sub>-Ascorbic acid (vitamin C, AA) exhibits anti-cancer effects with high-dose treatment through the generation of reactive oxygen species (ROS) and selective damage to cancer cells. The anti-cancer effects of &lt;sub>L&lt;/sub>-ascorbic acid are determined by sodium-dependent vitamin C transporter 2 (SVCT-2), a transporter of &lt;sub>L&lt;/sub>-ascorbic acid. In this study, we demonstrate that &lt;sub>L&lt;/sub>-ascorbic acid treatment showed efficient anti-cancer activity in cell lines with high expression levels of SVCT-2 for a gradient concentration of &lt;sub>L&lt;/sub>-ascorbic acid from 10 μM -2 mM. However, in low SVCT-2 expressing cell lines, high-dose &lt;sub>L&lt;/sub>-ascorbic acid (>1 mM) showed anti-cancer effects but low-dose (&lt;10 μM) treatment induced cell proliferation. Such conflicting results</pubmed_abstract><journal>Scientific reports</journal><pagination>11372</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6063950</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hormetic dose response to &lt;sub>L&lt;/sub>-ascorbic acid as an anti-cancer drug in colorectal cancer cell lines according to SVCT-2 expression.</pubmed_title><pmcid>PMC6063950</pmcid><pubmed_authors>Roh K</pubmed_authors><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Kil EJ</pubmed_authors><pubmed_authors>Byun HS</pubmed_authors><pubmed_authors>Yoo BC</pubmed_authors><pubmed_authors>Yeom CH</pubmed_authors><pubmed_authors>Cho SH</pubmed_authors><pubmed_authors>Song H</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Shin H</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Cho S</pubmed_authors><pubmed_authors>Chae JS</pubmed_authors><pubmed_authors>Shin Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hormetic dose response to &lt;sub>L&lt;/sub>-ascorbic acid as an anti-cancer drug in colorectal cancer cell lines according to SVCT-2 expression.</name><description>&lt;sub>L&lt;/sub>-Ascorbic acid (vitamin C, AA) exhibits anti-cancer effects with high-dose treatment through the generation of reactive oxygen species (ROS) and selective damage to cancer cells. The anti-cancer effects of &lt;sub>L&lt;/sub>-ascorbic acid are determined by sodium-dependent vitamin C transporter 2 (SVCT-2), a transporter of &lt;sub>L&lt;/sub>-ascorbic acid. In this study, we demonstrate that &lt;sub>L&lt;/sub>-ascorbic acid treatment showed efficient anti-cancer activity in cell lines with high expression levels of SVCT-2 for a gradient concentration of &lt;sub>L&lt;/sub>-ascorbic acid from 10 μM -2 mM. However, in low SVCT-2 expressing cell lines, high-dose &lt;sub>L&lt;/sub>-ascorbic acid (>1 mM) showed anti-cancer effects but low-dose (&lt;10 μM) treatment induced cell proliferation. Such conflicting results</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jul</publication><modification>2025-05-18T11:29:02.564Z</modification><creation>2025-05-18T11:29:02.564Z</creation></dates><accession>S-EPMC6063950</accession><cross_references><pubmed>30054560</pubmed><doi>10.1038/s41598-018-29386-7</doi></cross_references></HashMap>