<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Prasedya ES</submitter><funding>Ministry of Research, Technology and Higher Education</funding><pagination>6568</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8587204</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(21)</volume><pubmed_abstract>The red macroalga &lt;i>Gelidium latifolium&lt;/i> is widely distributed in the coastal areas of Indonesia. However, current knowledge on its potential biological activities is still limited. In this study, we investigated the potential bioactive compounds in &lt;i>Gelidium latifolium&lt;/i> ethanol extract (GLE), and its cytotoxic effects against the murine B16-F10 melanoma cell line. GLE shows high total phenolic content (107.06 ± 17.42 mg GAE/g) and total flavonoid content (151.77 ± 3.45 mg QE/g), which potentially contribute to its potential antioxidant activity (DPPH = 650.42 ± 2.01 µg/mL; ABTS = 557.01 ± 1.94 µg/mL). ESI-HR-TOF-MS analysis revealed large absorption in the [M-H]&lt;sup>-&lt;/sup> of 327.2339 m/z, corresponding to the monoisotopic molecular mass of brassicolene. The presence of this compound potentially contributes to GLE's cytotoxic activity (IC&lt;sub>50&lt;/sub> = 84.29 ± 1.93 µg/mL). Furthermore, GLE significantly increased the number of apoptotic cells (66.83 ± 3.06%) compared to controls (18.83 ± 3.76%). Apoptosis was also confirmed by changes in the expression levels of apoptosis-related genes (i.e., &lt;i>p53&lt;/i>, &lt;i>Bax&lt;/i>, &lt;i>Bak&lt;/i>, and &lt;i>Bcl2&lt;/i>). Downregulated expression of &lt;i>Bcl2&lt;/i> indicates an intrinsic apoptotic pathway. Current results suggest that components of &lt;i>Gelidium latifolium&lt;/i> should be further investigated as possible sources of novel antitumor drugs.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>The Antiproliferative and Apoptosis-Inducing Effects of the Red Macroalgae &lt;i>Gelidium latifolium&lt;/i> Extract against Melanoma Cells.</pubmed_title><pmcid>PMC8587204</pmcid><funding_grant_id>WCR 2021</funding_grant_id><pubmed_authors>Ardiana N</pubmed_authors><pubmed_authors>Prasedya ES</pubmed_authors><pubmed_authors>Nikmatullah A</pubmed_authors><pubmed_authors>Martyasari NWR</pubmed_authors><pubmed_authors>Sunarwidhi AL</pubmed_authors><pubmed_authors>Frediansyah A</pubmed_authors><pubmed_authors>Sunarpi H</pubmed_authors><pubmed_authors>Padmi H</pubmed_authors><pubmed_authors>Widyastuti S</pubmed_authors><pubmed_authors>Ilhami BTK</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Antiproliferative and Apoptosis-Inducing Effects of the Red Macroalgae &lt;i>Gelidium latifolium&lt;/i> Extract against Melanoma Cells.</name><description>The red macroalga &lt;i>Gelidium latifolium&lt;/i> is widely distributed in the coastal areas of Indonesia. However, current knowledge on its potential biological activities is still limited. In this study, we investigated the potential bioactive compounds in &lt;i>Gelidium latifolium&lt;/i> ethanol extract (GLE), and its cytotoxic effects against the murine B16-F10 melanoma cell line. GLE shows high total phenolic content (107.06 ± 17.42 mg GAE/g) and total flavonoid content (151.77 ± 3.45 mg QE/g), which potentially contribute to its potential antioxidant activity (DPPH = 650.42 ± 2.01 µg/mL; ABTS = 557.01 ± 1.94 µg/mL). ESI-HR-TOF-MS analysis revealed large absorption in the [M-H]&lt;sup>-&lt;/sup> of 327.2339 m/z, corresponding to the monoisotopic molecular mass of brassicolene. The presence of this compound potentially contributes to GLE's cytotoxic activity (IC&lt;sub>50&lt;/sub> = 84.29 ± 1.93 µg/mL). Furthermore, GLE significantly increased the number of apoptotic cells (66.83 ± 3.06%) compared to controls (18.83 ± 3.76%). Apoptosis was also confirmed by changes in the expression levels of apoptosis-related genes (i.e., &lt;i>p53&lt;/i>, &lt;i>Bax&lt;/i>, &lt;i>Bak&lt;/i>, and &lt;i>Bcl2&lt;/i>). Downregulated expression of &lt;i>Bcl2&lt;/i> indicates an intrinsic apoptotic pathway. Current results suggest that components of &lt;i>Gelidium latifolium&lt;/i> should be further investigated as possible sources of novel antitumor drugs.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2024-10-17T16:16:20.171Z</modification><creation>2022-02-11T12:55:44.367Z</creation></dates><accession>S-EPMC8587204</accession><cross_references><pubmed>34770978</pubmed><doi>10.3390/molecules26216568</doi></cross_references></HashMap>