<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jandova J</submitter><funding>National Institutes of Health</funding><pagination>605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7913703</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(4)</volume><pubmed_abstract>There are two stable isotopes of hydrogen, protium (1H) and deuterium (2H; D). Cellular stress response dysregulation in cancer represents both a major pathological driving force and a promising therapeutic target, but the molecular consequences and potential therapeutic impact of deuterium (2H)-stress on cancer cells remain largely unexplored. We have examined the anti-proliferative and apoptogenic effects of deuterium oxide (D2O; 'heavy water') together with stress response gene expression profiling in panels of malignant melanoma (A375V600E, A375NRAS, G361, LOX-IMVI), and pancreatic ductal adenocarcinoma (PANC-1, Capan-2, or MIA PaCa-2) cells with inclusion of human diploid Hs27 skin fibroblasts. Moreover, we have examined the efficacy of D2O-based pharmacological intervention in murine</pubmed_abstract><journal>Cancers</journal><pubmed_title>Deuterium Oxide (D2O) Induces Early Stress Response Gene Expression and Impairs Growth and Metastasis of Experimental Malignant Melanoma.</pubmed_title><pmcid>PMC7913703</pmcid><funding_grant_id>R01CA229418</funding_grant_id><funding_grant_id>ES007091</funding_grant_id><funding_grant_id>R21ES029579</funding_grant_id><funding_grant_id>ES006694</funding_grant_id><funding_grant_id>R03CA230949</funding_grant_id><funding_grant_id>CA023074</funding_grant_id><funding_grant_id>P01CA229112</funding_grant_id><pubmed_authors>Hua AB</pubmed_authors><pubmed_authors>Jandova J</pubmed_authors><pubmed_authors>Fimbres J</pubmed_authors><pubmed_authors>Wondrak GT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deuterium Oxide (D2O) Induces Early Stress Response Gene Expression and Impairs Growth and Metastasis of Experimental Malignant Melanoma.</name><description>There are two stable isotopes of hydrogen, protium (1H) and deuterium (2H; D). Cellular stress response dysregulation in cancer represents both a major pathological driving force and a promising therapeutic target, but the molecular consequences and potential therapeutic impact of deuterium (2H)-stress on cancer cells remain largely unexplored. We have examined the anti-proliferative and apoptogenic effects of deuterium oxide (D2O; 'heavy water') together with stress response gene expression profiling in panels of malignant melanoma (A375V600E, A375NRAS, G361, LOX-IMVI), and pancreatic ductal adenocarcinoma (PANC-1, Capan-2, or MIA PaCa-2) cells with inclusion of human diploid Hs27 skin fibroblasts. Moreover, we have examined the efficacy of D2O-based pharmacological intervention in murine</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2025-05-29T22:28:25.599Z</modification><creation>2021-03-02T08:09:11Z</creation></dates><accession>S-EPMC7913703</accession><cross_references><pubmed>33546433</pubmed><doi>10.3390/cancers13040605</doi></cross_references></HashMap>