<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Separovic D</submitter><funding>NCRR NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>372-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3123537</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>409(3)</volume><pubmed_abstract>Two anticancer agents, LCL85 and photodynamic therapy (PDT) were combined to test whether the combination PDT/LCL85 evokes changes in the sphingolipid (SL) profile and promotes cell death. Treatment of SCCVII mouse squamous carcinoma cells using the silicone phthalocyanine Pc 4 for PDT induced increases in the prodeath global ceramides/dihydroceramides (DHceramides), and no changes in the prosurvival sphingosine-1-phosphate (S1P). In contrast, after LCL85, the levels of most ceramides and DHceramides were reduced, whereas the levels of S1P were increased. After PDT/LCL85 the levels of global ceramides and DHceramides, and of S1P, were restored to resting levels. PDT/LCL85 also enhanced the levels of C18-, C20-, and C20:1-ceramide, and C18-DHceramide. Treatment with PDT, with or without LCL</pubmed_abstract><journal>Biochemical and biophysical research communications</journal><pubmed_title>Combining anticancer agents photodynamic therapy and LCL85 leads to distinct changes in the sphingolipid profile, autophagy, caspase-3 activation in the absence of cell death, and long-term sensitization.</pubmed_title><pmcid>PMC3123537</pmcid><funding_grant_id>P30 CA138313</funding_grant_id><funding_grant_id>P01 CA097132</funding_grant_id><funding_grant_id>R01 CA77475</funding_grant_id><funding_grant_id>IPO1CA097132</funding_grant_id><funding_grant_id>P30 CA 138313</funding_grant_id><funding_grant_id>P20 RR017677</funding_grant_id><funding_grant_id>C06 RR018823</funding_grant_id><funding_grant_id>R01 CA077475-11</funding_grant_id><funding_grant_id>R01 CA077475</funding_grant_id><pubmed_authors>Bhatti G</pubmed_authors><pubmed_authors>Bielawska A</pubmed_authors><pubmed_authors>Bai A</pubmed_authors><pubmed_authors>Separovic D</pubmed_authors><pubmed_authors>Joseph N</pubmed_authors><pubmed_authors>Buren EV</pubmed_authors><pubmed_authors>Breen P</pubmed_authors><pubmed_authors>Pierce JS</pubmed_authors><pubmed_authors>Saad ZH</pubmed_authors><pubmed_authors>Bielawski J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combining anticancer agents photodynamic therapy and LCL85 leads to distinct changes in the sphingolipid profile, autophagy, caspase-3 activation in the absence of cell death, and long-term sensitization.</name><description>Two anticancer agents, LCL85 and photodynamic therapy (PDT) were combined to test whether the combination PDT/LCL85 evokes changes in the sphingolipid (SL) profile and promotes cell death. Treatment of SCCVII mouse squamous carcinoma cells using the silicone phthalocyanine Pc 4 for PDT induced increases in the prodeath global ceramides/dihydroceramides (DHceramides), and no changes in the prosurvival sphingosine-1-phosphate (S1P). In contrast, after LCL85, the levels of most ceramides and DHceramides were reduced, whereas the levels of S1P were increased. After PDT/LCL85 the levels of global ceramides and DHceramides, and of S1P, were restored to resting levels. PDT/LCL85 also enhanced the levels of C18-, C20-, and C20:1-ceramide, and C18-DHceramide. Treatment with PDT, with or without LCL</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jun</publication><modification>2025-04-04T21:57:39.18Z</modification><creation>2019-03-27T00:43:01Z</creation></dates><accession>S-EPMC3123537</accession><cross_references><pubmed>21545791</pubmed><doi>10.1016/j.bbrc.2011.04.091</doi></cross_references></HashMap>