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Potential of Polar Lipids Isolated from the Marine Sponge Haliclona ( Halichoclona ) vansoesti against Melanoma
Marine sponges represent a good source of natural metabolites for biotechnological applications in the pharmacological, cosmeceutical, and nutraceutical fields. In the present work, we analyzed the biotechnological potential of the alien species ( ) de Weerdt, de Kluijver & Gomez, 1999, previous...
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Published in: | International journal of molecular sciences 2024-07, Vol.25 (13), p.7418 |
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creator | Ruocco, Nadia Nuzzo, Genoveffa Federico, Serena Esposito, Roberta Gallo, Carmela Ziaco, Marcello Manzo, Emiliano Fontana, Angelo Bertolino, Marco Zagami, Giacomo Zupo, Valerio Sansone, Clementina Costantini, Maria |
description | Marine sponges represent a good source of natural metabolites for biotechnological applications in the pharmacological, cosmeceutical, and nutraceutical fields. In the present work, we analyzed the biotechnological potential of the alien species
(
)
de Weerdt, de Kluijver & Gomez, 1999, previously collected in the Mediterranean Sea (Faro Lake, Sicily). The bioactivity and chemical content of this species has never been investigated, and information in the literature on its Caribbean counterpart is scarce. We show that an enriched extract of
induced cell death in human melanoma cells with an IC
value of 36.36 µg mL
, by (i) triggering a pro-inflammatory response, (ii) activating extrinsic apoptosis mediated by tumor necrosis factor receptors triggering the mitochondrial apoptosis via the involvement of Bcl-2 proteins and caspase 9, and (iii) inducing a significant reduction in several proteins promoting human angiogenesis. Through orthogonal SPE fractionations, we identified two active sphingoid-based lipid classes, also characterized by nuclear magnetic resonance and mass spectrometry, as the main components of two active fractions. Overall, our findings provide the first evaluation of the anti-cancer potential of polar lipids isolated from the marine sponge
(
)
, which may lead to new lead compounds with biotechnological applications in the pharmaceutical field. |
doi_str_mv | 10.3390/ijms25137418 |
format | article |
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(
)
de Weerdt, de Kluijver & Gomez, 1999, previously collected in the Mediterranean Sea (Faro Lake, Sicily). The bioactivity and chemical content of this species has never been investigated, and information in the literature on its Caribbean counterpart is scarce. We show that an enriched extract of
induced cell death in human melanoma cells with an IC
value of 36.36 µg mL
, by (i) triggering a pro-inflammatory response, (ii) activating extrinsic apoptosis mediated by tumor necrosis factor receptors triggering the mitochondrial apoptosis via the involvement of Bcl-2 proteins and caspase 9, and (iii) inducing a significant reduction in several proteins promoting human angiogenesis. Through orthogonal SPE fractionations, we identified two active sphingoid-based lipid classes, also characterized by nuclear magnetic resonance and mass spectrometry, as the main components of two active fractions. Overall, our findings provide the first evaluation of the anti-cancer potential of polar lipids isolated from the marine sponge
(
)
, which may lead to new lead compounds with biotechnological applications in the pharmaceutical field.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms25137418</identifier><identifier>PMID: 39000524</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animals ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - isolation & purification ; Antineoplastic Agents - pharmacology ; Apoptosis - drug effects ; Bioassays ; Cancer therapies ; Cell death ; Cell Line, Tumor ; Cytotoxicity ; FDA approval ; Haliclona - chemistry ; Humans ; Immunotherapy ; Lipids ; marine biotechnology ; Melanoma ; Melanoma - drug therapy ; Melanoma - metabolism ; Melanoma - pathology ; Metabolites ; porifera ; Porifera - chemistry ; SPE fractionation ; sphingoid lipids</subject><ispartof>International journal of molecular sciences, 2024-07, Vol.25 (13), p.7418</ispartof><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c310t-6dc082f5aacb5293b29b9a4f12f0b401ebbdea70cffe07dd99a630ecd88e412e3</cites><orcidid>0000-0002-0054-779X ; 0000-0001-7065-2379 ; 0000-0001-9766-8784 ; 0000-0002-3007-8154 ; 0000-0002-5453-461X ; 0000-0002-1665-2615 ; 0000-0003-3978-6170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3079320349/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3079320349?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39000524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ruocco, Nadia</creatorcontrib><creatorcontrib>Nuzzo, Genoveffa</creatorcontrib><creatorcontrib>Federico, Serena</creatorcontrib><creatorcontrib>Esposito, Roberta</creatorcontrib><creatorcontrib>Gallo, Carmela</creatorcontrib><creatorcontrib>Ziaco, Marcello</creatorcontrib><creatorcontrib>Manzo, Emiliano</creatorcontrib><creatorcontrib>Fontana, Angelo</creatorcontrib><creatorcontrib>Bertolino, Marco</creatorcontrib><creatorcontrib>Zagami, Giacomo</creatorcontrib><creatorcontrib>Zupo, Valerio</creatorcontrib><creatorcontrib>Sansone, Clementina</creatorcontrib><creatorcontrib>Costantini, Maria</creatorcontrib><title>Potential of Polar Lipids Isolated from the Marine Sponge Haliclona ( Halichoclona ) vansoesti against Melanoma</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Marine sponges represent a good source of natural metabolites for biotechnological applications in the pharmacological, cosmeceutical, and nutraceutical fields. In the present work, we analyzed the biotechnological potential of the alien species
(
)
de Weerdt, de Kluijver & Gomez, 1999, previously collected in the Mediterranean Sea (Faro Lake, Sicily). The bioactivity and chemical content of this species has never been investigated, and information in the literature on its Caribbean counterpart is scarce. We show that an enriched extract of
induced cell death in human melanoma cells with an IC
value of 36.36 µg mL
, by (i) triggering a pro-inflammatory response, (ii) activating extrinsic apoptosis mediated by tumor necrosis factor receptors triggering the mitochondrial apoptosis via the involvement of Bcl-2 proteins and caspase 9, and (iii) inducing a significant reduction in several proteins promoting human angiogenesis. Through orthogonal SPE fractionations, we identified two active sphingoid-based lipid classes, also characterized by nuclear magnetic resonance and mass spectrometry, as the main components of two active fractions. Overall, our findings provide the first evaluation of the anti-cancer potential of polar lipids isolated from the marine sponge
(
)
, which may lead to new lead compounds with biotechnological applications in the pharmaceutical field.</description><subject>Animals</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - isolation & purification</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Bioassays</subject><subject>Cancer therapies</subject><subject>Cell death</subject><subject>Cell Line, Tumor</subject><subject>Cytotoxicity</subject><subject>FDA approval</subject><subject>Haliclona - chemistry</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Lipids</subject><subject>marine biotechnology</subject><subject>Melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>Metabolites</subject><subject>porifera</subject><subject>Porifera - chemistry</subject><subject>SPE fractionation</subject><subject>sphingoid lipids</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkd1rFTEQxRdRbK2--SwBXyp46-RjP_JYitoLt7RQfQ6zyeQ2l93NNdkr-N-bdmspPmVm-OUwZ05VvedwJqWGL2E3ZlFz2SrevaiOuRJiBdC0L5_VR9WbnHcAQopav66Oyj-AWqjjKt7EmaY54MCiZzdxwMQ2YR9cZutcupkc8ymObL4jdoUpTMRu93HaErvEIdghTshOl_ouLu0n9hunHCnPgeEWw5RndkUDTnHEt9Urj0Omd4_vSfXz29cfF5erzfX39cX5ZmUlh3nVOAud8DWi7WuhZS90r1F5Ljz0Cjj1vSNswXpP0DqnNTYSyLquI8UFyZNqvei6iDuzT2HE9MdEDOZhENPWYJrL_mQaLrWqOXZOdso2oHupG-3LqWqpylmL1umitU_x16HYMmPIlobiiOIhGwmt7mqtVVvQj_-hu3hIU3H6QEkBUulCfV4om2LOifzTghzMfajmeagF__AoeuhHck_wvxTlX0ubm9c</recordid><startdate>20240706</startdate><enddate>20240706</enddate><creator>Ruocco, Nadia</creator><creator>Nuzzo, Genoveffa</creator><creator>Federico, Serena</creator><creator>Esposito, Roberta</creator><creator>Gallo, Carmela</creator><creator>Ziaco, Marcello</creator><creator>Manzo, Emiliano</creator><creator>Fontana, Angelo</creator><creator>Bertolino, Marco</creator><creator>Zagami, Giacomo</creator><creator>Zupo, Valerio</creator><creator>Sansone, Clementina</creator><creator>Costantini, Maria</creator><general>MDPI AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0054-779X</orcidid><orcidid>https://orcid.org/0000-0001-7065-2379</orcidid><orcidid>https://orcid.org/0000-0001-9766-8784</orcidid><orcidid>https://orcid.org/0000-0002-3007-8154</orcidid><orcidid>https://orcid.org/0000-0002-5453-461X</orcidid><orcidid>https://orcid.org/0000-0002-1665-2615</orcidid><orcidid>https://orcid.org/0000-0003-3978-6170</orcidid></search><sort><creationdate>20240706</creationdate><title>Potential of Polar Lipids Isolated from the Marine Sponge Haliclona ( Halichoclona ) vansoesti against Melanoma</title><author>Ruocco, Nadia ; Nuzzo, Genoveffa ; Federico, Serena ; Esposito, Roberta ; Gallo, Carmela ; Ziaco, Marcello ; Manzo, Emiliano ; Fontana, Angelo ; Bertolino, Marco ; Zagami, Giacomo ; Zupo, Valerio ; Sansone, Clementina ; Costantini, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-6dc082f5aacb5293b29b9a4f12f0b401ebbdea70cffe07dd99a630ecd88e412e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - 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In the present work, we analyzed the biotechnological potential of the alien species
(
)
de Weerdt, de Kluijver & Gomez, 1999, previously collected in the Mediterranean Sea (Faro Lake, Sicily). The bioactivity and chemical content of this species has never been investigated, and information in the literature on its Caribbean counterpart is scarce. We show that an enriched extract of
induced cell death in human melanoma cells with an IC
value of 36.36 µg mL
, by (i) triggering a pro-inflammatory response, (ii) activating extrinsic apoptosis mediated by tumor necrosis factor receptors triggering the mitochondrial apoptosis via the involvement of Bcl-2 proteins and caspase 9, and (iii) inducing a significant reduction in several proteins promoting human angiogenesis. Through orthogonal SPE fractionations, we identified two active sphingoid-based lipid classes, also characterized by nuclear magnetic resonance and mass spectrometry, as the main components of two active fractions. Overall, our findings provide the first evaluation of the anti-cancer potential of polar lipids isolated from the marine sponge
(
)
, which may lead to new lead compounds with biotechnological applications in the pharmaceutical field.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39000524</pmid><doi>10.3390/ijms25137418</doi><orcidid>https://orcid.org/0000-0002-0054-779X</orcidid><orcidid>https://orcid.org/0000-0001-7065-2379</orcidid><orcidid>https://orcid.org/0000-0001-9766-8784</orcidid><orcidid>https://orcid.org/0000-0002-3007-8154</orcidid><orcidid>https://orcid.org/0000-0002-5453-461X</orcidid><orcidid>https://orcid.org/0000-0002-1665-2615</orcidid><orcidid>https://orcid.org/0000-0003-3978-6170</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic Agents - chemistry Antineoplastic Agents - isolation & purification Antineoplastic Agents - pharmacology Apoptosis - drug effects Bioassays Cancer therapies Cell death Cell Line, Tumor Cytotoxicity FDA approval Haliclona - chemistry Humans Immunotherapy Lipids marine biotechnology Melanoma Melanoma - drug therapy Melanoma - metabolism Melanoma - pathology Metabolites porifera Porifera - chemistry SPE fractionation sphingoid lipids |
title | Potential of Polar Lipids Isolated from the Marine Sponge Haliclona ( Halichoclona ) vansoesti against Melanoma |
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