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Lipid Storage and Autophagy in Melanoma Cancer Cells
Cancer stem cells (CSC) represent a key cellular subpopulation controlling biological features such as cancer progression in all cancer types. By using melanospheres established from human melanoma patients, we compared less differentiated melanosphere-derived CSC to differentiating melanosphere-der...
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Published in: | International journal of molecular sciences 2017-06, Vol.18 (6), p.1271 |
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creator | Giampietri, Claudia Petrungaro, Simonetta Cordella, Martina Tabolacci, Claudio Tomaipitinca, Luana Facchiano, Antonio Eramo, Adriana Filippini, Antonio Facchiano, Francesco Ziparo, Elio |
description | Cancer stem cells (CSC) represent a key cellular subpopulation controlling biological features such as cancer progression in all cancer types. By using melanospheres established from human melanoma patients, we compared less differentiated melanosphere-derived CSC to differentiating melanosphere-derived cells. Increased lipid uptake was found in melanosphere-derived CSC vs. differentiating melanosphere-derived cells, paralleled by strong expression of lipogenic factors Sterol Regulatory Element-Binding Protein-1 (SREBP-1) and Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ). An inverse relation between lipid-storing phenotype and autophagy was also found, since microtubule-associated protein 1A/1B-Light Chain 3 (LC3) lipidation is reduced in melanosphere-derived CSC. To investigate upstream autophagy regulators, Phospho-AMP activated Protein Kinase (P-AMPK) and Phospho-mammalian Target of Rapamycin (P-mTOR) were analyzed; lower P-AMPK and higher P-mTOR expression in melanosphere-derived CSC were found, thus explaining, at least in part, their lower autophagic activity. In addition, co-localization of LC3-stained autophagosome spots and perilipin-stained lipid droplets was demonstrated mainly in differentiating melanosphere-derived cells, further supporting the role of autophagy in lipid droplets clearance. The present manuscript demonstrates an inverse relationship between lipid-storing phenotype and melanoma stem cells differentiation, providing novel indications involving autophagy in melanoma stem cells biology. |
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By using melanospheres established from human melanoma patients, we compared less differentiated melanosphere-derived CSC to differentiating melanosphere-derived cells. Increased lipid uptake was found in melanosphere-derived CSC vs. differentiating melanosphere-derived cells, paralleled by strong expression of lipogenic factors Sterol Regulatory Element-Binding Protein-1 (SREBP-1) and Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ). An inverse relation between lipid-storing phenotype and autophagy was also found, since microtubule-associated protein 1A/1B-Light Chain 3 (LC3) lipidation is reduced in melanosphere-derived CSC. To investigate upstream autophagy regulators, Phospho-AMP activated Protein Kinase (P-AMPK) and Phospho-mammalian Target of Rapamycin (P-mTOR) were analyzed; lower P-AMPK and higher P-mTOR expression in melanosphere-derived CSC were found, thus explaining, at least in part, their lower autophagic activity. In addition, co-localization of LC3-stained autophagosome spots and perilipin-stained lipid droplets was demonstrated mainly in differentiating melanosphere-derived cells, further supporting the role of autophagy in lipid droplets clearance. The present manuscript demonstrates an inverse relationship between lipid-storing phenotype and melanoma stem cells differentiation, providing novel indications involving autophagy in melanoma stem cells biology.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms18061271</identifier><identifier>PMID: 28617309</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>AMP-activated protein kinase ; AMP-Activated Protein Kinases - metabolism ; Autophagy ; Cancer ; Cell Differentiation ; Colorectal cancer ; Droplets ; Enzymes ; Fatty acids ; Genotype & phenotype ; Humans ; Kinases ; Lipid Metabolism ; Lipids ; Localization ; Melanoma ; Melanoma - metabolism ; Melanoma - pathology ; Metabolism ; Metastasis ; Microtubule-associated protein 1 ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Peroxisome proliferator-activated receptors ; Phenotypes ; Phosphorylation ; PPAR gamma - metabolism ; Proteins ; Rapamycin ; Skin cancer ; Stem cells ; Sterol Regulatory Element Binding Protein 1 - metabolism ; Sterol regulatory element-binding protein ; Sterols ; Storage ; TOR protein ; TOR Serine-Threonine Kinases - metabolism ; Triglycerides ; Tumor Cells, Cultured ; Tumors</subject><ispartof>International journal of molecular sciences, 2017-06, Vol.18 (6), p.1271</ispartof><rights>2017 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 (http://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><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-a58197555b5daf8f33d2e268876250dce3bfd07574caafd30c4d732080ea3a223</citedby><cites>FETCH-LOGICAL-c478t-a58197555b5daf8f33d2e268876250dce3bfd07574caafd30c4d732080ea3a223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2685299255/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2685299255?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28617309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giampietri, Claudia</creatorcontrib><creatorcontrib>Petrungaro, Simonetta</creatorcontrib><creatorcontrib>Cordella, Martina</creatorcontrib><creatorcontrib>Tabolacci, Claudio</creatorcontrib><creatorcontrib>Tomaipitinca, Luana</creatorcontrib><creatorcontrib>Facchiano, Antonio</creatorcontrib><creatorcontrib>Eramo, Adriana</creatorcontrib><creatorcontrib>Filippini, Antonio</creatorcontrib><creatorcontrib>Facchiano, Francesco</creatorcontrib><creatorcontrib>Ziparo, Elio</creatorcontrib><title>Lipid Storage and Autophagy in Melanoma Cancer Cells</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Cancer stem cells (CSC) represent a key cellular subpopulation controlling biological features such as cancer progression in all cancer types. By using melanospheres established from human melanoma patients, we compared less differentiated melanosphere-derived CSC to differentiating melanosphere-derived cells. Increased lipid uptake was found in melanosphere-derived CSC vs. differentiating melanosphere-derived cells, paralleled by strong expression of lipogenic factors Sterol Regulatory Element-Binding Protein-1 (SREBP-1) and Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ). An inverse relation between lipid-storing phenotype and autophagy was also found, since microtubule-associated protein 1A/1B-Light Chain 3 (LC3) lipidation is reduced in melanosphere-derived CSC. To investigate upstream autophagy regulators, Phospho-AMP activated Protein Kinase (P-AMPK) and Phospho-mammalian Target of Rapamycin (P-mTOR) were analyzed; lower P-AMPK and higher P-mTOR expression in melanosphere-derived CSC were found, thus explaining, at least in part, their lower autophagic activity. In addition, co-localization of LC3-stained autophagosome spots and perilipin-stained lipid droplets was demonstrated mainly in differentiating melanosphere-derived cells, further supporting the role of autophagy in lipid droplets clearance. The present manuscript demonstrates an inverse relationship between lipid-storing phenotype and melanoma stem cells differentiation, providing novel indications involving autophagy in melanoma stem cells biology.</description><subject>AMP-activated protein kinase</subject><subject>AMP-Activated Protein Kinases - metabolism</subject><subject>Autophagy</subject><subject>Cancer</subject><subject>Cell Differentiation</subject><subject>Colorectal cancer</subject><subject>Droplets</subject><subject>Enzymes</subject><subject>Fatty acids</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Kinases</subject><subject>Lipid Metabolism</subject><subject>Lipids</subject><subject>Localization</subject><subject>Melanoma</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>Metabolism</subject><subject>Metastasis</subject><subject>Microtubule-associated protein 1</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - 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By using melanospheres established from human melanoma patients, we compared less differentiated melanosphere-derived CSC to differentiating melanosphere-derived cells. Increased lipid uptake was found in melanosphere-derived CSC vs. differentiating melanosphere-derived cells, paralleled by strong expression of lipogenic factors Sterol Regulatory Element-Binding Protein-1 (SREBP-1) and Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ). An inverse relation between lipid-storing phenotype and autophagy was also found, since microtubule-associated protein 1A/1B-Light Chain 3 (LC3) lipidation is reduced in melanosphere-derived CSC. To investigate upstream autophagy regulators, Phospho-AMP activated Protein Kinase (P-AMPK) and Phospho-mammalian Target of Rapamycin (P-mTOR) were analyzed; lower P-AMPK and higher P-mTOR expression in melanosphere-derived CSC were found, thus explaining, at least in part, their lower autophagic activity. In addition, co-localization of LC3-stained autophagosome spots and perilipin-stained lipid droplets was demonstrated mainly in differentiating melanosphere-derived cells, further supporting the role of autophagy in lipid droplets clearance. The present manuscript demonstrates an inverse relationship between lipid-storing phenotype and melanoma stem cells differentiation, providing novel indications involving autophagy in melanoma stem cells biology.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28617309</pmid><doi>10.3390/ijms18061271</doi><oa>free_for_read</oa></addata></record> |
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subjects | AMP-activated protein kinase AMP-Activated Protein Kinases - metabolism Autophagy Cancer Cell Differentiation Colorectal cancer Droplets Enzymes Fatty acids Genotype & phenotype Humans Kinases Lipid Metabolism Lipids Localization Melanoma Melanoma - metabolism Melanoma - pathology Metabolism Metastasis Microtubule-associated protein 1 Neoplastic Stem Cells - metabolism Neoplastic Stem Cells - pathology Peroxisome proliferator-activated receptors Phenotypes Phosphorylation PPAR gamma - metabolism Proteins Rapamycin Skin cancer Stem cells Sterol Regulatory Element Binding Protein 1 - metabolism Sterol regulatory element-binding protein Sterols Storage TOR protein TOR Serine-Threonine Kinases - metabolism Triglycerides Tumor Cells, Cultured Tumors |
title | Lipid Storage and Autophagy in Melanoma Cancer Cells |
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