Ceramide Metabolism Balance, a Multifaceted Factor in Critical Steps of Breast Cancer Development
Ceramides are key lipids in energetic-metabolic pathways and signaling cascades, modulating critical physiological functions in cells. While synthesis of ceramides is performed in endoplasmic reticulum (ER), which is altered under overnutrition conditions, proteins associated with ceramide metabolis...
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creator | García-González, Victor Díaz-Villanueva, José Fernando Galindo-Hernández, Octavio Martínez-Navarro, Israel Hurtado-Ureta, Gustavo Pérez-Arias, Abril Alicia |
description | Ceramides are key lipids in energetic-metabolic pathways and signaling cascades, modulating critical physiological functions in cells. While synthesis of ceramides is performed in endoplasmic reticulum (ER), which is altered under overnutrition conditions, proteins associated with ceramide metabolism are located on membrane arrangement of mitochondria and ER (MAMs). However, ceramide accumulation in meta-inflammation, condition that associates obesity with a chronic low-grade inflammatory state, favors the deregulation of pathways such as insulin signaling, and induces structural rearrangements on mitochondrial membrane, modifying its permeability and altering the flux of ions and other molecules. Considering the wide biological processes in which sphingolipids are implicated, they have been associated with diseases that present abnormalities in their energetic metabolism, such as breast cancer. In this sense, sphingolipids could modulate various cell features, such as growth, proliferation, survival, senescence, and apoptosis in cancer progression; moreover, ceramide metabolism is associated to chemotherapy resistance, and regulation of metastasis. Cell⁻cell communication mediated by exosomes and lipoproteins has become relevant in the transport of several sphingolipids. Therefore, in this work we performed a comprehensive analysis of the state of the art about the multifaceted roles of ceramides, specifically the deregulation of ceramide metabolism pathways, being a key factor that could modulate neoplastic processes development. Under specific conditions, sphingolipids perform important functions in several cellular processes, and depending on the preponderant species and cellular and/or tissue status can inhibit or promote the development of metabolic and potentially breast cancer disease. |
doi_str_mv | 10.3390/ijms19092527 |
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While synthesis of ceramides is performed in endoplasmic reticulum (ER), which is altered under overnutrition conditions, proteins associated with ceramide metabolism are located on membrane arrangement of mitochondria and ER (MAMs). However, ceramide accumulation in meta-inflammation, condition that associates obesity with a chronic low-grade inflammatory state, favors the deregulation of pathways such as insulin signaling, and induces structural rearrangements on mitochondrial membrane, modifying its permeability and altering the flux of ions and other molecules. Considering the wide biological processes in which sphingolipids are implicated, they have been associated with diseases that present abnormalities in their energetic metabolism, such as breast cancer. In this sense, sphingolipids could modulate various cell features, such as growth, proliferation, survival, senescence, and apoptosis in cancer progression; moreover, ceramide metabolism is associated to chemotherapy resistance, and regulation of metastasis. Cell⁻cell communication mediated by exosomes and lipoproteins has become relevant in the transport of several sphingolipids. Therefore, in this work we performed a comprehensive analysis of the state of the art about the multifaceted roles of ceramides, specifically the deregulation of ceramide metabolism pathways, being a key factor that could modulate neoplastic processes development. Under specific conditions, sphingolipids perform important functions in several cellular processes, and depending on the preponderant species and cellular and/or tissue status can inhibit or promote the development of metabolic and potentially breast cancer disease.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms19092527</identifier><identifier>PMID: 30149660</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abnormalities ; Animals ; Apoptosis ; Autophagy ; Biological activity ; Breast cancer ; Breast Neoplasms - etiology ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cancer therapies ; Carbohydrate Metabolism ; Cascades ; Cell cycle ; Ceramide ; Ceramides - metabolism ; Chemoresistance ; Chemotherapy ; Deregulation ; Drug Resistance, Neoplasm ; Endoplasmic reticulum ; Endoplasmic Reticulum - metabolism ; Enzymes ; Epithelial-Mesenchymal Transition ; Exosomes ; Exosomes - metabolism ; Fatty acids ; Female ; Gene expression ; Humans ; Inflammation ; Inflammation - complications ; Inflammation - metabolism ; Insulin ; Kinases ; Lipid metabolism ; Lipids ; Lipoproteins ; Medical prognosis ; Membrane permeability ; Metabolic Networks and Pathways ; Metabolic pathways ; Metabolism ; Metastases ; Mitochondria ; Mitochondria - metabolism ; Neoplasm Metastasis ; Overnutrition ; Proteins ; Review ; Senescence ; Signal Transduction ; Sphingolipids ; Sphingolipids - metabolism ; State of the art ; Triglycerides</subject><ispartof>International journal of molecular sciences, 2018-08, Vol.19 (9), p.2527</ispartof><rights>2018. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 by the authors. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-15a13f518137ddad11c001cb95c2718bca89ba2d16dcbbd4e6782cb5ef9d32253</citedby><cites>FETCH-LOGICAL-c478t-15a13f518137ddad11c001cb95c2718bca89ba2d16dcbbd4e6782cb5ef9d32253</cites><orcidid>0000-0002-9421-3730 ; 0000-0003-4960-7551 ; 0000-0002-6847-4216</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163247/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163247/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30149660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García-González, Victor</creatorcontrib><creatorcontrib>Díaz-Villanueva, José Fernando</creatorcontrib><creatorcontrib>Galindo-Hernández, Octavio</creatorcontrib><creatorcontrib>Martínez-Navarro, Israel</creatorcontrib><creatorcontrib>Hurtado-Ureta, Gustavo</creatorcontrib><creatorcontrib>Pérez-Arias, Abril Alicia</creatorcontrib><title>Ceramide Metabolism Balance, a Multifaceted Factor in Critical Steps of Breast Cancer Development</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Ceramides are key lipids in energetic-metabolic pathways and signaling cascades, modulating critical physiological functions in cells. While synthesis of ceramides is performed in endoplasmic reticulum (ER), which is altered under overnutrition conditions, proteins associated with ceramide metabolism are located on membrane arrangement of mitochondria and ER (MAMs). However, ceramide accumulation in meta-inflammation, condition that associates obesity with a chronic low-grade inflammatory state, favors the deregulation of pathways such as insulin signaling, and induces structural rearrangements on mitochondrial membrane, modifying its permeability and altering the flux of ions and other molecules. Considering the wide biological processes in which sphingolipids are implicated, they have been associated with diseases that present abnormalities in their energetic metabolism, such as breast cancer. In this sense, sphingolipids could modulate various cell features, such as growth, proliferation, survival, senescence, and apoptosis in cancer progression; moreover, ceramide metabolism is associated to chemotherapy resistance, and regulation of metastasis. Cell⁻cell communication mediated by exosomes and lipoproteins has become relevant in the transport of several sphingolipids. Therefore, in this work we performed a comprehensive analysis of the state of the art about the multifaceted roles of ceramides, specifically the deregulation of ceramide metabolism pathways, being a key factor that could modulate neoplastic processes development. Under specific conditions, sphingolipids perform important functions in several cellular processes, and depending on the preponderant species and cellular and/or tissue status can inhibit or promote the development of metabolic and potentially breast cancer disease.</description><subject>Abnormalities</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Biological activity</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - etiology</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer therapies</subject><subject>Carbohydrate Metabolism</subject><subject>Cascades</subject><subject>Cell cycle</subject><subject>Ceramide</subject><subject>Ceramides - metabolism</subject><subject>Chemoresistance</subject><subject>Chemotherapy</subject><subject>Deregulation</subject><subject>Drug Resistance, Neoplasm</subject><subject>Endoplasmic reticulum</subject><subject>Endoplasmic Reticulum - 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etiology</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer therapies</topic><topic>Carbohydrate Metabolism</topic><topic>Cascades</topic><topic>Cell cycle</topic><topic>Ceramide</topic><topic>Ceramides - metabolism</topic><topic>Chemoresistance</topic><topic>Chemotherapy</topic><topic>Deregulation</topic><topic>Drug Resistance, Neoplasm</topic><topic>Endoplasmic reticulum</topic><topic>Endoplasmic Reticulum - metabolism</topic><topic>Enzymes</topic><topic>Epithelial-Mesenchymal Transition</topic><topic>Exosomes</topic><topic>Exosomes - metabolism</topic><topic>Fatty acids</topic><topic>Female</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammation - complications</topic><topic>Inflammation - metabolism</topic><topic>Insulin</topic><topic>Kinases</topic><topic>Lipid metabolism</topic><topic>Lipids</topic><topic>Lipoproteins</topic><topic>Medical prognosis</topic><topic>Membrane permeability</topic><topic>Metabolic Networks and Pathways</topic><topic>Metabolic pathways</topic><topic>Metabolism</topic><topic>Metastases</topic><topic>Mitochondria</topic><topic>Mitochondria - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García-González, Victor</au><au>Díaz-Villanueva, José Fernando</au><au>Galindo-Hernández, Octavio</au><au>Martínez-Navarro, Israel</au><au>Hurtado-Ureta, Gustavo</au><au>Pérez-Arias, Abril Alicia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ceramide Metabolism Balance, a Multifaceted Factor in Critical Steps of Breast Cancer Development</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2018-08-26</date><risdate>2018</risdate><volume>19</volume><issue>9</issue><spage>2527</spage><pages>2527-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Ceramides are key lipids in energetic-metabolic pathways and signaling cascades, modulating critical physiological functions in cells. While synthesis of ceramides is performed in endoplasmic reticulum (ER), which is altered under overnutrition conditions, proteins associated with ceramide metabolism are located on membrane arrangement of mitochondria and ER (MAMs). However, ceramide accumulation in meta-inflammation, condition that associates obesity with a chronic low-grade inflammatory state, favors the deregulation of pathways such as insulin signaling, and induces structural rearrangements on mitochondrial membrane, modifying its permeability and altering the flux of ions and other molecules. Considering the wide biological processes in which sphingolipids are implicated, they have been associated with diseases that present abnormalities in their energetic metabolism, such as breast cancer. In this sense, sphingolipids could modulate various cell features, such as growth, proliferation, survival, senescence, and apoptosis in cancer progression; moreover, ceramide metabolism is associated to chemotherapy resistance, and regulation of metastasis. Cell⁻cell communication mediated by exosomes and lipoproteins has become relevant in the transport of several sphingolipids. Therefore, in this work we performed a comprehensive analysis of the state of the art about the multifaceted roles of ceramides, specifically the deregulation of ceramide metabolism pathways, being a key factor that could modulate neoplastic processes development. Under specific conditions, sphingolipids perform important functions in several cellular processes, and depending on the preponderant species and cellular and/or tissue status can inhibit or promote the development of metabolic and potentially breast cancer disease.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>30149660</pmid><doi>10.3390/ijms19092527</doi><orcidid>https://orcid.org/0000-0002-9421-3730</orcidid><orcidid>https://orcid.org/0000-0003-4960-7551</orcidid><orcidid>https://orcid.org/0000-0002-6847-4216</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Animals Apoptosis Autophagy Biological activity Breast cancer Breast Neoplasms - etiology Breast Neoplasms - metabolism Breast Neoplasms - pathology Cancer therapies Carbohydrate Metabolism Cascades Cell cycle Ceramide Ceramides - metabolism Chemoresistance Chemotherapy Deregulation Drug Resistance, Neoplasm Endoplasmic reticulum Endoplasmic Reticulum - metabolism Enzymes Epithelial-Mesenchymal Transition Exosomes Exosomes - metabolism Fatty acids Female Gene expression Humans Inflammation Inflammation - complications Inflammation - metabolism Insulin Kinases Lipid metabolism Lipids Lipoproteins Medical prognosis Membrane permeability Metabolic Networks and Pathways Metabolic pathways Metabolism Metastases Mitochondria Mitochondria - metabolism Neoplasm Metastasis Overnutrition Proteins Review Senescence Signal Transduction Sphingolipids Sphingolipids - metabolism State of the art Triglycerides |
title | Ceramide Metabolism Balance, a Multifaceted Factor in Critical Steps of Breast Cancer Development |
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