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Oleate alters the immune response in non-small cell lung adenocarcinoma through regulation of HMGB1 release
Cancer cell evasion of the immune response is critical to cancer development and metastases. Clinicians' ability to kickstart the immune system to target these rogue cells is an ever-growing area of research and medicine. This study delved into the relationship between lipid metabolism, High Mo...
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Published in: | Frontiers in cell and developmental biology 2024-07, Vol.12, p.1348707 |
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container_title | Frontiers in cell and developmental biology |
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creator | Cole-Skinner, Breanna Andre, Nicole M Blankenheim, Zachary Root, Kate M Jafri, Kisa Simmons, Jr, Glenn E |
description | Cancer cell evasion of the immune response is critical to cancer development and metastases. Clinicians' ability to kickstart the immune system to target these rogue cells is an ever-growing area of research and medicine. This study delved into the relationship between lipid metabolism, High Mobility Group Box 1 protein (HMGB1)-a pro-inflammatory damage-associated molecular pattern protein-and immune regulation within non-small cell lung adenocarcinoma (NSCLC).
To address this question, we used a combination of proteomics, molecular biology, and bioinformatic techniques to investigate the relationship between fatty acids and immune signals within NSCLC.
We found that the expression of stearoyl CoA desaturase 1 (SCD1) was decreased in NSCLC tumors compared to normal tissues. This emphasized the critical role of lipid metabolism in tumor progression. Interestingly, monounsaturated fatty acid (MUFA) availability affected the expression of programmed death ligand-1 (PD-L1), a pivotal immune checkpoint target in lung cancer cells and immune cells, as well as HMGB1, suggesting a novel approach to modulating the immune response. This study uncovered a complex interplay between SCD1, PD-L1, and HMGB1, influencing the immunological sensitivity of tumors.
Our work underscores the critical importance of understanding the intricate relationships between lipid metabolism and immune modulation to develop more effective NSCLC treatments and personalized therapies. As we continue to explore these connections, we hope to contribute significantly to the ever-evolving field of cancer research, improving patient outcomes and advancing precision medicine in NSCLC. |
doi_str_mv | 10.3389/fcell.2024.1348707 |
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To address this question, we used a combination of proteomics, molecular biology, and bioinformatic techniques to investigate the relationship between fatty acids and immune signals within NSCLC.
We found that the expression of stearoyl CoA desaturase 1 (SCD1) was decreased in NSCLC tumors compared to normal tissues. This emphasized the critical role of lipid metabolism in tumor progression. Interestingly, monounsaturated fatty acid (MUFA) availability affected the expression of programmed death ligand-1 (PD-L1), a pivotal immune checkpoint target in lung cancer cells and immune cells, as well as HMGB1, suggesting a novel approach to modulating the immune response. This study uncovered a complex interplay between SCD1, PD-L1, and HMGB1, influencing the immunological sensitivity of tumors.
Our work underscores the critical importance of understanding the intricate relationships between lipid metabolism and immune modulation to develop more effective NSCLC treatments and personalized therapies. As we continue to explore these connections, we hope to contribute significantly to the ever-evolving field of cancer research, improving patient outcomes and advancing precision medicine in NSCLC.</description><identifier>ISSN: 2296-634X</identifier><identifier>EISSN: 2296-634X</identifier><identifier>DOI: 10.3389/fcell.2024.1348707</identifier><identifier>PMID: 39100092</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>fatty acid ; HMGB1 (high mobility group box 1) ; immunotherapy ; lung cancer ; tumor microenvironment</subject><ispartof>Frontiers in cell and developmental biology, 2024-07, Vol.12, p.1348707</ispartof><rights>Copyright © 2024 Cole-Skinner, Andre, Blankenheim, Root, Jafri and Simmons.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c294t-4eca74b58fe430510fcbe092716d1713bc526b10f881628fcf23957ce421d7593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39100092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cole-Skinner, Breanna</creatorcontrib><creatorcontrib>Andre, Nicole M</creatorcontrib><creatorcontrib>Blankenheim, Zachary</creatorcontrib><creatorcontrib>Root, Kate M</creatorcontrib><creatorcontrib>Jafri, Kisa</creatorcontrib><creatorcontrib>Simmons, Jr, Glenn E</creatorcontrib><title>Oleate alters the immune response in non-small cell lung adenocarcinoma through regulation of HMGB1 release</title><title>Frontiers in cell and developmental biology</title><addtitle>Front Cell Dev Biol</addtitle><description>Cancer cell evasion of the immune response is critical to cancer development and metastases. Clinicians' ability to kickstart the immune system to target these rogue cells is an ever-growing area of research and medicine. This study delved into the relationship between lipid metabolism, High Mobility Group Box 1 protein (HMGB1)-a pro-inflammatory damage-associated molecular pattern protein-and immune regulation within non-small cell lung adenocarcinoma (NSCLC).
To address this question, we used a combination of proteomics, molecular biology, and bioinformatic techniques to investigate the relationship between fatty acids and immune signals within NSCLC.
We found that the expression of stearoyl CoA desaturase 1 (SCD1) was decreased in NSCLC tumors compared to normal tissues. This emphasized the critical role of lipid metabolism in tumor progression. Interestingly, monounsaturated fatty acid (MUFA) availability affected the expression of programmed death ligand-1 (PD-L1), a pivotal immune checkpoint target in lung cancer cells and immune cells, as well as HMGB1, suggesting a novel approach to modulating the immune response. This study uncovered a complex interplay between SCD1, PD-L1, and HMGB1, influencing the immunological sensitivity of tumors.
Our work underscores the critical importance of understanding the intricate relationships between lipid metabolism and immune modulation to develop more effective NSCLC treatments and personalized therapies. As we continue to explore these connections, we hope to contribute significantly to the ever-evolving field of cancer research, improving patient outcomes and advancing precision medicine in NSCLC.</description><subject>fatty acid</subject><subject>HMGB1 (high mobility group box 1)</subject><subject>immunotherapy</subject><subject>lung cancer</subject><subject>tumor microenvironment</subject><issn>2296-634X</issn><issn>2296-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpNkc1u3CAUha2oVRKleYEsKpbdeMrlx8CyjdokUqpsWik7hPH1xCmGKdiLvH2ZzDTqCu7RPecgvqa5ArrhXJvPo8cQNowysQEutKLqpDlnzHRtx8Xju__uZ81lKc-UUmBSSc1PmzNuoM6GnTe_HwK6BYkLC-ZClick0zyvEUnGskux1DmSmGJbZhcC2beSsMYtcQPG5F32U0yzq86c1u1TtW3X4JYpRZJGcvvj5itUrZYU_NC8H10oeHk8L5pf37_9vL5t7x9u7q6_3LeeGbG0Ar1Topd6RMGpBDr6HutjFXQDKOC9l6zrq6w1dEyPfmTcSOVRMBiUNPyiuTvkDsk9212eZpdfbHKTfRVS3lqXl8kHtAB8YMBBOo1C8q7vsYfBGK208LLjNevTIWuX058Vy2Lnqew_wUVMa7Gcai2lkRzqKjus-pxKyTi-VQO1e2b2lZndM7NHZtX08Zi_9jMOb5Z_hPhfHvOSWQ</recordid><startdate>20240719</startdate><enddate>20240719</enddate><creator>Cole-Skinner, Breanna</creator><creator>Andre, Nicole M</creator><creator>Blankenheim, Zachary</creator><creator>Root, Kate M</creator><creator>Jafri, Kisa</creator><creator>Simmons, Jr, Glenn E</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20240719</creationdate><title>Oleate alters the immune response in non-small cell lung adenocarcinoma through regulation of HMGB1 release</title><author>Cole-Skinner, Breanna ; Andre, Nicole M ; Blankenheim, Zachary ; Root, Kate M ; Jafri, Kisa ; Simmons, Jr, Glenn E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c294t-4eca74b58fe430510fcbe092716d1713bc526b10f881628fcf23957ce421d7593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>fatty acid</topic><topic>HMGB1 (high mobility group box 1)</topic><topic>immunotherapy</topic><topic>lung cancer</topic><topic>tumor microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cole-Skinner, Breanna</creatorcontrib><creatorcontrib>Andre, Nicole M</creatorcontrib><creatorcontrib>Blankenheim, Zachary</creatorcontrib><creatorcontrib>Root, Kate M</creatorcontrib><creatorcontrib>Jafri, Kisa</creatorcontrib><creatorcontrib>Simmons, Jr, Glenn E</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in cell and developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cole-Skinner, Breanna</au><au>Andre, Nicole M</au><au>Blankenheim, Zachary</au><au>Root, Kate M</au><au>Jafri, Kisa</au><au>Simmons, Jr, Glenn E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oleate alters the immune response in non-small cell lung adenocarcinoma through regulation of HMGB1 release</atitle><jtitle>Frontiers in cell and developmental biology</jtitle><addtitle>Front Cell Dev Biol</addtitle><date>2024-07-19</date><risdate>2024</risdate><volume>12</volume><spage>1348707</spage><pages>1348707-</pages><issn>2296-634X</issn><eissn>2296-634X</eissn><abstract>Cancer cell evasion of the immune response is critical to cancer development and metastases. Clinicians' ability to kickstart the immune system to target these rogue cells is an ever-growing area of research and medicine. This study delved into the relationship between lipid metabolism, High Mobility Group Box 1 protein (HMGB1)-a pro-inflammatory damage-associated molecular pattern protein-and immune regulation within non-small cell lung adenocarcinoma (NSCLC).
To address this question, we used a combination of proteomics, molecular biology, and bioinformatic techniques to investigate the relationship between fatty acids and immune signals within NSCLC.
We found that the expression of stearoyl CoA desaturase 1 (SCD1) was decreased in NSCLC tumors compared to normal tissues. This emphasized the critical role of lipid metabolism in tumor progression. Interestingly, monounsaturated fatty acid (MUFA) availability affected the expression of programmed death ligand-1 (PD-L1), a pivotal immune checkpoint target in lung cancer cells and immune cells, as well as HMGB1, suggesting a novel approach to modulating the immune response. This study uncovered a complex interplay between SCD1, PD-L1, and HMGB1, influencing the immunological sensitivity of tumors.
Our work underscores the critical importance of understanding the intricate relationships between lipid metabolism and immune modulation to develop more effective NSCLC treatments and personalized therapies. As we continue to explore these connections, we hope to contribute significantly to the ever-evolving field of cancer research, improving patient outcomes and advancing precision medicine in NSCLC.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>39100092</pmid><doi>10.3389/fcell.2024.1348707</doi><oa>free_for_read</oa></addata></record> |
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subjects | fatty acid HMGB1 (high mobility group box 1) immunotherapy lung cancer tumor microenvironment |
title | Oleate alters the immune response in non-small cell lung adenocarcinoma through regulation of HMGB1 release |
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