Unveiling Disrupted Lipid Metabolism in Benign Prostate Hyperplasia, Prostate Cancer, and Metastatic Patients: Insights from a Colombian Nested Case–Control Study
Prostate cancer is a significant global health concern, and its prevalence is increasing worldwide. Despite extensive research efforts, the complexity of the disease remains challenging with respect to fully understanding it. Metabolomics has emerged as a powerful approach to understanding prostate...
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Veröffentlicht in: | Cancers 2023-11, Vol.15 (22), p.5465 |
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description | Prostate cancer is a significant global health concern, and its prevalence is increasing worldwide. Despite extensive research efforts, the complexity of the disease remains challenging with respect to fully understanding it. Metabolomics has emerged as a powerful approach to understanding prostate cancer by assessing comprehensive metabolite profiles in biological samples. In this study, metabolic profiles of patients with benign prostatic hyperplasia (BPH), prostate cancer (PCa), and metastatic prostate cancer (Met) were characterized using an untargeted approach that included metabolomics and lipidomics via liquid chromatography and gas chromatography coupled with high-resolution mass spectrometry. Comparative analysis among these groups revealed distinct metabolic profiles, primarily associated with lipid biosynthetic pathways, such as biosynthesis of unsaturated fatty acids, fatty acid degradation and elongation, and sphingolipid and linoleic acid metabolism. PCa patients showed lower levels of amino acids, glycerolipids, glycerophospholipids, sphingolipids, and carnitines compared to BPH patients. Compared to Met patients, PCa patients had reduced metabolites in the glycerolipid, glycerophospholipid, and sphingolipid groups, along with increased amino acids and carbohydrates. These altered metabolic profiles provide insights into the underlying pathways of prostate cancer’s progression, potentially aiding the development of new diagnostic, and therapeutic strategies. |
doi_str_mv | 10.3390/cancers15225465 |
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Despite extensive research efforts, the complexity of the disease remains challenging with respect to fully understanding it. Metabolomics has emerged as a powerful approach to understanding prostate cancer by assessing comprehensive metabolite profiles in biological samples. In this study, metabolic profiles of patients with benign prostatic hyperplasia (BPH), prostate cancer (PCa), and metastatic prostate cancer (Met) were characterized using an untargeted approach that included metabolomics and lipidomics via liquid chromatography and gas chromatography coupled with high-resolution mass spectrometry. Comparative analysis among these groups revealed distinct metabolic profiles, primarily associated with lipid biosynthetic pathways, such as biosynthesis of unsaturated fatty acids, fatty acid degradation and elongation, and sphingolipid and linoleic acid metabolism. PCa patients showed lower levels of amino acids, glycerolipids, glycerophospholipids, sphingolipids, and carnitines compared to BPH patients. Compared to Met patients, PCa patients had reduced metabolites in the glycerolipid, glycerophospholipid, and sphingolipid groups, along with increased amino acids and carbohydrates. These altered metabolic profiles provide insights into the underlying pathways of prostate cancer’s progression, potentially aiding the development of new diagnostic, and therapeutic strategies.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15225465</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Amino acids ; Benign ; Biomarkers ; Biopsy ; Cancer ; Cancer patients ; Carbohydrates ; Chemotherapy ; Comparative analysis ; Development and progression ; Disease ; Fatty acids ; Gas chromatography ; Health aspects ; Hyperplasia ; Instrument industry ; Linoleic acid ; Lipid metabolism ; Lipids ; Liquid chromatography ; Mass spectroscopy ; Metabolism ; Metabolites ; Metabolomics ; Metastases ; Metastasis ; Mortality ; Oncology, Experimental ; Patients ; Physiology ; Prostate cancer ; Public health ; Radiation therapy ; Sphingolipids ; Unsaturated fatty acids ; Urology ; World health</subject><ispartof>Cancers, 2023-11, Vol.15 (22), p.5465</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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><citedby>FETCH-LOGICAL-c410t-23a184a514b2f403daf06ef51723d8024606e8fd080321569beabcb7f6ece6353</citedby><cites>FETCH-LOGICAL-c410t-23a184a514b2f403daf06ef51723d8024606e8fd080321569beabcb7f6ece6353</cites><orcidid>0000-0001-6945-8261 ; 0000-0001-7011-9566 ; 0009-0008-9136-9626 ; 0000-0003-0783-5839 ; 0000-0001-6043-1521 ; 0000-0002-8198-726X</orcidid></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></links><search><creatorcontrib>Pardo-Rodriguez, Daniel</creatorcontrib><creatorcontrib>Santamaría-Torres, Mary</creatorcontrib><creatorcontrib>Salinas, Angela</creatorcontrib><creatorcontrib>Jiménez-Charris, Eliécer</creatorcontrib><creatorcontrib>Mosquera, Mildrey</creatorcontrib><creatorcontrib>Cala, Mónica P</creatorcontrib><creatorcontrib>García-Perdomo, Herney Andrés</creatorcontrib><title>Unveiling Disrupted Lipid Metabolism in Benign Prostate Hyperplasia, Prostate Cancer, and Metastatic Patients: Insights from a Colombian Nested Case–Control Study</title><title>Cancers</title><description>Prostate cancer is a significant global health concern, and its prevalence is increasing worldwide. Despite extensive research efforts, the complexity of the disease remains challenging with respect to fully understanding it. Metabolomics has emerged as a powerful approach to understanding prostate cancer by assessing comprehensive metabolite profiles in biological samples. In this study, metabolic profiles of patients with benign prostatic hyperplasia (BPH), prostate cancer (PCa), and metastatic prostate cancer (Met) were characterized using an untargeted approach that included metabolomics and lipidomics via liquid chromatography and gas chromatography coupled with high-resolution mass spectrometry. Comparative analysis among these groups revealed distinct metabolic profiles, primarily associated with lipid biosynthetic pathways, such as biosynthesis of unsaturated fatty acids, fatty acid degradation and elongation, and sphingolipid and linoleic acid metabolism. PCa patients showed lower levels of amino acids, glycerolipids, glycerophospholipids, sphingolipids, and carnitines compared to BPH patients. Compared to Met patients, PCa patients had reduced metabolites in the glycerolipid, glycerophospholipid, and sphingolipid groups, along with increased amino acids and carbohydrates. These altered metabolic profiles provide insights into the underlying pathways of prostate cancer’s progression, potentially aiding the development of new diagnostic, and therapeutic strategies.</description><subject>Amino acids</subject><subject>Benign</subject><subject>Biomarkers</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Cancer patients</subject><subject>Carbohydrates</subject><subject>Chemotherapy</subject><subject>Comparative analysis</subject><subject>Development and progression</subject><subject>Disease</subject><subject>Fatty acids</subject><subject>Gas chromatography</subject><subject>Health aspects</subject><subject>Hyperplasia</subject><subject>Instrument industry</subject><subject>Linoleic acid</subject><subject>Lipid metabolism</subject><subject>Lipids</subject><subject>Liquid chromatography</subject><subject>Mass spectroscopy</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Oncology, Experimental</subject><subject>Patients</subject><subject>Physiology</subject><subject>Prostate cancer</subject><subject>Public health</subject><subject>Radiation therapy</subject><subject>Sphingolipids</subject><subject>Unsaturated fatty acids</subject><subject>Urology</subject><subject>World health</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptks1u1DAUhSMEElXpmq0lNiw6rf-TYVdSoJUGqARdR45zPbhy7GA7SLPjHfoKfTKeBKeDVKiwJf8cfef6yLpV9ZLgE8bW-FQrryEmIigVXIon1QHFNV1JueZP_zo_r45SusFlMEZqWR9Ud9f-B1hn_Rad2xTnKcOANnayA_oIWfXB2TQi69Fb8Hbr0VUMKasM6GI3QZycSlYdP6jtfY5jpPzev6hWo6uygs_pDbr0yW6_5YRMDCNSqA0ujL1VHn2CtLzdqgS_ft62wecYHPqS52H3onpmlEtw9Gc_rK7fv_vaXqw2nz9ctmebleYE5xVlijRcCcJ7ajhmgzJYghGkpmxoMOWyXBsz4AYzSoRc96B63ddGggbJBDusXu_rTjF8n0uebrRJg3PKQ5hTR5s1a7jgnBT01SP0JszRl3T3FGZ1w-gDtVUOOutNyFHppWh3VteckUaQhTr5D1XmAKPVwYOxRf_HcLo36PLvKYLppmhHFXcdwd3SD92jfmC_Af-HqtA</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Pardo-Rodriguez, Daniel</creator><creator>Santamaría-Torres, Mary</creator><creator>Salinas, Angela</creator><creator>Jiménez-Charris, Eliécer</creator><creator>Mosquera, Mildrey</creator><creator>Cala, Mónica P</creator><creator>García-Perdomo, Herney Andrés</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</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><orcidid>https://orcid.org/0000-0001-6945-8261</orcidid><orcidid>https://orcid.org/0000-0001-7011-9566</orcidid><orcidid>https://orcid.org/0009-0008-9136-9626</orcidid><orcidid>https://orcid.org/0000-0003-0783-5839</orcidid><orcidid>https://orcid.org/0000-0001-6043-1521</orcidid><orcidid>https://orcid.org/0000-0002-8198-726X</orcidid></search><sort><creationdate>20231101</creationdate><title>Unveiling Disrupted Lipid Metabolism in Benign Prostate Hyperplasia, Prostate Cancer, and Metastatic Patients: Insights from a Colombian Nested Case–Control Study</title><author>Pardo-Rodriguez, Daniel ; 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Despite extensive research efforts, the complexity of the disease remains challenging with respect to fully understanding it. Metabolomics has emerged as a powerful approach to understanding prostate cancer by assessing comprehensive metabolite profiles in biological samples. In this study, metabolic profiles of patients with benign prostatic hyperplasia (BPH), prostate cancer (PCa), and metastatic prostate cancer (Met) were characterized using an untargeted approach that included metabolomics and lipidomics via liquid chromatography and gas chromatography coupled with high-resolution mass spectrometry. Comparative analysis among these groups revealed distinct metabolic profiles, primarily associated with lipid biosynthetic pathways, such as biosynthesis of unsaturated fatty acids, fatty acid degradation and elongation, and sphingolipid and linoleic acid metabolism. PCa patients showed lower levels of amino acids, glycerolipids, glycerophospholipids, sphingolipids, and carnitines compared to BPH patients. Compared to Met patients, PCa patients had reduced metabolites in the glycerolipid, glycerophospholipid, and sphingolipid groups, along with increased amino acids and carbohydrates. These altered metabolic profiles provide insights into the underlying pathways of prostate cancer’s progression, potentially aiding the development of new diagnostic, and therapeutic strategies.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/cancers15225465</doi><orcidid>https://orcid.org/0000-0001-6945-8261</orcidid><orcidid>https://orcid.org/0000-0001-7011-9566</orcidid><orcidid>https://orcid.org/0009-0008-9136-9626</orcidid><orcidid>https://orcid.org/0000-0003-0783-5839</orcidid><orcidid>https://orcid.org/0000-0001-6043-1521</orcidid><orcidid>https://orcid.org/0000-0002-8198-726X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amino acids Benign Biomarkers Biopsy Cancer Cancer patients Carbohydrates Chemotherapy Comparative analysis Development and progression Disease Fatty acids Gas chromatography Health aspects Hyperplasia Instrument industry Linoleic acid Lipid metabolism Lipids Liquid chromatography Mass spectroscopy Metabolism Metabolites Metabolomics Metastases Metastasis Mortality Oncology, Experimental Patients Physiology Prostate cancer Public health Radiation therapy Sphingolipids Unsaturated fatty acids Urology World health |
title | Unveiling Disrupted Lipid Metabolism in Benign Prostate Hyperplasia, Prostate Cancer, and Metastatic Patients: Insights from a Colombian Nested Case–Control Study |
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