Multi-omic molecular profiling of lung cancer in COPD
Chronic obstructive pulmonary disease (COPD) is a known risk factor for developing lung cancer but the underlying mechanisms remain unknown. We hypothesise that the COPD stroma contains molecular mechanisms supporting tumourigenesis.We conducted an unbiased multi-omic analysis to identify gene expre...
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Veröffentlicht in: | The European respiratory journal 2018-07, Vol.52 (1), p.1702665-1702665 |
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creator | Sandri, Brian J Kaplan, Adam Hodgson, Shane W Peterson, Mark Avdulov, Svetlana Higgins, LeeAnn Markowski, Todd Yang, Ping Limper, Andrew H Griffin, Timothy J Bitterman, Peter Lock, Eric F Wendt, Chris H |
description | Chronic obstructive pulmonary disease (COPD) is a known risk factor for developing lung cancer but the underlying mechanisms remain unknown. We hypothesise that the COPD stroma contains molecular mechanisms supporting tumourigenesis.We conducted an unbiased multi-omic analysis to identify gene expression patterns that distinguish COPD stroma in patients with or without lung cancer. We obtained lung tissue from patients with COPD and lung cancer (tumour and adjacent non-malignant tissue) and those with COPD without lung cancer for profiling of proteomic and mRNA (both cytoplasmic and polyribosomal). We used the Joint and Individual Variation Explained (JIVE) method to integrate and analyse across the three datasets.JIVE identified eight latent patterns that robustly distinguished and separated the three groups of tissue samples (tumour, adjacent and control). Predictive variables that associated with the tumour, compared to adjacent stroma, were mainly represented in the transcriptomic data, whereas predictive variables associated with adjacent tissue, compared to controls, were represented at the translatomic level. Pathway analysis revealed extracellular matrix and phosphatidylinositol-4,5-bisphosphate 3-kinase-protein kinase B signalling pathways as important signals in the tumour adjacent stroma.The multi-omic approach distinguishes tumour adjacent stroma in lung cancer and reveals two stromal expression patterns associated with cancer. |
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We hypothesise that the COPD stroma contains molecular mechanisms supporting tumourigenesis.We conducted an unbiased multi-omic analysis to identify gene expression patterns that distinguish COPD stroma in patients with or without lung cancer. We obtained lung tissue from patients with COPD and lung cancer (tumour and adjacent non-malignant tissue) and those with COPD without lung cancer for profiling of proteomic and mRNA (both cytoplasmic and polyribosomal). We used the Joint and Individual Variation Explained (JIVE) method to integrate and analyse across the three datasets.JIVE identified eight latent patterns that robustly distinguished and separated the three groups of tissue samples (tumour, adjacent and control). Predictive variables that associated with the tumour, compared to adjacent stroma, were mainly represented in the transcriptomic data, whereas predictive variables associated with adjacent tissue, compared to controls, were represented at the translatomic level. Pathway analysis revealed extracellular matrix and phosphatidylinositol-4,5-bisphosphate 3-kinase-protein kinase B signalling pathways as important signals in the tumour adjacent stroma.The multi-omic approach distinguishes tumour adjacent stroma in lung cancer and reveals two stromal expression patterns associated with cancer.</description><identifier>ISSN: 0903-1936</identifier><identifier>EISSN: 1399-3003</identifier><identifier>DOI: 10.1183/13993003.02665-2017</identifier><identifier>PMID: 29794131</identifier><language>eng</language><publisher>England: European Respiratory Society Journals Ltd</publisher><subject>AKT protein ; Chronic obstructive pulmonary disease ; Extracellular matrix ; Gene expression ; Kinases ; Lung cancer ; Lung diseases ; Molecular modelling ; Obstructive lung disease ; Phosphatidylinositol 4,5-diphosphate ; Proteomics ; Signal transduction ; Stroma ; Tumorigenesis ; Tumors</subject><ispartof>The European respiratory journal, 2018-07, Vol.52 (1), p.1702665-1702665</ispartof><rights>The content of this work is not subject to copyright. Design and branding are copyright ©ERS 2018.</rights><rights>Copyright European Respiratory Society Journals Ltd. Jul 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-de7b6c3f9a6437ddae59e8106ecc7b0ca2bb54b55469b5ba9ad8de75143cf2323</citedby><cites>FETCH-LOGICAL-c433t-de7b6c3f9a6437ddae59e8106ecc7b0ca2bb54b55469b5ba9ad8de75143cf2323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29794131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sandri, Brian J</creatorcontrib><creatorcontrib>Kaplan, Adam</creatorcontrib><creatorcontrib>Hodgson, Shane W</creatorcontrib><creatorcontrib>Peterson, Mark</creatorcontrib><creatorcontrib>Avdulov, Svetlana</creatorcontrib><creatorcontrib>Higgins, LeeAnn</creatorcontrib><creatorcontrib>Markowski, Todd</creatorcontrib><creatorcontrib>Yang, Ping</creatorcontrib><creatorcontrib>Limper, Andrew H</creatorcontrib><creatorcontrib>Griffin, Timothy J</creatorcontrib><creatorcontrib>Bitterman, Peter</creatorcontrib><creatorcontrib>Lock, Eric F</creatorcontrib><creatorcontrib>Wendt, Chris H</creatorcontrib><title>Multi-omic molecular profiling of lung cancer in COPD</title><title>The European respiratory journal</title><addtitle>Eur Respir J</addtitle><description>Chronic obstructive pulmonary disease (COPD) is a known risk factor for developing lung cancer but the underlying mechanisms remain unknown. We hypothesise that the COPD stroma contains molecular mechanisms supporting tumourigenesis.We conducted an unbiased multi-omic analysis to identify gene expression patterns that distinguish COPD stroma in patients with or without lung cancer. We obtained lung tissue from patients with COPD and lung cancer (tumour and adjacent non-malignant tissue) and those with COPD without lung cancer for profiling of proteomic and mRNA (both cytoplasmic and polyribosomal). We used the Joint and Individual Variation Explained (JIVE) method to integrate and analyse across the three datasets.JIVE identified eight latent patterns that robustly distinguished and separated the three groups of tissue samples (tumour, adjacent and control). Predictive variables that associated with the tumour, compared to adjacent stroma, were mainly represented in the transcriptomic data, whereas predictive variables associated with adjacent tissue, compared to controls, were represented at the translatomic level. Pathway analysis revealed extracellular matrix and phosphatidylinositol-4,5-bisphosphate 3-kinase-protein kinase B signalling pathways as important signals in the tumour adjacent stroma.The multi-omic approach distinguishes tumour adjacent stroma in lung cancer and reveals two stromal expression patterns associated with cancer.</description><subject>AKT protein</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Extracellular matrix</subject><subject>Gene expression</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Lung diseases</subject><subject>Molecular modelling</subject><subject>Obstructive lung disease</subject><subject>Phosphatidylinositol 4,5-diphosphate</subject><subject>Proteomics</subject><subject>Signal transduction</subject><subject>Stroma</subject><subject>Tumorigenesis</subject><subject>Tumors</subject><issn>0903-1936</issn><issn>1399-3003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkU9LxDAQxYMo7rr6CQQpePHSNck0aXMRZP0LK-tBzyFN0zVL2qxpK_jtbd11UU8DM--9meGH0CnBU0IyuCQgBGAMU0w5ZzHFJN1D46EbD-19NMYCQ0wE8BE6apoVxoQnQA7RiIpUJATIGLGnzrU29pXVUeWd0Z1TIVoHX1pn62Xky8h1fdWq1iZEto5mi-ebY3RQKteYk22doNe725fZQzxf3D_OruexTgDauDBpzjWUQvV706JQhgmTEcyN1mmOtaJ5zpKcsYSLnOVKqCLrPYwkoEsKFCboapO77vLKFNrUbVBOroOtVPiUXln5d1LbN7n0H5JzklEBfcDFNiD49840raxso41zqja-ayTFCaMpw3jYdf5PuvJdqPv3elUGPCMC814FG5UOvmmCKXfHECwHLPIHi_zGIgcsvevs9x87zw8H-ALlOYd3</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Sandri, Brian J</creator><creator>Kaplan, Adam</creator><creator>Hodgson, Shane W</creator><creator>Peterson, Mark</creator><creator>Avdulov, Svetlana</creator><creator>Higgins, LeeAnn</creator><creator>Markowski, Todd</creator><creator>Yang, Ping</creator><creator>Limper, Andrew H</creator><creator>Griffin, Timothy J</creator><creator>Bitterman, Peter</creator><creator>Lock, Eric F</creator><creator>Wendt, Chris H</creator><general>European Respiratory Society Journals Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201807</creationdate><title>Multi-omic molecular profiling of lung cancer in COPD</title><author>Sandri, Brian J ; Kaplan, Adam ; Hodgson, Shane W ; Peterson, Mark ; Avdulov, Svetlana ; Higgins, LeeAnn ; Markowski, Todd ; Yang, Ping ; Limper, Andrew H ; Griffin, Timothy J ; Bitterman, Peter ; Lock, Eric F ; Wendt, Chris H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-de7b6c3f9a6437ddae59e8106ecc7b0ca2bb54b55469b5ba9ad8de75143cf2323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>AKT protein</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Extracellular matrix</topic><topic>Gene expression</topic><topic>Kinases</topic><topic>Lung cancer</topic><topic>Lung diseases</topic><topic>Molecular modelling</topic><topic>Obstructive lung disease</topic><topic>Phosphatidylinositol 4,5-diphosphate</topic><topic>Proteomics</topic><topic>Signal transduction</topic><topic>Stroma</topic><topic>Tumorigenesis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sandri, Brian J</creatorcontrib><creatorcontrib>Kaplan, Adam</creatorcontrib><creatorcontrib>Hodgson, Shane W</creatorcontrib><creatorcontrib>Peterson, Mark</creatorcontrib><creatorcontrib>Avdulov, Svetlana</creatorcontrib><creatorcontrib>Higgins, LeeAnn</creatorcontrib><creatorcontrib>Markowski, Todd</creatorcontrib><creatorcontrib>Yang, Ping</creatorcontrib><creatorcontrib>Limper, Andrew H</creatorcontrib><creatorcontrib>Griffin, Timothy J</creatorcontrib><creatorcontrib>Bitterman, Peter</creatorcontrib><creatorcontrib>Lock, Eric F</creatorcontrib><creatorcontrib>Wendt, Chris H</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sandri, Brian J</au><au>Kaplan, Adam</au><au>Hodgson, Shane W</au><au>Peterson, Mark</au><au>Avdulov, Svetlana</au><au>Higgins, LeeAnn</au><au>Markowski, Todd</au><au>Yang, Ping</au><au>Limper, Andrew H</au><au>Griffin, Timothy J</au><au>Bitterman, Peter</au><au>Lock, Eric F</au><au>Wendt, Chris H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-omic molecular profiling of lung cancer in COPD</atitle><jtitle>The European respiratory journal</jtitle><addtitle>Eur Respir J</addtitle><date>2018-07</date><risdate>2018</risdate><volume>52</volume><issue>1</issue><spage>1702665</spage><epage>1702665</epage><pages>1702665-1702665</pages><issn>0903-1936</issn><eissn>1399-3003</eissn><abstract>Chronic obstructive pulmonary disease (COPD) is a known risk factor for developing lung cancer but the underlying mechanisms remain unknown. We hypothesise that the COPD stroma contains molecular mechanisms supporting tumourigenesis.We conducted an unbiased multi-omic analysis to identify gene expression patterns that distinguish COPD stroma in patients with or without lung cancer. We obtained lung tissue from patients with COPD and lung cancer (tumour and adjacent non-malignant tissue) and those with COPD without lung cancer for profiling of proteomic and mRNA (both cytoplasmic and polyribosomal). We used the Joint and Individual Variation Explained (JIVE) method to integrate and analyse across the three datasets.JIVE identified eight latent patterns that robustly distinguished and separated the three groups of tissue samples (tumour, adjacent and control). Predictive variables that associated with the tumour, compared to adjacent stroma, were mainly represented in the transcriptomic data, whereas predictive variables associated with adjacent tissue, compared to controls, were represented at the translatomic level. Pathway analysis revealed extracellular matrix and phosphatidylinositol-4,5-bisphosphate 3-kinase-protein kinase B signalling pathways as important signals in the tumour adjacent stroma.The multi-omic approach distinguishes tumour adjacent stroma in lung cancer and reveals two stromal expression patterns associated with cancer.</abstract><cop>England</cop><pub>European Respiratory Society Journals Ltd</pub><pmid>29794131</pmid><doi>10.1183/13993003.02665-2017</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AKT protein Chronic obstructive pulmonary disease Extracellular matrix Gene expression Kinases Lung cancer Lung diseases Molecular modelling Obstructive lung disease Phosphatidylinositol 4,5-diphosphate Proteomics Signal transduction Stroma Tumorigenesis Tumors |
title | Multi-omic molecular profiling of lung cancer in COPD |
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