Generation of in situ sequencing based OncoMaps to spatially resolve gene expression profiles of diagnostic and prognostic markers in breast cancer
Gene expression analysis of breast cancer largely relies on homogenized tissue samples. Due to the high degree of cellular and molecular heterogeneity of tumor tissues, bulk tissue-based analytical approaches can only provide very limited system-level information about different signaling mechanisms...
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description | Gene expression analysis of breast cancer largely relies on homogenized tissue samples. Due to the high degree of cellular and molecular heterogeneity of tumor tissues, bulk tissue-based analytical approaches can only provide very limited system-level information about different signaling mechanisms and cellular interactions within the complex tissue context.
We describe an analytical approach using in situ sequencing (ISS), enabling highly multiplexed, spatially and morphologically resolved gene expression profiling. Ninety-one genes including prognostic and predictive marker profiles, as well as genes involved in specific cellular pathways were mapped within whole breast cancer tissue sections, covering luminal A/B-like, HER2-positive and triple negative tumors. Finally, all these features were combined and assembled into a molecular-morphological OncoMap for each tumor tissue.
Our in situ approach spatially revealed intratumoral heterogeneity with regard to tumor subtype as well as to the OncotypeDX recurrence score and even uncovered areas of minor cellular subpopulations. Since ISS-resolved molecular profiles are linked to their histological context, a deeper analysis of the core and periphery of tumor foci enabled identification of specific gene expression patterns associated with these morphologically relevant regions.
ISS generated OncoMaps represent useful tools to extend our general understanding of the biological processes behind tumor progression and can further support the identification of novel therapeutical targets as well as refine tumor diagnostics.
Swedish Cancerfonden, UCAN, Vetenskapsrådet, Cancer Genomics Netherlands, Iris, Stig och Gerry Castenbäcks Stiftelse, BRECT, PCM Program, King Gustaf V Jubilee Fund, BRO, KI and Stockholm County Council, Alice Wallenberg Foundation. |
doi_str_mv | 10.1016/j.ebiom.2019.09.009 |
format | Article |
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We describe an analytical approach using in situ sequencing (ISS), enabling highly multiplexed, spatially and morphologically resolved gene expression profiling. Ninety-one genes including prognostic and predictive marker profiles, as well as genes involved in specific cellular pathways were mapped within whole breast cancer tissue sections, covering luminal A/B-like, HER2-positive and triple negative tumors. Finally, all these features were combined and assembled into a molecular-morphological OncoMap for each tumor tissue.
Our in situ approach spatially revealed intratumoral heterogeneity with regard to tumor subtype as well as to the OncotypeDX recurrence score and even uncovered areas of minor cellular subpopulations. Since ISS-resolved molecular profiles are linked to their histological context, a deeper analysis of the core and periphery of tumor foci enabled identification of specific gene expression patterns associated with these morphologically relevant regions.
ISS generated OncoMaps represent useful tools to extend our general understanding of the biological processes behind tumor progression and can further support the identification of novel therapeutical targets as well as refine tumor diagnostics.
Swedish Cancerfonden, UCAN, Vetenskapsrådet, Cancer Genomics Netherlands, Iris, Stig och Gerry Castenbäcks Stiftelse, BRECT, PCM Program, King Gustaf V Jubilee Fund, BRO, KI and Stockholm County Council, Alice Wallenberg Foundation.</description><identifier>ISSN: 2352-3964</identifier><identifier>EISSN: 2352-3964</identifier><identifier>DOI: 10.1016/j.ebiom.2019.09.009</identifier><identifier>PMID: 31526717</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Biomarkers, Tumor ; Breast cancer ; Breast Neoplasms - diagnosis ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - mortality ; Cell Line, Tumor ; Diagnostic ; Female ; Gene expression analysis ; Gene Expression Profiling - methods ; Gene Expression Regulation, Neoplastic ; Humans ; Immunohistochemistry ; Oncogenes ; Polymorphism, Single Nucleotide ; Prognosis ; Prognostic ; Reproducibility of Results ; Research paper ; Transcriptome ; Tumor heterogeneity</subject><ispartof>EBioMedicine, 2019-10, Vol.48, p.212-223</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.</rights><rights>2019 The Authors 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-585956ff1760bd59a42d521ac654bd0015321eee03dc83f6e85c0cecc025328b3</citedby><cites>FETCH-LOGICAL-c571t-585956ff1760bd59a42d521ac654bd0015321eee03dc83f6e85c0cecc025328b3</cites><orcidid>0000-0001-5526-1847</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/PMC6838368/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838368/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31526717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-176757$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-492452$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:142197250$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Svedlund, Jessica</creatorcontrib><creatorcontrib>Strell, Carina</creatorcontrib><creatorcontrib>Qian, Xiaoyan</creatorcontrib><creatorcontrib>Zilkens, Kilian J.C.</creatorcontrib><creatorcontrib>Tobin, Nicholas P.</creatorcontrib><creatorcontrib>Bergh, Jonas</creatorcontrib><creatorcontrib>Sieuwerts, Anieta M.</creatorcontrib><creatorcontrib>Nilsson, Mats</creatorcontrib><title>Generation of in situ sequencing based OncoMaps to spatially resolve gene expression profiles of diagnostic and prognostic markers in breast cancer</title><title>EBioMedicine</title><addtitle>EBioMedicine</addtitle><description>Gene expression analysis of breast cancer largely relies on homogenized tissue samples. Due to the high degree of cellular and molecular heterogeneity of tumor tissues, bulk tissue-based analytical approaches can only provide very limited system-level information about different signaling mechanisms and cellular interactions within the complex tissue context.
We describe an analytical approach using in situ sequencing (ISS), enabling highly multiplexed, spatially and morphologically resolved gene expression profiling. Ninety-one genes including prognostic and predictive marker profiles, as well as genes involved in specific cellular pathways were mapped within whole breast cancer tissue sections, covering luminal A/B-like, HER2-positive and triple negative tumors. Finally, all these features were combined and assembled into a molecular-morphological OncoMap for each tumor tissue.
Our in situ approach spatially revealed intratumoral heterogeneity with regard to tumor subtype as well as to the OncotypeDX recurrence score and even uncovered areas of minor cellular subpopulations. Since ISS-resolved molecular profiles are linked to their histological context, a deeper analysis of the core and periphery of tumor foci enabled identification of specific gene expression patterns associated with these morphologically relevant regions.
ISS generated OncoMaps represent useful tools to extend our general understanding of the biological processes behind tumor progression and can further support the identification of novel therapeutical targets as well as refine tumor diagnostics.
Swedish Cancerfonden, UCAN, Vetenskapsrådet, Cancer Genomics Netherlands, Iris, Stig och Gerry Castenbäcks Stiftelse, BRECT, PCM Program, King Gustaf V Jubilee Fund, BRO, KI and Stockholm County Council, Alice Wallenberg Foundation.</description><subject>Biomarkers, Tumor</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - diagnosis</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - mortality</subject><subject>Cell Line, Tumor</subject><subject>Diagnostic</subject><subject>Female</subject><subject>Gene expression analysis</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Oncogenes</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prognosis</subject><subject>Prognostic</subject><subject>Reproducibility of Results</subject><subject>Research paper</subject><subject>Transcriptome</subject><subject>Tumor heterogeneity</subject><issn>2352-3964</issn><issn>2352-3964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqNkttu1DAQhi0EotXSJ0BCvuSCLD7EOVyAVBUoSEW9AW4tx5kEb7N28CQLfQ5eGKe7rdoLEJIVH-abfyb2T8hzztac8eL1Zg2NC9u1YLxeszRY_YgcC6lEJusif3xvfUROEDeMMa7ydFg9JUeSK1GUvDwmv8_BQzSTC56GjjpP0U0zRfgxg7fO97QxCC299DZ8NiPSKVAcE2-G4ZpGwDDsgPZJhMKvMe1xURpj6NwAuEi2zvQ-4OQsNb5dQrfbrYlXEHEp2kQwOFFrvIX4jDzpzIBwcphX5OuH91_OPmYXl-efzk4vMqtKPmWqUrUquo6XBWtaVZtctEpwYwuVN-3yu1JwAGCytZXsCqiUZRasZSJFqkauSLbXxZ8wzo0eo0stXetgnD4cXaUV6Lws0j0m_tVf-Xfu26kOsdfzrPNa5Er8H46zTv2Xqkz42z2e2C20FvwUzfAg62HEu--6DztdVLKS6bMiLw8CMaTXw0lvHVoYBuMhzKiFqEVdVfymltyjNgbECN1dGc704i-90Tf-0ou_NEuD1Snrxf0O73Ju3ZSAN3sA0qvtHESN1iUbQesi2Em3wf2zwB-sUeee</recordid><startdate>20191001</startdate><enddate>20191001</enddate><creator>Svedlund, Jessica</creator><creator>Strell, Carina</creator><creator>Qian, Xiaoyan</creator><creator>Zilkens, Kilian J.C.</creator><creator>Tobin, Nicholas P.</creator><creator>Bergh, Jonas</creator><creator>Sieuwerts, Anieta M.</creator><creator>Nilsson, Mats</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>ABAVF</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DG7</scope><scope>ZZAVC</scope><scope>DF2</scope><orcidid>https://orcid.org/0000-0001-5526-1847</orcidid></search><sort><creationdate>20191001</creationdate><title>Generation of in situ sequencing based OncoMaps to spatially resolve gene expression profiles of diagnostic and prognostic markers in breast cancer</title><author>Svedlund, Jessica ; Strell, Carina ; Qian, Xiaoyan ; Zilkens, Kilian J.C. ; Tobin, Nicholas P. ; Bergh, Jonas ; Sieuwerts, Anieta M. ; Nilsson, Mats</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-585956ff1760bd59a42d521ac654bd0015321eee03dc83f6e85c0cecc025328b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biomarkers, Tumor</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - diagnosis</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - mortality</topic><topic>Cell Line, Tumor</topic><topic>Diagnostic</topic><topic>Female</topic><topic>Gene expression analysis</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Oncogenes</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prognosis</topic><topic>Prognostic</topic><topic>Reproducibility of Results</topic><topic>Research paper</topic><topic>Transcriptome</topic><topic>Tumor heterogeneity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Svedlund, Jessica</creatorcontrib><creatorcontrib>Strell, Carina</creatorcontrib><creatorcontrib>Qian, Xiaoyan</creatorcontrib><creatorcontrib>Zilkens, Kilian J.C.</creatorcontrib><creatorcontrib>Tobin, Nicholas P.</creatorcontrib><creatorcontrib>Bergh, Jonas</creatorcontrib><creatorcontrib>Sieuwerts, Anieta M.</creatorcontrib><creatorcontrib>Nilsson, Mats</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Stockholms universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Stockholms universitet</collection><collection>SwePub Articles full text</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>EBioMedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Svedlund, Jessica</au><au>Strell, Carina</au><au>Qian, Xiaoyan</au><au>Zilkens, Kilian J.C.</au><au>Tobin, Nicholas P.</au><au>Bergh, Jonas</au><au>Sieuwerts, Anieta M.</au><au>Nilsson, Mats</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of in situ sequencing based OncoMaps to spatially resolve gene expression profiles of diagnostic and prognostic markers in breast cancer</atitle><jtitle>EBioMedicine</jtitle><addtitle>EBioMedicine</addtitle><date>2019-10-01</date><risdate>2019</risdate><volume>48</volume><spage>212</spage><epage>223</epage><pages>212-223</pages><issn>2352-3964</issn><eissn>2352-3964</eissn><abstract>Gene expression analysis of breast cancer largely relies on homogenized tissue samples. Due to the high degree of cellular and molecular heterogeneity of tumor tissues, bulk tissue-based analytical approaches can only provide very limited system-level information about different signaling mechanisms and cellular interactions within the complex tissue context.
We describe an analytical approach using in situ sequencing (ISS), enabling highly multiplexed, spatially and morphologically resolved gene expression profiling. Ninety-one genes including prognostic and predictive marker profiles, as well as genes involved in specific cellular pathways were mapped within whole breast cancer tissue sections, covering luminal A/B-like, HER2-positive and triple negative tumors. Finally, all these features were combined and assembled into a molecular-morphological OncoMap for each tumor tissue.
Our in situ approach spatially revealed intratumoral heterogeneity with regard to tumor subtype as well as to the OncotypeDX recurrence score and even uncovered areas of minor cellular subpopulations. Since ISS-resolved molecular profiles are linked to their histological context, a deeper analysis of the core and periphery of tumor foci enabled identification of specific gene expression patterns associated with these morphologically relevant regions.
ISS generated OncoMaps represent useful tools to extend our general understanding of the biological processes behind tumor progression and can further support the identification of novel therapeutical targets as well as refine tumor diagnostics.
Swedish Cancerfonden, UCAN, Vetenskapsrådet, Cancer Genomics Netherlands, Iris, Stig och Gerry Castenbäcks Stiftelse, BRECT, PCM Program, King Gustaf V Jubilee Fund, BRO, KI and Stockholm County Council, Alice Wallenberg Foundation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31526717</pmid><doi>10.1016/j.ebiom.2019.09.009</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5526-1847</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers, Tumor Breast cancer Breast Neoplasms - diagnosis Breast Neoplasms - genetics Breast Neoplasms - metabolism Breast Neoplasms - mortality Cell Line, Tumor Diagnostic Female Gene expression analysis Gene Expression Profiling - methods Gene Expression Regulation, Neoplastic Humans Immunohistochemistry Oncogenes Polymorphism, Single Nucleotide Prognosis Prognostic Reproducibility of Results Research paper Transcriptome Tumor heterogeneity |
title | Generation of in situ sequencing based OncoMaps to spatially resolve gene expression profiles of diagnostic and prognostic markers in breast cancer |
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