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Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion
Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to...
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Published in: | Neoplasia (New York, N.Y.) N.Y.), 2019-05, Vol.21 (5), p.482-493 |
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creator | Hao, Jing Zeltz, Cédric Pintilie, Melania Li, Quan Sakashita, Shingo Wang, Tao Cabanero, Michael Martins-Filho, Sebastiao N. Wang, Dennis Y. Pasko, Elena Venkat, Kalpana Joseph, Joella Raghavan, Vibha Zhu, Chang-Qi Wang, Yu-Hui Moghal, Nadeem Tsao, Ming-Sound Navab, Roya |
description | Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value < .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. In summary, our studies show that functional heterogeneity in CAF plays key role in promoting cancer cell invasion in NSCLC. |
doi_str_mv | 10.1016/j.neo.2019.03.009 |
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Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value < .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. In summary, our studies show that functional heterogeneity in CAF plays key role in promoting cancer cell invasion in NSCLC.</description><identifier>ISSN: 1476-5586</identifier><identifier>EISSN: 1476-5586</identifier><identifier>DOI: 10.1016/j.neo.2019.03.009</identifier><identifier>PMID: 30978569</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cancer-Associated Fibroblasts - metabolism ; Cancer-Associated Fibroblasts - pathology ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Movement ; Cell Proliferation ; Cohort Studies ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Humans ; Lung Neoplasms - genetics ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Male ; Mice ; Mice, SCID ; Neoplasm Invasiveness ; Neoplasm Recurrence, Local - genetics ; Neoplasm Recurrence, Local - metabolism ; Neoplasm Recurrence, Local - pathology ; Prognosis ; Sialyltransferases - genetics ; Sialyltransferases - metabolism ; Stromal Cells - metabolism ; Stromal Cells - pathology ; Survival Rate ; Tumor Cells, Cultured ; Xenograft Model Antitumor Assays</subject><ispartof>Neoplasia (New York, N.Y.), 2019-05, Vol.21 (5), p.482-493</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-8fd92a98c39446b6327599c70258273c509082ba266859b98384a97eac5f99f83</citedby><cites>FETCH-LOGICAL-c528t-8fd92a98c39446b6327599c70258273c509082ba266859b98384a97eac5f99f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1476558618305748$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3536,27905,27906,45761</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30978569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hao, Jing</creatorcontrib><creatorcontrib>Zeltz, Cédric</creatorcontrib><creatorcontrib>Pintilie, Melania</creatorcontrib><creatorcontrib>Li, Quan</creatorcontrib><creatorcontrib>Sakashita, Shingo</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Cabanero, Michael</creatorcontrib><creatorcontrib>Martins-Filho, Sebastiao N.</creatorcontrib><creatorcontrib>Wang, Dennis Y.</creatorcontrib><creatorcontrib>Pasko, Elena</creatorcontrib><creatorcontrib>Venkat, Kalpana</creatorcontrib><creatorcontrib>Joseph, Joella</creatorcontrib><creatorcontrib>Raghavan, Vibha</creatorcontrib><creatorcontrib>Zhu, Chang-Qi</creatorcontrib><creatorcontrib>Wang, Yu-Hui</creatorcontrib><creatorcontrib>Moghal, Nadeem</creatorcontrib><creatorcontrib>Tsao, Ming-Sound</creatorcontrib><creatorcontrib>Navab, Roya</creatorcontrib><title>Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion</title><title>Neoplasia (New York, N.Y.)</title><addtitle>Neoplasia</addtitle><description>Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value < .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. In summary, our studies show that functional heterogeneity in CAF plays key role in promoting cancer cell invasion in NSCLC.</description><subject>Animals</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer-Associated Fibroblasts - metabolism</subject><subject>Cancer-Associated Fibroblasts - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Cohort Studies</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Recurrence, Local - genetics</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Prognosis</subject><subject>Sialyltransferases - genetics</subject><subject>Sialyltransferases - metabolism</subject><subject>Stromal Cells - metabolism</subject><subject>Stromal Cells - pathology</subject><subject>Survival Rate</subject><subject>Tumor Cells, Cultured</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1476-5586</issn><issn>1476-5586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kUGO1DAQRSMEYoaBA7BBXrJJcJzYscWq1TDQUgsQPaytilMZ3ErixnZaghV34AqcjJPgngwDKzZ2qfTfL1X9LHta0qKkpXixLyZ0BaOlKmhVUKruZedl3Yiccynu_1OfZY9C2NPElE3zMDurqGokF-o8-7n-DB5MRG-_QbRuIq4nr2yIdjKRfHCHebhph1N_Dd7YyY2Qr0JwxkLEjlza1rt2gBAD6b0byTs3_fr-YzfCMJA1pmc7T9d_WfIRjwhDIKlyA5LeebK7krvNihE7Jd1k0C_gZjpCSMMfZw_6ROCT2_8i-3T5-mr9Nt--f7NZr7a54UzGXPadYqCkqVRdi1ZUrOFKmYYyLllTGU4VlawFJoTkqlWykjWoBsHwXqleVhfZZvHtHOz1wdsR_FftwOqbhvPXGny0ZkDdITJVcuhaWddGtK1M7qbkAqgQqjfJ6_nidfDuy4wh6tEGk7aClNkcNGNUcdVUnCVpuUiNdyF47O9Gl1SfgtZ7nSB9ClrTSqegE_Ps1n5uR-zuiD_JJsHLRYDpYEeLXgdjMd22sx5NTBvZ_9j_Bn-queM</recordid><startdate>201905</startdate><enddate>201905</enddate><creator>Hao, Jing</creator><creator>Zeltz, Cédric</creator><creator>Pintilie, Melania</creator><creator>Li, Quan</creator><creator>Sakashita, Shingo</creator><creator>Wang, Tao</creator><creator>Cabanero, Michael</creator><creator>Martins-Filho, Sebastiao N.</creator><creator>Wang, Dennis Y.</creator><creator>Pasko, Elena</creator><creator>Venkat, Kalpana</creator><creator>Joseph, Joella</creator><creator>Raghavan, Vibha</creator><creator>Zhu, Chang-Qi</creator><creator>Wang, Yu-Hui</creator><creator>Moghal, Nadeem</creator><creator>Tsao, Ming-Sound</creator><creator>Navab, Roya</creator><general>Elsevier Inc</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>DOA</scope></search><sort><creationdate>201905</creationdate><title>Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion</title><author>Hao, Jing ; Zeltz, Cédric ; Pintilie, Melania ; Li, Quan ; Sakashita, Shingo ; Wang, Tao ; Cabanero, Michael ; Martins-Filho, Sebastiao N. ; Wang, Dennis Y. ; Pasko, Elena ; Venkat, Kalpana ; Joseph, Joella ; Raghavan, Vibha ; Zhu, Chang-Qi ; Wang, Yu-Hui ; Moghal, Nadeem ; Tsao, Ming-Sound ; Navab, Roya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-8fd92a98c39446b6327599c70258273c509082ba266859b98384a97eac5f99f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer-Associated Fibroblasts - metabolism</topic><topic>Cancer-Associated Fibroblasts - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Cohort Studies</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Recurrence, Local - genetics</topic><topic>Neoplasm Recurrence, Local - metabolism</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Prognosis</topic><topic>Sialyltransferases - genetics</topic><topic>Sialyltransferases - metabolism</topic><topic>Stromal Cells - metabolism</topic><topic>Stromal Cells - pathology</topic><topic>Survival Rate</topic><topic>Tumor Cells, Cultured</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hao, Jing</creatorcontrib><creatorcontrib>Zeltz, Cédric</creatorcontrib><creatorcontrib>Pintilie, Melania</creatorcontrib><creatorcontrib>Li, Quan</creatorcontrib><creatorcontrib>Sakashita, Shingo</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Cabanero, Michael</creatorcontrib><creatorcontrib>Martins-Filho, Sebastiao N.</creatorcontrib><creatorcontrib>Wang, Dennis Y.</creatorcontrib><creatorcontrib>Pasko, Elena</creatorcontrib><creatorcontrib>Venkat, Kalpana</creatorcontrib><creatorcontrib>Joseph, Joella</creatorcontrib><creatorcontrib>Raghavan, Vibha</creatorcontrib><creatorcontrib>Zhu, Chang-Qi</creatorcontrib><creatorcontrib>Wang, Yu-Hui</creatorcontrib><creatorcontrib>Moghal, Nadeem</creatorcontrib><creatorcontrib>Tsao, Ming-Sound</creatorcontrib><creatorcontrib>Navab, Roya</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>Directory of Open Access Journals</collection><jtitle>Neoplasia (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hao, Jing</au><au>Zeltz, Cédric</au><au>Pintilie, Melania</au><au>Li, Quan</au><au>Sakashita, Shingo</au><au>Wang, Tao</au><au>Cabanero, Michael</au><au>Martins-Filho, Sebastiao N.</au><au>Wang, Dennis Y.</au><au>Pasko, Elena</au><au>Venkat, Kalpana</au><au>Joseph, Joella</au><au>Raghavan, Vibha</au><au>Zhu, Chang-Qi</au><au>Wang, Yu-Hui</au><au>Moghal, Nadeem</au><au>Tsao, Ming-Sound</au><au>Navab, Roya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion</atitle><jtitle>Neoplasia (New York, N.Y.)</jtitle><addtitle>Neoplasia</addtitle><date>2019-05</date><risdate>2019</risdate><volume>21</volume><issue>5</issue><spage>482</spage><epage>493</epage><pages>482-493</pages><issn>1476-5586</issn><eissn>1476-5586</eissn><abstract>Carcinoma-associated fibroblasts (CAFs) are abundant stromal cells in tumor microenvironment that are critically involved in cancer progression. Contrasting reports have shown that CAFs can have either pro- or antitumorigenic roles, indicating that CAFs are functionally heterogeneous. Therefore, to precisely target the cancer-promoting CAF subsets, it is necessary to identify specific markers to define these subpopulations and understand their functions. We characterized two CAFs subsets from 28 non–small cell lung cancer (NSCLC) patient tumors that were scored and classified based on desmoplasia [mainly characterized by proliferating CAFs; high desmoplastic CAFs (HD-CAF; n = 15) and low desmoplastic CAFs (LD-CAF; n = 13)], which is an independent prognostic factor. Here, for the first time, we demonstrate that HD-CAFs and LD-CAFs show different tumor-promoting abilities. HD-CAFs showed higher rate of collagen matrix remodeling, invasion, and tumor growth compared to LD-CAFs. Transcriptomic analysis identified 13 genes that were differentially significant (fold ≥1.5; adjusted P value < .1) between HD-CAFs and LD-CAFs. The top upregulated differentially expressed gene, ST8SIA2 (11.3 fold; adjusted P value = .02), enhanced NSCLC tumor cell invasion in 3D culture compared to control when it was overexpressed in CAFs, suggesting an important role of ST8SIA2 in cancer cell invasion. We confirmed the protumorigenic role of ST8SIA2, showing that ST8SIA2 was significantly associated with the risk of relapse in three independent NSCLC clinical datasets. In summary, our studies show that functional heterogeneity in CAF plays key role in promoting cancer cell invasion in NSCLC.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30978569</pmid><doi>10.1016/j.neo.2019.03.009</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Cancer-Associated Fibroblasts - metabolism Cancer-Associated Fibroblasts - pathology Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - pathology Cell Movement Cell Proliferation Cohort Studies Gene Expression Profiling Gene Expression Regulation, Neoplastic Humans Lung Neoplasms - genetics Lung Neoplasms - metabolism Lung Neoplasms - pathology Male Mice Mice, SCID Neoplasm Invasiveness Neoplasm Recurrence, Local - genetics Neoplasm Recurrence, Local - metabolism Neoplasm Recurrence, Local - pathology Prognosis Sialyltransferases - genetics Sialyltransferases - metabolism Stromal Cells - metabolism Stromal Cells - pathology Survival Rate Tumor Cells, Cultured Xenograft Model Antitumor Assays |
title | Characterization of Distinct Populations of Carcinoma-Associated Fibroblasts from Non–Small Cell Lung Carcinoma Reveals a Role for ST8SIA2 in Cancer Cell Invasion |
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