Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Phenotypic plasticity refers to a phenomenon in which cells transiently gain traits of another lineage. During carcinoma progression, phenotypic plasticity drives invasion, dissemination and metastasis. Indeed, while most of the studies of phenotypic plasticity have been in the context of epithelial...
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creator | Ware, Kathryn E. Gilja, Shivee Xu, Shenghan Shetler, Samantha Jolly, Mohit K. Wang, Xueyang Bartholf Dewitt, Suzanne Hish, Alexander J. Jordan, Sarah Eward, William Levine, Herbert Armstrong, Andrew J. Somarelli, Jason A. |
description | Phenotypic plasticity refers to a phenomenon in which cells transiently gain traits of another lineage. During carcinoma progression, phenotypic plasticity drives invasion, dissemination and metastasis. Indeed, while most of the studies of phenotypic plasticity have been in the context of epithelial-derived carcinomas, it turns out sarcomas, which are mesenchymal in origin, also exhibit phenotypic plasticity, with a subset of sarcomas undergoing a phenomenon that resembles a mesenchymal-epithelial transition (MET). Here, we developed a method comprising the miR-200 family and grainyhead-like 2 (GRHL2) to mimic this MET-like phenomenon observed in sarcoma patient samples.We sequentially express GRHL2 and the miR-200 family using cell transduction and transfection, respectively, to better understand the molecular underpinnings of these phenotypic transitions in sarcoma cells. Sarcoma cells expressing miR-200s and GRHL2 demonstrated enhanced epithelial characteristics in cell morphology and alteration of epithelial and mesenchymal biomarkers. Future studies using these methods can be used to better understand the phenotypic consequences of MET-like processes on sarcoma cells, such as migration, invasion, metastatic propensity, and therapy resistance. |
doi_str_mv | 10.3791/55520 |
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During carcinoma progression, phenotypic plasticity drives invasion, dissemination and metastasis. Indeed, while most of the studies of phenotypic plasticity have been in the context of epithelial-derived carcinomas, it turns out sarcomas, which are mesenchymal in origin, also exhibit phenotypic plasticity, with a subset of sarcomas undergoing a phenomenon that resembles a mesenchymal-epithelial transition (MET). Here, we developed a method comprising the miR-200 family and grainyhead-like 2 (GRHL2) to mimic this MET-like phenomenon observed in sarcoma patient samples.We sequentially express GRHL2 and the miR-200 family using cell transduction and transfection, respectively, to better understand the molecular underpinnings of these phenotypic transitions in sarcoma cells. Sarcoma cells expressing miR-200s and GRHL2 demonstrated enhanced epithelial characteristics in cell morphology and alteration of epithelial and mesenchymal biomarkers. Future studies using these methods can be used to better understand the phenotypic consequences of MET-like processes on sarcoma cells, such as migration, invasion, metastatic propensity, and therapy resistance.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/55520</identifier><identifier>PMID: 28448023</identifier><language>eng</language><publisher>United States: MyJove Corporation</publisher><subject>Cell Count ; Cell Line, Tumor ; Developmental Biology ; DNA-Binding Proteins - metabolism ; Epithelial Cells - pathology ; Epithelial-Mesenchymal Transition - physiology ; Gene Expression Regulation ; Humans ; MicroRNAs - metabolism ; Sarcoma - pathology ; Transcription Factors - metabolism ; Transfection</subject><ispartof>Journal of Visualized Experiments, 2017-04 (122)</ispartof><rights>Copyright © 2017, Journal of Visualized Experiments</rights><rights>Copyright © 2017, Journal of Visualized Experiments 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-f9fb9890add4d19f06fd65bea3d7116ba232d92bcdbe1b6c30050cfd8e059d083</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://www.jove.com/files/email_thumbs/55520.png</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564486/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564486/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3829,27903,27904,53769,53771</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/55520$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28448023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ware, Kathryn E.</creatorcontrib><creatorcontrib>Gilja, Shivee</creatorcontrib><creatorcontrib>Xu, Shenghan</creatorcontrib><creatorcontrib>Shetler, Samantha</creatorcontrib><creatorcontrib>Jolly, Mohit K.</creatorcontrib><creatorcontrib>Wang, Xueyang</creatorcontrib><creatorcontrib>Bartholf Dewitt, Suzanne</creatorcontrib><creatorcontrib>Hish, Alexander J.</creatorcontrib><creatorcontrib>Jordan, Sarah</creatorcontrib><creatorcontrib>Eward, William</creatorcontrib><creatorcontrib>Levine, Herbert</creatorcontrib><creatorcontrib>Armstrong, Andrew J.</creatorcontrib><creatorcontrib>Somarelli, Jason A.</creatorcontrib><title>Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells</title><title>Journal of Visualized Experiments</title><addtitle>J Vis Exp</addtitle><description>Phenotypic plasticity refers to a phenomenon in which cells transiently gain traits of another lineage. During carcinoma progression, phenotypic plasticity drives invasion, dissemination and metastasis. Indeed, while most of the studies of phenotypic plasticity have been in the context of epithelial-derived carcinomas, it turns out sarcomas, which are mesenchymal in origin, also exhibit phenotypic plasticity, with a subset of sarcomas undergoing a phenomenon that resembles a mesenchymal-epithelial transition (MET). Here, we developed a method comprising the miR-200 family and grainyhead-like 2 (GRHL2) to mimic this MET-like phenomenon observed in sarcoma patient samples.We sequentially express GRHL2 and the miR-200 family using cell transduction and transfection, respectively, to better understand the molecular underpinnings of these phenotypic transitions in sarcoma cells. Sarcoma cells expressing miR-200s and GRHL2 demonstrated enhanced epithelial characteristics in cell morphology and alteration of epithelial and mesenchymal biomarkers. Future studies using these methods can be used to better understand the phenotypic consequences of MET-like processes on sarcoma cells, such as migration, invasion, metastatic propensity, and therapy resistance.</description><subject>Cell Count</subject><subject>Cell Line, Tumor</subject><subject>Developmental Biology</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Epithelial Cells - pathology</subject><subject>Epithelial-Mesenchymal Transition - physiology</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>MicroRNAs - metabolism</subject><subject>Sarcoma - pathology</subject><subject>Transcription Factors - metabolism</subject><subject>Transfection</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE9LAzEQxYMottZ-AQ-yF8HLapLdbJOLKKVqoeLBCt5CNn9sym5Sk91Cv71bW4ueZmB-82beA2CI4E02YuiWEILhEegjlsMU0tHH8Z--B85iXEJYYEjoKehhmucU4qwP7qdOtbKx3iXeJC86aicXm1pU6WRlm4WurKiSeRAu2i0UE-uSNxGkr0Uy1lUVz8GJEVXUw30dgPfHyXz8nM5en6bjh1kqM4qb1DBTMsqgUCpXiBlYGFWQUotMjRAqSoEzrBgupSo1KguZQUigNIpqSJiCNBuAu53uqi1rraR2TRAVXwVbi7DhXlj-f-Lsgn_6NSek6MwWncD1XiD4r1bHhtc2ys6CcNq3kSPK8AhnlGzRqx0qg48xaHM4gyDfps1_0u64y78_HajfeDvgYgcs_VrzpW-D6zLab38DGbmD2w</recordid><startdate>20170407</startdate><enddate>20170407</enddate><creator>Ware, Kathryn E.</creator><creator>Gilja, Shivee</creator><creator>Xu, Shenghan</creator><creator>Shetler, Samantha</creator><creator>Jolly, Mohit K.</creator><creator>Wang, Xueyang</creator><creator>Bartholf Dewitt, Suzanne</creator><creator>Hish, Alexander J.</creator><creator>Jordan, Sarah</creator><creator>Eward, William</creator><creator>Levine, Herbert</creator><creator>Armstrong, Andrew J.</creator><creator>Somarelli, Jason A.</creator><general>MyJove Corporation</general><scope>BEELZ</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></search><sort><creationdate>20170407</creationdate><title>Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells</title><author>Ware, Kathryn E. ; Gilja, Shivee ; Xu, Shenghan ; Shetler, Samantha ; Jolly, Mohit K. ; Wang, Xueyang ; Bartholf Dewitt, Suzanne ; Hish, Alexander J. ; Jordan, Sarah ; Eward, William ; Levine, Herbert ; Armstrong, Andrew J. ; Somarelli, Jason A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-f9fb9890add4d19f06fd65bea3d7116ba232d92bcdbe1b6c30050cfd8e059d083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cell Count</topic><topic>Cell Line, Tumor</topic><topic>Developmental Biology</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Epithelial Cells - pathology</topic><topic>Epithelial-Mesenchymal Transition - physiology</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>MicroRNAs - metabolism</topic><topic>Sarcoma - pathology</topic><topic>Transcription Factors - metabolism</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ware, Kathryn E.</creatorcontrib><creatorcontrib>Gilja, Shivee</creatorcontrib><creatorcontrib>Xu, Shenghan</creatorcontrib><creatorcontrib>Shetler, Samantha</creatorcontrib><creatorcontrib>Jolly, Mohit K.</creatorcontrib><creatorcontrib>Wang, Xueyang</creatorcontrib><creatorcontrib>Bartholf Dewitt, Suzanne</creatorcontrib><creatorcontrib>Hish, Alexander J.</creatorcontrib><creatorcontrib>Jordan, Sarah</creatorcontrib><creatorcontrib>Eward, William</creatorcontrib><creatorcontrib>Levine, Herbert</creatorcontrib><creatorcontrib>Armstrong, Andrew J.</creatorcontrib><creatorcontrib>Somarelli, Jason A.</creatorcontrib><collection>JoVE Journal: Developmental Biology</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><jtitle>Journal of Visualized Experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Ware, Kathryn E.</au><au>Gilja, Shivee</au><au>Xu, Shenghan</au><au>Shetler, Samantha</au><au>Jolly, Mohit K.</au><au>Wang, Xueyang</au><au>Bartholf Dewitt, Suzanne</au><au>Hish, Alexander J.</au><au>Jordan, Sarah</au><au>Eward, William</au><au>Levine, Herbert</au><au>Armstrong, Andrew J.</au><au>Somarelli, Jason A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells</atitle><jtitle>Journal of Visualized Experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2017-04-07</date><risdate>2017</risdate><issue>122</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>Phenotypic plasticity refers to a phenomenon in which cells transiently gain traits of another lineage. During carcinoma progression, phenotypic plasticity drives invasion, dissemination and metastasis. Indeed, while most of the studies of phenotypic plasticity have been in the context of epithelial-derived carcinomas, it turns out sarcomas, which are mesenchymal in origin, also exhibit phenotypic plasticity, with a subset of sarcomas undergoing a phenomenon that resembles a mesenchymal-epithelial transition (MET). Here, we developed a method comprising the miR-200 family and grainyhead-like 2 (GRHL2) to mimic this MET-like phenomenon observed in sarcoma patient samples.We sequentially express GRHL2 and the miR-200 family using cell transduction and transfection, respectively, to better understand the molecular underpinnings of these phenotypic transitions in sarcoma cells. Sarcoma cells expressing miR-200s and GRHL2 demonstrated enhanced epithelial characteristics in cell morphology and alteration of epithelial and mesenchymal biomarkers. Future studies using these methods can be used to better understand the phenotypic consequences of MET-like processes on sarcoma cells, such as migration, invasion, metastatic propensity, and therapy resistance.</abstract><cop>United States</cop><pub>MyJove Corporation</pub><pmid>28448023</pmid><doi>10.3791/55520</doi><oa>free_for_read</oa></addata></record> |
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subjects | Cell Count Cell Line, Tumor Developmental Biology DNA-Binding Proteins - metabolism Epithelial Cells - pathology Epithelial-Mesenchymal Transition - physiology Gene Expression Regulation Humans MicroRNAs - metabolism Sarcoma - pathology Transcription Factors - metabolism Transfection |
title | Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells |
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