Using the Chicken Chorioallantoic Membrane In Vivo Model to Study Gynecological and Urological Cancers
Mouse models are the benchmark tests for in vivo cancer studies. However, cost, time, and ethical considerations have led to calls for alternative in vivo cancer models. The chicken chorioallantoic membrane (CAM) model provides an inexpensive, rapid alternative that permits direct visualization of t...
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description | Mouse models are the benchmark tests for in vivo cancer studies. However, cost, time, and ethical considerations have led to calls for alternative in vivo cancer models. The chicken chorioallantoic membrane (CAM) model provides an inexpensive, rapid alternative that permits direct visualization of tumor development and is suitable for in vivo imaging. As such, we sought to develop an optimized protocol for engrafting gynecological and urological tumors into this model, which we present here. Approximately 7 days postfertilization, the air cell is moved to the vascularized side of the egg, where an opening is created in the shell. Tumors from murine and human cell lines and primary tissues can then be engrafted. These are typically seeded in a mixture of extracellular matrix and medium to avoid cellular dispersal and provide nutrient support until the cells recruit a vascular supply. Tumors may then grow for up to an additional 14 days prior to the eggs hatching. By implanting cells stably transduced with firefly luciferase, bioluminescence imaging can be used for the sensitive detection of tumor growth on the membrane and cancer cell spread throughout the embryo. This model can potentially be used to study tumorigenicity, invasion, metastasis, and therapeutic effectiveness. The chicken CAM model requires significantly less time and financial resources compared to traditional murine models. Because the eggs are immunocompromised and immune tolerant, tissues from any organism can potentially be implanted without costly transgenic animals (e.g., mice) required for implantation of human tissues. However, many of the advantages of this model could potentially also be limitations, including the short tumor generation time and immunocompromised/immune tolerant status. Additionally, although all tumor types presented here engraft in the chicken chorioallantoic membrane model, they do so with varying degrees of tumor growth. |
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However, cost, time, and ethical considerations have led to calls for alternative in vivo cancer models. The chicken chorioallantoic membrane (CAM) model provides an inexpensive, rapid alternative that permits direct visualization of tumor development and is suitable for in vivo imaging. As such, we sought to develop an optimized protocol for engrafting gynecological and urological tumors into this model, which we present here. Approximately 7 days postfertilization, the air cell is moved to the vascularized side of the egg, where an opening is created in the shell. Tumors from murine and human cell lines and primary tissues can then be engrafted. These are typically seeded in a mixture of extracellular matrix and medium to avoid cellular dispersal and provide nutrient support until the cells recruit a vascular supply. Tumors may then grow for up to an additional 14 days prior to the eggs hatching. By implanting cells stably transduced with firefly luciferase, bioluminescence imaging can be used for the sensitive detection of tumor growth on the membrane and cancer cell spread throughout the embryo. This model can potentially be used to study tumorigenicity, invasion, metastasis, and therapeutic effectiveness. The chicken CAM model requires significantly less time and financial resources compared to traditional murine models. Because the eggs are immunocompromised and immune tolerant, tissues from any organism can potentially be implanted without costly transgenic animals (e.g., mice) required for implantation of human tissues. However, many of the advantages of this model could potentially also be limitations, including the short tumor generation time and immunocompromised/immune tolerant status. Additionally, although all tumor types presented here engraft in the chicken chorioallantoic membrane model, they do so with varying degrees of tumor growth.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/60651</identifier><identifier>PMID: 32065133</identifier><language>eng</language><publisher>CAMBRIDGE: MyJove Corporation</publisher><subject>Animals ; Cancer Research ; Chickens ; Chorioallantoic Membrane - metabolism ; Disease Models, Animal ; Female ; Genital Neoplasms, Female - diagnosis ; Genital Neoplasms, Female - pathology ; Humans ; Multidisciplinary Sciences ; Science & Technology ; Science & Technology - Other Topics ; Urologic Neoplasms - diagnosis ; Urologic Neoplasms - pathology</subject><ispartof>Journal of Visualized Experiments, 2020-01 (155), Article 60651</ispartof><rights>Copyright © 2020, Journal of Visualized Experiments</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>9</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000535305900025</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c448t-d96ba6372850c4788c61cb46d6362b484227595b10ee74d84f3e94fd0366501d3</citedby><cites>FETCH-LOGICAL-c448t-d96ba6372850c4788c61cb46d6362b484227595b10ee74d84f3e94fd0366501d3</cites><orcidid>0000-0003-3893-2666</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://www.jove.com/files/email_thumbs/60651.png</thumbnail><link.rule.ids>230,315,782,786,887,3847,27933,27934,28257</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/60651$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32065133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sharrow, Allison C.</creatorcontrib><creatorcontrib>Ishihara, Moe</creatorcontrib><creatorcontrib>Hu, Junhui</creatorcontrib><creatorcontrib>Kim, Il Hyun</creatorcontrib><creatorcontrib>Wu, Lily</creatorcontrib><title>Using the Chicken Chorioallantoic Membrane In Vivo Model to Study Gynecological and Urological Cancers</title><title>Journal of Visualized Experiments</title><addtitle>JOVE-J VIS EXP</addtitle><addtitle>J Vis Exp</addtitle><description>Mouse models are the benchmark tests for in vivo cancer studies. However, cost, time, and ethical considerations have led to calls for alternative in vivo cancer models. The chicken chorioallantoic membrane (CAM) model provides an inexpensive, rapid alternative that permits direct visualization of tumor development and is suitable for in vivo imaging. As such, we sought to develop an optimized protocol for engrafting gynecological and urological tumors into this model, which we present here. Approximately 7 days postfertilization, the air cell is moved to the vascularized side of the egg, where an opening is created in the shell. Tumors from murine and human cell lines and primary tissues can then be engrafted. These are typically seeded in a mixture of extracellular matrix and medium to avoid cellular dispersal and provide nutrient support until the cells recruit a vascular supply. Tumors may then grow for up to an additional 14 days prior to the eggs hatching. By implanting cells stably transduced with firefly luciferase, bioluminescence imaging can be used for the sensitive detection of tumor growth on the membrane and cancer cell spread throughout the embryo. This model can potentially be used to study tumorigenicity, invasion, metastasis, and therapeutic effectiveness. The chicken CAM model requires significantly less time and financial resources compared to traditional murine models. Because the eggs are immunocompromised and immune tolerant, tissues from any organism can potentially be implanted without costly transgenic animals (e.g., mice) required for implantation of human tissues. However, many of the advantages of this model could potentially also be limitations, including the short tumor generation time and immunocompromised/immune tolerant status. Additionally, although all tumor types presented here engraft in the chicken chorioallantoic membrane model, they do so with varying degrees of tumor growth.</description><subject>Animals</subject><subject>Cancer Research</subject><subject>Chickens</subject><subject>Chorioallantoic Membrane - metabolism</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Genital Neoplasms, Female - diagnosis</subject><subject>Genital Neoplasms, Female - pathology</subject><subject>Humans</subject><subject>Multidisciplinary Sciences</subject><subject>Science & Technology</subject><subject>Science & Technology - Other Topics</subject><subject>Urologic Neoplasms - diagnosis</subject><subject>Urologic Neoplasms - pathology</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkU1vEzEQhi0EoiX0D3BAviAhVQGvv9Z7QUIrWiq14gBB3CyvdzZx2Nit7Q3Kv8chISo3TjOjeeZD74vQRUXesbqp3ksiRfUEnVcNJ3Oi6h9PH-Vn6EVKa0IkJUI9R2eM7mnGztGwSM4vcV4BblfO_gRfYogumHE0Pgdn8R1sumg84BuPv7ttwHehhxHngL_mqd_h650HG8awdNaM2PgeL-KpbI23ENNL9GwwY4KLY5yhxdWnb-3n-e2X65v24-3ccq7yvG9kZySrqRLE8lopKyvbcdlLJmnHFae0Fo3oKgJQ817xgUHDh54wKQWpejZDHw5776duA70Fn6MZ9X10GxN3Ohin_-14t9LLsNU1E40qkszQ2-OCGB4mSFlvXLKwFwPClDRlQgpVc8oL-uaA2hhSijCczlRE7z3Rfzwp3OvHP52ovyYU4PIA_IIuDMk6KJqdMEKIYIIR0ZSMikKr_6dbl012wbdh8rmMvjqMrsMW9DpM0Rczjm_-Bldmr-s</recordid><startdate>20200128</startdate><enddate>20200128</enddate><creator>Sharrow, Allison C.</creator><creator>Ishihara, Moe</creator><creator>Hu, Junhui</creator><creator>Kim, Il Hyun</creator><creator>Wu, Lily</creator><general>MyJove Corporation</general><general>Journal Of Visualized Experiments</general><scope>AULCJ</scope><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</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><orcidid>https://orcid.org/0000-0003-3893-2666</orcidid></search><sort><creationdate>20200128</creationdate><title>Using the Chicken Chorioallantoic Membrane In Vivo Model to Study Gynecological and Urological Cancers</title><author>Sharrow, Allison C. ; Ishihara, Moe ; Hu, Junhui ; Kim, Il Hyun ; Wu, Lily</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-d96ba6372850c4788c61cb46d6362b484227595b10ee74d84f3e94fd0366501d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cancer Research</topic><topic>Chickens</topic><topic>Chorioallantoic Membrane - metabolism</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Genital Neoplasms, Female - diagnosis</topic><topic>Genital Neoplasms, Female - pathology</topic><topic>Humans</topic><topic>Multidisciplinary Sciences</topic><topic>Science & Technology</topic><topic>Science & Technology - Other Topics</topic><topic>Urologic Neoplasms - diagnosis</topic><topic>Urologic Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sharrow, Allison C.</creatorcontrib><creatorcontrib>Ishihara, Moe</creatorcontrib><creatorcontrib>Hu, Junhui</creatorcontrib><creatorcontrib>Kim, Il Hyun</creatorcontrib><creatorcontrib>Wu, Lily</creatorcontrib><collection>JoVE Journal: Cancer Research</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</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>Sharrow, Allison C.</au><au>Ishihara, Moe</au><au>Hu, Junhui</au><au>Kim, Il Hyun</au><au>Wu, Lily</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Using the Chicken Chorioallantoic Membrane In Vivo Model to Study Gynecological and Urological Cancers</atitle><jtitle>Journal of Visualized Experiments</jtitle><stitle>JOVE-J VIS EXP</stitle><addtitle>J Vis Exp</addtitle><date>2020-01-28</date><risdate>2020</risdate><issue>155</issue><artnum>60651</artnum><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>Mouse models are the benchmark tests for in vivo cancer studies. 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By implanting cells stably transduced with firefly luciferase, bioluminescence imaging can be used for the sensitive detection of tumor growth on the membrane and cancer cell spread throughout the embryo. This model can potentially be used to study tumorigenicity, invasion, metastasis, and therapeutic effectiveness. The chicken CAM model requires significantly less time and financial resources compared to traditional murine models. Because the eggs are immunocompromised and immune tolerant, tissues from any organism can potentially be implanted without costly transgenic animals (e.g., mice) required for implantation of human tissues. However, many of the advantages of this model could potentially also be limitations, including the short tumor generation time and immunocompromised/immune tolerant status. 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subjects | Animals Cancer Research Chickens Chorioallantoic Membrane - metabolism Disease Models, Animal Female Genital Neoplasms, Female - diagnosis Genital Neoplasms, Female - pathology Humans Multidisciplinary Sciences Science & Technology Science & Technology - Other Topics Urologic Neoplasms - diagnosis Urologic Neoplasms - pathology |
title | Using the Chicken Chorioallantoic Membrane In Vivo Model to Study Gynecological and Urological Cancers |
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