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Evaluating the use of optical coherence tomography for the detection of epithelial cancers in vitro
Optical coherence tomography (OCT) is a noninvasive imaging methodology that is able to image tissue to depths of over 1 mm. Many epithelial conditions, such as melanoma and oral cancers, require an invasive biopsy for diagnosis. A noninvasive, real-time, point of care method of imaging depth-resolv...
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Published in: | Journal of biomedical optics 2011-11, Vol.16 (11), p.116015-116015 |
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container_end_page | 116015 |
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container_title | Journal of biomedical optics |
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creator | Smith, Louise E Hearnden, Vanessa Lu, Zenghai Smallwood, Rod Hunter, Keith D Matcher, Stephen J Thornhill, Martin H Murdoch, Craig MacNeil, Sheila |
description | Optical coherence tomography (OCT) is a noninvasive imaging methodology that is able to image tissue to depths of over 1 mm. Many epithelial conditions, such as melanoma and oral cancers, require an invasive biopsy for diagnosis. A noninvasive, real-time, point of care method of imaging depth-resolved epithelial structure could greatly improve early diagnosis and long-term monitoring in patients. Here, we have used tissue-engineered (TE) models of normal skin and oral mucosa to generate models of melanoma and oral cancer. We have used these to determine the ability of OCT to image epithelial differences in vitro. We report that while in vivo OCT gives reasonable depth information for both skin and oral mucosa, in vitro the information provided is less detailed but still useful. OCT can provide reassurance on the development of TE models of skin and oral mucosa as they develop in vitro. OCT was able to detect the gross alteration in the epithelium of skin and mucosal models generated with malignant cell lines but was less able to detect alteration in the epithelium of TE models that mimicked oral dysplasia or, in models where tumor cells had penetrated into the dermis. |
doi_str_mv | 10.1117/1.3652708 |
format | article |
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OCT was able to detect the gross alteration in the epithelium of skin and mucosal models generated with malignant cell lines but was less able to detect alteration in the epithelium of TE models that mimicked oral dysplasia or, in models where tumor cells had penetrated into the dermis.</description><subject>Carcinoma, Squamous Cell - chemistry</subject><subject>Cell Line, Tumor</subject><subject>Cells, Cultured</subject><subject>Fingers</subject><subject>Histocytochemistry</subject><subject>Humans</subject><subject>Melanoma - chemistry</subject><subject>Models, Biological</subject><subject>Mouth Mucosa - chemistry</subject><subject>Mouth Neoplasms - chemistry</subject><subject>Skin - chemistry</subject><subject>Skin Neoplasms - chemistry</subject><subject>Tomography, Optical Coherence - methods</subject><issn>1083-3668</issn><issn>1560-2281</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNo9kEtPwzAQhC0EoqVw4A8g3xCHFD8SxzmiqjykSlzgHKWbdWuUxMF2KvXfk9LCaVe738xIQ8gtZ3POef7I51JlImf6jEx5plgihObn4860TKRSekKuQvhijGlVqEsyEYJzwQWbEljuqmaoou02NG6RDgGpM9T10ULVUHBb9NgB0uhat_FVv91T4_wvW2NEiNZ1BwX2drw19iCqRoEP1HZ0Z6N31-TCVE3Am9Ockc_n5cfiNVm9v7wtnlYJiLSISVHkEoXJYK1zxUHkoA1IaVKhC2VSw7AGBVID1kVtBNZKQaoYSr6GYnzKGbk_-vbefQ8YYtnaANg0VYduCGXBUzGG8GwkH44keBeCR1P23raV35eclYdKS16eKh3Zu5PrsG6x_if_OpQ_-ChyFg</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Smith, Louise E</creator><creator>Hearnden, Vanessa</creator><creator>Lu, Zenghai</creator><creator>Smallwood, Rod</creator><creator>Hunter, Keith D</creator><creator>Matcher, Stephen J</creator><creator>Thornhill, Martin H</creator><creator>Murdoch, Craig</creator><creator>MacNeil, Sheila</creator><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></search><sort><creationdate>20111101</creationdate><title>Evaluating the use of optical coherence tomography for the detection of epithelial cancers in vitro</title><author>Smith, Louise E ; Hearnden, Vanessa ; Lu, Zenghai ; Smallwood, Rod ; Hunter, Keith D ; Matcher, Stephen J ; Thornhill, Martin H ; Murdoch, Craig ; MacNeil, Sheila</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c249t-9973e2f5cb8761c27c8fc33f42896f4f0edc6c38ced9df2ed66c460e31bc90ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Carcinoma, Squamous Cell - chemistry</topic><topic>Cell Line, Tumor</topic><topic>Cells, Cultured</topic><topic>Fingers</topic><topic>Histocytochemistry</topic><topic>Humans</topic><topic>Melanoma - chemistry</topic><topic>Models, Biological</topic><topic>Mouth Mucosa - chemistry</topic><topic>Mouth Neoplasms - chemistry</topic><topic>Skin - chemistry</topic><topic>Skin Neoplasms - chemistry</topic><topic>Tomography, Optical Coherence - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Louise E</creatorcontrib><creatorcontrib>Hearnden, Vanessa</creatorcontrib><creatorcontrib>Lu, Zenghai</creatorcontrib><creatorcontrib>Smallwood, Rod</creatorcontrib><creatorcontrib>Hunter, Keith D</creatorcontrib><creatorcontrib>Matcher, Stephen J</creatorcontrib><creatorcontrib>Thornhill, Martin H</creatorcontrib><creatorcontrib>Murdoch, Craig</creatorcontrib><creatorcontrib>MacNeil, Sheila</creatorcontrib><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><jtitle>Journal of biomedical optics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Louise E</au><au>Hearnden, Vanessa</au><au>Lu, Zenghai</au><au>Smallwood, Rod</au><au>Hunter, Keith D</au><au>Matcher, Stephen J</au><au>Thornhill, Martin H</au><au>Murdoch, Craig</au><au>MacNeil, Sheila</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating the use of optical coherence tomography for the detection of epithelial cancers in vitro</atitle><jtitle>Journal of biomedical optics</jtitle><addtitle>J Biomed Opt</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>16</volume><issue>11</issue><spage>116015</spage><epage>116015</epage><pages>116015-116015</pages><issn>1083-3668</issn><eissn>1560-2281</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>Optical coherence tomography (OCT) is a noninvasive imaging methodology that is able to image tissue to depths of over 1 mm. 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OCT was able to detect the gross alteration in the epithelium of skin and mucosal models generated with malignant cell lines but was less able to detect alteration in the epithelium of TE models that mimicked oral dysplasia or, in models where tumor cells had penetrated into the dermis.</abstract><cop>United States</cop><pmid>22112120</pmid><doi>10.1117/1.3652708</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Carcinoma, Squamous Cell - chemistry Cell Line, Tumor Cells, Cultured Fingers Histocytochemistry Humans Melanoma - chemistry Models, Biological Mouth Mucosa - chemistry Mouth Neoplasms - chemistry Skin - chemistry Skin Neoplasms - chemistry Tomography, Optical Coherence - methods |
title | Evaluating the use of optical coherence tomography for the detection of epithelial cancers in vitro |
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