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The c-MYC Protooncogene Expression in Cholesteatoma
Cholesteatoma is an epidermoid cyst, which is most frequently found in the middle ear. The matrix of cholesteatoma is histologically similar to the matrix of the epidermoid cyst of the skin (atheroma); their epithelium is characterized by hyperproliferation. The c-MYC protooncogene located on chromo...
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Published in: | BioMed research international 2014-01, Vol.2014 (2014), p.1-6 |
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description | Cholesteatoma is an epidermoid cyst, which is most frequently found in the middle ear. The matrix of cholesteatoma is histologically similar to the matrix of the epidermoid cyst of the skin (atheroma); their epithelium is characterized by hyperproliferation. The c-MYC protooncogene located on chromosome 8q24 encodes a transcription factor involved in the regulation of cell proliferation and differentiation. Previous studies have found aneuploidy of chromosome 8, copy number variation of c-MYC gene, and the presence of elevated level c-MYC protein in cholesteatoma. In this study we have compared the expression of c-MYC gene in samples taken from the matrix of 26 acquired cholesteatomas (15 children and 11 adults), 15 epidermoid cysts of the skin (atheromas; head and neck region) and 5 normal skin samples (retroauricular region) using RT-qPCR, providing the first precise measurement of the expression of c-MYC gene in cholesteatoma. We have found significantly elevated c-MYC gene expression in cholesteatoma compared to atheroma and to normal skin samples. There was no significant difference, however, in c-MYC gene expression between cholesteatoma samples of children and adults. The significant difference in c-MYC gene expression level in cholesteatoma compared to that of atheroma implies a more prominent hyperproliferative phenotype which may explain the clinical behavior typical of cholesteatoma. |
doi_str_mv | 10.1155/2014/639896 |
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The matrix of cholesteatoma is histologically similar to the matrix of the epidermoid cyst of the skin (atheroma); their epithelium is characterized by hyperproliferation. The c-MYC protooncogene located on chromosome 8q24 encodes a transcription factor involved in the regulation of cell proliferation and differentiation. Previous studies have found aneuploidy of chromosome 8, copy number variation of c-MYC gene, and the presence of elevated level c-MYC protein in cholesteatoma. In this study we have compared the expression of c-MYC gene in samples taken from the matrix of 26 acquired cholesteatomas (15 children and 11 adults), 15 epidermoid cysts of the skin (atheromas; head and neck region) and 5 normal skin samples (retroauricular region) using RT-qPCR, providing the first precise measurement of the expression of c-MYC gene in cholesteatoma. We have found significantly elevated c-MYC gene expression in cholesteatoma compared to atheroma and to normal skin samples. There was no significant difference, however, in c-MYC gene expression between cholesteatoma samples of children and adults. The significant difference in c-MYC gene expression level in cholesteatoma compared to that of atheroma implies a more prominent hyperproliferative phenotype which may explain the clinical behavior typical of cholesteatoma.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2014/639896</identifier><identifier>PMID: 24683550</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject>Adolescent ; Adult ; Aged ; Aggressiveness ; Case-Control Studies ; Cell growth ; Child ; Child, Preschool ; Children & youth ; Cholesteatoma ; Cholesteatoma, Middle Ear - genetics ; Cholesteatoma, Middle Ear - surgery ; Chromosomes ; Cysts ; Demography ; Experiments ; Female ; Gene expression ; Gene Expression Regulation ; Hospitals ; Humans ; Male ; Middle Aged ; Otolaryngology ; Patients ; Pediatrics ; Plaque, Atherosclerotic - genetics ; Proto-Oncogene Proteins c-myc - genetics ; Proto-Oncogene Proteins c-myc - metabolism ; Proto-oncogenes ; Science ; Skin - pathology ; Studies ; Surgery ; Young Adult</subject><ispartof>BioMed research international, 2014-01, Vol.2014 (2014), p.1-6</ispartof><rights>Copyright © 2014 Enikő Palkó et al.</rights><rights>COPYRIGHT 2014 John Wiley & Sons, Inc.</rights><rights>Copyright © 2014 Eniko Palkó et al. Eniko Palkó et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2014 Enikő Palkó et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-34683480accfaebc77f6da5f1f002f34ecf49be81d5b98f7b60257ffda98956a3</citedby><cites>FETCH-LOGICAL-c461t-34683480accfaebc77f6da5f1f002f34ecf49be81d5b98f7b60257ffda98956a3</cites><orcidid>0000-0001-8609-5765</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1566048634/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1566048634?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,25753,27924,27925,37012,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24683550$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Maune, Steffen</contributor><creatorcontrib>Palkó, Enikő</creatorcontrib><creatorcontrib>Póliska, Szilárd</creatorcontrib><creatorcontrib>Csákányi, Zsuzsanna</creatorcontrib><creatorcontrib>Katona, Gábor</creatorcontrib><creatorcontrib>Karosi, Tamás</creatorcontrib><creatorcontrib>Helfferich, Frigyes</creatorcontrib><creatorcontrib>Penyige, András</creatorcontrib><creatorcontrib>Sziklai, István</creatorcontrib><title>The c-MYC Protooncogene Expression in Cholesteatoma</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Cholesteatoma is an epidermoid cyst, which is most frequently found in the middle ear. The matrix of cholesteatoma is histologically similar to the matrix of the epidermoid cyst of the skin (atheroma); their epithelium is characterized by hyperproliferation. The c-MYC protooncogene located on chromosome 8q24 encodes a transcription factor involved in the regulation of cell proliferation and differentiation. Previous studies have found aneuploidy of chromosome 8, copy number variation of c-MYC gene, and the presence of elevated level c-MYC protein in cholesteatoma. In this study we have compared the expression of c-MYC gene in samples taken from the matrix of 26 acquired cholesteatomas (15 children and 11 adults), 15 epidermoid cysts of the skin (atheromas; head and neck region) and 5 normal skin samples (retroauricular region) using RT-qPCR, providing the first precise measurement of the expression of c-MYC gene in cholesteatoma. We have found significantly elevated c-MYC gene expression in cholesteatoma compared to atheroma and to normal skin samples. There was no significant difference, however, in c-MYC gene expression between cholesteatoma samples of children and adults. 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The matrix of cholesteatoma is histologically similar to the matrix of the epidermoid cyst of the skin (atheroma); their epithelium is characterized by hyperproliferation. The c-MYC protooncogene located on chromosome 8q24 encodes a transcription factor involved in the regulation of cell proliferation and differentiation. Previous studies have found aneuploidy of chromosome 8, copy number variation of c-MYC gene, and the presence of elevated level c-MYC protein in cholesteatoma. In this study we have compared the expression of c-MYC gene in samples taken from the matrix of 26 acquired cholesteatomas (15 children and 11 adults), 15 epidermoid cysts of the skin (atheromas; head and neck region) and 5 normal skin samples (retroauricular region) using RT-qPCR, providing the first precise measurement of the expression of c-MYC gene in cholesteatoma. We have found significantly elevated c-MYC gene expression in cholesteatoma compared to atheroma and to normal skin samples. There was no significant difference, however, in c-MYC gene expression between cholesteatoma samples of children and adults. The significant difference in c-MYC gene expression level in cholesteatoma compared to that of atheroma implies a more prominent hyperproliferative phenotype which may explain the clinical behavior typical of cholesteatoma.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>24683550</pmid><doi>10.1155/2014/639896</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-8609-5765</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aggressiveness Case-Control Studies Cell growth Child Child, Preschool Children & youth Cholesteatoma Cholesteatoma, Middle Ear - genetics Cholesteatoma, Middle Ear - surgery Chromosomes Cysts Demography Experiments Female Gene expression Gene Expression Regulation Hospitals Humans Male Middle Aged Otolaryngology Patients Pediatrics Plaque, Atherosclerotic - genetics Proto-Oncogene Proteins c-myc - genetics Proto-Oncogene Proteins c-myc - metabolism Proto-oncogenes Science Skin - pathology Studies Surgery Young Adult |
title | The c-MYC Protooncogene Expression in Cholesteatoma |
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