p16 INK4A genetic and epigenetic profiles differ in relation to age and site in head and neck squamous cell carcinomas
Head and neck squamous cell carcinoma (HNSCC) typically affects male smokers older than 55 years. Recently, an increase in the incidence of HNSCC in young adults has been recognized, many of them nonsmokers and females. Functional inactivation of p16 is known to be a common event in HNSCC, mainly by...
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Veröffentlicht in: | Human pathology 2008-03, Vol.39 (3), p.452-458 |
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creator | O'Regan, Esther M. Toner, Mary E. Finn, Stephen P. Fan, Chun Yang Ring, Martina Hagmar, Bjorn Timon, Conrad Smyth, Paul Cahill, Susanne Flavin, Richard Sheils, Orla M. O'Leary, John J. |
description | Head and neck squamous cell carcinoma (HNSCC) typically affects male smokers older than 55 years. Recently, an increase in the incidence of HNSCC in young adults has been recognized, many of them nonsmokers and females. Functional inactivation of
p16 is known to be a common event in HNSCC, mainly by either deletion or methylation. A previous study by this group has shown that
p16 deletions in HNSCC are significantly associated with age. The primary objective of this study was to evaluate additional molecular alterations of
p16 in HNSCC, specifically in relation to age, site, and human papillomavirus (HPV) status. Patients ranging in age from 22 to 76 years with HNSCC were prospectively identified (n = 24). Methylation-specific polymerase chain reaction and immunohistochemistry were used to evaluate
p16 gene inactivation and p16 protein expression, respectively. HPV 16 status was determined for each case. Overall,
p16 inactivation was a frequent event detected in 46% of cases. Methylation of
p16 was more often detected in females than males (
P = .05). All cases showing
p16 methylation were from the anterior tongue, and 75% of them were young patients. The results indicate that
p16 methylation is a more common event in those younger than 40 years in contrast to
p16 deletions, which are more common in those older than 40 years. Consequently, it appears that specific modes of inactivation of
p16 in HNSCC are related to specific patient risk profiles. Interestingly, HPV 16 messenger RNA was detected exclusively in HNSCC from the base of tongue lesions and was only found in males. This differs from the patient profile of HNSCC in the young, which affects the anterior tongue and commonly females, thus, making it highly unlikely that this virus is a primary causative agent of HNSCC in these young adults. |
doi_str_mv | 10.1016/j.humpath.2007.08.004 |
format | Article |
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p16 is known to be a common event in HNSCC, mainly by either deletion or methylation. A previous study by this group has shown that
p16 deletions in HNSCC are significantly associated with age. The primary objective of this study was to evaluate additional molecular alterations of
p16 in HNSCC, specifically in relation to age, site, and human papillomavirus (HPV) status. Patients ranging in age from 22 to 76 years with HNSCC were prospectively identified (n = 24). Methylation-specific polymerase chain reaction and immunohistochemistry were used to evaluate
p16 gene inactivation and p16 protein expression, respectively. HPV 16 status was determined for each case. Overall,
p16 inactivation was a frequent event detected in 46% of cases. Methylation of
p16 was more often detected in females than males (
P = .05). All cases showing
p16 methylation were from the anterior tongue, and 75% of them were young patients. The results indicate that
p16 methylation is a more common event in those younger than 40 years in contrast to
p16 deletions, which are more common in those older than 40 years. Consequently, it appears that specific modes of inactivation of
p16 in HNSCC are related to specific patient risk profiles. Interestingly, HPV 16 messenger RNA was detected exclusively in HNSCC from the base of tongue lesions and was only found in males. This differs from the patient profile of HNSCC in the young, which affects the anterior tongue and commonly females, thus, making it highly unlikely that this virus is a primary causative agent of HNSCC in these young adults.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2007.08.004</identifier><language>eng</language><publisher>Philadelphia: Elsevier Inc</publisher><subject>Cervical cancer ; CGH ; Deoxyribonucleic acid ; DNA ; DNA methylation ; Epigenetics ; Genetic testing ; Head & neck cancer ; HNSCC young ; HPV ; Human papillomavirus ; Methylation ; p16 ; Polymerase chain reaction ; Young adults</subject><ispartof>Human pathology, 2008-03, Vol.39 (3), p.452-458</ispartof><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.humpath.2007.08.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids></links><search><creatorcontrib>O'Regan, Esther M.</creatorcontrib><creatorcontrib>Toner, Mary E.</creatorcontrib><creatorcontrib>Finn, Stephen P.</creatorcontrib><creatorcontrib>Fan, Chun Yang</creatorcontrib><creatorcontrib>Ring, Martina</creatorcontrib><creatorcontrib>Hagmar, Bjorn</creatorcontrib><creatorcontrib>Timon, Conrad</creatorcontrib><creatorcontrib>Smyth, Paul</creatorcontrib><creatorcontrib>Cahill, Susanne</creatorcontrib><creatorcontrib>Flavin, Richard</creatorcontrib><creatorcontrib>Sheils, Orla M.</creatorcontrib><creatorcontrib>O'Leary, John J.</creatorcontrib><title>p16 INK4A genetic and epigenetic profiles differ in relation to age and site in head and neck squamous cell carcinomas</title><title>Human pathology</title><description>Head and neck squamous cell carcinoma (HNSCC) typically affects male smokers older than 55 years. Recently, an increase in the incidence of HNSCC in young adults has been recognized, many of them nonsmokers and females. Functional inactivation of
p16 is known to be a common event in HNSCC, mainly by either deletion or methylation. A previous study by this group has shown that
p16 deletions in HNSCC are significantly associated with age. The primary objective of this study was to evaluate additional molecular alterations of
p16 in HNSCC, specifically in relation to age, site, and human papillomavirus (HPV) status. Patients ranging in age from 22 to 76 years with HNSCC were prospectively identified (n = 24). Methylation-specific polymerase chain reaction and immunohistochemistry were used to evaluate
p16 gene inactivation and p16 protein expression, respectively. HPV 16 status was determined for each case. Overall,
p16 inactivation was a frequent event detected in 46% of cases. Methylation of
p16 was more often detected in females than males (
P = .05). All cases showing
p16 methylation were from the anterior tongue, and 75% of them were young patients. The results indicate that
p16 methylation is a more common event in those younger than 40 years in contrast to
p16 deletions, which are more common in those older than 40 years. Consequently, it appears that specific modes of inactivation of
p16 in HNSCC are related to specific patient risk profiles. Interestingly, HPV 16 messenger RNA was detected exclusively in HNSCC from the base of tongue lesions and was only found in males. This differs from the patient profile of HNSCC in the young, which affects the anterior tongue and commonly females, thus, making it highly unlikely that this virus is a primary causative agent of HNSCC in these young adults.</description><subject>Cervical cancer</subject><subject>CGH</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>Epigenetics</subject><subject>Genetic testing</subject><subject>Head & neck cancer</subject><subject>HNSCC young</subject><subject>HPV</subject><subject>Human papillomavirus</subject><subject>Methylation</subject><subject>p16</subject><subject>Polymerase chain reaction</subject><subject>Young adults</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo1kFtPwyAUx4nRxDn9CCYkPrdCgUKfzLJ4WVz0Ze-E0cNG7WhX2n1-Wzefzu1_bj-EHilJKaH5c5Xuh0Nr-n2aESJTolJC-BWaUcGyRLEiu0azMZMnikp5i-5irAihVHAxQ6eW5nj19ckXeAcBem-xCSWG1v-Hbdc4X0PEpXcOOuwD7qA2vW8C7htsdvDXEX0PU20PpvxLBLA_OB4Hc2iGiC3UNbamsz40BxPv0Y0zdYSHi52jzdvrZvmRrL_fV8vFOgHFVeIMWMYyCYQJblUhCDGZEkpIxq0zBSuME6PjTEk426rMSkHyUsmtgG3mFJujp_PY8YnjALHXVTN0YdyoKWFcSZ4Vk-rlrILxkpOHTkfrIVgofQe212XjR7meWOtKX1jribUmSo9k2S-eq3WL</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>O'Regan, Esther M.</creator><creator>Toner, Mary E.</creator><creator>Finn, Stephen P.</creator><creator>Fan, Chun Yang</creator><creator>Ring, Martina</creator><creator>Hagmar, Bjorn</creator><creator>Timon, Conrad</creator><creator>Smyth, Paul</creator><creator>Cahill, Susanne</creator><creator>Flavin, Richard</creator><creator>Sheils, Orla M.</creator><creator>O'Leary, John J.</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>K9.</scope></search><sort><creationdate>20080301</creationdate><title>p16 INK4A genetic and epigenetic profiles differ in relation to age and site in head and neck squamous cell carcinomas</title><author>O'Regan, Esther M. ; Toner, Mary E. ; Finn, Stephen P. ; Fan, Chun Yang ; Ring, Martina ; Hagmar, Bjorn ; Timon, Conrad ; Smyth, Paul ; Cahill, Susanne ; Flavin, Richard ; Sheils, Orla M. ; O'Leary, John J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e848-faec3327e0354c89500a28585734cfa939af5cfafad043b82c7506d87b5eb2f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Cervical cancer</topic><topic>CGH</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>Epigenetics</topic><topic>Genetic testing</topic><topic>Head & neck cancer</topic><topic>HNSCC young</topic><topic>HPV</topic><topic>Human papillomavirus</topic><topic>Methylation</topic><topic>p16</topic><topic>Polymerase chain reaction</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Regan, Esther M.</creatorcontrib><creatorcontrib>Toner, Mary E.</creatorcontrib><creatorcontrib>Finn, Stephen P.</creatorcontrib><creatorcontrib>Fan, Chun Yang</creatorcontrib><creatorcontrib>Ring, Martina</creatorcontrib><creatorcontrib>Hagmar, Bjorn</creatorcontrib><creatorcontrib>Timon, Conrad</creatorcontrib><creatorcontrib>Smyth, Paul</creatorcontrib><creatorcontrib>Cahill, Susanne</creatorcontrib><creatorcontrib>Flavin, Richard</creatorcontrib><creatorcontrib>Sheils, Orla M.</creatorcontrib><creatorcontrib>O'Leary, John J.</creatorcontrib><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Regan, Esther M.</au><au>Toner, Mary E.</au><au>Finn, Stephen P.</au><au>Fan, Chun Yang</au><au>Ring, Martina</au><au>Hagmar, Bjorn</au><au>Timon, Conrad</au><au>Smyth, Paul</au><au>Cahill, Susanne</au><au>Flavin, Richard</au><au>Sheils, Orla M.</au><au>O'Leary, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>p16 INK4A genetic and epigenetic profiles differ in relation to age and site in head and neck squamous cell carcinomas</atitle><jtitle>Human pathology</jtitle><date>2008-03-01</date><risdate>2008</risdate><volume>39</volume><issue>3</issue><spage>452</spage><epage>458</epage><pages>452-458</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Head and neck squamous cell carcinoma (HNSCC) typically affects male smokers older than 55 years. Recently, an increase in the incidence of HNSCC in young adults has been recognized, many of them nonsmokers and females. Functional inactivation of
p16 is known to be a common event in HNSCC, mainly by either deletion or methylation. A previous study by this group has shown that
p16 deletions in HNSCC are significantly associated with age. The primary objective of this study was to evaluate additional molecular alterations of
p16 in HNSCC, specifically in relation to age, site, and human papillomavirus (HPV) status. Patients ranging in age from 22 to 76 years with HNSCC were prospectively identified (n = 24). Methylation-specific polymerase chain reaction and immunohistochemistry were used to evaluate
p16 gene inactivation and p16 protein expression, respectively. HPV 16 status was determined for each case. Overall,
p16 inactivation was a frequent event detected in 46% of cases. Methylation of
p16 was more often detected in females than males (
P = .05). All cases showing
p16 methylation were from the anterior tongue, and 75% of them were young patients. The results indicate that
p16 methylation is a more common event in those younger than 40 years in contrast to
p16 deletions, which are more common in those older than 40 years. Consequently, it appears that specific modes of inactivation of
p16 in HNSCC are related to specific patient risk profiles. Interestingly, HPV 16 messenger RNA was detected exclusively in HNSCC from the base of tongue lesions and was only found in males. This differs from the patient profile of HNSCC in the young, which affects the anterior tongue and commonly females, thus, making it highly unlikely that this virus is a primary causative agent of HNSCC in these young adults.</abstract><cop>Philadelphia</cop><pub>Elsevier Inc</pub><doi>10.1016/j.humpath.2007.08.004</doi><tpages>7</tpages></addata></record> |
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subjects | Cervical cancer CGH Deoxyribonucleic acid DNA DNA methylation Epigenetics Genetic testing Head & neck cancer HNSCC young HPV Human papillomavirus Methylation p16 Polymerase chain reaction Young adults |
title | p16 INK4A genetic and epigenetic profiles differ in relation to age and site in head and neck squamous cell carcinomas |
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