Detection of HPV DNA in oral carcinoma using polymerase chain reaction together with in situ hybridization

Craig S. Miller; Maria S. Zeuss; Dean K. White

doi:10.1016/0030-4220(94)90227-5

Detection of HPV DNA in oral carcinoma using polymerase chain reaction together with in situ hybridization

Craig S. Miller, Maria S. Zeuss, Dean K. White

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Abstract

This study determined the prevalence of human papillomavirus16/18 DNA in deparaffinized oral carcinoma specimens on slides with the use of the different sensitivities of in situ hybridization and a technique that combines polyermase chain reaction and in situ hybridization. Human papillomavirus DNA was not detected in the 30 biopsy specimens analyzed by in situ hybridization alone using biotinylated DNA probes specific for human papillomavirus16/18. Twenty of 30 specimens (66.7%) were found to have human papillomavirus DNA (p < 0.001) with the use of the polymerase chain reaction-in situ hybridization technique. Human papillomavirus 16 was detected in 18 of 26 specimens (69.2%), and 7 of 25 carcinomas (28%) were found to contain human papillomavirus 18. Dual infections were present in 5 of 21 (23.8%) specimens. Human papillomavirus DNA was more prevalent in men (75%) than women (57.1%). However, there was no difference in the mean age of patients with oral carcinoma (men, 67.8 years; women, 67.5 years) who had human papillomavirus and those who did not (67.2 years). Carcinomas associated with dual infections occurred at a lower mean age (59.4 years) than those associated with a single human papillomavirus type (p < 0.005). We conclude that the polymerase chain reaction-in situ hybridization technique enhances our ability to demonstrate human papillomavirus types highly associated with oral squamous cell carcinoma.

Original language	English
Pages (from-to)	480-486
Number of pages	7
Journal	Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
Volume	77
Issue number	5
DOIs	https://doi.org/10.1016/0030-4220(94)90227-5
State	Published - May 1994

Bibliographical note

Funding Information:
This work was supported in part by grant (DE09885-OlAl) from the National Institutes of Dental Research and a grant from Di-gene Diagnostics. aAssistant Professor, Oral Medicine Section, Department of Oral Health Science, University of Kentucky College of Dentistry. bProfessor, Departamento de Atencion Odontologica Integral al Adult0 (Patologia Bucal), Facultad de Odontologia, University of Carabobo College of Dentistry. cProfessor, Oral Pathology Section, University of Kentucky College of Dentistry. Copyright @ 1994 by Mosby-Year Book, Inc. OO30-4220/94/$3.00 + 0 l/14/53169

ASJC Scopus subject areas

Pathology and Forensic Medicine
General Dentistry

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10.1016/0030-4220(94)90227-5

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@article{d0d19cc7ddf34ce9b9ba8c7dfe0e96cc,

title = "Detection of HPV DNA in oral carcinoma using polymerase chain reaction together with in situ hybridization",

abstract = "This study determined the prevalence of human papillomavirus16/18 DNA in deparaffinized oral carcinoma specimens on slides with the use of the different sensitivities of in situ hybridization and a technique that combines polyermase chain reaction and in situ hybridization. Human papillomavirus DNA was not detected in the 30 biopsy specimens analyzed by in situ hybridization alone using biotinylated DNA probes specific for human papillomavirus16/18. Twenty of 30 specimens (66.7%) were found to have human papillomavirus DNA (p < 0.001) with the use of the polymerase chain reaction-in situ hybridization technique. Human papillomavirus 16 was detected in 18 of 26 specimens (69.2%), and 7 of 25 carcinomas (28%) were found to contain human papillomavirus 18. Dual infections were present in 5 of 21 (23.8%) specimens. Human papillomavirus DNA was more prevalent in men (75%) than women (57.1%). However, there was no difference in the mean age of patients with oral carcinoma (men, 67.8 years; women, 67.5 years) who had human papillomavirus and those who did not (67.2 years). Carcinomas associated with dual infections occurred at a lower mean age (59.4 years) than those associated with a single human papillomavirus type (p < 0.005). We conclude that the polymerase chain reaction-in situ hybridization technique enhances our ability to demonstrate human papillomavirus types highly associated with oral squamous cell carcinoma.",

author = "Miller, {Craig S.} and Zeuss, {Maria S.} and White, {Dean K.}",

note = "Funding Information: This work was supported in part by grant (DE09885-OlAl) from the National Institutes of Dental Research and a grant from Di-gene Diagnostics. aAssistant Professor, Oral Medicine Section, Department of Oral Health Science, University of Kentucky College of Dentistry. bProfessor, Departamento de Atencion Odontologica Integral al Adult0 (Patologia Bucal), Facultad de Odontologia, University of Carabobo College of Dentistry. cProfessor, Oral Pathology Section, University of Kentucky College of Dentistry. Copyright @ 1994 by Mosby-Year Book, Inc. OO30-4220/94/$3.00 + 0 l/14/53169",

year = "1994",

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AU - Miller, Craig S.

AU - Zeuss, Maria S.

AU - White, Dean K.

N1 - Funding Information: This work was supported in part by grant (DE09885-OlAl) from the National Institutes of Dental Research and a grant from Di-gene Diagnostics. aAssistant Professor, Oral Medicine Section, Department of Oral Health Science, University of Kentucky College of Dentistry. bProfessor, Departamento de Atencion Odontologica Integral al Adult0 (Patologia Bucal), Facultad de Odontologia, University of Carabobo College of Dentistry. cProfessor, Oral Pathology Section, University of Kentucky College of Dentistry. Copyright @ 1994 by Mosby-Year Book, Inc. OO30-4220/94/$3.00 + 0 l/14/53169

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N2 - This study determined the prevalence of human papillomavirus16/18 DNA in deparaffinized oral carcinoma specimens on slides with the use of the different sensitivities of in situ hybridization and a technique that combines polyermase chain reaction and in situ hybridization. Human papillomavirus DNA was not detected in the 30 biopsy specimens analyzed by in situ hybridization alone using biotinylated DNA probes specific for human papillomavirus16/18. Twenty of 30 specimens (66.7%) were found to have human papillomavirus DNA (p < 0.001) with the use of the polymerase chain reaction-in situ hybridization technique. Human papillomavirus 16 was detected in 18 of 26 specimens (69.2%), and 7 of 25 carcinomas (28%) were found to contain human papillomavirus 18. Dual infections were present in 5 of 21 (23.8%) specimens. Human papillomavirus DNA was more prevalent in men (75%) than women (57.1%). However, there was no difference in the mean age of patients with oral carcinoma (men, 67.8 years; women, 67.5 years) who had human papillomavirus and those who did not (67.2 years). Carcinomas associated with dual infections occurred at a lower mean age (59.4 years) than those associated with a single human papillomavirus type (p < 0.005). We conclude that the polymerase chain reaction-in situ hybridization technique enhances our ability to demonstrate human papillomavirus types highly associated with oral squamous cell carcinoma.

AB - This study determined the prevalence of human papillomavirus16/18 DNA in deparaffinized oral carcinoma specimens on slides with the use of the different sensitivities of in situ hybridization and a technique that combines polyermase chain reaction and in situ hybridization. Human papillomavirus DNA was not detected in the 30 biopsy specimens analyzed by in situ hybridization alone using biotinylated DNA probes specific for human papillomavirus16/18. Twenty of 30 specimens (66.7%) were found to have human papillomavirus DNA (p < 0.001) with the use of the polymerase chain reaction-in situ hybridization technique. Human papillomavirus 16 was detected in 18 of 26 specimens (69.2%), and 7 of 25 carcinomas (28%) were found to contain human papillomavirus 18. Dual infections were present in 5 of 21 (23.8%) specimens. Human papillomavirus DNA was more prevalent in men (75%) than women (57.1%). However, there was no difference in the mean age of patients with oral carcinoma (men, 67.8 years; women, 67.5 years) who had human papillomavirus and those who did not (67.2 years). Carcinomas associated with dual infections occurred at a lower mean age (59.4 years) than those associated with a single human papillomavirus type (p < 0.005). We conclude that the polymerase chain reaction-in situ hybridization technique enhances our ability to demonstrate human papillomavirus types highly associated with oral squamous cell carcinoma.

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VL - 77

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JO - Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

JF - Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

IS - 5

ER -

Detection of HPV DNA in oral carcinoma using polymerase chain reaction together with in situ hybridization

Abstract

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