Human papillomaviruses in normal oral mucosa: a comparison of methods for sample collection.

The prevalence of six genital genotypes of HPV was assessed in the clinically normal oral mucosa of an adult Caucasian population, and three methods of sample collection compared. HPV DNA was detected in the mouth of 60% of 60 subjects. HPV 16 was the most prevalent genotype, and positive samples were found most frequently in men over 50. A 3% sucrose mouthwash produced more positive results (51%) than mucosal scrapes of three separate sites (45%) or buccal mucosal biopsies (12%). There was no association of a positive result for HPV DNA with any particular mucosal site. A mouthwash was the preferred single screening method for epidemiologic studies of HPV DNA in the mouth, but the greatest yield of positive samples was obtained if multiple sampling techniques were employed.

[1]  K. Münger,et al.  The state of the p53 and retinoblastoma genes in human cervical carcinoma cell lines. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[2]  W. A. Yeudall,et al.  Human papillomavirus DNA in biopsies of oral tissues. , 1991, The Journal of general virology.

[3]  Arnold J. Levine,et al.  The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53 , 1990, Cell.

[4]  S. Syrjänen,et al.  Oral mucosal changes in women with genital HPV infection. , 1990, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

[5]  S. Syrjänen Basic concepts and practical applications of recombinant DNA techniques in detection of human papillomavirus (HPV) infections , 1990 .

[6]  M. Wells,et al.  Demonstration of multiple HPV types in normal cervix and in cervical squamous cell carcinoma using the polymerase chain reaction on paraffin wax embedded material. , 1990, Journal of clinical pathology.

[7]  Y. Soong,et al.  Detection of human papillomaviruses in cervicovaginal cells using polymerase chain reaction. , 1990, The Journal of infectious diseases.

[8]  W. Lancaster,et al.  Amplification of human papillomavirus DNA sequences by using conserved primers , 1989, Journal of clinical microbiology.

[9]  E. Villiers Heterogeneity of the human papillomavirus group. , 1989 .

[10]  J. Brandsma,et al.  Association of papillomavirus with cancers of the head and neck. , 1989, Archives of otolaryngology--head & neck surgery.

[11]  Che-Shoa Chang,et al.  High prevalence of human papillomavirus infection and possible association with betel quid chewing and smoking in oral epidermoid carcinomas in taiwan , 1989, Journal of medical virology.

[12]  K. Münger,et al.  The human papilloma virus-16 E7 oncoprotein is able to bind to the retinoblastoma gene product. , 1989, Science.

[13]  S. Syrjänen,et al.  Concept of the Existence of Human Papillomavirus (HPV) DNA in Histologically Normal Squamous Epithelium of the Genital Tract Should be Re‐Evaluated , 1989, Acta obstetricia et gynecologica Scandinavica.

[14]  J. Macnab,et al.  Human papillomavirus in paired normal and abnormal cervical biopsies–implications for treatment , 1988, British journal of obstetrics and gynaecology.

[15]  S. Syrjänen,et al.  Human papillomavirus (HPV) DNA sequences in oral precancerous lesions and squamous cell carcinoma demonstrated by in situ hybridization. , 1988, Journal of oral pathology.

[16]  R. Williamson,et al.  SIMPLE NON-INVASIVE METHOD TO OBTAIN DNA FOR GENE ANALYSIS , 1988, The Lancet.

[17]  W. Rawls,et al.  Comparison of the Cytobrush and cotton swabs in sampling cervical cells for filter in situ hybridization detection of human papillomavirus types 16 and 18 DNA. , 1988, Acta cytologica.

[18]  N. Maitland,et al.  Papillomaviruses: the current status in relation to oral disease. , 1988, Oral surgery, oral medicine, and oral pathology.

[19]  K. Mullis,et al.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.

[20]  N. Maitland,et al.  Detection of human papillomavirus DNA in biopsies of human oral tissue. , 1987, British Journal of Cancer.

[21]  N. Maitland,et al.  HPV 16 DNA IN NORMAL AND MALIGNANT CERVICAL EPITHELIUM: IMPLICATIONS FOR THE AETIOLOGY AND BEHAVIOUR OF CERVICAL NEOPLASIA , 1987, The Lancet.

[22]  N. Maitland,et al.  HUMAN PAPILLOMAVIRUS DNA AND ORAL MUCOSA , 1987, The Lancet.

[23]  J. Bidwell,et al.  HLA-DR allogenotyping using exon-specific cDNA probes and application of rapid minigel methods. , 1986, Molecular immunology.

[24]  N. Maitland,et al.  HUMAN PAPILLOMAVIRUS TYPE-16 HOMOLOGOUS DNA IN NORMAL HUMAN ECTOCERVIX , 1986, The Lancet.

[25]  E. de Villiers,et al.  Papillomavirus DNA in human tongue carcinomas , 1985, International journal of cancer.

[26]  L. Gissmann,et al.  Papillomavirus infection of the lower genital tract: Detection of viral DNA in gynecological swabs , 1985, International journal of cancer.

[27]  J. Feldman,et al.  A case-control investigation of alcohol, tobacco, and diet in head and neck cancer. , 1975, Preventive medicine.

[28]  E. Southern Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.