The Relation of HPV Infection and Expression of p53 and p16 Proteins in Esophageal Squamous Cells Carcinoma

To investigate the HPV prevalence and characterize the expression of potential molecular surrogate markers of HPV infection in esophageal squamous cell carcinoma. The prevalence of HPV in individuals with and without esophageal cancer (EC) was determined by using multiplex PCR; p16 and p53 protein l...

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Published inJournal of Cancer Vol. 8; no. 6; pp. 1062 - 1070
Main Authors Pastrez, Paula Roberta Aguiar, Mariano, Vânia Sammartino, da Costa, Allini Mafra, Silva, Estela Maria, Scapulatempo-Neto, Cristovam, Guimarães, Denise Peixoto, Fava, Gilberto, Neto, Said Abdala Zemi, Nunes, Emily Montosa, Sichero, Laura, Villa, Luisa Lina, Syrjanen, Kari Juhani, Longatto-Filho, Adhemar
Format Journal Article
LanguageEnglish
Published Australia Ivyspring International Publisher 01.01.2017
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Summary:To investigate the HPV prevalence and characterize the expression of potential molecular surrogate markers of HPV infection in esophageal squamous cell carcinoma. The prevalence of HPV in individuals with and without esophageal cancer (EC) was determined by using multiplex PCR; p16 and p53 protein levels were assessed by immunohistochemistry (IHC). High-risk HPV (hr-HPV) was found in the same frequency (13.8%) in esophageal squamous cell carcinoma (ESCC) and in healthy individuals. The p53 expression was positive in 67.5% of tumor tissue, 20.0% of adjacent non-tumoral tissue and 1.8% of normal esophageal tissue. p16 was positive in 11.6% of esophageal cancer cases and 4.7% of adjacent non-tumoral tissue. p16 was undetectable among control group samples. p53 and p16 levels were not significantly associated with the HPV status. These results suggest that hr-HPV types are not associated with the development of ESCC and that p53 and p16 protein expression have no relationship with HPV infection in normal or cancerous esophagus.
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Competing Interests: The authors have declared that no competing interest exists.
ISSN:1837-9664
1837-9664
DOI:10.7150/jca.17080