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Frequency of Human Papillomavirus Detection in Chagasic Megaesophagus Associated or Not with Esophageal Squamous Cell Carcinoma

巨食道 医学 共感染 内科学 食管鳞状细胞癌 人乳头瘤病毒 多重聚合酶链反应 胃肠病学 食管癌 基因分型 癌症 聚合酶链反应 食管 肿瘤科 人类免疫缺陷病毒(HIV) 病毒学 生物 基因型 生物化学 基因
作者
Fernanda Franco Munari,Laura Sichero,Adriana Cruvinel Carloni,Croider Franco Lacerda,Emily Montosa Nunes,Antônio Talvane Torres de Oliveira,Cristovam Scapulatempo‐Neto,Sandra Regina Morini da Silva,Eduardo Crema,Sheila Jorge Adad,Maria Aparecida Marchesan Rodrigues,Maria Aparecida Coelho Arruda Henry,Denise Peixoto Guimarães,Rui Manuel Reis,Luisa L. Villa,Adhemar Longatto‐Filho
出处
期刊:Pathobiology [Karger Publishers]
卷期号:89 (1): 29-37 被引量:1
标识
DOI:10.1159/000518697
摘要

Chagasic megaesophagus (CM) as well as the presence of human papillomavirus (HPV) has been reported as etiological factors for esophageal squamous cell carcinoma (ESCC).We assessed the prevalence of HPV DNA in a series of ESCCs associated or not with CM. Data obtained were further correlated to the pathological and clinical data of affected individuals.A retrospective study was performed on 92 formalin-fixed and paraffin-embedded tissues collected from patients referred to 3 different hospitals in São Paulo, Brazil: Barretos Cancer Hospital, Barretos, São Paulo; Federal University of Triângulo Mineiro, Uberaba, Minas Gerais; and São Paulo State University, Botucatu, São Paulo. Cases were divided into 3 groups: (i) 24 patients with CM associated with ESCC (CM/ESCC); (ii) 37 patients with ESCC without CM (ESCC); and (iii) 31 patients with CM without ESCC (CM). Detection of HPV DNA was assessed in all samples by a genotyping assay combining multiplex polymerase chain reaction and bead-based Luminex technology.We identified a high prevalence of high-risk HPV in patients in the CM group (12/31, 38.8%) and CM/ESCC (8/24, 33.3%), compared to individuals in the ESCC group (6/37, 16.3%). The individuals in the groups with cancer (ESCC and CM/ESCC) had a higher frequency of HPV-16 (4/9, 44.5% and 2/8, 25.0%). The other types of high-risk HPVs detected were HPV-31, 45, 51, 53, 56, 66, and 73. We also observed in some samples HPV coinfection by more than one viral type. Despite the high incidence of HPV, it did not show any association with the patient's clinical-pathological and molecular (TP53 mutation status) characteristics.This is the first report of the presence of HPV DNA in CM associated with ESCC. HPV infection was more presence in megaesophagus lesions. Further studies are needed to confirm and better understand the role of persistent HPV infection in patients with CM.
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