Prevalence of human papillomavirus in esophageal carcinoma in Tangshan, China

被引:8
作者
Mehryar, Mohammadreza Mohammadzad [1 ,2 ]
Li, Shu-Ying [3 ]
Liu, Hong-Wei [4 ]
Li, Fan [1 ,2 ]
Zhang, Fang [1 ,2 ]
Zhou, Yu-Bai [2 ]
Zeng, Yi [1 ,2 ,5 ,6 ]
Li, Jin-Tao [1 ,2 ,5 ,6 ]
机构
[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing Key Lab Environm & Viral Oncol, Beijing 100124, Peoples R China
[2] Sichuan Univ, West China Hosp, Collaborat Innovat Ctr Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[3] Hebei United Univ, Coll Basic Med, Dept Pathogen Biol, Tangshan 063000, Hebei Province, Peoples R China
[4] China West Normal Univ, Coll Life Sci, Key Lab Southwest China Wildlife Resources Conser, Minist Educ, Nanchong 637000, Sichuan, Peoples R China
[5] Chinese Ctr Dis Control & Prevent, Natl Inst Viral Dis Control & Prevent, Beijing 100052, Peoples R China
[6] Key Lab Infect Dis Prevent & Control, Beijing 100052, Peoples R China
关键词
Esophageal carcinoma; Formalin-fixed; paraffin-embedded tissue; Esophageal squamous cell carcinoma; Human papillomavirus; Polymerase chain reaction; SQUAMOUS-CELL CARCINOMA; HIGH-RISK REGION; CANCER; VIRUS; DNA; INFECTION; TYPE-16; LESIONS; HPV; ETIOLOGY;
D O I
10.3748/wjg.v21.i10.2905
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: to study the prevalence of human papillomavirus (HPV) in esophageal carcinoma in Tangshan, China, a high-incidence area. METHODS: Formalin-fixed, paraffin-embedded tissue specimens from 198 patients who were pathologically diagnosed with esophageal squamous cell carcinoma from 2011 to 2013 were obtained from a pathology department in Tangshan. DNA was extracted from all 198 specimens to detect HPV by polymerase chain reaction (PCR). beta-globin PCR was performed to check the quality of the DNA extraction procedure. PCR was performed to detect a wide range of HPV types, and type-specific PCR was performed to detect HPV types 16 and 18. Negative and positive controls were used for HPV 16 and 18 detection. RESULTS: The DNA extraction method in this study appeared to be more effective than other previously reported methods. After DNA extraction, more than 98% of the tissue specimens had an acceptable result in the DNA qualification test (beta-globin PCR). The overall prevalence of HPV in tumor tissues by GP6+/GP5+ PCR was 79.79%, and the prevalence of HPV types 16 and 18 was 40.40% and 47.47%, respectively. PCR demonstrated the presence of HPV, and direct sequencing confirmed the HPV genotypes. All HPV-positive PCR products were checked by DNA sequence analysis using DNAman and compared with the known HPV sequences listed in the Basic Local Alignment Search Tool database to evaluate the HPV types. This analysis confirmed the presence of HPV types 16 and 18. CONCLUSION: DNA of high-risk HPV types 16 and 18 is present in esophageal tumors, implicating HPV as a possible etiologic factor for esophageal squamous cell carcinoma.
引用
收藏
页码:2905 / 2911
页数:7
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