人细小病毒B19感染不同头颈部解剖亚位的恶性和良性组织标本。

IF 3.1 2区 医学 Q3 IMMUNOLOGY
Haniyeh Abuei, Sepide Namdari, Tahereh Pakdel, Fatemeh Pakdel, Azadeh Andishe-Tadbir, Abbas Behzad-Behbahani, Mohammad J Ashraf, Parnian Alavi, Ali Farhadi
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引用次数: 0

摘要

背景:人细小病毒B19 (B19V)感染在头颈部鳞状细胞癌(HNSCCs)和口腔黏液囊肿等恶性和良性病变中的作用尚未确定。在此,我们首次检测了B19V在伊朗HNSCCs中的存在。方法:采用巢式聚合酶链反应(nPCR)和TaqMan定量PCR法对108例HNSCC标本进行B19V检测。采用免疫组化方法评价B19V VP1/VP2蛋白、p16INK4a、NF-κB在肿瘤组织及其邻近非肿瘤组织中的表达。另外,选取健康成人40例口腔黏液囊肿、30例口腔口腔黏膜拭子和30例鼻咽拭子作为对照分析。结果:36.1%的HNSCCs检出B19V DNA。此外,23.3%的HNSCC标本对B19V VP1/VP2蛋白表现出免疫反应性。结论:综上所述,B19V在伊朗HNSCC患者的组织中经常存在,而在健康受试者的邻近非肿瘤组织以及口腔黏液囊肿病变、口腔和鼻咽拭子中大多不存在。HPV可能导致B19V在HNSCC组织中持续存在。需要进一步的研究来调查B19V在HNSCCs发展中的潜在病因学或辅助因素作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Human parvovirus B19 infection in malignant and benign tissue specimens of different head and neck anatomical subsites.

Human parvovirus B19 infection in malignant and benign tissue specimens of different head and neck anatomical subsites.

Human parvovirus B19 infection in malignant and benign tissue specimens of different head and neck anatomical subsites.

Background: The role of human parvovirus B19 (B19V) infection in malignant and benign lesions such as head and neck squamous cell carcinomas (HNSCCs) and oral mucocele lesions has not been established. Herein, we examined, for the first time, the presence of B19V in HNSCCs from Iranian subjects.

Methods: One hundred and eight HNSCC specimens were analyzed for the presence of B19V using nested polymerase chain reaction (nPCR) and TaqMan quantitative PCR assays. Immunohistochemistry procedures were performed to evaluate the expression of B19V VP1/VP2 proteins, p16INK4a, and NF-κB in tumor tissues and their adjacent non-tumor tissues. In addition, 40 oral mucocele, 30 oral buccal mucosa swabs, and 30 nasopharyngeal swabs obtained from healthy adults were analyzed as controls.

Results: B19V DNA was detected in 36.1% of HNSCCs. Further, 23.3% of HNSCC specimens showed immunoreactivity against B19V VP1/VP2 proteins. There was a significant difference in the frequency of B19V DNA-positive cases between the patient and control groups (p < 0.0001). Moreover, comparing tumoral tissues and their adjacent non-tumor tissues in terms of immunoreactivity against B19V structural proteins, a significant association was found between tumor tissues and B19V infection (p < 0.0001). Finally, investigating the simultaneous presence of B19V and high-risk human papillomaviruses (HPV) DNA, we found a significant association between these two viral infections in HNSCCs (p = 0.031).

Conclusions: To sum up, B19V was frequently present in HNSCC tissues of Iranian patients but mostly absent in the adjacent non-tumor tissues as well as oral mucocele lesions, buccal, and nasopharyngeal swabs of healthy subjects. HPV possibly contributes to B19V persistence in HNSCC tissues. Additional research is required to investigate potential etiological or cofactor roles of B19V in the development of HNSCCs.

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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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