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本文引用的文献

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Human papillomavirus type-distribution in cervical cancer in China: the importance of HPV 16 and 18.中国宫颈癌中人类乳头瘤病毒型别分布:HPV16 和 18 的重要性。
Cancer Causes Control. 2009 Nov;20(9):1705-13. doi: 10.1007/s10552-009-9422-z. Epub 2009 Aug 25.
2
A review of human carcinogens--Part B: biological agents.人类致癌物综述——B部分:生物制剂
Lancet Oncol. 2009 Apr;10(4):321-2. doi: 10.1016/s1470-2045(09)70096-8.
3
[Detection of human papillomavirus in tissues of esophageal carcinomas by polymerase chain reaction].[应用聚合酶链反应检测食管癌组织中的人乳头瘤病毒]
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2008 Aug;22(4):251-3.
4
HPV prophylactic vaccines and the potential prevention of noncervical cancers in both men and women.人乳头瘤病毒预防性疫苗与男性和女性非宫颈癌的潜在预防
Cancer. 2008 Nov 15;113(10 Suppl):3036-46. doi: 10.1002/cncr.23764.
5
Comparison of two PCR-based human papillomavirus genotyping methods.两种基于聚合酶链反应的人乳头瘤病毒基因分型方法的比较。
J Clin Microbiol. 2008 Oct;46(10):3437-45. doi: 10.1128/JCM.00620-08. Epub 2008 Aug 20.
6
Human papillomavirus accounts both for increased incidence and better prognosis in tonsillar cancer.人乳头瘤病毒既导致扁桃体癌发病率上升,也使其预后更佳。
Anticancer Res. 2008 Mar-Apr;28(2B):1133-8.
7
Case-control study of human papillomavirus and oropharyngeal cancer.人乳头瘤病毒与口咽癌的病例对照研究
N Engl J Med. 2007 May 10;356(19):1944-56. doi: 10.1056/NEJMoa065497.
8
A prospective study of tobacco, alcohol, and the risk of esophageal and gastric cancer subtypes.一项关于烟草、酒精与食管癌和胃癌亚型风险的前瞻性研究。
Am J Epidemiol. 2007 Jun 15;165(12):1424-33. doi: 10.1093/aje/kwm051. Epub 2007 Apr 9.
9
Human papillomavirus type distribution in invasive cervical cancer and high-grade cervical lesions: a meta-analysis update.浸润性宫颈癌和高级别宫颈病变中人类乳头瘤病毒的类型分布:一项Meta分析的更新
Int J Cancer. 2007 Aug 1;121(3):621-32. doi: 10.1002/ijc.22527.
10
No association between HPV infection and the neoplastic progression of esophageal squamous cell carcinoma: result from a cross-sectional study in a high-risk region of China.人乳头瘤病毒感染与食管鳞状细胞癌肿瘤进展之间无关联:来自中国高危地区的一项横断面研究结果
Int J Cancer. 2006 Sep 15;119(6):1354-9. doi: 10.1002/ijc.21980.

在中国,人乳头瘤病毒(HPV)与食管鳞状细胞癌(ESCC)无关。

No role for human papillomavirus in esophageal squamous cell carcinoma in China.

机构信息

Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, Bethesda, MD 20852-7248, USA.

出版信息

Int J Cancer. 2010 Jul 1;127(1):93-100. doi: 10.1002/ijc.25023.

DOI:10.1002/ijc.25023
PMID:19918949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3069961/
Abstract

Certain regions of China have high rates of esophageal squamous cell carcinoma (ESCC). Previous studies of human papillomavirus (HPV), a proposed causal factor, have produced highly variable results. We attempted to evaluate HPV and ESCC more definitively using extreme care to prevent DNA contamination. We collected tissue and serum in China from 272 histopathologically-confirmed ESCC cases with rigorous attention to good molecular biology technique. We tested for HPV DNA in fresh-frozen tumor tissue using PCR with PGMY L1 consensus primers and HPV16 and 18 type-specific E6 and E7 primers, and in formalin-fixed paraffin-embedded tumor tissue using SPF(10) L1 primers. In HPV-positive cases, we evaluated p16(INK4a) overexpression and HPV E6/E7 seropositivity as evidence of carcinogenic HPV activity. beta-globin, and thus DNA, was adequate in 98.2% of the frozen tumor tissues (267/272). Of these, 99.6% (95% confidence interval (CI) = 97.9-100.0%) were negative for HPV DNA by PGMY, and 100% (95% CI = 98.6-100%) were negative by HPV16/18 E6/E7 PCR. In the corresponding formalin-fixed paraffin-embedded tumor specimens, 99.3% (95% CI = 97.3-99.9%) were HPV negative by SPF(10). By PGMY, 1 case tested weakly positive for HPV89, a noncancer causing HPV type. By SPF(10), 2 cases tested weakly positive: 1 for HPV16 and 1 for HPV31. No HPV DNA-positive case had evidence of HPV oncogene activity as measured by p16(INK4a) overexpression or E6/E7 seropositivity. This study provides the most definitive evidence to date that HPV is not involved in ESCC carcinogenesis in China. HPV DNA contamination cannot be ruled out as an explanation for high HPV prevalence in ESCC tissue studies with less stringent tissue procurement and processing protocols.

摘要

中国某些地区的食管鳞状细胞癌(ESCC)发病率很高。先前关于人乳头瘤病毒(HPV)的研究结果差异很大,HPV 是一种被认为的致癌因素。我们试图通过严格防止 DNA 污染,更明确地评估 HPV 和 ESCC。我们在中国收集了 272 例经组织病理学证实的 ESCC 病例的组织和血清,非常注重良好的分子生物学技术。我们使用聚合酶链反应(PCR)用 PGMY L1 通用引物和 HPV16 和 18 型特异性 E6 和 E7 引物检测新鲜冷冻肿瘤组织中的 HPV DNA,并用 SPF(10) L1 引物检测福尔马林固定石蜡包埋肿瘤组织中的 HPV DNA。在 HPV 阳性病例中,我们评估了 p16(INK4a)过表达和 HPV E6/E7 血清阳性作为致癌 HPV 活性的证据。β-球蛋白,因此 DNA,在 98.2%的冷冻肿瘤组织(267/272)中充足。其中,99.6%(95%置信区间(CI)=97.9-100.0%)PGMY 检测 HPV DNA 阴性,100%(95%CI=98.6-100%)HPV16/18 E6/E7 PCR 检测 HPV DNA 阴性。在相应的福尔马林固定石蜡包埋肿瘤标本中,99.3%(95%CI=97.3-99.9%)SPF(10)检测 HPV 阴性。PGMY 检测到 1 例 HPV89 弱阳性,HPV89 是非致癌 HPV 型。SPF(10)检测到 2 例弱阳性:1 例为 HPV16,1 例为 HPV31。没有 HPV DNA 阳性病例有 p16(INK4a)过表达或 E6/E7 血清阳性作为 HPV 致癌基因活性的证据。本研究提供了迄今为止最明确的证据,表明 HPV 在中国并非 ESCC 致癌作用的原因。HPV DNA 污染不能排除作为组织采集和处理协议不太严格的 ESCC 组织研究中 HPV 高流行率的解释。