Infections and Immunoepidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892-7248, USA.
J Natl Cancer Inst. 2011 Mar 16;103(6):501-7. doi: 10.1093/jnci/djr003. Epub 2011 Feb 3.
Lung cancer kills more than 1 million people worldwide each year. Whereas several human papillomavirus (HPV)-associated cancers have been identified, the role of HPV in lung carcinogenesis remains controversial.
We selected 450 lung cancer patients from an Italian population-based case-control study, the Environment and Genetics in Lung Cancer Etiology. These patients were selected from those with an adequate number of unstained tissue sections and included all those who had never smoked and a random sample of the remaining patients. We used real-time polymerase chain reaction (PCR) to test specimens from these patients for HPV DNA, specifically for E6 gene sequences from HPV16 and E7 gene sequences from HPV18. We also tested a subset of 92 specimens from all never-smokers and a random selection of smokers for additional HPV types by a PCR-based test for at least 54 mucosal HPV genotypes. DNA was extracted from ethanol- or formalin-fixed paraffin-embedded tumor tissue under strict PCR clean conditions. The prevalence of HPV in tumor tissue was investigated.
Specimens from 399 of 450 patients had adequate DNA for analysis. Most patients were current (220 patients or 48.9%) smokers, and 92 patients (20.4%) were women. When HPV16 and HPV18 type-specific primers were used, two specimens were positive for HPV16 at low copy number but were negative on additional type-specific HPV16 testing. Neither these specimens nor the others examined for a broad range of HPV types were positive for any HPV type.
When DNA contamination was avoided and state-of-the-art highly sensitive HPV DNA detection assays were used, we found no evidence that HPV was associated with lung cancer in a representative Western population. Our results provide the strongest evidence to date to rule out a role for HPV in lung carcinogenesis in Western populations.
每年,肺癌在全球范围内导致超过 100 万人死亡。虽然已经确定了几种与人类乳头瘤病毒(HPV)相关的癌症,但 HPV 在肺癌发生中的作用仍存在争议。
我们从意大利一项基于人群的病例对照研究“环境与肺癌病因学中的遗传因素”中选择了 450 名肺癌患者。这些患者是从那些有足够数量未染色组织切片的患者中选择的,包括所有从未吸烟的患者和其余患者的随机样本。我们使用实时聚合酶链反应(PCR)检测这些患者的标本中的 HPV DNA,具体来说是 HPV16 的 E6 基因序列和 HPV18 的 E7 基因序列。我们还通过基于 PCR 的检测对从未吸烟的 92 例标本和吸烟者的随机样本检测了其他 HPV 类型,该检测至少检测了 54 种黏膜 HPV 基因型。在严格的 PCR 清洁条件下,从乙醇或福尔马林固定的石蜡包埋肿瘤组织中提取 DNA。研究了肿瘤组织中 HPV 的流行情况。
450 名患者中有 399 名患者的标本有足够的 DNA 进行分析。大多数患者为当前吸烟者(220 名患者或 48.9%),92 名患者为女性(20.4%)。当使用 HPV16 和 HPV18 型特异性引物时,两个标本 HPV16 的低拷贝数为阳性,但在其他 HPV16 型特异性检测中为阴性。这些标本和其他广泛检测 HPV 类型的标本均未检测到任何 HPV 型阳性。
当避免 DNA 污染并使用最先进的高灵敏度 HPV DNA 检测方法时,我们没有发现 HPV 与代表性西方人群肺癌相关的证据。我们的结果提供了迄今为止最有力的证据,排除了 HPV 在西方人群肺癌发生中的作用。