Campisi Giuseppina, Panzarella Vera, Giuliani Michele, Lajolo Carlo, Di Fede Olga, Falaschini Silvia, Di Liberto Chiara, Scully Crispian, Lo Muzio Lorenzo
Department of Oral Sciences, University of Palermo, Palermo, Italy.
Int J Oncol. 2007 Apr;30(4):813-23.
Human papillomaviruses (HPVs) are a group of host-specific DNA viruses, with a remarkable epithelial cell specificity: they have been reported principally in the ano-genital tract, urethra, skin, larynx, tracheo-bronchial and oral mucosa. More than 100 different HPV types have been identified and classified as high (e.g. 16, 18, 31) or low (e.g. 11, 42, 36) -risk (HR and LR), based on their association with cervical carcinoma. The carcinogenic role of HR-HPV revolves mainly around two of its oncoproteins: HPV-E6 which promotes degradation of the p53 tumour suppressor gene product and HPV-E7 which modifies the pRb tumour suppressor gene product, inhibiting the activity of TGF-beta2. Since these viral oncoproteins are capable of transforming primary human keratinocytes from either genital or upper respiratory tract epithelia, they have been considered to play a role in disrupting cell-cycle regulatory pathways leading to a genetic progression to ano-genital cancer and, possibly, also to oral squamous cell carcinoma (OSCC). Recently, the oncogene HPV-E5 has also been found to transform cells by modulating growth factor receptors. On the basis of the high, although very variable, frequency of HR-HPV in OSCC, an oral malignant potential of HPV infection has been hypothesised but not definitively confirmed. Major aims of this review are to update the understanding of HPV activities with respect to oral oncology and to comment on the HPV DNA reported frequencies in OSCC and potentially malignant oral lesions. A computer database search was performed, through the use of MEDLINE (PubMED) and Cochrane Library, for the last three decades. Search key words used were: human papillomavirus, HPV and cancer, HPV and oral lesions, HPV and oral premalignant lesions, HPV and oral cancer, HPV and HNSCC, HPV and oral mucosa. The search was of all fields, all languages and all dates available.
人乳头瘤病毒(HPV)是一组宿主特异性DNA病毒,具有显著的上皮细胞特异性:主要见于肛门生殖道、尿道、皮肤、喉、气管支气管和口腔黏膜。已鉴定出100多种不同的HPV类型,并根据其与宫颈癌的关联分为高风险(如16、18、31型)或低风险(如11、42、36型)(HR和LR)。HR-HPV的致癌作用主要围绕其两种癌蛋白:促进p53肿瘤抑制基因产物降解的HPV-E6和修饰pRb肿瘤抑制基因产物、抑制TGF-β2活性的HPV-E7。由于这些病毒癌蛋白能够转化来自生殖器或上呼吸道上皮的原代人角质形成细胞,它们被认为在破坏细胞周期调节途径中起作用,导致肛门生殖器癌的遗传进展,也可能导致口腔鳞状细胞癌(OSCC)。最近,还发现癌基因HPV-E5通过调节生长因子受体来转化细胞。基于OSCC中HR-HPV的高频率(尽管变化很大),有人推测HPV感染具有口腔恶性潜能,但尚未得到明确证实。本综述的主要目的是更新对HPV在口腔肿瘤学方面活性的认识,并对OSCC和潜在恶性口腔病变中报道的HPV DNA频率进行评论。通过使用MEDLINE(PubMED)和Cochrane图书馆,对过去三十年进行了计算机数据库搜索。使用的搜索关键词为:人乳头瘤病毒、HPV与癌症、HPV与口腔病变、HPV与口腔癌前病变、HPV与口腔癌、HPV与头颈部鳞状细胞癌、HPV与口腔黏膜。搜索涵盖所有领域、所有语言和所有可用日期。