Syrjänen K J
Laboratory of Pathology and Cancer Research, Finnish Cancer Society, Kuopio, Finland.
Arch Geschwulstforsch. 1987;57(6):417-44.
Current data implicating an etiological role of Human papillomavirus (HPV) infections in precancer lesions (intraepithelial neoplasia) and squamous cell carcinoma of both the genital tract and other sites (oral cavity, larynx, skin, esophagus, nasal cavity, bronchus) can be summarized as follows: a) HPV involvement in benign, precancer, and malignant genital squamous cell lesions has been demonstrated by morphological, immunohistochemical and DNA hybridization techniques; b) HPV infections in the genital tract are sexually transmitted (STD) and associated with the same risk factors as development of cervical carcinoma; c) natural history of cervical HPV lesions is equivalent to that of CIN, i.e. they are potentially progressive to carcinoma in situ; d) latent HPV infections exist in the genital tract of both sexes; e) animal models exist, where papillomaviruses induce malignant transformation; f) HPV 11 induces transformation of human squamous epithelium in vivo (nude mouse renal subcapsule assay); g) malignant transformation of HPV lesions seems to depend on virus type and the physical state of its DNA, i.e. whether or not integrated in the host cell DNA; h) malignant transformation most probably requires synergistic actions between HPV and chemical or physical carcinogens or other infectious agents; i) genetic disposition (at least in animals) significantly contributes to malignant transformation; j) immunological defence mechanisms of the host probably are capable of modifying the course of HPV infection (efficacy in man remains to be elucidated). Many details of the molecular mechanisms still remain to be clarified, however. No applicable model systems exist to elucidate these issues, or the mechanisms leading to the progression to invasive cancer. Improved tissue culture systems for in vitro differentiation of keratinocytes should help in elucidating the biology of papillomaviruses and their interaction with cell division and differentiation.
目前有数据表明,人乳头瘤病毒(HPV)感染在癌前病变(上皮内瘤变)以及生殖道和其他部位(口腔、喉、皮肤、食管、鼻腔、支气管)的鳞状细胞癌中具有病因学作用,相关情况可总结如下:a)通过形态学、免疫组织化学和DNA杂交技术已证实HPV与良性、癌前及恶性生殖器鳞状细胞病变有关;b)生殖道HPV感染通过性传播(性传播疾病),且与宫颈癌发生的风险因素相同;c)宫颈HPV病变的自然史与宫颈上皮内瘤变(CIN)相同,即它们有可能进展为原位癌;d)男女两性的生殖道均存在HPV潜伏感染;e)存在动物模型,乳头瘤病毒可在其中诱导恶性转化;f)HPV 11可在体内诱导人鳞状上皮转化(裸鼠肾被膜下接种试验);g)HPV病变的恶性转化似乎取决于病毒类型及其DNA的物理状态,即是否整合到宿主细胞DNA中;h)恶性转化很可能需要HPV与化学或物理致癌物或其他感染因子之间的协同作用;i)遗传易感性(至少在动物中)对恶性转化有显著影响;j)宿主的免疫防御机制可能能够改变HPV感染的进程(在人类中的效果尚待阐明)。然而,分子机制的许多细节仍有待澄清。目前不存在适用的模型系统来阐明这些问题,或导致进展为浸润性癌的机制。用于角质形成细胞体外分化的改良组织培养系统应有助于阐明乳头瘤病毒的生物学特性及其与细胞分裂和分化的相互作用。