Pecoraro G, Lee M, Morgan D, Defendi V
Department of Pathology, New York University Medical Center, New York.
Am J Pathol. 1991 Jan;138(1):1-8.
Cervical carcinoma develops through a progressive spectrum of premalignant intraepithelial lesions (CIN I-III), the majority of which are associated with human papillomavirus (HPV) types 16 and 18. We established HPV16 and HPV18 immortalized human cervical epithelial cell lines and used them as a model to investigate the genesis and progression of cervical malignancy. The cell lines when cultured in vitro in a system mimicking their in vivo environment exhibit cytologic atypia and a variety of defects in morphologic differentiation at early passage compared to their normal counterparts. With increased passage, these alterations progress to more severe grades, histologically similar to CIN III; however only a limited number of the cell lines are tumorigenic, mimicking the epidemiologic evidence on the rate of conversion from premalignant to invasive carcinoma. The observed changes are not associated with alterations of viral DNA integration or expression and may reflect specific cellular events or changes in virus-host interactions associated with malignant progression.
宫颈癌通过一系列逐渐发展的癌前上皮内病变(CIN I - III)演变而来,其中大多数与16型和18型人乳头瘤病毒(HPV)相关。我们建立了HPV16和HPV18永生化人宫颈上皮细胞系,并将其用作研究宫颈恶性肿瘤发生和发展的模型。与正常对应细胞相比,这些细胞系在模拟其体内环境的体外系统中培养时,在传代早期表现出细胞学异型性和形态分化方面的各种缺陷。随着传代次数增加,这些改变进展到更严重的程度,组织学上类似于CIN III;然而,只有少数细胞系具有致瘤性,这与从癌前病变转化为浸润性癌的发生率的流行病学证据相符。观察到的变化与病毒DNA整合或表达的改变无关,可能反映了与恶性进展相关的特定细胞事件或病毒 - 宿主相互作用的变化。