Puranen M, Saarikoski S, Syrjänen K, Syrjänen S
Department of Pathology, University of Kuopio, Finland.
Acta Cytol. 1996 May-Jun;40(3):391-5. doi: 10.1159/000333842.
To test the applicability of four protocols in recovering DNA suitable for amplification with the polymerase chain reaction (PCR) in archival, Papanicolaou-stained cervical smears.
The most efficient method was used to isolate DNA from 11 archival, Papanicolaou-stained smears with cytopathic changes due to human papillomavirus (HPV) infection to confirm the presence of HPV DNA.
beta-Globin was successfully amplified in all smears, while HPV DNA was detected in 6 of 11. Four of the four HPV DNA-negative smears were classified as high grade squamous intraepithelial lesions. Failure to detect HPV DNA might have been due to the low copy number of HPV DNA or deletion of the L1 region.
High cellularity and the method of recovering DNA from the smear are important determinants of successful amplification of HPV DNA in archival cervical smears.
检测四种方法在从存档的巴氏染色宫颈涂片中提取适用于聚合酶链反应(PCR)扩增的DNA方面的适用性。
采用最有效的方法从11份因人类乳头瘤病毒(HPV)感染而有细胞病变的存档巴氏染色涂片中分离DNA,以确认HPV DNA的存在。
所有涂片均成功扩增出β-珠蛋白,11份中有6份检测到HPV DNA。4份HPV DNA阴性涂片中有4份被归类为高级别鳞状上皮内病变。未能检测到HPV DNA可能是由于HPV DNA拷贝数低或L1区域缺失。
细胞数量多以及从涂片中提取DNA的方法是存档宫颈涂片中成功扩增HPV DNA的重要决定因素。