Nishikawa A, Shimada M, Fukushima M
Department of Obstetrics and Gynecology, Sapporo Medical College.
Nihon Sanka Fujinka Gakkai Zasshi. 1991 Dec;43(12):1660-6.
We analyzed HPV-16 E6/E7 mRNA in human uterine cervical carcinomas and cervical intraepithelial neoplasias (CINs) by polymerase chain reaction (PCR) with reverse transcription (RT-PCR). Simultaneously total RNA and DNA were extracted from 6 cervical carcinomas, 14 CINs and 2 normal cervical tissues by the guanidium isothiocyanate/CsCl method. HPV-16 DNA was detected in 3 cervical carcinomas and 6 CINs. HPV-16 E6/E7 transcripts were detected in all HPV-16 DNA positive cervical carcinomas and CINs. In 2 cervical carcinomas and 5 CINs, 2 spliced E6 mRNA (E6I and E6II) and full length E6 mRNA were detected. In one cervical carcinoma and in one CIN, only full length E6-E7 mRNA was detected. Sequence analysis of cloned PCR products showed that both transcripts were generated by splicing out an intron in E6, from nucleotides (nt) 226 to 409 in E6I and from nt 226 to 526 in E6II. There was no significance difference in HPV-16 E6/E7 mRNA patterns between cervical carcinomas and CINs. This sensitive RT-PCR technique was available for analysis of HPV-16 mRNA in the small specimens.
我们采用逆转录聚合酶链反应(RT-PCR)对人子宫颈癌和子宫颈上皮内瘤变(CIN)中的人乳头瘤病毒16型(HPV-16)E6/E7信使核糖核酸(mRNA)进行了分析。同时,采用异硫氰酸胍/CsCl法从6例宫颈癌、14例CIN和2例正常宫颈组织中提取了总RNA和DNA。在3例宫颈癌和6例CIN中检测到HPV-16 DNA。在所有HPV-16 DNA阳性的宫颈癌和CIN中均检测到HPV-16 E6/E7转录本。在2例宫颈癌和5例CIN中,检测到2种剪接的E6 mRNA(E6I和E6II)和全长E6 mRNA。在1例宫颈癌和1例CIN中,仅检测到全长E6-E7 mRNA。对克隆的PCR产物进行序列分析表明,这两种转录本都是通过去除E6中的一个内含子产生的,E6I中从核苷酸(nt)226到409,E6II中从nt 226到526。宫颈癌和CIN之间HPV-16 E6/E7 mRNA模式无显著差异。这种灵敏的RT-PCR技术可用于分析小标本中的HPV-16 mRNA。