Shimano S, Fukushima M, Nishikawa A, Yamakawa Y, Takashima S, Satoh M, Minase T, Kutuzawa T, Hashimoto M
Department of Obstetrics and Gynecology, Sapporo Medical College.
Jpn J Clin Oncol. 1991 Feb;21(1):8-12.
Using in situ hybridization, human papillomavirus (HPV 6, 16, 18, 31, 33) DNAs were detected in a cervical severe dysplasia accompanied by squamous metaplasia. It was found that, only HPV 31 DNA was harbored in the cervical severe dysplasia, but HPV DNAs were not identified in a lesion of squamous metaplasia. The in situ hybridization method will be of use, therefore, when dysplasia with squamous metaplasia or other lesions are examined for HPV DNA. In a cervical smear, HPV 31 DNA could be detected on the nuclei of dysplastic cells, so this method is applicable to cervical smears. If squamous metaplasia is to be considered as a precursor lesion to cervical dysplasia, the HPV DNA harbored in the dysplasia must also be detected in the accompanying squamous metaplasia. Our results suggested that not all squamous metaplasias were involved with HPV, as far as we were able to detect using five types of HPV DNA probe.
采用原位杂交技术,在伴有鳞状化生的宫颈重度发育异常中检测到人乳头瘤病毒(HPV 6、16、18、31、33)DNA。结果发现,仅在宫颈重度发育异常中检测到HPV 31 DNA,而在鳞状化生病变中未发现HPV DNA。因此,当检查伴有鳞状化生的发育异常或其他病变中的HPV DNA时,原位杂交方法将很有用。在宫颈涂片检查中,可在发育异常细胞的细胞核上检测到HPV 31 DNA,所以该方法适用于宫颈涂片检查。如果将鳞状化生视为宫颈发育异常的前驱病变,那么在发育异常中检测到的HPV DNA也必须在伴随的鳞状化生中检测到。我们的结果表明,就我们能够使用五种HPV DNA探针检测而言,并非所有的鳞状化生都与HPV有关。