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生殖器病毒感染与宫颈肿瘤

Genital virus infection and cervical neoplasia.

作者信息

Kitchener H C

机构信息

Department of Midwifery, University of Glasgow, Queen Mother's Hospital, Yorkhill.

出版信息

Br J Obstet Gynaecol. 1988 Feb;95(2):182-91. doi: 10.1111/j.1471-0528.1988.tb06849.x.

DOI:10.1111/j.1471-0528.1988.tb06849.x
PMID:2831934
Abstract

The reported association between genital infection by herpes simplex virus (HSV) type 2 and cervical neoplasia has been investigated at a molecular level. Tissue culture of over 50 cervical cancers resulted in the development of several cell lines but none of these expressed HSV information. The permanent cell line, Cx106, which was generated was found to contain multiple genome copies of human papillomavirus (HPV) type 16. Southern blot analysis of nine cervical cancers showed an authentic 2.8 Kb fragment of HSV-2 DNA in one of the tumours. This piece of viral DNA maps in a morphological transforming region of the HSV genome. Superinfection of cervical cancers with temperature-sensitive (ts) mutants of HSV 1 and 2 did not generate recombinant virus, suggesting tht HSV DNA was not present in the tumours studied. An attempt to identify latent HSV close to the cervix in organ cultures of uterosacral ligament tissues resulted in reactivation of virus in several instances. These results are discussed against a background of decline in acceptance by many, for the HSV link with cervical cancer, and the dramatic impact of the discovery of a close relation between HPV type 16 and lower genital tract neoplasia.

摘要

已在分子水平上对报告的2型单纯疱疹病毒(HSV)生殖器感染与宫颈癌之间的关联进行了研究。对50多种宫颈癌进行组织培养,产生了几种细胞系,但这些细胞系均未表达HSV信息。所产生的永久性细胞系Cx106被发现含有16型人乳头瘤病毒(HPV)的多个基因组拷贝。对9例宫颈癌进行的Southern印迹分析显示,其中1例肿瘤中有一条真实的2.8kb HSV-2 DNA片段。这段病毒DNA定位于HSV基因组的一个形态转化区域。用HSV 1和2的温度敏感(ts)突变体对宫颈癌进行超感染未产生重组病毒,这表明在所研究的肿瘤中不存在HSV DNA。在子宫骶韧带组织的器官培养中,试图在宫颈附近鉴定潜伏性HSV,结果在若干情况下导致病毒重新激活。在许多人对HSV与宫颈癌之间联系的认可度下降以及发现16型HPV与下生殖道肿瘤之间密切关系所产生的巨大影响的背景下,对这些结果进行了讨论。

相似文献

1
Genital virus infection and cervical neoplasia.生殖器病毒感染与宫颈肿瘤
Br J Obstet Gynaecol. 1988 Feb;95(2):182-91. doi: 10.1111/j.1471-0528.1988.tb06849.x.
2
[The possibility of viral etiology in cervical carcinogenesis].[宫颈癌发生中病毒病因的可能性]
Nihon Sanka Fujinka Gakkai Zasshi. 1990 Aug;42(8):802-11.
3
[Correlation of human papilloma virus (HPV) and herpes simplex virus-2 (HSV-2)in the viral etiology of carcinoma of uterine cervix].[人乳头瘤病毒(HPV)与单纯疱疹病毒2型(HSV-2)在子宫颈癌病毒病因学中的相关性]
Zhonghua Zhong Liu Za Zhi. 1989 Mar;11(2):108-10.
4
Viral etiology of cervical carcinoma. Human papilloma virus and herpes simplex virus type 2.
Chin Med J (Engl). 1989 Feb;102(2):94-9.
5
Herpes simplex virus. An expanding relationship to human cancer.
J Reprod Med. 1983 Feb;28(2):116-22.
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Carcinoma of the cervix: can a viral etiology be confirmed?
IARC Sci Publ. 1984(63):433-50.
7
Search for human papillomavirus, herpes simplex virus and c-myc oncogene in human genital tumors.在人类生殖器肿瘤中检测人乳头瘤病毒、单纯疱疹病毒和c-myc癌基因。
Int J Cancer. 1989 Apr 15;43(4):570-7. doi: 10.1002/ijc.2910430407.
8
[Herpes simplex virus type 2 infection. Etiology, clinical aspects, diagnosis, therapy, HSV-2 and cervix cancer].[单纯疱疹病毒2型感染。病因、临床症状、诊断、治疗、HSV-2与宫颈癌]
Zentralbl Gynakol. 1985;107(24):1473-8.
9
Detection of herpes simplex virus type-2 DNA and human papilloma virus DNA sequences in cervical carcinoma tissue by molecular hybridization.通过分子杂交检测宫颈癌组织中的单纯疱疹病毒2型DNA和人乳头瘤病毒DNA序列。
J Exp Pathol. 1992;6(1-2):55-64.
10
The presence of RNA complementary to HSV-2 (herpes simplex virus) DNA in cervical intraepithelial neoplasia after laser therapy.激光治疗后宫颈上皮内瘤变中与单纯疱疹病毒2型(HSV-2)DNA互补的RNA的存在情况。
Br J Obstet Gynaecol. 1984 Mar;91(3):265-9. doi: 10.1111/j.1471-0528.1984.tb04765.x.

引用本文的文献

1
In situ hybridization analysis of HPV DNA in cervical precancer and cervical cancers from China.中国宫颈癌前病变和宫颈癌中HPV DNA的原位杂交分析
Arch Gynecol Obstet. 1990;247(1):21-9. doi: 10.1007/BF02390651.
2
Long term follow up of women with borderline cervical smear test results: effects of age and viral infection on progression to high grade dyskaryosis.宫颈涂片检查结果为临界状态的女性的长期随访:年龄和病毒感染对进展为高级别核异质的影响。
BMJ. 1992 May 9;304(6836):1209-12. doi: 10.1136/bmj.304.6836.1209.