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人乳头瘤病毒激活的细胞转录因子Brn-3a在CIN3宫颈病变中过表达。

The HPV-activating cellular transcription factor Brn-3a is overexpressed in CIN3 cervical lesions.

作者信息

Ndisdang D, Morris P J, Chapman C, Ho L, Singer A, Latchman D S

机构信息

Windeyer Institute of Medical Sciences, University College London Medical School, The Windeyer Building, Cleveland Street, London W1P 6DB, United Kingdom.

出版信息

J Clin Invest. 1998 Apr 15;101(8):1687-92. doi: 10.1172/JCI1089.

Abstract

The cervical cellular transcription factors Brn-3a and Brn-3b have antagonistic effects on transcription of the human papilloma virus types 16 and 18 E6 and E7 oncogenes, with Brn-3a activating expression and Brn-3b repressing it. We therefore measured expression of Brn-3a and Brn-3b mRNAs in biopsies from 16 women with no detectable cervical abnormality, and in 14 women with cervical intraepithelial neoplasia grade 3 (CIN3) lesions. Although the mean level of Brn-3b expression was similar in both groups, the mean level of Brn-3a expression was over 300-fold higher in the CIN3 samples when compared with normals. Elevated expression of Brn-3a was also detected in 16 histologically normal regions of the cervix adjacent to the CIN3 lesions, indicating that elevation of Brn-3a levels is not confined to the lesion in women with CIN3, and is thus not a consequence of the oncogenic process. The elevated levels of Brn-3a in the CIN3 patient samples, together with the activating effect of Brn-3a on HPV-16 and -18 oncogene expression, suggest that induction of this factor is involved in activating HPV-16 and -18 oncogene expression in the cervix, and hence in the production of cervical cancers induced by HPV.

摘要

宫颈细胞转录因子Brn-3a和Brn-3b对人乳头瘤病毒16型和18型E6和E7癌基因的转录具有拮抗作用,其中Brn-3a激活其表达,而Brn-3b抑制其表达。因此,我们检测了16名未检测到宫颈异常的女性活检组织以及14名患有宫颈上皮内瘤变3级(CIN3)病变的女性活检组织中Brn-3a和Brn-3b mRNA的表达。尽管两组中Brn-3b的平均表达水平相似,但与正常样本相比,CIN3样本中Brn-3a的平均表达水平高出300多倍。在与CIN3病变相邻的16个宫颈组织学正常区域也检测到Brn-3a表达升高,这表明Brn-3a水平升高并不局限于CIN3女性的病变部位,因此不是致癌过程的结果。CIN3患者样本中Brn-3a水平升高,以及Brn-3a对HPV-16和-18癌基因表达的激活作用,表明该因子的诱导参与了宫颈中HPV-16和-18癌基因表达的激活,进而参与了HPV诱导的宫颈癌的发生。

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