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精液中的端粒酶激活恶性和正常宫颈上皮细胞。

Activation of telomerase by seminal plasma in malignant and normal cervical epithelial cells.

机构信息

Ageing and Health Centre, Nursing School, Shandong University, Jinan, People's Republic of China.

出版信息

J Pathol. 2011 Oct;225(2):203-11. doi: 10.1002/path.2914. Epub 2011 May 18.

Abstract

Seminal fluids are involved in the development of cervical cancer but the underlying mechanism is unclear. Because cellular transformation requires telomerase activation by expression of the telomerase reverse transcriptase (hTERT) gene, we examined the role of seminal fluids in telomerase activation. Significantly elevated hTERT mRNA and telomerase activity were observed in cervical cell lines (HeLa, SiHa and Caski) treated with seminal plasma. Normal cervical epithelial cells expressed minimal levels of hTERT mRNA and telomerase activity, and seminal plasma substantially enhanced both expression and activity. The hTERT promoter activity was similarly increased in seminal plasma-treated HeLa cells and this effect was closely correlated with increased Sp1 expression and binding to the hTERT promoter. Cyclooxygenase-2 (COX-2) was simultaneously increased in HeLa cells exposed to seminal plasma, and blockade of COX-2 induction abolished seminal plasma stimulation of the hTERT promoter activity, hTERT expression and telomerase activity. Prostaglandin E2 (PGE2) mimics the effect of seminal plasma, stimulating Sp1 expression, enhancing Sp1 occupancy on the hTERT promoter and promoter activity. Moreover, tumour growth was robustly enhanced when HeLa cells together with seminal plasma were injected into nude-mice. Taken together, seminal plasma stimulates COX-2-PGE2-Sp1-dependent hTERT transcription, which provides insights into the putative mechanism underlying telomerase activation in cervical epithelial and cancer cells.

摘要

精液与宫颈癌的发生有关,但具体机制尚不清楚。由于细胞转化需要端粒酶的激活,端粒酶逆转录酶(hTERT)基因的表达,我们研究了精液在端粒酶激活中的作用。用精液处理宫颈细胞系(HeLa、SiHa 和 Caski)后,观察到 hTERT mRNA 和端粒酶活性显著升高。正常宫颈上皮细胞表达的 hTERT mRNA 和端粒酶活性很低,而精液则显著增强了两者的表达和活性。在精液处理的 HeLa 细胞中,hTERT 启动子活性也相似增加,这种效应与 Sp1 表达和与 hTERT 启动子的结合增加密切相关。HeLa 细胞暴露于精液时,环氧化酶-2(COX-2)同时增加,阻断 COX-2 诱导可消除精液对 hTERT 启动子活性、hTERT 表达和端粒酶活性的刺激作用。前列腺素 E2(PGE2)模拟精液的作用,刺激 Sp1 表达,增强 Sp1 对 hTERT 启动子和启动子活性的占据。此外,当将 HeLa 细胞与精液一起注射到裸鼠中时,肿瘤生长得到了显著增强。总之,精液刺激 COX-2-PGE2-Sp1 依赖性 hTERT 转录,这为宫颈上皮细胞和癌细胞中端粒酶激活的潜在机制提供了新的认识。

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