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Seminal plasma activates cyclooxygenase-2 and prostaglandin E2 receptor expression and signalling in cervical adenocarcinoma cells

机译:精浆激活宫颈腺癌细胞中的环氧合酶2和前列腺素E2受体表达及信号传导

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摘要

Enhanced cyclooxygenase (COX) expression and prostaglandin E2 (PGE2) synthesis are regarded as promoters of neoplastic cell proliferation and angiogenesis. Expression of COX-2 and synthesis of PGE2 are up-regulated in cervical carcinomas. In sexually active women, growth and invasiveness of neoplastic cervical epithelial cells may be also under the direct influence of PGE2 present in seminal plasma. The aims of this study were to investigate the effect of seminal plasma and PGE2 on the expression of COX-2 and expression and signalling of the PGE2 receptor subtypes (EP1–EP4) in HeLa (cervical adenocarcinoma) cells. Treatment of HeLa cells with seminal plasma or PGE2 resulted in up-regulation of COX-2 expression (P < 0.05). In addition, seminal plasma induced the mRNA expression of EP1, EP2 and EP4 receptors, whilst PGE2 treatment of HeLa cells induced the expression of the EP4 receptor (P < 0.05). This was coincident with a rapid accumulation of adenosine 3′,5′-cyclic monophosphate (cAMP) in HeLa cells stimulated with seminal plasma or PGE2, which was greater in seminal plasma stimulated cells compared with PGE2 stimulated cells (P < 0.05). Subsequently, we investigated whether the effect of seminal plasma on cAMP signalling in HeLa cells was mediated via the cAMP-linked EP2/EP4 receptors. Stimulation of HeLa cells with seminal plasma or PGE2 resulted in an augmented cAMP accumulation in cells transfected with the EP2 or EP4 receptor cDNA compared with control transfected cells (P < 0.05). These data suggest that, in sexually active women, seminal plasma may play a role in modulating neoplastic cell function and cervical tumorigenesis.
机译:增强的环氧合酶(COX)表达和前列腺素E2(PGE2)合成被认为是肿瘤细胞增殖和血管生成的促进剂。宫颈癌中COX-2的表达和PGE2的合成上调。在性活跃的女性中,肿瘤宫颈上皮细胞的生长和侵袭性也可能受精浆中PGE2的直接影响。本研究的目的是研究精浆和PGE2对宫颈癌HeLa细胞中COX-2表达以及PGE2受体亚型(EP1-EP4)的表达和信号传导的影响。用精浆或PGE2处理HeLa细胞导致COX-2表达上调(P <0.05)。此外,精浆诱导EP1,EP2和EP4受体的mRNA表达,而PGE2处理HeLa细胞则诱导EP4受体的表达(P <0.05)。这与精浆或PGE2刺激的HeLa细胞中腺苷3',5'-环一磷酸(cAMP)的快速积累相吻合,精浆刺激的细胞中PAMP2刺激的细胞中腺苷3',5'-环一磷酸酯(P <0.05)更大。随后,我们调查了精浆对HeLa细胞中cAMP信号转导的影响是否通过cAMP连接的EP2 / EP4受体介导。与对照转染细胞相比,用精浆或PGE2刺激HeLa细胞导致在用EP2或EP4受体cDNA转染的细胞中cAMP积累增加(P <0.05)。这些数据表明,在从事性活动的女性中,精浆可能在调节肿瘤细胞功能和宫颈肿瘤发生中起作用。

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