Gubbay O, Guo W, Rae M T, Niven D, Langdon S P, Hillier S G
Centre for Reproductive Biology, The Chancellor's Building, University of Edinburgh, 49 Little France Crescent, Old Dalkeith Road, Edinburgh EH16 4SB, UK.
Br J Cancer. 2005 May 23;92(10):1927-33. doi: 10.1038/sj.bjc.6602568.
Ovulation is believed to contribute to the development of ovarian cancers that derive from the ovarian surface epithelium (OSE). The process of ovulation is synonymous with inflammation and inflammatory cytokines such as interleukin-1alpha (IL-1alpha) have recently been shown to induce both inflammatory and anti-inflammatory responses in human OSE (HOSE) cells. In this study we directly compared levels of IL-1alpha-induced gene expression by analysing the levels of 11beta-hydroxysteroid dehydrogenase (11betaHSD) types 1 (11betaHSD-1) and 2 (11betaHSD-2), cyclooxygenase-2 (COX-2), IL-1 receptor (IL-1R) and glucocorticoid receptor alpha (GRalpha) mRNA between normal HOSE cells and cell lines derived from poorly differentiated (SKOV-3, BG-1, PEO-4) and well-differentiated (PEO-14) ovarian adenocarcinoma. In HOSE cell cultures, and to a lesser extent PEO-14 cells, the basal mRNA levels of COX-2 and 11betaHSD-1 were relatively high and further shown to be induced in response to IL-1alpha (for HOSE cells; >20-fold, P<0.05 and PEO-14 cells; >3fold, P<0.05). However, whereas HOSE cells expressed a low level of 11betaHSD-2 mRNA that was only mildly responsive to IL-1alpha (1.3-fold, P<0.001), all cell lines exhibited a higher basal level of 11betaHSD-2 mRNA that was in some cases further stimulated in PEO-4 cells (five-fold; P<0.05) or suppressed in SKOV-3 cells (two-fold; P<0.01) in response to IL-1alpha. All cells tested expressed IL-1R and, with the exception of BG-1, GRalpha. These results indicate that cell lines derived from ovarian cancers have lost the ability to respond normally to inflammatory cytokines such as IL-1alpha. The finding that normal OSE cells, in contrast to cell lines derived from patients with ovarian adenocarcinoma, abundantly express 11betaHSD-1 mRNA but are essentially devoid of 11betaHSD-2 mRNA supports the concept that the pattern of 11betaHSD isoform gene expression is a defining feature of neoplastic cellular transformation, which might have particular relevance to the ovary.
排卵被认为与源自卵巢表面上皮(OSE)的卵巢癌的发生有关。排卵过程等同于炎症,近期研究表明,诸如白细胞介素 - 1α(IL - 1α)等炎性细胞因子可在人OSE(HOSE)细胞中诱导炎性和抗炎反应。在本研究中,我们通过分析11β - 羟基类固醇脱氢酶(11βHSD)1型(11βHSD - 1)和2型(11βHSD - 2)、环氧化酶 - 2(COX - 2)、IL - 1受体(IL - 1R)以及糖皮质激素受体α(GRα)mRNA的水平,直接比较了正常HOSE细胞与源自低分化(SKOV - 3、BG - 1、PEO - 4)和高分化(PEO - 14)卵巢腺癌的细胞系中IL - 1α诱导的基因表达水平。在HOSE细胞培养物中,以及在较小程度上在PEO - 14细胞中,COX - 2和11βHSD - 1的基础mRNA水平相对较高,并且进一步显示在对IL - 1α的反应中被诱导(对于HOSE细胞;>20倍,P<0.05;对于PEO - 14细胞;>3倍,P<0.05)。然而,虽然HOSE细胞表达低水平的11βHSD - 2 mRNA,且对IL - 1α仅有轻微反应(1.3倍,P<0.001),但所有细胞系均表现出较高的11βHSD - 2 mRNA基础水平,在某些情况下,PEO - 4细胞中该水平进一步受到刺激(5倍;P<0.05),而SKOV - 3细胞中则受到抑制(2倍;P<0.01)。所有测试细胞均表达IL - 1R,除BG - 1外,还表达GRα。这些结果表明,源自卵巢癌的细胞系已丧失对诸如IL - 1α等炎性细胞因子正常反应的能力。与源自卵巢腺癌患者的细胞系相比,正常OSE细胞大量表达11βHSD - 1 mRNA但基本不表达11βHSD - 2 mRNA这一发现支持了11βHSD同工型基因表达模式是肿瘤细胞转化的决定性特征这一概念,这可能与卵巢具有特别的相关性。