Division of Oncology, Department of Medicine, University Hospital of Patras, Rion 26504, Greece.
Mol Cancer. 2009 Nov 24;8:109. doi: 10.1186/1476-4598-8-109.
Recent evidence suggests that estrogen signaling may be involved in the pathogenesis of non-small cell lung cancer (NSCLC). Aromatase is an enzyme complex that catalyses the final step in estrogen synthesis and is present in several tissues, including the lung. In the current study we investigated the activity of the aromatase inhibitor exemestane in human NSCLC cell lines H23 and A549.
Aromatase expression was detected in both cell lines. H23 cells showed lower protein and mRNA levels of aromatase, compared to A549 cells. Exemestane decreased cell proliferation and increased apoptosis in both cell lines, 48 h after its application, with A549 exhibiting higher sensitivity than H23 cells. Aromatase protein and mRNA levels were not affected by exemestane in A549 cells, whereas an increase in both protein and mRNA levels was observed in H23 cells, 48 h after exemestane application. Moreover, an increase in cAMP levels was found in both cell lines, 15 min after the administration of exemestane. In addition, we studied the effect of exemestane on epidermal growth factor receptor (EGFR) localization and activation. Exemestane increased EGFR activation 15 min after its application in H23 cells. Furthermore, we demonstrated a translocation of EGFR from cell membrane, 24 h after the addition of exemestane in H23 cells. No changes in EGFR activation or localization were observed in A549 cells.
Our findings suggest an antiproliferative effect of exemestane on NSCLC cell lines. Exemestane may be more effective in cells with higher aromatase levels. Further studies are needed to assess the activity of exemestane in NSCLC.
最近的证据表明,雌激素信号可能参与非小细胞肺癌(NSCLC)的发病机制。芳香酶是一种酶复合物,催化雌激素合成的最后一步,存在于包括肺在内的几种组织中。在目前的研究中,我们研究了芳香酶抑制剂依西美坦在人 NSCLC 细胞系 H23 和 A549 中的活性。
在这两种细胞系中都检测到了芳香酶的表达。与 A549 细胞相比,H23 细胞的芳香酶蛋白和 mRNA 水平较低。依西美坦在应用 48 小时后,降低了两种细胞系的细胞增殖并增加了细胞凋亡,A549 细胞的敏感性高于 H23 细胞。依西美坦未影响 A549 细胞中的芳香酶蛋白和 mRNA 水平,但在应用依西美坦 48 小时后观察到这两种水平均增加。此外,在应用依西美坦 15 分钟后,两种细胞系的 cAMP 水平均增加。此外,我们研究了依西美坦对表皮生长因子受体(EGFR)定位和激活的影响。依西美坦在应用后 15 分钟增加了 H23 细胞中 EGFR 的激活。此外,我们在 H23 细胞中证明,依西美坦添加 24 小时后,EGFR 从细胞膜易位。在 A549 细胞中,未观察到 EGFR 激活或定位的变化。
我们的研究结果表明依西美坦对 NSCLC 细胞系具有抗增殖作用。在芳香酶水平较高的细胞中,依西美坦可能更有效。需要进一步研究来评估依西美坦在 NSCLC 中的活性。