共 44 条
Antiproliferative effect of exemestane in lung cancer cells
被引:38
作者:
Koutras, Angelos
[1
]
Giannopoulou, Efstathia
[2
]
Kritikou, Ismini
[2
]
Antonacopoulou, Anna
[2
]
Evans, T. R. Jeffry
[3
]
Papavassiliou, Athanasios G.
[4
]
Kalofonos, Haralabos
[1
]
机构:
[1] Univ Hosp Patras, Dept Med, Div Oncol, Rion 26504, Greece
[2] Univ Hosp Patras, Patras Med Sch, Clin Oncol Lab, Rion 26504, Greece
[3] Univ Glasgow, Canc Res UK Beatson Labs, Glasgow G61 1BD, Lanark, Scotland
[4] Univ Athens, Sch Med, Dept Biol Chem, GR-11527 Athens, Greece
来源:
关键词:
GROWTH-FACTOR RECEPTOR;
HORMONE REPLACEMENT THERAPY;
ESTROGEN-RECEPTOR;
AROMATASE INHIBITORS;
BREAST-CANCER;
POSTMENOPAUSAL WOMEN;
SIGNALING PATHWAYS;
APOPTOTIC ACTION;
EXPRESSION;
TAMOXIFEN;
D O I:
10.1186/1476-4598-8-109
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
070307 [化学生物学];
071010 [生物化学与分子生物学];
摘要:
Background: 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. Results: 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. Conclusion: 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.
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