Galectin-3: differential expression between small-cell and non-small-cell lung cancer

被引:30
作者
Buttery, R
Monaghan, H
Salter, DM
Sethi, T
机构
[1] Univ Edinburgh, Ctr Inflammat Res, Rayne Lab, Edinburgh EH8 9AG, Midlothian, Scotland
[2] Univ Edinburgh, Sch Sci & Mol Med, Div Pathol, Edinburgh EH8 9AG, Midlothian, Scotland
关键词
galectin-3; lung cancer; histology; chemotherapy;
D O I
10.1111/j.1365-2559.2004.01815.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To compare the histological expression of galectin-3 in different lung cancers, including small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC). Lung cancer is the leading cause of cancer deaths in the UK. Galectin-3 is a beta-galactoside binding protein with a controversial role in malignant transformation. SCLC metastasizes early and is initially chemosensitive; NSCLC metastasizes later, offering the chance of surgical cure, but is much less chemosensitive. Mixed tumours present a diagnostic and therapeutic problem, with a poorer response to therapy. Insight into the cellular mechanisms that govern metastasis and chemoresistance will profoundly influence the future management of this disease. Methods and results: In this study the histological expression of galectin-3 was assessed in a panel of lung tumour specimens, using the indirect streptavidin-biotin method. A striking difference in galectin-3 expression was observed between tumours, with high expression in NSCLC (42/47 samples) and low expression in SCLC (negative in 13/18, weak in 5/18). Conclusion: This differential expression of galectin-3 between histological types of lung carcinoma suggests that galectin-3 may have an important influence on tumour cell adhesion, apoptosis and the response of tumours to chemotherapy.
引用
收藏
页码:339 / 344
页数:6
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