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Prognostic role of galectin-3 expression in patients with solid tumors: a meta-analysis of 36 eligible studies

BACKGROUND: Galectin-3 as a β-galactoside-binding protein, has been found to be involved in tumor cell growth, anti-apoptosis, adhesion, angiogenesis, invasion, and distant metastases, indicating that it may play a pivotal role in cancer development and progression. However, their results remain deb...

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Detalles Bibliográficos
Autores principales: Wang, Yi, Liu, Shiwei, Tian, Ye, Wang, Yamin, Zhang, Qijie, Zhou, Xiang, Meng, Xianghu, Song, Ninghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215616/
https://www.ncbi.nlm.nih.gov/pubmed/30410421
http://dx.doi.org/10.1186/s12935-018-0668-y
Descripción
Sumario:BACKGROUND: Galectin-3 as a β-galactoside-binding protein, has been found to be involved in tumor cell growth, anti-apoptosis, adhesion, angiogenesis, invasion, and distant metastases, indicating that it may play a pivotal role in cancer development and progression. However, their results remain debatable and inconclusive. Hence, this meta-analysis was performed to clarify the precise predictive value of galectin-3 in various cancers. METHODS: PubMed, Web of Science, Embase, Cochrane Library, CNKI and Wanfang databases were searched comprehensively for eligible studies up to July 15, 2018. Pooled hazard ratios (HRs) with 95% confidence intervals (CIs) of OS or DFS/PFS/RFS were calculated to demonstrate their associations. RESULTS: A total of 36 relevant studies were ultimately enrolled in this meta-analysis. Our results shed light on the significant association of elevated galectin-3 expression with reduced OS or DFS/RFS/PFS in overall cancer patients (pooled HR = 1.79, 95% CI 1.42–2.27, I(2)= 67.3%, p < 0.01; pooled HR = 1.57, 95% CI 1.04–2.37, I(2)= 67.1%, p = 0.001). In tumor type subgroup analysis, we found high expression of galectin-3 was correlated with shorter OS or DFS/RFS/PFS in colorectal cancer (pooled HR = 3.05, 95% CI 2.13–4.35, I(2)= 0.0%, p = 0.734; pooled HR = 2.49, 95% CI 1.82–3.41, I(2) = 0.0%, p = 0.738; respectively) and meanwhile it merely associated with reduced OS in ovarian cancer or non-small cell lung cancer (pooled HR = 2.24, 95% CI 1.38–3.64, I(2)= 0.0%, p = 0.910; pooled HR = 2.07, 95% CI 1.48–2.88, I(2)= 0.0%, p = 0.563; separately). CONCLUSIONS: Taken together, our results suggested that galectin-3 played an oncogenic role in colorectal cancer, ovarian cancer and non-small cell lung cancer, indicating it could be a promising biomarker and a novel therapeutic target for them. Further studies were warranted to validate our findings.