TY - JOUR
T1 - Galectin-3 expression is associated with bladder cancer progression and clinical outcome
AU - Canesin, Giacomo
AU - Gonzalez-Peramato, Pilar
AU - Palou, Joan
AU - Urrutia, Manuel
AU - Cordón-Cardo, Carlos
AU - Sánchez-Carbayo, Marta
PY - 2010/8
Y1 - 2010/8
N2 - Galectin-3 belongs to a family of carbohydratebinding proteins whose function is not fully characterized. However, it is believed to play a role in adhesion, proliferation and apoptosis in solid tumors. We aimed at investigating galectin-3 expression in bladder cancer. Galectin-3 expression was assessed by transcript profiling (U133A arrays) in a series or frozen bladder tumors (n=105). Immunohistochemistry was performed on tissue arrays containing bladder tumors (n=389) to evaluate associations of protein expression patterns of galectin-3 with proliferation (Ki67), apoptosis (apopdetek), bcl-2, and clinicopathologic variables. Galectin- 3 protein levels were then quantified in 160 urinary specimens of bladder cancer patients and controls by enzymeimmunoanalysis. Galectin-3 gene expression levels increased in invasive tumours as compared with non-muscle invasive lesions (p=0.001) and were associated with poor survival in patients with advanced disease (p=0.03). Protein expression patterns also correlated galectin-3 with tumor stage (p< 0.001), grade (p=0.03), Ki67 and apopdetek (p<0.001), and overall survival in patients with T1G3 tumors (p<0.001). Furthermore, galectin-3 urinary levels segregated bladder cancer patients from controls with high diagnostic accuracy (AUC=0.7). Independent series of bladder tumors showed that transcript and protein levels of galectin-3 were differentially expressed along bladder cancer progression. Urinary protein levels served to identify bladder cancer patients. These observations suggest a role for galectin-3 as a biomarker for bladder cancer diagnostics, staging, and outcome prognosis.
AB - Galectin-3 belongs to a family of carbohydratebinding proteins whose function is not fully characterized. However, it is believed to play a role in adhesion, proliferation and apoptosis in solid tumors. We aimed at investigating galectin-3 expression in bladder cancer. Galectin-3 expression was assessed by transcript profiling (U133A arrays) in a series or frozen bladder tumors (n=105). Immunohistochemistry was performed on tissue arrays containing bladder tumors (n=389) to evaluate associations of protein expression patterns of galectin-3 with proliferation (Ki67), apoptosis (apopdetek), bcl-2, and clinicopathologic variables. Galectin- 3 protein levels were then quantified in 160 urinary specimens of bladder cancer patients and controls by enzymeimmunoanalysis. Galectin-3 gene expression levels increased in invasive tumours as compared with non-muscle invasive lesions (p=0.001) and were associated with poor survival in patients with advanced disease (p=0.03). Protein expression patterns also correlated galectin-3 with tumor stage (p< 0.001), grade (p=0.03), Ki67 and apopdetek (p<0.001), and overall survival in patients with T1G3 tumors (p<0.001). Furthermore, galectin-3 urinary levels segregated bladder cancer patients from controls with high diagnostic accuracy (AUC=0.7). Independent series of bladder tumors showed that transcript and protein levels of galectin-3 were differentially expressed along bladder cancer progression. Urinary protein levels served to identify bladder cancer patients. These observations suggest a role for galectin-3 as a biomarker for bladder cancer diagnostics, staging, and outcome prognosis.
KW - Biomarker
KW - Bladder cancer
KW - Galectin-3
UR - http://www.scopus.com/inward/record.url?scp=77954632902&partnerID=8YFLogxK
U2 - 10.1007/s13277-010-0033-9
DO - 10.1007/s13277-010-0033-9
M3 - Article
C2 - 20401558
AN - SCOPUS:77954632902
SN - 1010-4283
VL - 31
SP - 277
EP - 285
JO - Tumor Biology
JF - Tumor Biology
IS - 4
ER -