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Decreased DBC1 Expression Is Associated With Poor Prognosis in Patients With Non-Muscle-Invasive Bladder Cancer

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½ÉÀÇÀç, ÀÌÀϼ®, °­È£¿ø, ±èÀÚ¿µ, ±è¿øÅÂ, Kim Isaac-Yi, ·ù±ÙÈ£, ÃÖ¿µÇö, ¹®¼º±Ç, ±è¿ëÁØ, À±¼®Áß, ÀÌ»óö, ±è¿øÀç,
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½ÉÀÇÀç ( Shim Ui-Jae ) 
Chungbuk National University College of Medicine Department of Urology

ÀÌÀϼ® ( Lee Il-Seok ) 
Chungbuk National University College of Medicine Department of Urology
°­È£¿ø ( Kang Ho-Won ) 
Chungbuk National University College of Medicine Department of Urology
±èÀÚ¿µ ( Kim Ja-Young ) 
USA Children¡¯s Hospital Boston The Urological Diseases Research Center
±è¿øÅ ( Kim Won-Tae ) 
Chungbuk National University College of Medicine Department of Urology
 ( Kim Isaac-Yi ) 
USA Robert Wood Johnson Medical School The Cancer Institute of New Jersey Section of Urologic Oncology
·ù±ÙÈ£ ( Ryu Keun-Ho ) 
Chungbuk National University
ÃÖ¿µÇö ( Choi Yung-Hyun ) 
Dong-Eui University College of Oriental Medicine Department of Biochemistry
¹®¼º±Ç ( Moon Sung-Kwon ) 
Chungang University Department of Food and Biotechnology
±è¿ëÁØ ( Kim Yong-June ) 
Chungbuk National University College of Medicine Department of Urology
À±¼®Áß ( Yun Seok-Joong ) 
Chungbuk National University College of Medicine Department of Urology
ÀÌ»óö ( Lee Sang-Cheol ) 
Chungbuk National University College of Medicine Department of Urology
±è¿øÀç ( Kim Wun-Jae ) 
Chungbuk National University College of Medicine Department of Urology

Abstract


Purpose: The deleted in bladder cancer 1 (DBC1) gene is located within chromosome 9 (9q32-33), a chromosomal region that frequently shows loss of heterozygosity in bladder cancer (BC). It is suspected that it acts as a tumor suppressor gene, but its prognostic value remains unclear. The aim of the present study was to investigate the value of DBC1 as a prognostic marker in BC. Materials and Methods: The expression of DBC1 was determined by real-time polymerase chain reaction analysis in 344 patients with BC (220 non-muscle-invasive BC [NMIBC] and 124 muscle-invasive BC [MIBC]) and in 34 patients with normal bladder mucosa. The results were compared with clinicopathologic parameters, and the prognostic value of DBC1 was evaluated by Kaplan-Meier analysis and a multivariate Cox regression model. Results: DBC1 expression was significantly decreased in patients with MIBC compared with those diagnosed with NMIBC (p=0.010). Patients with aggressive tumor characteristics had lower DBC1 expression levels in NMIBC (each, p<0.05). By multivariate Cox regression analysis, low DBC1 expression was a predictor of progression to MIBC (hazard ratio, 7.104; p=0.013). Kaplan-Meier estimates revealed a significant difference in tumor recurrence, progression to MIBC, and cancer-specific survival depending on the level of DBC1 expression in NMIBC (log-rank test, each, p<0.05). Conclusions: The expression of DBC1 was associated with tumor aggressiveness, progression to MIBC, and survival in NMIBC. Our results suggest that DBC1 expression can be a useful prognostic marker for patients with NMIBC.

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Bladder cancer; Human DBC1 protein; Prognosis

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