Overexpression of clusterin in transitional cell carcinoma of the bladder is related to disease progression and recurrence

被引:108
作者
Miyake, H
Gleave, M
Kamidono, S
Hara, I
机构
[1] Kobe Univ, Sch Med, Dept Urol, Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Univ British Columbia, Div Urol, Vancouver, BC, Canada
关键词
D O I
10.1016/S0090-4295(01)01484-4
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To determine whether the expression level of clusterin in transitional cell carcinoma (TCC) of the bladder could be used as a predictor of tumor recurrence and prognosis. Methods. Total RNA samples were extracted from 89 specimens of TCC of the bladder, and the expression level of clusterin mRNA in these specimens was measured by Northern blot analysis. The results were evaluated with respect to several clinicopathologic factors. Results. The mean level of clusterin mRNA expression in invasive TCC of the bladder was fourfold and fivefold higher than that in superficial TCC and normal urothelial tissue, respectively. The expression level of clusterin mRNA showed no significant correlation with sex, age, tumor size, or multiplicity, and the pathologic stage and tumor grade showed close associations with clusterin expression. The overall survival rate of patients with strong clusterin expression was significantly lower than that of patients with weak expression. Among the 43 patients with invasive TCC who underwent complete resection, the recurrence-free survival rate of patients with strong clusterin expression was significantly lower than that of patients with weak expression. Moreover, multivariate analyses indicated that among these 43 patients, strong expression of clusterin was an independent predictor of tumor recurrence. Conclusions. These findings indicate that clusterin mRNA is strongly expressed in invasive TCC of the bladder compared with the expression in superficial TCC and that strong clusterin expression could be used as a novel predictor of prognosis of patients with TCC of the bladder. Urology 59: 150-154, 2002. (C) 2002, Elsevier Science Inc.
引用
收藏
页码:150 / 154
页数:5
相关论文
共 19 条
[1]  
[Anonymous], HISTOLOGICAL TYPING
[2]   SGP-2 EXPRESSION AS A GENETIC-MARKER OF PROGRESSIVE CELLULAR PATHOLOGY IN EXPERIMENTAL HYDRONEPHROSIS [J].
CONNOR, J ;
BUTTYAN, R ;
OLSSON, CA ;
DAGATI, V ;
OTOOLE, K ;
SAWCZUK, IS .
KIDNEY INTERNATIONAL, 1991, 39 (06) :1098-1103
[3]   DISTINCT SITES OF PRODUCTION AND DEPOSITION OF THE PUTATIVE CELL-DEATH MARKER CLUSTERIN IN THE HUMAN THYMUS [J].
FRENCH, LE ;
SAPPINO, AP ;
TSCHOPP, J ;
SCHIFFERLI, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) :1919-1925
[4]   Prognostic variables in patients who have undergone radical cystectomy for transitional cell carcinoma of the bladder [J].
Hara, S ;
Miyake, H ;
Fujisawa, M ;
Okada, H ;
Arakawa, S ;
Kamidono, S ;
Hara, I .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2001, 31 (08) :399-402
[5]   Absence of p53 overexpression and favorable response to cisplatin-based neoadjuvant chemotherapy in urothelial carcinomas [J].
Kakehi, Y ;
Özdemir, E ;
Habuchi, T ;
Yamabe, H ;
Hashimura, H ;
Katsura, Y ;
Yoshida, O .
JAPANESE JOURNAL OF CANCER RESEARCH, 1998, 89 (02) :214-220
[6]  
Keegan PE, 1998, BRIT J UROL, V82, P710
[7]  
KYPRIANOU N, 1991, CANCER RES, V51, P162
[8]  
MALKOWICZ SB, 1990, J UROLOGY, V144, P641
[9]  
Miyake H, 2000, CLIN CANCER RES, V6, P1655
[10]  
Miyake H, 2000, CANCER RES, V60, P2547