GATA3 immunohistochemistry in urothelial carcinoma of the upper urinary tract as a urothelial marker and a prognosticator

被引:45
作者
Inoue, Satoshi [1 ,2 ,3 ,4 ]
Mizushima, Taichi [1 ,2 ,3 ,4 ]
Fujita, Kazutoshi [4 ,5 ]
Meliti, Abdelrazak [3 ]
Ide, Hiroki [3 ,4 ]
Yamaguchi, Seiji [6 ]
Fushimi, Hiroaki [7 ]
Netto, George J. [3 ,4 ]
Nonomura, Norio [5 ]
Miyamoto, Hiroshi [1 ,2 ,3 ,4 ,8 ]
机构
[1] Univ Rochester, Med Ctr, Dept Pathol & Lab Med, 601 Elmwood Ave,Box 626, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, James P Wilmot Canc Inst, Rochester, NY 14642 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Sch Med, James Buchanan Brady Urol Inst, Baltimore, MD 21287 USA
[5] Osaka Univ, Grad Sch Med, Dept Urol, Suita, Osaka 5650871, Japan
[6] Osaka Gen Med Ctr, Dept Urol, Osaka 5588558, Japan
[7] Osaka Gen Med Ctr, Dept Pathol, Osaka 5588558, Japan
[8] Univ Rochester, Med Ctr, Dept Urol, Rochester, NY 14642 USA
关键词
GATA3; Immunohistochemistry; Prognosis; Upper urinary tract urothelial carcinoma; Sex hormone receptors; BINDING-PROTEIN; 3; ANDROGEN RECEPTOR; BLADDER-CANCER; ESTROGEN-RECEPTORS; CELL-CARCINOMA; EXPRESSION; TRANSCRIPTION; DIAGNOSIS; PATHWAY; TARGET;
D O I
10.1016/j.humpath.2017.04.003
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Immunohistochemistry of a transcription factor, GATA3, has been widely used as a promising urothelial marker in diagnostic surgical pathology practice. However, the expression status of GATA3 in upper urinary tract urothelial carcinomas (UUTUCs) and its prognostic significance have not been fully investigated. We immunohistochemically stained for GATA3 in 99 UUTUC samples and paired nonneoplastic urothelial tissues. GATA3 was positive in 51 (5 I.5%; 32 [32.3%] weak, I I [11.1%] moderate, 8 [8. 1%] strong) of 99 UUTUCs, which was significantly lower than in benign urothelium (79 [96.3%] of 82; 33 [40.2%] weak, 35 [42.7%] moderate, 11 [13.4%] strong; P < .001). However, there were no statistically significant associations between GATA3 expression and tumor grade, pT stage, lymph node involvement, or distant metastasis. Meanwhile, the rate of GATA3 positivity was significantly higher (P = .004) in ureteral tumors (66.0%) than in renal pelvic tumors (35.6%). Kaplan-Meier and log-rank tests revealed that GATA3 negativity was significantly associated with lower recurrence-free survival (P = .037 for all cases, P = .026 for muscle-invasive tumors) and cancer-specific survival (P = .007 for all cases, P = .012 for muscle invasive tumors, P = .035 for cases with adjuvant chemotherapy) rates. Multivariate analysis further identified strong correlations of GATA3 expression with tumor progression (all cases: hazard ratio [HR],0.479 [95% confidence interval {CI}, 0.229-1.003; P = .051]; muscle-invasive tumors: HR, 0.387 [95% CI, 0.166-0.903; P = .028) or cancer-specific mortality (all cases: HR, 0.354 [95% CI, 0.135-0.925; P = .034]; muscle-invasive tumors: HR, 0.402 [95% CI, 0.149-1.086; P = .072]). Thus, compared with nonneoplastic urothelium, a significant decrease in the expression of GATA3 in UUTUC was seen. Moreover, loss of GATA3 expression was found to be an independent predictor of poor patient outcomes. Of note was that only roughly half of high-grade and/or muscle-invasive UUTUCs were immunoreactive for GATA3. (C) 2017 Elsevier Inc. All rights reserved.
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收藏
页码:83 / 90
页数:8
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