Uroplakin gene expression by normal and neoplastic human urothelium

被引:113
作者
Lobban, ED
Smith, BA
Hall, GD
Harnden, P
Roberts, P
Selby, PJ
Trejdosiewicz, LK
Southgate, J [1 ]
机构
[1] St James Univ Hosp, Imperial Canc Res Fund, Canc Med Res Unit, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Dept Pathol, Leeds LS9 7TF, W Yorkshire, England
[3] St James Univ Hosp, Dept Cytogenet, Leeds LS9 7TF, W Yorkshire, England
关键词
D O I
10.1016/S0002-9440(10)65709-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
cDNA sequences for human uroplakins UPIa, UPIb, UPII, and UPIII were cloned and used to investigate uroplakin transcription by normal and neoplastic urothelial cells. Normal urothelium expressed mRNA for all four uroplakins, although UPIII could be detected only by ribonuclease protection assay. By irt situ hybridization, UPIa and UPII were confined to superficial cells and UPIb was also expressed by intermediate cells. Cultured normal human urothelial cells showed a proliferative basal/intermediate cell phenotype and constitutive expression of UPIb only. Uroplakin expression by transitional cell carcinoma cell Lines was related to their differentiated phenotype in vitro. RT4 cells expressed all uroplakins, VM-CUB-3 expressed three uroplakins, RT112 and HT1376 cells expressed only UPIb in high abundance, and COLO232, KK47, and EJ cells had no detectable expression. These results correlated with patterns of uroplakin expression in tumors. UPIa and UPII were detected superficially only in well differentiated transitional cell carcinoma papillae, UPIb was positive in seven of nine and overexpressed in five of nine non-invasive transitional cell carcinomas and was also present in four of eight invasive transitional cell carcinomas. Lymph node metastases retained the same pattern of UPIb expression as the primary tumor. Unlike the three differentiation-regulated uroplakins, UPIb may have an alternative role in urothelial cell/tissue processes.
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页码:1957 / 1967
页数:11
相关论文
共 33 条
[1]   CYTOGENETIC STUDY OF 10 CARCINOMAS OF THE BLADDER - INVOLVEMENT OF CHROMOSOME-1 AND CHROMOSOME-11 [J].
ATKIN, NB ;
BAKER, MC .
CANCER GENETICS AND CYTOGENETICS, 1985, 15 (3-4) :253-268
[2]   Growth factors in bladder wound healing [J].
Baskin, LS ;
Sutherland, RS ;
Thomson, AA ;
Nguyen, HT ;
Morgan, DM ;
Hayward, SW ;
Hom, YK ;
DiSandro, M ;
Cunha, GR .
JOURNAL OF UROLOGY, 1997, 157 (06) :2388-2395
[3]  
Booth C, 1997, LAB INVEST, V76, P843
[4]   KAI1, A METASTASIS SUPPRESSOR GENE FOR PROSTATE-CANCER ON HUMAN-CHROMOSOME 11P11.2 [J].
DONG, JT ;
LAMB, PW ;
RINKERSCHAEFFER, CW ;
VUKANOVIC, J ;
ICHIKAWA, T ;
ISAACS, JT ;
BARRETT, JC .
SCIENCE, 1995, 268 (5212) :884-886
[5]   Chromosomal localization of the human urothelial ''tetraspan'' gene, UPK1B, to 3q13.3-q21 and detection of a TaqI polymorphism [J].
Finch, JL ;
Webb, GC ;
Evdokiou, A ;
Cowled, PA .
GENOMICS, 1997, 40 (03) :501-503
[6]   CYTOKERATIN-20 EXPRESSION BY NONINVASIVE TRANSITIONAL-CELL CARCINOMAS - POTENTIAL FOR DISTINGUISHING RECURRENT FROM NONRECURRENT DISEASE [J].
HARNDEN, P ;
ALLAM, A ;
JOYCE, AD ;
PATEL, A ;
SELBY, P ;
SOUTHGATE, J .
HISTOPATHOLOGY, 1995, 27 (02) :169-174
[7]  
HARNDEN P, 1996, CURR DIAGN PATHOL, V3, P109
[8]  
HARNDEN P, 1998, IN PRESS LANCET
[9]  
HODGES GM, 1979, BIOMEDICAL RES APPL, P307
[10]   CLONING OF A GROWTH ARREST-SPECIFIC AND TRANSFORMING GROWTH-FACTOR BETA-REGULATED GENE, TI-1, FROM AN EPITHELIAL-CELL LINE [J].
KALLIN, B ;
DEMARTIN, R ;
ETZOLD, T ;
SORRENTINO, V ;
PHILIPSON, L .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (10) :5338-5345