Lobban E D, Smith B A, Hall G D, Harnden P, Roberts P, Selby P J, Trejdosiewicz L K, Southgate J
ICRF Cancer Medicine Research Unit, St. James's University Hospital, Leeds, United Kingdom.
Am J Pathol. 1998 Dec;153(6):1957-67. doi: 10.1016/S0002-9440(10)65709-4.
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 in 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 noninvasive 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.
克隆了人尿血小板溶素UPIa、UPIb、UPII和UPIII的cDNA序列,并用于研究正常和肿瘤性尿路上皮细胞的尿血小板溶素转录情况。正常尿路上皮表达所有四种尿血小板溶素的mRNA,尽管仅通过核糖核酸酶保护试验才能检测到UPIII。通过原位杂交,UPIa和UPII局限于表层细胞,UPIb也由中层细胞表达。培养的正常人尿路上皮细胞表现出增殖性基底/中层细胞表型,且仅组成性表达UPIb。移行细胞癌细胞系的尿血小板溶素表达与其体外分化表型相关。RT4细胞表达所有尿血小板溶素,VM-CUB-3表达三种尿血小板溶素,RT112和HT1376细胞仅高丰度表达UPIb,而COLO232、KK47和EJ细胞未检测到表达。这些结果与肿瘤中尿血小板溶素的表达模式相关。仅在高分化移行细胞癌乳头的表层检测到UPIa和UPII。UPIb在9例非侵袭性移行细胞癌中的7例呈阳性,在9例中的5例过表达,在8例侵袭性移行细胞癌中的4例也存在。淋巴结转移保留了与原发肿瘤相同的UPIb表达模式。与三种受分化调节的尿血小板溶素不同,UPIb可能在尿路上皮细胞/组织过程中具有其他作用。