Cloning of the human uroplakin 1B cDNA and analysis of its expression in urothelial‐tumor cell lines and bladder‐carcinoma tissue

• Published in: International journal of cancer Vol. 80; no. 4; pp. 533 - 538
• Main Authors: Finch, Jennie L., Miller, John, Aspinall, James O., Cowled, Prudence A.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 09.02.1999; Wiley-Liss
• Subjects: Amino Acid Sequence; Animals; Biological and medical sciences; Carcinoma, Transitional Cell - genetics; Carcinoma, Transitional Cell - metabolism; Cattle; Cloning, Molecular; DNA, Complementary - genetics; Gene Deletion; Gene Rearrangement - genetics; Humans; Medical sciences; Membrane Glycoproteins - chemistry; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; Molecular Sequence Data; Neoplasm Proteins - chemistry; Neoplasm Proteins - genetics; Neoplasm Proteins - metabolism; Nephrology. Urinary tract diseases; Open Reading Frames - genetics; RNA, Messenger - metabolism; Tumor Cells, Cultured; Tumors of the urinary system; Urinary Bladder - metabolism; Urinary Bladder Neoplasms - genetics; Urinary Bladder Neoplasms - metabolism; Urinary tract. Prostate gland; Uroplakin Ib; Urothelium - metabolism; Human; Urinary system disease; Carcinoma; Malignant tumor; Urinary tract disease; Gene expression; Complementary DNA; Urinary bladder; Established cell line; Gene rearrangement; Genetics; Bladder disease; Molecular biology; Molecular cloning
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/(SICI)1097-0215(19990209)80:4<533::AID-IJC9>3.0.CO;2-5

The human uroplakin 1B (UPK1B) gene codes for a structural protein which is a terminal differentiation component of the asymmetric unit membrane on the apical surface of the mammalian bladder. UPK1B is a member of the tetraspan family of proteins, many of which have de‐regulated patterns of expression in cancer. Using polymerase‐chain‐reaction techniques, we have cloned a partial human UPK1B cDNA which codes for the putative full open reading frame for the UPK1B protein. The deduced human UPK1B protein sequence has 92% and 93% amino‐acid homology with bovine UPK1b and mink TI1 proteins respectively. Using Northern analysis, we show that the human UPK1B gene is highly expressed in normal human urothelium. However, expression of UPK1B mRNA was undetectable or markedly reduced in 11 out of 16 samples of transitional‐cell‐bladder‐carcinoma tissue and in all 5 bladder‐carcinoma cell lines when compared with normal urothelial tissue. The molecular mechanism of down‐regulation of RNA expression does not appear to involve gross gene rearrangements or allelic loss. Int. J. Cancer 80:533–538, 1999. © 1999 Wiley‐Liss, Inc.