| International Journal of Molecular Sciences | |
| Expression and Role of GPR87 in Urothelial Carcinoma of the Bladder | |
| Homare Okazoe1  Xia Zhang1  Dage Liu2  Shinsuke Shibuya3  Nobufumi Ueda1  Mikio Sugimoto1  | |
| [1] Department of Urology, Kagawa University Faculty of Medicine, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan; E-Mails:;Department of General Thoracic Surgery, Kagawa University Faculty of Medicine, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan; E-Mail:;Department of Diagnostic Pathology, Kagawa University Faculty of Medicine, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan; E-Mail: | |
| 关键词: GPR87; non-muscle-invasive bladder cancer; intravesical recurrence; progression; | |
| DOI : 10.3390/ijms140612367 | |
| 来源: mdpi | |
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【 摘 要 】
The orphan GPR87 has recently been matched with its ligand LPA, which is a lipid mediator with multiple physiological functions, including cancer cell proliferation. This study aimed to clarify the role of GPR87 in urothelial carcinoma of the bladder. GPR87 expression was assessed in seven human bladder cancer cell lines. A replication-deficient recombinant adenoviral vector expressing shRNA targeting GPR87 (Ad-shGPR87), was constructed. Gene silencing was carried out using Ad-shGPR87. Immunohistochemical analysis was performed for transurethral resection of bladder tumor samples from 71 patients with non-muscle-invasive bladder cancer. We observed GPR87 expression in five of the seven cell lines, and silencing GPR87 gene expression significantly reduced cell viability. GPR87 expression was positive in 38 (54%) of 71 tumors. Ki-67 index was associated with positive GPR87 staining status (
【 授权许可】
CC BY
© 2013 by the authors; licensee MDPI, Basel, Switzerland
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190035849ZK.pdf | 497KB |
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