Role of peroxisome proliferator-activated receptor γ and its ligands in non-neoplastic and neoplastic human urothelial cells

K Nakashiro, Y Hayashi, A Kita, T Tamatani… - The American journal of …, 2001 - Elsevier
K Nakashiro, Y Hayashi, A Kita, T Tamatani, A Chlenski, N Usuda, K Hattori, JK Reddy…
The American journal of pathology, 2001Elsevier
Peroxisome proliferator-activated receptor γ (PPARγ) is a member of the nuclear receptor
superfamily of ligand-activated transcription factors and is expressed in several types of
tissue. Although PPARγ reportedly is expressed in normal urothelium, its function is
unknown. We examined the expression of PPARγ in normal urothelium and bladder cancer
in an attempt to assess its functional role. Immunohistochemical staining revealed normal
urothelium to express PPARγ uniformly. All low-grade carcinomas were positive either …
Peroxisome proliferator-activated receptor γ (PPARγ) is a member of the nuclear receptor superfamily of ligand-activated transcription factors and is expressed in several types of tissue. Although PPARγ reportedly is expressed in normal urothelium, its function is unknown. We examined the expression of PPARγ in normal urothelium and bladder cancer in an attempt to assess its functional role. Immunohistochemical staining revealed normal urothelium to express PPARγ uniformly. All low-grade carcinomas were positive either diffusely or focally, whereas staining was primarily focal or absent in high-grade carcinomas. A nonneoplastic urothelial cell line (1T-1), a low-grade (RT4) carcinoma cell line, and two high-grade (T24 and 253J) carcinoma cell lines in culture expressed PPARγ mRNA and protein. Luciferase assay indicated that PPARγ was functional. PPARγ ligands (15-deoxy-Δ12,14-prostaglandin J2, troglitazone and pioglitazone) suppressed the growth of nonneoplastic and neoplastic urothelial cells in a dose-dependent manner. However, neoplastic cells were more resistant than were nonneoplastic cells. Failure to express PPARγ or ineffective transcriptional activity may be some of the mechanisms responsible for resistance to the inhibitory action of PPARγ ligands.
Elsevier