» Articles » PMID: 17296438

Expression of Cyclooxygenase-2 in Normal Urothelium, and Superficial and Advanced Transitional Cell Carcinoma of Bladder

Overview
Journal J Urol
Publisher Wolters Kluwer
Specialty Urology
Date 2007 Feb 14
PMID 17296438
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: We compared the differential expression of cyclooxygenase-2 in normal bladder tissue, primary bladder transitional cell carcinoma and transitional cell carcinoma metastases to lymph nodes, and determined whether cyclooxygenase-2 expression is associated with molecular alterations commonly found in bladder transitional cell carcinoma and clinical outcomes after radical cystectomy.

Materials And Methods: Immunohistochemical staining for cyclooxygenase-2, survivin (Novus Biologicals, Littleton, Colorado), p21, p27, pRB, p53, MIB-1, Bax, Bcl-2, cyclin D(1) (Dakotrade mark), cyclin E (Oncogene, Cambridge, Massachusetts) and caspase-3 (Cell Signaling, Beverley, Massachusetts) was performed on archival bladder specimens from 9 subjects who underwent cystectomy for benign causes, 21 patients who underwent transurethral resection and 157 consecutive patients after radical cystectomy, and on 41 positive lymph nodes.

Results: Cyclooxygenase-2 was expressed in none of the 9 normal bladder specimens (0%), 52% of transurethral resection specimens, 62% of cystectomy specimens and 80% of lymph nodes involved with transitional cell carcinoma. Cyclooxygenase-2 expression was associated with higher pathological stage, lymphovascular invasion and metastases to lymph nodes (p=0.001, 0.045 and 0.002, respectively). Cyclooxygenase-2 expression was associated with altered expression of p53 (p=0.039), pRB (p=0.025), cyclin D1 (p=0.034) and caspase-3 (p=0.014). On univariate analysis cyclooxygenase-2 expression was associated with an increased risk of disease recurrence and bladder cancer specific mortality (p=0.0189 and 0.0472, respectively). However, on multivariate analysis only pathological stage and metastases to lymph nodes were associated with disease recurrence (p<0.001 and <0.001) and survival (p<0.001 and 0.015, respectively).

Conclusions: Cyclooxygenase-2 is not expressed in normal bladder urothelium. Cyclooxygenase-2 over expression is associated with pathological and molecular features of biologically aggressive disease, suggesting a role for cyclooxygenase-2 in bladder cancer development and invasion.

Citing Articles

Preoperative oral treatment with cyclooxygenase-2 inhibitor for cystitis glandularis.

Yanagi M, Motoda N, Katsu A, Kono H, Kimata R, Hamasaki T IJU Case Rep. 2024; 7(4):297-300.

PMID: 38966771 PMC: 11221942. DOI: 10.1002/iju5.12728.


Inflammation in Urological Malignancies: The Silent Killer.

Catalano M, Roviello G, Santi R, Villari D, Spatafora P, Galli I Int J Mol Sci. 2023; 24(1).

PMID: 36614308 PMC: 9821648. DOI: 10.3390/ijms24010866.


High COX-2 immunostaining in papillary thyroid carcinoma is associated with adverse survival outcomes.

Al-Maghrabi J, Gomaa W Ann Saudi Med. 2022; 42(6):359-365.

PMID: 36444921 PMC: 9706716. DOI: 10.5144/0256-4947.2022.359.


Regulatory Components of Oxidative Stress and Inflammation and Their Complex Interplay in Carcinogenesis.

Dharshini L, Rasmi R, Kathirvelan C, Kumar K, Saradhadevi K, Sakthivel K Appl Biochem Biotechnol. 2022; 195(5):2893-2916.

PMID: 36441404 DOI: 10.1007/s12010-022-04266-z.


Non-muscle invasive bladder cancer biomarkers beyond morphology.

De Carlo C, Valeri M, Corbitt D, Cieri M, Colombo P Front Oncol. 2022; 12:947446.

PMID: 35992775 PMC: 9382689. DOI: 10.3389/fonc.2022.947446.