Key result
High expression of TIMP-1 mRNA in urothelial cancer cells was significantly correlated with higher pathological stage, increased tumor cell growth activity, and poorer prognosis.
Observational (n=33)
High expression of TIMP-1 mRNA in urothelial cancer cells correlates with higher malignant potential and poorer prognosis.
May support risk stratification in urothelial cancer; leaves open therapeutic targeting pending validation.
PURPOSE: We evaluated the role of tissue inhibitor of metalloproteinase-1 (TIMP-1) in the invasion and metastasis of human urothelial cancer. MATERIALS AND METHODS: The expression level of TIMP-1 messenger (m)RNA was determined in 33 urothelial carcinomas, including upper urothelial cancer in 15 cases and bladder cancer in 18, by Northern blot analysis. Localization of TIMP-1 mRNA was analyzed by in situ hybridization. These data were compared with clinicopathological features. We also determined the growth activity of tumor cells using immunohistochemical staining for Ki-67 and compared it with the expression levels of TIMP-1 mRNA. These data were also compared with clinicopathological features. RESULTS: The expression level of TIMP-1 mRNA significantly correlated with pathological stage and histological differentiation. In situ hybridization showed that TIMP-1 mRNA was expressed in the cytoplasm of urothelial cancer cells. The Ki-67 labeling index significantly correlated with the expression level of TIMP-1 mRNA in urothelial cancer. Patients with high expression of TIMP-1 mRNA had a poorer prognosis than those with low expression. CONCLUSIONS: TIMP-1 mRNA is expressed in the cytoplasm of cancer cells and high expression indicates more malignant potential in cases of urothelial cancer.
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Yano et al. (2002) conducted an observational in Urothelial cancer (n=33). High TIMP-1 mRNA expression vs. Low TIMP-1 mRNA expression was evaluated on Correlation with pathological stage, histological differentiation, and prognosis. High expression of TIMP-1 mRNA in urothelial cancer cells was significantly correlated with higher pathological stage, increased tumor cell growth activity, and poorer prognosis.
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