MMP-9 overexpression due to TIMP-1 and RECK underexpression is associated with prognosis in prostate cancer

Author(s):Show less -

Reis, Sabrina Thalita ^{[1, 2, 3]} ; Pontes-Junior, Jose ^{[1, 2, 3]} ; Antunes, Alberto Azoubel ^{[1, 2, 3]} ; de Sousa-Canavez, Juliana Moreira ^[4] ; Dall'Oglio, Marcos Francisco ^{[1, 2, 3]} ; Passerotti, Carlo C. ^[2] ; Abe, Daniel Kanda ^{[1, 3]} ; Crippa, Alexandre ^{[1, 3]} ; Shiomi da Cruz, Jose Arnaldo ^[2] ; Timoszczuk, Luciana M. S. ^[2] ; Srougi, Miguel ^{[1, 2, 3]} ; Leite, Katia R. M. ^{[1, 2, 3]}

Affiliation

^[1] ICESP, Sao Paulo - Brazil

^[2] Univ Sao Paulo, Sch Med, Dept Urol, Lab Med Invest LIM55, Sao Paulo - Brazil

^[3] Univ Sao Paulo, Sch Med, Dept Urol, Urooncol Grp, Sao Paulo - Brazil

^[4] Genoa Biotechnol SA, Sao Paulo - Brazil

• Document type: Journal article
• Source: International Journal of Biological Markers; v. 26, n. 4, p. 255-261, OCT-DEC 2011.
• Web of Science Citations: 19

Abstract

Background: Extracellular matrix homeostasis is strictly maintained by a coordinated balance between the expression of metalloproteinases (MMPs) and their inhibitors. The purpose of this study was to investigate whether the expression of MMP-9 and its specific inhibitors, TIMP-1 and RECK, are expressed in a reproducible, specific pattern and if the profiles are related to prognosis and clinical outcome in prostate cancer (PC). Methods: MMP-9, TIMP-1, and RECK expression levels were analyzed by quantitative real-time polymerase chain reaction (qRT-PCR) in fresh-frozen malignant tissue specimens collected from 79 patients with clinically localized PC submitted to radical prostatectorny (RP). Frozen benign prostatic tissue from another 10 men with prostate cancer, also submitted to RP, was analyzed to determine if the profile of gene expression was maintained. The control group consisted of 11 patients with benign prostate hyperplasia (BPH). Results: In the tumor samples, MMP-9 was overexpressed by 9.2 times, and TIMP-1 and RECK were underexpressed (0.75 and 0.80 times, respectively). Overexpression of MMP-9 was significantly related to PSA levels above 10 ng/mL (p=0.033). In addition, MMP-9 overexpression was related to biochemical recurrence, with a marginal statistical significance (p=0.089). MMP-9 was also overexpressed in benign tissues of patients with PC, as were TIMP-1 and RECK, in contrast to their underexpression in tumor samples. Conclusion: Our results show that MMP-9 is overexpressed and its negative regulators are underexpressed in PC tissue, emphasizing a possible role of MMP-9 in the carcinogenesis process. Additionally, we noticed a relationship between MMP-9 overexpression and increased levels of PSA, an important prognostic factor. In benign tissue adjacent to tumors, the MMP-9 equilibrium is likely maintained because the expression of its negative regulators is preserved. (AU)