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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Tissue expression of MMP-9, TIMP-1, RECK, and miR338-3p in prostate gland: can it predict cancer?

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de Moraes, Rodolfo Pacheco [1] ; Pimenta, Ruan [2, 1] ; Mori, Fernando Noboru Cabral [1] ; dos Santos, Gabriel Arantes [2, 1] ; Viana, Nayara Izabel [1] ; Guimaraes, Vanessa Ribeiro [1] ; de Camargo, Juliana Alves [1] ; Moreira-Leite', Katia Ramos [1] ; Srougi, Miguel [2, 1] ; Nahas, William Carlos [3] ; Reis, Sabrina T. [1]
Total Authors: 11
Affiliation:
[1] Fac Med Sao Paulo FMUSP, Lab Med Invest LIM55, Urol Dept, Sao Paulo - Brazil
[2] DOr Inst Res & Educ IDOR, Sao Paulo - Brazil
[3] Univ Sao Paulo, Inst Canc Estado Sao Paulo ICESP, Sao Paulo - Brazil
Total Affiliations: 3
Document type: Journal article
Source: MOLECULAR BIOLOGY RESEARCH COMMUNICATIONS; v. 10, n. 4, p. 149-156, DEC 2021.
Web of Science Citations: 0
Abstract

Prostate cancer is the most frequent malignancy affecting men worldwide. Due to the low sensitivity and specificity of the prostate-specific antigen test and the digital rectal exam as screening modalities, several alternatives are being studied. This study aimed to evaluate the application of MMP-9 and its regulators (TIMP-1, RECK, and miR-338-3p) as diagnostic and prognostic indicators of prostate cancer. A total of 134 randomly selected patients under investigation for prostate cancer submitted to a transrectal ultrasound-guided prostate biopsy were enrolled in the study; of these, 61 were positive for the disease (cases), and 73 were negative (control group). The tissue samples were further analyzed by gene and miR-338-3p expression analysis using qRT-PCR (one randomly selected fragment of each patient). Approximately 58% of the patients with prostate cancer presented MMP9 upregulation, while 73%, 65%, and 69% downregulated IMP-1, RECK, and miR-338-3p, respectively. MiR-338-3p was expressed at lower levels in patients with PSA concentrations exceeding 20 ng/mL (p=0.045) and abnormal DRE (p=0.006), while the RECK was more expressed in patients with abnormal DRE (p=0.01). We found that most patients with prostate cancer overexpressed MMP-9; on the other hand, most of them underexpressed TIMP-1, RECK, and miR-338-3p. MiR-338-3p presented as a possible predictor of poor prognosis. Further studies are warranted to evaluate these biomarkers as prognosis factors better. (AU)

FAPESP's process: 17/17489-3 - The role of MMP-9, TIMP-1 and RECK in the diagnostic and prognostic of prostate cancer
Grantee:Fernando Noboru Cabral Mori
Support Opportunities: Scholarships in Brazil - Scientific Initiation