Literature DB >> 22740956

Clinical role of pleural effusion MMP-3 levels in malignant pleural mesothelioma.

Aki Murakami1, Chiharu Tabata, Rie Tabata, Hisaya Okuwa, Takashi Nakano.   

Abstract

Malignant pleural mesothelioma (MPM) is an aggressive malignant tumor of mesothelial origin associated with asbestos exposure. MPM exhibits a limited response to conventional chemotherapy and radiotherapy. This, early diagnosis of MPM is essential. Malignant tumor progression requires the destruction of the basement membrane, which is constructed from extracellular matrix (ECM) materials. Various types of human tumor cells are reported to produce ECM-degrading proteases that are important in tumor progression. Among this group of proteolytic enzymes, matrix metalloproteinases (MMPs) are thought to be important due to their wide degrading function. We investigated the pleural effusion MMP-3 levels of patients with MPM and compared them with those of a population with non-malignant pleuritis or lung cancer involving malignant pleural effusion. The pleural effusion MMP-3 concentrations of 52 MPM patients and 67 non-MPM patients were measured. The results showed that the MPM patients had significantly higher pleural effusion MMP-3 levels than the population with non-malignant pleuritis. The overall survival of the MPM patients with lower pleural effusion MMP-3 levels was longer than that of patients with higher pleural effusion MMP-3 levels. Our data therefore suggest a clinical role of pleural effusion MMP-3 levels in malignant pleural mesothelioma.

Entities:  

Year:  2011        PMID: 22740956      PMCID: PMC3362431          DOI: 10.3892/ol.2011.536

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  36 in total

1.  Diffuse pleural mesothelioma and asbestos exposure in the North Western Cape Province.

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2.  Use of tumor markers for differential diagnosis of mesothelioma and secondary pleural malignancies.

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Review 3.  New approaches for mesothelioma: biologics, vaccines, gene therapy, and other novel agents.

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Journal:  Semin Oncol       Date:  2002-02       Impact factor: 4.929

4.  Increased matrix metalloproteinase activation in esophageal squamous cell carcinoma.

Authors:  Sumana Mukherjee; Mark J Roth; Sanford M Dawsey; Wusheng Yan; Jaime Rodriguez-Canales; Heidi S Erickson; Nan Hu; Alisa M Goldstein; Philip R Taylor; Annely M Richardson; Michael A Tangrea; Rodrigo F Chuaqui; Michael R Emmert-Buck
Journal:  J Transl Med       Date:  2010-10-05       Impact factor: 5.531

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Authors:  V W Rusch
Journal:  Chest       Date:  1995-10       Impact factor: 9.410

6.  Inhibition of MMP-3 activity and invasion of the MDA-MB-231 human invasive breast carcinoma cell line by bioflavonoids.

Authors:  Kanokkarn Phromnoi; Supachai Yodkeeree; Songyot Anuchapreeda; Pornngarm Limtrakul
Journal:  Acta Pharmacol Sin       Date:  2009-07-20       Impact factor: 6.150

7.  Mesothelin-family proteins and diagnosis of mesothelioma.

Authors:  Bruce W S Robinson; Jenette Creaney; Richard Lake; Anna Nowak; A William Musk; Nick de Klerk; Pernilla Winzell; Karl Erik Hellstrom; Ingegerd Hellstrom
Journal:  Lancet       Date:  2003-11-15       Impact factor: 79.321

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Journal:  Cancer       Date:  1987-06-15       Impact factor: 6.860

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Journal:  Growth Factors       Date:  1994       Impact factor: 2.511

10.  Interleukin 8: an autocrine growth factor for malignant mesothelioma.

Authors:  G Galffy; K A Mohammed; P A Dowling; N Nasreen; M J Ward; V B Antony
Journal:  Cancer Res       Date:  1999-01-15       Impact factor: 12.701

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  1 in total

Review 1.  The role of VEGF in the diagnosis and treatment of malignant pleural effusion in patients with non‑small cell lung cancer (Review).

Authors:  Yao Chen; Nicholas W Mathy; Hongda Lu
Journal:  Mol Med Rep       Date:  2018-04-23       Impact factor: 2.952

  1 in total

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