Overexpression of peroxiredoxins I, II, III, V, and VI in malignant mesothelioma
- PMID: 11857495
- DOI: 10.1002/path.1042
Overexpression of peroxiredoxins I, II, III, V, and VI in malignant mesothelioma
Abstract
Peroxiredoxins (Prxs) are a recently characterized group of thiol-containing proteins with efficient antioxidant capacity, capable of consuming hydrogen peroxide in living cells. Altogether six distinct Prxs have been characterized in mammalian tissues. Their expression was investigated in histological samples of mesothelioma and in cell lines established from the tumours of mesothelioma patients. Four cases with histopathologically healthy pleura from non-smokers were used as controls. Healthy pleural mesothelium was negative or very weakly positive for all Prxs. In mesothelioma, the most prominent reactivity was observed with Prxs I, II, V, and VI. Prx I was highly or moderately expressed in 25/36 cases, the corresponding figures for Prxs II-VI being 27/36 (Prx II), 13/36 (Prx III), 2/36 (Prx IV), 24/36 (Prx V), and 30/36 (Prx VI). Positive staining was observed both in the cytosolic and the nuclear compartment, with the exception of Prx III, which showed no nuclear reactivity. The staining pattern of Prxs III and V was granular. Immunoelectron microscopic localization of Prxs was in accordance with the immunohistochemical findings, showing diffuse cytoplasmic localization for Prxs I, II, IV, and VI and distinct mitochondrial labelling for Prxs III and V. There was no significant association between the extent of staining and different Prxs. It appeared that Prxs may not have prognostic significance, but being prominently expressed in most mesotheliomas these proteins, at least in theory, may play a role in the primary drug resistance of this disease.
Copyright 2002 John Wiley & Sons, Ltd.
Similar articles
-
Peroxiredoxins in breast carcinoma.Clin Cancer Res. 2003 Aug 15;9(9):3418-24. Clin Cancer Res. 2003. PMID: 12960131
-
Characterization of neural cell types expressing peroxiredoxins in mouse brain.Neurosci Lett. 2005 Jun 24;381(3):252-7. doi: 10.1016/j.neulet.2005.02.048. Neurosci Lett. 2005. PMID: 15896479
-
Expression of peroxiredoxin and thioredoxin in human lung cancer and paired normal lung.Respirology. 2006 May;11(3):269-75. doi: 10.1111/j.1440-1843.2006.00849.x. Respirology. 2006. PMID: 16635084
-
Mitochondrial peroxiredoxin involvement in antioxidant defence and redox signalling.Biochem J. 2009 Dec 23;425(2):313-25. doi: 10.1042/BJ20091541. Biochem J. 2009. PMID: 20025614 Review.
-
The function of peroxiredoxins in plant organelle redox metabolism.J Exp Bot. 2006;57(8):1697-709. doi: 10.1093/jxb/erj160. Epub 2006 Apr 10. J Exp Bot. 2006. PMID: 16606633 Review.
Cited by
-
Peroxiredoxin 3 is a redox-dependent target of thiostrepton in malignant mesothelioma cells.PLoS One. 2012;7(6):e39404. doi: 10.1371/journal.pone.0039404. Epub 2012 Jun 25. PLoS One. 2012. PMID: 22761781 Free PMC article.
-
Redox Homeostasis and Cellular Antioxidant Systems: Crucial Players in Cancer Growth and Therapy.Oxid Med Cell Longev. 2016;2016:6235641. doi: 10.1155/2016/6235641. Epub 2016 Jun 21. Oxid Med Cell Longev. 2016. PMID: 27418953 Free PMC article. Review.
-
Peroxiredoxins - Urinary Surveillance Biomarkers in Urothelial Cancer.J Cancer. 2022 Jun 13;13(9):2751-2756. doi: 10.7150/jca.69811. eCollection 2022. J Cancer. 2022. PMID: 35812179 Free PMC article.
-
Stage-related alterations in renal cell carcinoma--comprehensive quantitative analysis by 2D-DIGE and protein network analysis.PLoS One. 2011;6(7):e21867. doi: 10.1371/journal.pone.0021867. Epub 2011 Jul 7. PLoS One. 2011. PMID: 21760917 Free PMC article.
-
Overexpression of peroxiredoxin-3 and -5 is a potential biomarker for prognosis in endometrial cancer.Oncol Lett. 2018 Apr;15(4):5111-5118. doi: 10.3892/ol.2018.7909. Epub 2018 Jan 31. Oncol Lett. 2018. PMID: 29541251 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials