Oncotarget

Research Papers:

Annexin A2 is a novel Cellular Redox Regulatory Protein involved in Tumorigenesis

Patricia Alexandra Madureira, Richard Hill, Victoria Ann Miller, Carman Giacomantonio, Patrick WK Lee and David Morton Waisman _

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Oncotarget. 2011; 2:1075-1093. https://doi.org/10.18632/oncotarget.375

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Abstract

Patricia Alexandra Madureira1, Richard Hill2, Victoria Ann Miller1, Carman Giacomantonio3, Patrick Wing Kwong Lee2 and David Morton Waisman1

1Departments of Biochemistry & Molecular Biology and Pathology

2Department of Microbiology and Immunology

3Department of Medicine, Dalhousie University Halifax, Nova Scotia, B3H 4R2, Canada

Received: December 1, 2011; Accepted: December 9, 2011; Published: December 20, 2011;

Keywords: ANXA2, reactive oxygen species (ROS), redox regulation, oxidative stress, tumorigenesis

Correspondence:

David Morton Waisman, email:

Abstract

Annexins are a structurally related family of calcium and phospholipid-binding proteins that are involved in the regulation of a wide range of molecular and cellular processes. Annexin A2 is unique among the annexins in that it possesses redox sensitive cysteine(s). The ubiquitous and abundant expression of ANXA2 in cells and its reactivity with hydrogen peroxide led us to hypothesize that this protein could play a role in cellular redox regulation. Here we show that ANXA2 protein levels are induced by hydrogen peroxide. Furthermore, depletion of ANXA2 resulted in the elevation of cellular reactive oxygen species (ROS) upon oxidative stress, increased activation of the ROS-induced pro-apoptotic kinases, JNK, p38 and Akt and elevated sensitivity to ROS-mediated cellular damage/death. ANXA2-null mice showed significantly elevated protein oxidation in the liver and lung tissues compared to WT mice. ANXA2 depleted cancer cells showed enhanced cellular protein oxidation concomitant with decreased tumor growth compared to control cancer cells and both the protein oxidation and tumor growth deficit were reversed by the antioxidant N-acetyl cysteine, indicating that ANXA2 redox regulatory function plays a major role in tumorigenesis. Ex-vivo human cancer studies showed that up-regulation of the reduced form of ANXA2 is associated with protection of the tumor proteins from oxidation. In summary, our results indicate that ANXA2 redox regulatory function plays an important role protecting cells from oxidative stress, particularly during tumorigenesis.


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