Annexin A1 (ANXA1) is a Ca2+-regulated phospholipid-binding protein involved in various cell processes. ANXA1 was initially widely studied in inflammation resolution, but its overexpression was later reported in a large number of cancers. Further in-depth investigations have revealed that this protein could have many roles in cancer progression and act at different levels (from cancer initiation to metastasis). This is partly due to the location of ANXA1 in different cell compartments. ANXA1 can be nuclear, cytoplasmic and/or membrane associated. This last location allows ANXA1 to be proteolytically cleaved and/or to become accessible to its cognate partners, the formyl-peptide receptors. Indeed, in some cancers, ANXA1 is found at the cell surface, where it stimulates formyl-peptide receptors to trigger oncogenic pathways. In the present review, we look at the different locations of ANXA1 and their association with the deregulated pathways often observed in cancers. We have specifically detailed the non-classic pathways of ANXA1 externalization, the significance of its cleavage and the role of the ANXA1–formyl-peptide receptor complex in cancer progression.
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February 2016
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Cover Image
Image modified from a figure representing the 5 mechanisms of annexin A1 externalization through non-classic secretory pathways, discussed by Boudhraa et al in issue 130(4) of Clinical Science. For further details please see pp. 205–220. Image kindly provided by Z. Boudhraa, B. Bouchon, C. Viallard, M. D'Incan and F. Degoul.
Review Article|
January 14 2016
Annexin A1 localization and its relevance to cancer
Zied Boudhraa;
*Clermont Université, Université d'Auvergne, Imagerie Moléculaire et Thérapie Vectorisée, BP 10448, F-63000 Clermont-Ferrand, France
†INSERM, U 990, F-63000 Clermont-Ferrand, France
Correspondence: Zied Boudhraa ([email protected]).
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Bernadette Bouchon;
Bernadette Bouchon
*Clermont Université, Université d'Auvergne, Imagerie Moléculaire et Thérapie Vectorisée, BP 10448, F-63000 Clermont-Ferrand, France
†INSERM, U 990, F-63000 Clermont-Ferrand, France
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Claire Viallard;
Claire Viallard
*Clermont Université, Université d'Auvergne, Imagerie Moléculaire et Thérapie Vectorisée, BP 10448, F-63000 Clermont-Ferrand, France
†INSERM, U 990, F-63000 Clermont-Ferrand, France
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Michel D'Incan;
Michel D'Incan
*Clermont Université, Université d'Auvergne, Imagerie Moléculaire et Thérapie Vectorisée, BP 10448, F-63000 Clermont-Ferrand, France
†INSERM, U 990, F-63000 Clermont-Ferrand, France
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Françoise Degoul
Françoise Degoul
*Clermont Université, Université d'Auvergne, Imagerie Moléculaire et Thérapie Vectorisée, BP 10448, F-63000 Clermont-Ferrand, France
†INSERM, U 990, F-63000 Clermont-Ferrand, France
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Publisher: Portland Press Ltd
Received:
June 10 2015
Revision Received:
October 12 2015
Accepted:
October 20 2015
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2016 Authors; published by Portland Press Limited
2016
Clin Sci (Lond) (2016) 130 (4): 205–220.
Article history
Received:
June 10 2015
Revision Received:
October 12 2015
Accepted:
October 20 2015
Citation
Zied Boudhraa, Bernadette Bouchon, Claire Viallard, Michel D'Incan, Françoise Degoul; Annexin A1 localization and its relevance to cancer. Clin Sci (Lond) 1 February 2016; 130 (4): 205–220. doi: https://doi.org/10.1042/CS20150415
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