Annexin A1 localization and its relevance to cancer

膜联蛋白A1 受体 癌细胞 细胞生物学 癌症研究 癌症 生物 细胞 细胞表面受体 细胞质 膜联蛋白 生物化学 遗传学
作者
Zied Boudhraa,Bernadette Bouchon,Claire Viallard,M. D’Incan,Françoise Degoul
出处
期刊:Clinical Science [Portland Press]
卷期号:130 (4): 205-220 被引量:126
标识
DOI:10.1042/cs20150415
摘要

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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