| Literature DB >> 25866182 |
Pradeep Bist1, Qian Hui Phua1, Shinla Shu1, Yuan Yi1, Durkeshwari Anbalagan1, Lay Hoon Lee1, Gautam Sethi2, Boon Chuan Low3, Lina H K Lim4.
Abstract
Wound healing is critical for normal development and pathological processes including cancer cell metastasis. MAPK, Rho-GTPases and NFκB are important regulators of wound healing, but mechanisms for their integration are incompletely understood. Annexin-A1 (ANXA1) is upregulated in invasive breast cancer cells resulting in constitutive activation of NFκB. We show here that silencing ANXA1 increases the formation of stress fibers and focal adhesions, which may inhibit wound healing. ANXA1 regulated wound healing is dependent on the activation of ERK1/2. ANXA1 increases the activation of RhoA, which is dependent on ERK activation. Furthermore, active RhoA is important in NF-κB activation, where constitutively active RhoA potentiates NFκB activation, while dominant negative RhoA inhibits NFκB activation in response to CXCL12 stimulation and active MEKK plasmids. These findings establish a central role for ANXA1 in the cell migration through the activation of NFκB, ERK1/2 and RhoA.Entities:
Keywords: Annexin-1 (ANXA1); ERK; Metastasis; Nuclear factor-kappa B (NF-κB); RhoA; Stress fibers
Mesh:
Substances:
Year: 2015 PMID: 25866182 DOI: 10.1016/j.bbrc.2015.03.166
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575