S100A4 Elevation Empowers Expression of Metastasis Effector Molecules in Human Breast Cancer.



Ismail, TM, Bennett, D, Platt-Higgins, AM, Al-Medhity, M, Barraclough, R and Rudland, PS ORCID: 0000-0002-7491-0846
(2016) S100A4 Elevation Empowers Expression of Metastasis Effector Molecules in Human Breast Cancer. Cancer research, 77 (3). 780 - 789.

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Abstract

Many human glandular cancers metastasize along nerve tracts, but the mechanisms involved are generally poorly understood. The calcium-binding protein S100A4 is expressed at elevated levels in human cancers, where it has been linked to increased invasion and metastasis. Here we report genetic studies in a Drosophila model to define S100A4 effector functions that mediate metastatic dissemination of mutant Ras-induced tumors in the developing nervous system. In flies overexpressing mutant RasVal12 and S100A4, there was a significant increase in activation of the stress kinase JNK and production of the matrix metalloproteinase MMP1. Genetic or chemical blockades of JNK and MMP1 suppressed metastatic dissemination associated with S100A4 elevation, defining required signaling pathway(s) for S100A4 in this setting. In clinical specimens of human breast cancer, elevated levels of the mammalian paralogs MMP2, MMP9, and MMP13 are associated with a 4- to 9-fold relative decrease in patient survival. In individual tumors, levels of MMP2 and MMP13 correlated more closely with levels of S100A4, whereas MMP9 levels correlated more closely with the S100 family member S100P. Overall, our results suggest the existence of evolutionarily conserved pathways used by S100A4 to promote metastatic dissemination, with potential prognostic and therapeutic implications for metastasis by cancers that preferentially exploit nerve tract migration routes. Cancer Res; 77(3); 1-10. ©2016 AACR.

Item Type: Article
Uncontrolled Keywords: S100A4/JNK, MMPs/Drosophila/human breast cancer
Depositing User: Symplectic Admin
Date Deposited: 06 Dec 2016 15:00
Last Modified: 16 Apr 2021 11:14
DOI: 10.1158/0008-5472.can-16-1802
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3004779