Format

Send to

Choose Destination
Mol Cell Proteomics. 2019 May 6. pii: mcp.RA119.001496. doi: 10.1074/mcp.RA119.001496. [Epub ahead of print]

Proteomic profiling of human prostate cancer-associated fibroblasts (CAF) reveals LOXL2-dependent regulation of the tumor microenvironment.

Author information

1
Biochemistry and Molecular Biology, Monash University, Australia.
2
Monash University, Australia.
3
The Garvan Institute of Medical Research, Australia.
4
Peking University Cancer Hospital & Institute, China.
5
The Garvan Institute of Medical Research and the Kinghorn Cancer Centre, Australia.
6
Biochemistry and Molecular Biology, Monash University, Australia roger.daly@monash.edu.

Abstract

In prostate cancer, cancer-associated fibroblasts (CAF) exhibit contrasting biological properties to non-malignant prostate fibroblasts (NPF) and promote tumorigenesis. Resolving intercellular signaling pathways between CAF and prostate tumor epithelium may offer novel opportunities for research translation. To this end, the proteome and phosphoproteome of four pairs of patient-matched CAF and NPF were characterized to identify discriminating proteomic signatures. Samples were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) with a hyper reaction monitoring data-independent acquisition (HRM-DIA) workflow. Proteins that exhibited a significant increase in CAF versus NPF were enriched for the functional categories 'cell adhesion' and the 'extracellular matrix'. The CAF phosphoproteome exhibited enhanced phosphorylation of proteins associated with the 'spliceosome' and 'actin binding'. STRING analysis of the CAF proteome revealed a prominent interaction hub associated with collagen synthesis, modification, and signaling. It contained multiple collagens, including the fibrillar types COL1A1/2 and COL5A1; the receptor tyrosine kinase discoidin domaincontaining receptor 2 (DDR2), a receptor for fibrillar collagens; and lysyl oxidase-like 2 (LOXL2), an enzyme which promotes collagen crosslinking. Increased activity and/or expression of LOXL2 and DDR2 in CAF were confirmed by enzymatic assays and Western blot analyses. Pharmacological inhibition of CAF-derived LOXL2 perturbed extracellular matrix (ECM) organization and decreased CAF migration in a wound healing assay. Furthermore, it significantly impaired the motility of co-cultured RWPE-2 prostate tumor epithelial cells. These results indicate that CAF-derived LOXL2 is an important mediator of intercellular communication within the prostate tumor microenvironment and is a potential therapeutic target.

KEYWORDS:

Cancer biomarker(s); Cancer-associated fibroblasts; Fibroblasts; LOXL2; Non-malignant prostate fibroblasts; Phosphoproteome; Prostate cancer; Prostate cancer biomarkers; Tumor microenvironment*

PMID:
31061140
DOI:
10.1074/mcp.RA119.001496
Free full text

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center