Desmoglein 2 modulates extracellular vesicle release from squamous cell carcinoma keratinocytes

Authors:
Open Access
Publisher website
Google Scholar
Abstract
Extracellular vesicles (EVs) are nanoscale membrane‐derived vesicles that serve as intercellular messengers carrying lipids, proteins, and genetic material. Substantial evidence has shown that cancer‐derived EVs, secreted by tumor cells into the blood and other bodily fluids, play a critical role in modulating the tumor microenvironment and affecting the pathogenesis of cancer. Here we demonstrate for the first time that squamous cell carcinoma (SCC) EVs were enriched with the C‐terminal fragment of desmoglein 2 (Dsg2), a desmosomal cadherin often overexpressed in malignancies. Overexpression of Dsg2 increased EV release and mitogenic + fibroblasts. Furthermore, SCC EVs activated Erk1/2 and Akt signaling and enhanced fibroblast cell proliferation. In vivo, Dsg2 was highly up‐regulated in the head and neck SCCs, and EVs isolated from sera of patients with SCC were enriched in Dsg2 C‐terminal fragment and epidermal growth factor receptor. This study defines a mechanism by which Dsg2 expression in cancer cells can modulate the tumor microenvironment, a step critical for tumor progression.—Overmiller, A. M., Pierluissi, J. A., Wermuth, P. J., Sauma, S., Martinez‐Outschoorn, U., Tuluc, M., Luginbuhl, A., Curry, J., Harshyne, L. A., Wahl, J. K. III, South, A. P., Mahoney, M. G. Desmoglein 2 modulates extracellular vesicle release from squamous cell carcinoma keratinocytes. FASEB J . 31, 3412–3424 (2017). www.fasebj.org
Funding Information
  • National Institutes of Health
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR056067)
  • Thomas Jefferson University

This publication has 54 references indexed in Scilit: