Published April 1, 2014 | Version v1
Journal article

Effects of activated fibroblasts on phenotype modulation, EGFR signalling and cell cycle regulation in OSCC cells

  • 1. Center for Molecular Biomedicine, Institute of Pathology, Jena University Hospital, 07740 Jena (Germany)
  • 2. Institute of Biochemistry and Biophysics, Friedrich Schiller University Jena, 07740 Jena (Germany)
  • 3. Clinic of Internal Medicine I, Jena University Hospital, 07740 Jena (Germany)

Description

Crosstalk between carcinoma associated fibroblasts (CAFs) and oral squamous cell carcinoma (OSCC) cells is suggested to mediate phenotype transition of cancer cells as a prerequisite for tumour progression, to predict patients’ outcome, and to influence the efficacy of EGFR inhibitor therapies. Here we investigate the influence of activated fibroblasts as a model for CAFs on phenotype and EGFR signalling in OSCC cells in vitro. For this, immortalised hTERT-BJ1 fibroblasts were activated with TGFβ1 and PDGFAB to generate a myofibroblast or proliferative phenotype, respectively. Conditioned media (FCMTGF, FCMPDGF) were used to stimulate PE/CA-PJ15 OSCC cells. Results were compared to the effect of conditioned media of non-stimulated fibroblasts (FCMB). FCMTGF stimulation leads to an up-regulation of vimentin in the OSCC cells and an enhancement of invasive behaviour, indicating EMT-like effects. Similarly, FCMTGF≫FCMPDGF induced up-regulation of EGFR, but not of ErbB2/ErbB3. In addition, we detected an increase in basal activities of ERK, PI3K/Akt and Stat3 (FCMTGF>FCMPDGF) accompanied by protein interaction of vimentin with pERK. These effects are correlated with an increased proliferation. In summary, our results suggest that the activated myofibroblast phenotype provides soluble factors which are able to induce EMT-like phenomena and to increase EGFR signalling as well as cell proliferation in OSCC cells. Our results indicate a possible influence of activated myofibroblasts on EGFR-inhibitor therapy. Therefore, CAFs may serve as promising novel targets for combined therapy strategies. - Highlights: • A cell culture model for cancer associated fibroblasts is described. • The mutual interaction with OSCC cells leads to up-regulation of EGFR in tumour cells. • mCAF induces EGFR downstream signalling with increased proliferation in OSCC. • Erk activation is associated with protein interaction with vimentin as sign of EMT. • Results qualify CAF as promising new therapeutic targets in OSCC

Availability note (English)

Available from http://dx.doi.org/10.1016/j.yexcr.2013.12.024

Additional details

Identifiers

DOI
10.1016/j.yexcr.2013.12.024;
PII
S0014-4827(13)00559-4;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
322
Journal Issue
2
Journal Page Range
p. 402-414
ISSN
0014-4827
CODEN
ECREAL

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46101578
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
CARCINOMAS; CELL CULTURES; CELL PROLIFERATION; COMBINED THERAPY; FIBROBLASTS; GROWTH FACTORS; IN VITRO; PHENOTYPE; RECEPTORS; TRANSCRIPTION
Descriptors DEC
ANIMAL CELLS; CONNECTIVE TISSUE CELLS; DISEASES; MEDICINE; MEMBRANE PROTEINS; MITOGENS; NEOPLASMS; ORGANIC COMPOUNDS; PROTEINS; SOMATIC CELLS; THERAPY

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.