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Cell-line-specific stimulation of tumor cell aggressiveness by wound healing factors - a central role for STAT3

Ekblad, Lars LU orcid ; Lindgren, Gustaf LU ; Persson, Emma ; Kjellén, Elisabeth LU and Wennerberg, Johan LU orcid (2013) In BMC Cancer 13.
Abstract
Background: Local recurrence is a major factor affecting survival after treatment for head and neck squamous cell carcinoma (HNSCC). It is possible that the normal processes involved in wound healing after surgical removal of a primary tumor can boost the regrowth of residual cancer cells, thereby contributing to the recurrent growth. In this work, we collected human wound fluids and used them to investigate the effect of wound healing factors on HNSCC cell lines in vitro. Methods: Wound fluids were collected from thyroidectomized patients diagnosed with benign disease and were included in assays of cell proliferation, migration, cell scattering, and invasion. The involvement of intracellular signaling pathways and membrane receptors were... (More)
Background: Local recurrence is a major factor affecting survival after treatment for head and neck squamous cell carcinoma (HNSCC). It is possible that the normal processes involved in wound healing after surgical removal of a primary tumor can boost the regrowth of residual cancer cells, thereby contributing to the recurrent growth. In this work, we collected human wound fluids and used them to investigate the effect of wound healing factors on HNSCC cell lines in vitro. Methods: Wound fluids were collected from thyroidectomized patients diagnosed with benign disease and were included in assays of cell proliferation, migration, cell scattering, and invasion. The involvement of intracellular signaling pathways and membrane receptors were investigated by western blotting and the inclusion of specific inhibitors. Results: One out of four cell lines was greatly stimulated in proliferation, migration, cell scattering, and invasion by the addition of wound fluid as compared with addition of fetal bovine or human serum. These effects were accompanied by a sharp increase in activation of signal transducer and activator of transcription 3 (STAT3). Inhibition of STAT3 activation abolished the wound fluid response, showing that STAT3 plays an important role in the wound healing response. Several of the observed phenotypic changes were epithelial-to-mesenchymal transition (EMT)-like, but the appropriate changes were not seen in any of the EMT markers investigated. The involvement of c-Met or epidermal growth factor receptor family members was excluded, while the interleukin-6 receptor was found to be partly responsible for the activation of STAT3. Conclusions: In conclusion, we found cell-line-specific effects of wound healing factors on HNSCC, setting the stage for therapy development and predictive opportunities. (Less)
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author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Head and neck cancer, Local recurrence, Wound healing, Proliferation, Invasion, Migration, STAT3, IL-6, IL6R, Tocilizumab
in
BMC Cancer
volume
13
article number
33
publisher
BioMed Central (BMC)
external identifiers
  • wos:000315636000001
  • scopus:84872760879
  • pmid:23351302
ISSN
1471-2407
DOI
10.1186/1471-2407-13-33
project
Local recurrences in head and neck cancer – etiology and prevention
language
English
LU publication?
yes
id
b7d4e7e9-5aab-48c5-be05-09dbd57b5bbd (old id 3671311)
date added to LUP
2016-04-01 14:51:05
date last changed
2022-01-28 02:53:20
@article{b7d4e7e9-5aab-48c5-be05-09dbd57b5bbd,
  abstract     = {{Background: Local recurrence is a major factor affecting survival after treatment for head and neck squamous cell carcinoma (HNSCC). It is possible that the normal processes involved in wound healing after surgical removal of a primary tumor can boost the regrowth of residual cancer cells, thereby contributing to the recurrent growth. In this work, we collected human wound fluids and used them to investigate the effect of wound healing factors on HNSCC cell lines in vitro. Methods: Wound fluids were collected from thyroidectomized patients diagnosed with benign disease and were included in assays of cell proliferation, migration, cell scattering, and invasion. The involvement of intracellular signaling pathways and membrane receptors were investigated by western blotting and the inclusion of specific inhibitors. Results: One out of four cell lines was greatly stimulated in proliferation, migration, cell scattering, and invasion by the addition of wound fluid as compared with addition of fetal bovine or human serum. These effects were accompanied by a sharp increase in activation of signal transducer and activator of transcription 3 (STAT3). Inhibition of STAT3 activation abolished the wound fluid response, showing that STAT3 plays an important role in the wound healing response. Several of the observed phenotypic changes were epithelial-to-mesenchymal transition (EMT)-like, but the appropriate changes were not seen in any of the EMT markers investigated. The involvement of c-Met or epidermal growth factor receptor family members was excluded, while the interleukin-6 receptor was found to be partly responsible for the activation of STAT3. Conclusions: In conclusion, we found cell-line-specific effects of wound healing factors on HNSCC, setting the stage for therapy development and predictive opportunities.}},
  author       = {{Ekblad, Lars and Lindgren, Gustaf and Persson, Emma and Kjellén, Elisabeth and Wennerberg, Johan}},
  issn         = {{1471-2407}},
  keywords     = {{Head and neck cancer; Local recurrence; Wound healing; Proliferation; Invasion; Migration; STAT3; IL-6; IL6R; Tocilizumab}},
  language     = {{eng}},
  publisher    = {{BioMed Central (BMC)}},
  series       = {{BMC Cancer}},
  title        = {{Cell-line-specific stimulation of tumor cell aggressiveness by wound healing factors - a central role for STAT3}},
  url          = {{https://lup.lub.lu.se/search/files/4198720/4016075.pdf}},
  doi          = {{10.1186/1471-2407-13-33}},
  volume       = {{13}},
  year         = {{2013}},
}