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Radioresistant laryngeal cancers upregulate type 1 IGF receptor and exhibit increased cellular dependence on IGF and EGF signalling

Abstract:

Objectives Patients failing radiotherapy for laryngeal squamous cell carcinoma (LSCC) often require salvage total laryngectomy which has major functional consequences, highlighting a need for biomarkers of radiotherapy resistance. In other tumour types, radioresistance has been linked to epidermal growth factor receptor (EGFR) and type 1 insulin‐like growth factor receptor (IGF‐1R). Here, we evaluated IGF‐1R and EGFR as predictors and mediators of LSCC radioresistance.

Design We compared IGF‐1R and EGFR immunohistochemical scores in LSCC patients achieving long‐term remission post‐radiotherapy (n=23), patients treated with primary laryngectomy (n=22) or salvage laryngectomy following radiotherapy recurrence (n=18). To model radioresistance in vitro, two LSCC cell lines underwent clinically‐relevant irradiation to 55 Gy in 2.75 Gy fractions.

Results IGF‐1R expression was higher in pre‐treatment biopsies of radiotherapy‐failures compared with those in long‐term remission, and was upregulated post‐radiotherapy. Patients undergoing primary laryngectomy had more advanced T/N stage and greater tumour IGF‐1R content than those achieving long‐term remission. Pre‐treatment EGFR did not associate with radiotherapy outcomes but showed a trend to upregulation post‐irradiation. In vitro, radiosensitivity was enhanced by inhibition of EGFR but not IGF. Repeated irradiation upregulated IGF‐1R in BICR18 and SQ20B cells and EGFR in SQ20B, and enhanced SQ20B radioresistance. Repeatedly‐irradiated SQ20B_55 cells were not radiosensitised by inhibition of IGF and/or EGFR, but IGF‐1R:EGFR co‐inhibition suppressed baseline cell survival more effectively than blockade of either pathway alone, and more effectively than in parental cells.

Conclusions Radiation upregulates IGF‐1R and may enhance IGF/EGFR dependence, suggesting that IGF/EGFR blockade may have activity in LSCCs that recur post‐radiotherapy.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1111/coa.13434

Authors

More by this author
Institution:
University of Oxford
Department:
Surgical Sciences
Role:
Author
ORCID:
0000-0001-8654-6888
More by this author
Institution:
University of Oxford
Department:
Oncology
Role:
Author
More by this author
Institution:
University of Oxford
Department:
Oncology
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Surgical Sciences
Role:
Author
ORCID:
0000-0002-8152-816X


Publisher:
Wiley
Journal:
Clinical Otolaryngology More from this journal
Volume:
44
Issue:
6
Pages:
1026-1036
Publication date:
2019-09-19
Acceptance date:
2019-09-19
DOI:
EISSN:
1749-4486
ISSN:
1749-4478


Language:
English
Keywords:
Pubs id:
pubs:1054449
UUID:
uuid:a607e373-b6bc-4b0a-b6d0-2588738cd127
Local pid:
pubs:1054449
Source identifiers:
1054449
Deposit date:
2019-09-20
ARK identifier:

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