G B Fogarty1, N M Conus, J Chu, G McArthur. 1. Division of Radioation Oncology, Translational Research Laboratory, Division of Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia. gerald.fogarty@mia.net.au
Abstract
BACKGROUND: Locally advanced skin cancers including squamous cell carcinoma (SCC) of the skin are increasing in incidence. Patients are often elderly with significant comorbidities and therapy can be difficult. New targeted therapies, such as treatment directed at the epidermal growth factor receptor (EGFR), may be effective and less toxic in these patients. However, before designing appropriate clinical trials it is necessary to characterize the expression and activation of targets such as the EGFR to evaluate the rationale of using EGFR inhibitors (EGFRIs) in the treatment of this type of cancer. OBJECTIVES: To characterize the expression and activation by phosphorylation of EGFR in SCC of the skin by quantitative Western blotting using the LiCor immunofluorescence detection system with validation by immunohistochemistry. Secondary objectives were to evaluate downstream targets of EGFR expression and activation in SCC of the skin and to examine the associations between EGFR, pathological features and clinical behaviour of these tumours. METHODS: Twenty-one mainly locally advanced skin SCCs collected in our institution and stored in our tissue bank over a 4-year period were used for the study. RESULTS: Nine of 21 (43%) tumours expressed EGFR above background. Of those nine, five expressed phosphorylated EGFR. There was no correlation with downstream activation of canonical signalling pathways, pathological features or clinical behaviour. CONCLUSIONS: EGFR is expressed in a minority of tumours and then is not always activated. These results show that, before designing a trial with a targeted agent such as an EGFRI in SCC of the skin, it is important to verify the presence of the appropriate target to maximize the best outcome.
BACKGROUND: Locally advanced skin cancers including squamous cell carcinoma (SCC) of the skin are increasing in incidence. Patients are often elderly with significant comorbidities and therapy can be difficult. New targeted therapies, such as treatment directed at the epidermal growth factor receptor (EGFR), may be effective and less toxic in these patients. However, before designing appropriate clinical trials it is necessary to characterize the expression and activation of targets such as the EGFR to evaluate the rationale of using EGFR inhibitors (EGFRIs) in the treatment of this type of cancer. OBJECTIVES: To characterize the expression and activation by phosphorylation of EGFR in SCC of the skin by quantitative Western blotting using the LiCor immunofluorescence detection system with validation by immunohistochemistry. Secondary objectives were to evaluate downstream targets of EGFR expression and activation in SCC of the skin and to examine the associations between EGFR, pathological features and clinical behaviour of these tumours. METHODS: Twenty-one mainly locally advanced skin SCCs collected in our institution and stored in our tissue bank over a 4-year period were used for the study. RESULTS: Nine of 21 (43%) tumours expressed EGFR above background. Of those nine, five expressed phosphorylated EGFR. There was no correlation with downstream activation of canonical signalling pathways, pathological features or clinical behaviour. CONCLUSIONS:EGFR is expressed in a minority of tumours and then is not always activated. These results show that, before designing a trial with a targeted agent such as an EGFRI in SCC of the skin, it is important to verify the presence of the appropriate target to maximize the best outcome.
Authors: Laure Rittié; Sanjay Kansra; Stefan W Stoll; Yong Li; Johann E Gudjonsson; Yuan Shao; Lowell E Michael; Gary J Fisher; Timothy M Johnson; James T Elder Journal: Am J Pathol Date: 2007-06 Impact factor: 4.307
Authors: William N William; Lei Feng; Renata Ferrarotto; Lawrence Ginsberg; Merrill Kies; Scott Lippman; Bonnie Glisson; Edward S Kim Journal: J Am Acad Dermatol Date: 2017-09-28 Impact factor: 11.527
Authors: de Lima Vazquez Vinicius; Cristovam Scapulatempo; Natalia Martins Perpetuo; Faheez Mohamed; Teóclito Sachetto de Carvalho; Antônio Talvane Torres de Oliveira; José Getúlio Martins Segalla; André Lopes Carvalho Journal: J Skin Cancer Date: 2011-05-19
Authors: Sara Falivene; Francesca Maria Giugliano; Antonio Maria Grimaldi; Rossella Di Franco; Diego Toledo; Matteo Muto; Fabrizio Cammarota; Valentina Borzillo; Paolo Antonio Ascierto; Paolo Muto Journal: BMC Dermatol Date: 2014-09-30
Authors: Sherene Loi; Christos Sotiriou; Benjamin Haibe-Kains; Francoise Lallemand; Nelly M Conus; Martine J Piccart; Terence P Speed; Grant A McArthur Journal: BMC Med Genomics Date: 2009-06-24 Impact factor: 3.063