Fogarty G B, Conus N M, Chu J, McArthur G
Division of Radioation Oncology, Translational Research Laboratory, Division of Research, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
Br J Dermatol. 2007 Jan;156(1):92-8. doi: 10.1111/j.1365-2133.2006.07603.x.
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.
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.
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.
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.
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.
包括皮肤鳞状细胞癌(SCC)在内的局部晚期皮肤癌发病率正在上升。患者通常为老年人,伴有严重的合并症,治疗可能具有挑战性。新的靶向治疗,如针对表皮生长因子受体(EGFR)的治疗,在这些患者中可能有效且毒性较小。然而,在设计合适的临床试验之前,有必要对诸如EGFR等靶点的表达和激活情况进行表征,以评估使用EGFR抑制剂(EGFRIs)治疗这类癌症的理论依据。
使用LiCor免疫荧光检测系统通过定量蛋白质免疫印迹法对皮肤SCC中EGFR的表达和磷酸化激活情况进行表征,并通过免疫组织化学进行验证。次要目的是评估皮肤SCC中EGFR表达和激活的下游靶点,并研究EGFR、这些肿瘤的病理特征与临床行为之间的关联。
本研究使用了在4年期间收集于我们机构并存储在我们组织库中的21例主要为局部晚期的皮肤SCC。
21例肿瘤中有9例(43%)EGFR表达高于背景水平。在这9例中,有5例表达磷酸化EGFR。与经典信号通路的下游激活、病理特征或临床行为均无相关性。
EGFR在少数肿瘤中表达,且并非总是被激活。这些结果表明,在设计针对皮肤SCC的靶向药物(如EGFRIs)的试验之前,重要的是要验证合适靶点的存在,以实现最佳疗效。