Exp Dermatol. 2010 Feb;19(2):151-3. doi: 10.1111/j.1600-0625.2009.01028.x.
Epidermal growth factor receptor (EGFR) gene amplification and protein overexpression are common in several cancers. EGFR status has seldom been studied in cutaneous squamous carcinomas (SCCs), or their precursors, actinic keratoses (AKs). We evaluated the presence of EGFR genomic aberrations and EGFR protein overexpression in 25 AKs and 35 invasive SCCs by means of fluorescence in situ hybridization (FISH) and immunohistochemistry. EGFR numerical aberrations were detected in 52% of AKs and 77.1% of SCCs (P = 0.042). EGFR amplification was identified in 12% of AKs and 20% of SCCs. No differences regarding EGFR numerical aberrations were observed when AKs with high-grade dysplasia were compared with SCCs. A good correlation was observed between EGFR numerical aberrations and EGFR overexpression. Our results suggest that EGFR numerical aberrations occur in the early stages of epithelial carcinogenesis in skin, not playing a role in the progression from low-grade SCCs into more aggressive phenotypes.
表皮生长因子受体 (EGFR) 基因扩增和蛋白过表达在几种癌症中很常见。EGFR 状态在皮肤鳞状细胞癌 (SCC) 或其前体光化性角化病 (AK) 中很少被研究。我们通过荧光原位杂交 (FISH) 和免疫组织化学评估了 25 例 AK 和 35 例浸润性 SCC 中 EGFR 基因异常和 EGFR 蛋白过表达的情况。在 52%的 AK 和 77.1%的 SCC 中检测到 EGFR 数量异常 (P = 0.042)。在 12%的 AK 和 20%的 SCC 中发现了 EGFR 扩增。在高级别发育不良的 AK 与 SCC 相比时,EGFR 数量异常没有差异。EGFR 数量异常与 EGFR 过表达之间存在良好的相关性。我们的结果表明,EGFR 数量异常发生在皮肤上皮癌发生的早期阶段,在从低级别 SCC 进展为更具侵袭性表型的过程中不起作用。