Schmitz Sandra, Bindea Gabriela, Albu Roxana Irina, Mlecnik Bernhard, Machiels Jean-Pascal
Institut Roi Albert II, Department of Medical Oncology, Cliniques Universitaires Saint-Luc and Institut de Recherche Clinique et Expérimentale (Pole MIRO), Université Catholique de Louvain, Brussels, Belgium.
Department of Head and Neck Surgery, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
Oncotarget. 2015 Oct 27;6(33):34288-99. doi: 10.18632/oncotarget.5924.
To investigate if cetuximab induces epithelial to mesenchymal transition (EMT) and activation of cancer associated fibroblast (CAF) in the tumors of patients with squamous cell carcinoma of the head and neck (SCCHN).
Cetuximab was administered for two weeks prior to surgery to 20 treatment-naïve patients. Five untreated patients were included as controls. Tumor biopsies were performed at baseline and before surgery. Gene expression profiles and quantitative real-time PCR (qRT-PCR) analysis of the pre-and post-treatment biopsies were compared. To further investigate EMT and CAF, correlations between previously described EMT and CAF markers and our microarray data set were calculated.
Gene expression profile analyses and qRT-PCR showed that some of the genes modified by cetuximab were related to CAFs and EMT (ZNF521, CXCL12, ASPN, OLFML3, OLFM1, TWIST1, LEF1, ZEB1, FAP). We identified 2 patient clusters with different EMT and CAF characteristics. Whereas one cluster showed clear upregulation of expression of genes implicated in CAF and EMT including markers of embryologic pathways like NOTCH and Wnt, the other did not.
Even if EMT and CAFs are implicated in cetuximab resistance in pre-clinical models, we demonstrate for the first time that these molecular processes may occur clinically early on.
研究西妥昔单抗是否会在头颈部鳞状细胞癌(SCCHN)患者的肿瘤中诱导上皮-间质转化(EMT)以及激活癌症相关成纤维细胞(CAF)。
对20例未经治疗的患者在手术前两周给予西妥昔单抗。纳入5例未接受治疗的患者作为对照。在基线期和手术前进行肿瘤活检。比较治疗前后活检组织的基因表达谱和定量实时PCR(qRT-PCR)分析。为进一步研究EMT和CAF,计算先前描述的EMT和CAF标志物与我们的微阵列数据集之间的相关性。
基因表达谱分析和qRT-PCR显示,西妥昔单抗改变的一些基因与CAF和EMT相关(ZNF521、CXCL12、ASPN、OLFML3、OLFM1、TWIST1、LEF1、ZEB1、FAP)。我们鉴定出2个具有不同EMT和CAF特征的患者聚类。其中一个聚类显示与CAF和EMT相关的基因表达明显上调,包括NOTCH和Wnt等胚胎学途径的标志物,而另一个聚类则没有。
即使在临床前模型中EMT和CAF与西妥昔单抗耐药有关,但我们首次证明这些分子过程可能在临床上早期就会发生。