Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Ave., Detroit, MI 48201, USA.
Anticancer Res. 2012 Mar;32(3):753-60.
The effectiveness of photodynamic therapy (PDT) for cancer treatment correlates with apoptosis. We observed that suppression of de novo-generated sphingolipids, e.g. ceramide, renders cells resistant to apoptosis post-PDT. Ceramide synthase 6 (CerS6) has been implicated in apoptosis after various stimuli.
To investigate the involvement of down-regulation of CerS6 in apoptosis and its impact on the sphingolipid profile post-PDT with the silicone phthalocyanine Pc 4 in a human head and neck squamous carcinoma cell line.
Besides siRNA transfections and PDT treatment, immunoblotting for protein expression, mass spectrometry for sphingolipid analysis, spectroflurometry and flow cytometry for apoptotic marker detection, and trypan blue assay for cytotoxicity assessment, were used.
CerS6 knockdown led to reduction in PDT-induced DEVDase activation, mitochondrial depolarization, apoptosis and cell death. CerS6 knockdown was associated with selective decreases in ceramides and dihydroceramides, markedly of C18-dihydroceramide, post-PDT.
CerS6 might be a novel therapeutic target for regulating apoptotic resistance to PDT.
光动力疗法(PDT)治疗癌症的效果与细胞凋亡相关。我们观察到,抑制从头合成的鞘脂,如神经酰胺,可使细胞在 PDT 后对细胞凋亡产生抗性。在各种刺激后,神经酰胺合酶 6(CerS6)已被牵连到细胞凋亡中。
研究下调 CerS6 在凋亡中的作用及其对人头颈鳞癌细胞系在用硅酞菁 Pc 4 进行 PDT 后鞘脂谱的影响。
除了 siRNA 转染和 PDT 处理外,还使用免疫印迹法检测蛋白表达、质谱法检测鞘脂分析、分光光度法和流式细胞术检测凋亡标志物、台盼蓝法检测细胞毒性评估。
CerS6 敲低导致 PDT 诱导的 DEVDase 激活、线粒体去极化、凋亡和细胞死亡减少。CerS6 敲低与 PDT 后神经酰胺和二氢神经酰胺选择性减少有关,尤其是 C18-二氢神经酰胺。
CerS6 可能是调节 PDT 诱导的细胞凋亡抗性的新的治疗靶点。