Fan Zhichao, Cui Xiaojun, Wei Dan, Liu Wei, Li Buhong, He Hao, Ye Huamao, Zhu Naishuo, Wei Xunbin
State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Sci Rep. 2016 May 6;6:25353. doi: 10.1038/srep25353.
Photodynamic therapy (PDT) with protoporphyrin IX (PpIX), which is endogenously derived from 5-aminolevulinic acid (5-ALA) or its derivatives, is a promising modality for the treatment of both pre-malignant and malignant lesions. However, the mechanisms of how ALA-induced PpIX selectively accumulated in the tumors are not fully elucidated. Here we discovered that eukaryotic translation elongation factor 1 alpha 1 (eEF1A1) interacted with PpIX (with an affinity constant of 2.96 × 10(6) M(-1)). Microscopy imaging showed that ALA-induced PpIX was co-localized with eEF1A1 in cancer cells. eEF1A1 was found to enrich ALA-induced PpIX in cells by competitively blocking the downstream bioavailability of PpIX. Taken together, our study discovered eEF1A1 as a novel photosensitizer binding protein, which may play an essential role in the enrichment of ALA-induced PpIX in cancer cells during PDT. These suggested eEF1A1 as a molecular marker to predict the selectivity and efficiency of 5-ALA based PDT in cancer therapy.
基于内源性源自5-氨基乙酰丙酸(5-ALA)或其衍生物的原卟啉IX(PpIX)的光动力疗法(PDT)是一种用于治疗癌前病变和恶性病变的有前景的方法。然而,ALA诱导的PpIX如何在肿瘤中选择性积累的机制尚未完全阐明。在此,我们发现真核翻译延伸因子1α1(eEF1A1)与PpIX相互作用(亲和常数为2.96×10⁶ M⁻¹)。显微镜成像显示,ALA诱导的PpIX与癌细胞中的eEF1A1共定位。发现eEF1A1通过竞争性阻断PpIX的下游生物利用度在细胞中富集ALA诱导的PpIX。综上所述,我们的研究发现eEF1A1是一种新型的光敏剂结合蛋白,其可能在PDT期间癌细胞中ALA诱导的PpIX的富集中起重要作用。这些表明eEF1A1作为一种分子标志物,可预测基于5-ALA的PDT在癌症治疗中的选择性和效率。