Janczar Karolina, Su Zhangjie, Raccagni Isabella, Anfosso Andrea, Kelly Charlotte, Durrenberger Pascal F, Gerhard Alexander, Roncaroli Federico
Division of Brain Science, Wolfson Neuroscience Laboratories, Imperial College London, Du Cane Road, London W12 0NN, U.K.
Wolfson Molecular Imaging Center, Institute of Brain, Behaviour and Mental Health, University of Manchester, 27 Palatine Road, Withington, Manchester M20 3LJ, U.K.
Biochem Soc Trans. 2015 Aug;43(4):579-85. doi: 10.1042/BST20150064. Epub 2015 Aug 3.
The 18-kDa mitochondrial translocator protein (TSPO) is known to be highly expressed in several types of cancer, including gliomas, whereas expression in normal brain is low. TSPO functions in glioma are still incompletely understood. The TSPO can be quantified pre-operatively with molecular imaging making it an ideal candidate for personalized treatment of patient with glioma. Studies have proposed to exploit the TSPO as a transporter of chemotherapics to selectively target tumour cells in the brain. Our studies proved that positron emission tomography (PET)-imaging can contribute to predict progression of patients with glioma and that molecular imaging with TSPO-specific ligands is suitable to stratify patients in view of TSPO-targeted treatment. Finally, we proved that TSPO in gliomas is predominantly expressed by tumour cells.
已知18 kDa的线粒体转位蛋白(TSPO)在包括神经胶质瘤在内的多种癌症中高表达,而在正常脑组织中表达较低。TSPO在神经胶质瘤中的功能仍未完全明确。术前可通过分子成像对TSPO进行定量,这使其成为神经胶质瘤患者个性化治疗的理想候选物。研究提出利用TSPO作为化疗药物的转运体,以选择性地靶向脑内肿瘤细胞。我们的研究证明,正电子发射断层扫描(PET)成像有助于预测神经胶质瘤患者的病情进展,并且使用TSPO特异性配体的分子成像适用于根据TSPO靶向治疗对患者进行分层。最后,我们证明神经胶质瘤中的TSPO主要由肿瘤细胞表达。