Arias-Ramos Nuria, Ferrer-Font Laura, Lope-Piedrafita Silvia, Mocioiu Victor, Julià-Sapé Margarida, Pumarola Martí, Arús Carles, Candiota Ana Paula
Departament de Bioquímica i Biologia Molecular, Unitat de Bioquímica de Biociències, Edifici Cs, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Spain.
Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), 28029 Madrid, Spain.
Metabolites. 2017 May 18;7(2):20. doi: 10.3390/metabo7020020.
Glioblastoma (GBM) is the most common aggressive primary brain tumor in adults, with a short survival time even after aggressive therapy. Non-invasive surrogate biomarkers of therapy response may be relevant for improving patient survival. Previous work produced such biomarkers in preclinical GBM using semi-supervised source extraction and single-slice Magnetic Resonance Spectroscopic Imaging (MRSI). Nevertheless, GBMs are heterogeneous and single-slice studies could prevent obtaining relevant information. The purpose of this work was to evaluate whether a multi-slice MRSI approach, acquiring consecutive grids across the tumor, is feasible for preclinical models and may produce additional insight into therapy response. Nosological images were analyzed pixel-by-pixel and a relative responding volume, the (), was defined to quantify response. Heterogeneous response levels were observed and treated animals were ascribed to three arbitrary predefined groups: high response (HR, = 2), = 68.2 ± 2.8%, intermediate response (IR, = 6), = 41.1 ± 4.2% and low response (LR, = 2), = 13.4 ± 14.3%, producing therapy response categorization which had not been fully registered in single-slice studies. Results agreed with the multi-slice approach being feasible and producing an inverse correlation between and Ki67 immunostaining. Additionally, ca. 7-day oscillations of were observed, suggesting that host immune system activation in response to treatment could contribute to the responding patterns detected.
胶质母细胞瘤(GBM)是成人中最常见的侵袭性原发性脑肿瘤,即使经过积极治疗,生存期也很短。治疗反应的非侵入性替代生物标志物可能与提高患者生存率相关。先前的研究使用半监督源提取和单切片磁共振波谱成像(MRSI)在临床前GBM模型中产生了此类生物标志物。然而,GBM具有异质性,单切片研究可能无法获取相关信息。本研究的目的是评估一种多切片MRSI方法,即在肿瘤上获取连续的网格,对于临床前模型是否可行,以及是否能对治疗反应产生更多见解。对疾病分类图像进行逐像素分析,并定义一个相对反应体积()来量化反应。观察到了异质性反应水平,并将接受治疗的动物分为三个任意预定义组:高反应组(HR,=2),=68.2±2.8%;中度反应组(IR,=6),=41.1±4.2%;低反应组(LR,=2),=13.4±14.3%,从而得出了单切片研究中未完全记录的治疗反应分类。结果表明多切片方法可行,且与Ki67免疫染色呈负相关。此外,还观察到约7天的振荡,这表明宿主免疫系统对治疗的激活可能有助于检测到的反应模式。