Lu Fa-Ke, Calligaris David, Olubiyi Olutayo I, Norton Isaiah, Yang Wenlong, Santagata Sandro, Xie X Sunney, Golby Alexandra J, Agar Nathalie Y R
Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts.
Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Cancer Res. 2016 Jun 15;76(12):3451-62. doi: 10.1158/0008-5472.CAN-16-0270. Epub 2016 Apr 12.
The goal of brain tumor surgery is to maximize tumor removal without injuring critical brain structures. Achieving this goal is challenging as it can be difficult to distinguish tumor from nontumor tissue. While standard histopathology provides information that could assist tumor delineation, it cannot be performed iteratively during surgery as freezing, sectioning, and staining of the tissue require too much time. Stimulated Raman scattering (SRS) microscopy is a powerful label-free chemical imaging technology that enables rapid mapping of lipids and proteins within a fresh specimen. This information can be rendered into pathology-like images. Although this approach has been used to assess the density of glioma cells in murine orthotopic xenografts models and human brain tumors, tissue heterogeneity in clinical brain tumors has not yet been fully evaluated with SRS imaging. Here we profile 41 specimens resected from 12 patients with a range of brain tumors. By evaluating large-scale stimulated Raman imaging data and correlating this data with current clinical gold standard of histopathology for 4,422 fields of view, we capture many essential diagnostic hallmarks for glioma classification. Notably, in fresh tumor samples, we observe additional features, not seen by conventional methods, including extensive lipid droplets within glioma cells, collagen deposition in gliosarcoma, and irregularity and disruption of myelinated fibers in areas infiltrated by oligodendroglioma cells. The data are freely available in a public resource to foster diagnostic training and to permit additional interrogation. Our work establishes the methodology and provides a significant collection of reference images for label-free neurosurgical pathology. Cancer Res; 76(12); 3451-62. ©2016 AACR.
脑肿瘤手术的目标是在不损伤关键脑结构的情况下最大限度地切除肿瘤。实现这一目标具有挑战性,因为很难区分肿瘤组织和非肿瘤组织。虽然标准组织病理学可提供有助于肿瘤轮廓勾勒的信息,但由于组织冷冻、切片和染色耗时过长,无法在手术过程中反复进行。受激拉曼散射(SRS)显微镜检查是一种强大的无标记化学成像技术,能够对新鲜标本中的脂质和蛋白质进行快速成像。这些信息可转化为类似病理的图像。尽管这种方法已用于评估小鼠原位异种移植模型和人脑肿瘤中胶质瘤细胞的密度,但SRS成像尚未对临床脑肿瘤中的组织异质性进行全面评估。在此,我们剖析了从12例患有一系列脑肿瘤的患者身上切除的41个标本。通过评估大规模受激拉曼成像数据,并将这些数据与4422个视野的组织病理学当前临床金标准相关联,我们获取了许多用于胶质瘤分类的重要诊断特征。值得注意的是,在新鲜肿瘤样本中,我们观察到了传统方法未发现的其他特征,包括胶质瘤细胞内广泛的脂滴、胶质肉瘤中的胶原沉积以及少突胶质细胞瘤细胞浸润区域中髓鞘纤维的不规则性和破坏。这些数据可在公共资源中免费获取,以促进诊断培训并允许进一步研究。我们的工作建立了该方法,并为无标记神经外科病理学提供了大量参考图像集。《癌症研究》;76(12);3451 - 62。©2016美国癌症研究协会。