Department of Neurosurgery, Kitasato University School of Medicine, Kanagawa, Japan.
Department of Cell Pathology, Graduate School of Life Sciences, Kumamoto University, Kumamoto, Japan.
Adv Exp Med Biol. 2020;1234:107-122. doi: 10.1007/978-3-030-37184-5_8.
Glioblastoma (GBM) develops from adult brain white matter and is the most common and lethal primary brain tumor, characterized by rapid growth and invasion. GBM tumors frequently spread into the contralateral hemisphere, including in the beginning of tumor development. However, after complete resection of the tumor mass and chemo-radiotherapy, GBM commonly recurs around the tumor removal site, suggesting that the microenvironment at the tumor border provides therapeutic resistance to GBM cells. To improve patient prognosis, understanding the microenvironment at the tumor border is critical. Several microRNAs (miRNAs) show higher expression at the tumor border, with the top three involved in oligodendrocyte differentiation. Oligodendrocyte progenitor cells (OPCs) may induce stemness and chemo-radioresistance in GBM cells, providing a supportive function to promote GBM. This review describes important features of OPCs and insights into the "border niche," a unique microenvironment that allows GBM cells to survive and recur at the tumor border.
胶质母细胞瘤(GBM)起源于成人脑白质,是最常见和致命的原发性脑肿瘤,其特征为快速生长和侵袭。GBM 肿瘤常扩散到对侧半球,包括在肿瘤发展的早期。然而,在肿瘤肿块的完全切除和化疗-放疗后,GBM 通常在肿瘤切除部位周围复发,这表明肿瘤边界的微环境为 GBM 细胞提供了治疗抗性。为了改善患者的预后,了解肿瘤边界的微环境至关重要。有几种 microRNAs(miRNAs)在肿瘤边界处表达更高,其中前三种与少突胶质细胞分化有关。少突胶质前体细胞(OPCs)可能在 GBM 细胞中诱导干细胞特性和化疗-放疗抗性,为 GBM 提供支持功能以促进其生长。本综述描述了 OPCs 的重要特征,并深入探讨了“边界生态位”,这是一种独特的微环境,允许 GBM 细胞在肿瘤边界处存活和复发。