Department of Applied Cell Sciences, Kashan University of Medical Sciences, Kashan, Iran; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Department of Human Anatomy & Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada; Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada; Research Institute of Oncology and Hematology, Cancer Care Manitoba, University of Manitoba, Winnipeg, Canada.
Drug Resist Updat. 2019 Jan;42:35-45. doi: 10.1016/j.drup.2018.03.003. Epub 2019 Mar 8.
Glioblastoma multiforme (GBM) is among the most incurable cancers. GBMs survival rate has not markedly improved, despite new radical surgery protocols, the introduction of new anticancer drugs, new treatment protocols, and advances in radiation techniques. The low efficacy of therapy, and short interval between remission and recurrence, could be attributed to the resistance of a small fraction of tumorigenic cells to treatment. The existence and importance of cancer stem cells (CSCs) is perceived by some as controversial. Experimental evidences suggest that the presence of therapy-resistant glioblastoma stem cells (GSCs) could explain tumor recurrence and metastasis. Some scientists, including most of the authors of this review, believe that GSCs are the driving force behind GBM relapses, whereas others however, question the existence of GSCs. Evidence has accumulated indicating that non-tumorigenic cancer cells with high heterogeneity, could undergo reprogramming and become GSCs. Hence, targeting GSCs as the "root cells" initiating malignancy has been proposed to eradicate this devastating disease. Most standard treatments fail to completely eradicate GSCs, which can then cause the recurrence of the disease. To effectively target GSCs, a comprehensive understanding of the biology of GSCs as well as the mechanisms by which these cells survive during treatment and develop into new tumor, is urgently needed. Herein, we provide an overview of the molecular features of GSCs, and elaborate how to facilitate their detection and efficient targeting for therapeutic interventions. We also discuss GBM classifications based on the molecular stem cell subtypes with a focus on potential therapeutic approaches.
多形性胶质母细胞瘤(GBM)是最难治愈的癌症之一。尽管采用了新的根治性手术方案、引入了新的抗癌药物、制定了新的治疗方案并改进了放射技术,但 GBM 的生存率并没有显著提高。治疗效果不佳以及缓解与复发之间的间隔很短,可能归因于一小部分肿瘤细胞对治疗具有抗性。一些人认为癌症干细胞(CSC)的存在和重要性存在争议。实验证据表明,存在对治疗有抗性的胶质母细胞瘤干细胞(GSC)可能解释了肿瘤的复发和转移。一些科学家,包括本综述的大多数作者,认为 GSC 是 GBM 复发的驱动力,而其他人则对 GSC 的存在提出了质疑。有证据表明,具有高度异质性的非肿瘤性癌细胞可以重新编程并成为 GSC。因此,将 GSC 作为引发恶性肿瘤的“根源细胞”进行靶向治疗,已被提出用于根除这种毁灭性疾病。大多数标准治疗方法都无法完全根除 GSC,这可能导致疾病复发。为了有效地靶向 GSC,迫切需要全面了解 GSC 的生物学特性,以及这些细胞在治疗期间生存并发展为新肿瘤的机制。在此,我们概述了 GSC 的分子特征,并详细阐述了如何促进其检测和有效靶向治疗干预。我们还讨论了基于分子干细胞亚型的 GBM 分类,重点介绍了潜在的治疗方法。