Tian Guofeng, Song Yifu, Zhang Yaochuan, Kan Liang, Hou Ana, Han Sheng
Department of Neurosurgery, The First Hospital of China Medical University, No. 115 Nanjing North Street, Shenyang, 110001, China.
Department of Geriatrics, Shengjing Hospital of China Medical University, No. 36 Sanhao Street, Shenyang, 110004, China.
J Transl Med. 2025 Sep 2;23(1):984. doi: 10.1186/s12967-025-07034-9.
Glioma represents the most prevalent primary tumors of the central nervous system, originating from glial cells. Cancer stem cells have the ability to extensively proliferate, self-renew, and form colonies, which contribute to tumorigenesis. Studies have found a population of cells within glioblastoma exhibiting characteristics similar to those of cancer cells, termed glioma stem cells (GSCs). GSCs have two distinct phenotypes: mesenchymal subtype (MES) and proneural subtype (PN). Despite the vital role of these subtypes in glioma biology, there is a significant lack of comprehensive reviews focusing on the regulatory mechanisms underlying each phenotype.This review integrates emerging insights into the regulatory mechanisms underlying GSCs plasticity, with dedicated analysis of novel pathways governing PN and MES phenotypes and their dynamic transition. By examining these critical elements, we aim to contribute to the development of novel therapeutic strategies in the ongoing fight against gliomas.
胶质瘤是中枢神经系统最常见的原发性肿瘤,起源于神经胶质细胞。癌症干细胞具有广泛增殖、自我更新和形成集落的能力,这些能力有助于肿瘤发生。研究发现,胶质母细胞瘤中有一群细胞表现出与癌细胞相似的特征,称为胶质瘤干细胞(GSCs)。GSCs有两种不同的表型:间充质亚型(MES)和神经前体细胞亚型(PN)。尽管这些亚型在胶质瘤生物学中起着至关重要的作用,但目前严重缺乏对每种表型潜在调控机制的全面综述。本综述整合了对GSCs可塑性潜在调控机制的新见解,专门分析了控制PN和MES表型及其动态转变的新途径。通过研究这些关键因素,我们旨在为正在进行的对抗胶质瘤的新型治疗策略的开发做出贡献。