Decoding the Glioblastoma Microenvironment: AI-Driven Analysis of Cellular MRI Signatures for Targeted Therapy.

IF 7.4 4区 医学 Q3 CELL BIOLOGY
Yao Sun, Kai Wang, Tiantao Ye
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引用次数: 0

Abstract

Glioblastoma (GB), the most aggressive primary brain tumor, is characterized by profound inter- and intratumoral heterogeneity and a highly immunosuppressive tumor microenvironment (TME), both of which contribute to its poor prognosis and resistance to conventional therapies. The dynamic interplay between malignant cells and diverse TME constituents including immune cells, neural elements, and extracellular matrix components drives tumor progression, clonal evolution, and therapeutic failure. Traditional treatment modalities such as surgery, radiotherapy, and chemotherapy often fall short due to their inability to address the spatial and temporal complexity of the TME. Recent advances in artificial intelligence (AI) and cellular MRI profiling offer promising avenues for decoding the GB microenvironment at unprecedented resolution. By integrating AI-driven analysis of cellular MRI signatures, researchers can identify distinct microenvironmental niches and resistant subclones, enabling the development of targeted therapies that simultaneously disrupt tumor cells and their supportive ecosystems. This approach holds potential to overcome current therapeutic limitations and pave the way for personalized, microenvironment-informed interventions in GB management.

解码胶质母细胞瘤微环境:人工智能驱动的靶向治疗细胞MRI特征分析。
胶质母细胞瘤(GB)是最具侵袭性的原发性脑肿瘤,其特点是肿瘤间和肿瘤内的异质性和高度免疫抑制的肿瘤微环境(TME),这两者都导致了其预后差和对常规治疗的抵抗。恶性细胞与多种TME成分(包括免疫细胞、神经细胞和细胞外基质成分)之间的动态相互作用驱动肿瘤进展、克隆进化和治疗失败。传统的治疗方式,如手术、放疗和化疗,由于无法解决TME的空间和时间复杂性,往往达不到预期的效果。人工智能(AI)和细胞MRI分析的最新进展为以前所未有的分辨率解码GB微环境提供了有希望的途径。通过整合人工智能驱动的细胞MRI特征分析,研究人员可以识别不同的微环境生态位和耐药亚克隆,从而开发出同时破坏肿瘤细胞及其支持性生态系统的靶向治疗方法。这种方法有潜力克服目前的治疗局限性,并为个性化、微环境知情干预GB管理铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
0.00%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Cellular and Molecular Neurobiology publishes original research concerned with the analysis of neuronal and brain function at the cellular and subcellular levels. The journal offers timely, peer-reviewed articles that describe anatomic, genetic, physiologic, pharmacologic, and biochemical approaches to the study of neuronal function and the analysis of elementary mechanisms. Studies are presented on isolated mammalian tissues and intact animals, with investigations aimed at the molecular mechanisms or neuronal responses at the level of single cells. Cellular and Molecular Neurobiology also presents studies of the effects of neurons on other organ systems, such as analysis of the electrical or biochemical response to neurotransmitters or neurohormones on smooth muscle or gland cells.
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