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脊索瘤的分子图谱:从多组学到人工智能的当前前沿

英文原题:The molecular landscape of chordoma: Current frontiers from multi-omics to artificial intelligence.

查看英文原题

The molecular landscape of chordoma: Current frontiers from multi-omics to artificial intelligence.

PubMed 2026/08/09(内容时间) Biochim Biophys Acta Rev Cancer Q1 · IF 11.2(JCR 2025)

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中文摘要

脊索瘤是一种发生于中轴骨的罕见且侵袭性强的恶性骨肿瘤,由于其复杂的解剖位置以及高达85%的高复发率,长期以来对临床医生构成挑战。本综述综合了脊索瘤研究的最新进展,并概述了多组学、先进免疫学以及人工智能如何重塑其治疗范式。其发病机制的核心是T-box转录因子Brachyury,本综述强调其既是特征性诊断标志物,也是主要的治疗脆弱靶点。针对这一驱动因子的前沿创新包括共价小分子结合剂、靶向蛋白降解以及旨在攻击细胞内癌蛋白的肽中心CAR-T 细胞。肿瘤免疫微环境在功能上是动态的,细胞治疗的新维度,如双特异性CAR构建体和NK细胞平台,正在被设计用于中和免疫抑制因子。除生物学见解外,本综述还强调了计算生物学的作用,特别是深度学习和机器学习模型如何在肿瘤分割和个体化生存预测中达到专家级精度。通过整合基因组、转录组、表观基因组和蛋白质组数据,多组学方法能够充分阐明脊索瘤亚型及其潜在耐药机制,最终为更精准和个体化的治疗策略铺平道路。

展开英文摘要原文

Chordoma is a rare and aggressive malignant bone tumor of the axial skeleton that has historically challenged clinicians due to its complex anatomical locations and a high recurrence rate of up to 85%. This review synthesizes the most recent advances in chordoma research and offers an overview of how multi-omics, advanced immunology, and artificial intelligence are reshaping the treatment paradigm. Central to its pathogenesis is the T-box transcription factor Brachyury, which this review highlights as both the pathognomonic diagnostic marker and the primary therapeutic vulnerability. Cutting-edge innovations targeting this driver include covalent small-molecule binders, targeted protein degradation, and peptide-centric CAR-T cells designed to attack the intracellular oncoprotein.

The tumor immune microenvironment is functionally dynamic, and new dimensions in cellular therapy, such as dual-specific CAR constructs and NK-cell platforms, are being engineered to neutralize immunosuppressive factors. Beyond biological insights, the review emphasizes the role of computational biology, specifically how deep-learning and machine-learning models achieve expert-level precision in tumor segmentation and personalized survival forecasting.

By integrating genomic, transcriptomic, epigenomic, and proteomic data, multiomics approaches can fully elucidate chordoma subtypes and underlying resistance mechanisms, ultimately paving the way for more precise and personalized therapeutic strategies.

论文信息

作者
Tecimel D、Seven D、Türe U、Bayrak ÖF
第一作者单位
Faculty of Engineering, Genetics and Bioengineering Department, Yeditepe University, İstanbul 34755, Turkey; Department of Medical Genetics, School of Medicine, Yeditepe University, İstanbul, 34755, Turkey. Electronic address: didem.tecimel@yeditepe.edu.tr.Turkey
通讯作者单位
Department of Medical Genetics, School of Medicine, Yeditepe University, İstanbul, 34755, Turkey. Electronic address: ofbayrak@yeditepe.edu.tr.Turkey
文献类型
综述
期刊
Biochimica et biophysica acta. Reviews on cancer2026 Oct
原文标识
PubMed 42571860 · DOI 10.1016/j.bbcan.2026.189678