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从实验室到临床:推进我们对直肠癌放射抗拒性的理解

英文原题:From bench to bedside: advancing our understanding of radioresistance in rectal cancer.

PubMed 2026/07/22(内容时间) Cancer Metastasis Rev Q1 · IF 12.7(JCR 2025)

研究概要

直肠癌(RC)的全球发病率正以惊人的速度增长,尽管早期检测有所改善,但仍有超过50%的病例在晚期才被诊断。

中文摘要

直肠癌(RC)的全球发病率正以惊人的速度增长,尽管早期检测有所改善,仍有超过50%的病例在晚期才被诊断。虽然新辅助(放)化疗方案仍是治疗的基石,但高达20-40%的肿瘤表现出或产生对电离辐射的抵抗,限制了治疗选择并导致疾病进展。本综述在放射生物学基本6R框架内——即修复(Repair)、再氧合(Reoxygenation)、再分布(Redistribution)、放射敏感性(Radiosensitivity)、再增殖(Repopulation)和再激活(Reactivation)——对RC放射抵抗背后复杂的生物学和分子机制提供了全面的见解。更具体地说,本文全面综述了DNA损伤修复通路、细胞周期调控、缺氧、转录可塑性调控因子如癌症干细胞以及非编码RNA。此外,还剖析了TIL(肿瘤浸润淋巴细胞)、癌症相关巨噬细胞和炎症性癌症相关成纤维细胞在放射抵抗中的关键作用,这些因素共同在放疗后塑造了一个免疫抑制和促转移的微环境。此外,一个较少被探索的机制,即放疗后癌细胞的代谢重编程,被提出作为放射生物学的第7个R,即“重编程”(Reprogramming),它使肿瘤得以存活并促进侵袭性表型。这一新视角为RC抵抗的分子理解增添了新的复杂性层面,并提供了目前放射生物学研究中缺失的机制性见解。此外,还讨论了先进的实验模型,如球体、患者来源的类器官和动物模型,作为临床前研究和治疗测试的宝贵平台。本综述还将机制见解与生物标志物指导的临床决策相结合,以支持RC管理。通过揭示这些多因素机制,我们强调了开发预测性生物标志物和定制治疗策略以克服耐药并改善患者预后的机会。

展开英文摘要原文

The global incidence of rectal cancer (RC) is increasing at an alarming rate, with over 50% of cases still diagnosed at advanced stages, despite improvements in early detection. While neoadjuvant (chemo)radiotherapy regimens remain a cornerstone of treatment, up to 20-40% of tumours exhibit or develop resistance to ionising radiation, limiting therapeutic options and leading to disease evolution. This review offers a comprehensive insight into the complex biological and molecular mechanisms underlying RC radioresistance within the fundamental 6Rs of radiobiology: Repair, Reoxygenation, Redistribution, Radiosensitivity, Repopulation, and Reactivation. More specifically, DNA damage repair pathways, cell cycle regulation, hypoxia, transcriptional plasticity regulators such as cancer stem cells, and non-coding RNAs are comprehensively reviewed. Additionally, the critical roles of tumour-infiltrating lymphocytes, cancer-associated macrophages, and inflammatory cancer-associated fibroblasts in radioresistance are also dissected, which collectively shape an immunosuppressive and pro-metastatic niche following radiotherapy. Furthermore, a less explored mechanism, namely the metabolic rewiring of cancer cells after radiotherapy, is proposed as a new 7th R of Radiobiology, namely "Reprogramming", that enables tumour survival and promotes aggressive phenotypes. This new perspective adds a new layer of complexity to the molecular understanding of RC resistance and provides a mechanistic insight currently missing in radiobiology research. Additionally, advanced experimental models, such as spheroids, patient-derived organoids, and animal models, are discussed as valuable platforms for pre-clinical research and therapeutic testing. This review also integrates mechanistic insights with biomarker-guided clinical decision-making to support RC management. By unravelling these multifactorial mechanisms, we highlight opportunities to develop predictive biomarkers and tailored therapeutic strategies to overcome resistance and improve patient outcomes.

论文信息

作者
Estêvão D、da Cruz-Ribeiro M、Coelho D、Lencart J、Sousa O、Sarmento B、de Wever O、Oliveira MJ
第一作者单位
i3S - Institute for Research and Innovation in Health, University of Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.Portugal
通讯作者单位
i3S - Institute for Research and Innovation in Health, University of Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal. mariajo@ineb.up.pt.Portugal
文献类型
综述
期刊
Cancer metastasis reviews2026 Jul 22
原文标识
PubMed 42481817 · DOI 10.1007/s10555-026-10359-6