Aberrant Notch signaling in gliomas: a potential landscape of actionable converging targets for combination approach in therapies resistance.

IF 4.6 Q1 ONCOLOGY 癌症耐药(英文) Pub Date : 2022-01-01 DOI:10.20517/cdr.2022.46
Maria D'Amico, Francesca De Amicis
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引用次数: 5

Abstract

The current therapeutic protocols and prognosis of gliomas still depend on clinicopathologic and radiographic characteristics. For high-grade gliomas, the standard of care is resection followed by radiotherapy plus temozolomide chemotherapy. However, treatment resistance develops due to different mechanisms, among which is the dynamic interplay between the tumor and its microenvironment. Different signaling pathways cause the proliferation of so-called glioma stem cells, a minor cancer cell population with stem cell-like characteristics and aggressive phenotype. In the last decades, numerous studies have indicated that Notch is a crucial pathway that maintains the characteristics of resistant glioma stem cells. Data obtained from preclinical models indicate that downregulation of the Notch pathway could induce multifaceted drug sensitivity, acting on the expression of drug-transporter proteins, inducing epithelial-mesenchymal transition, and shaping the tumor microenvironment. This review provides a brief overview of the published data supporting the roles of Notch in drug resistance and demonstrates how potential novel strategies targeting Notch could become an efficacious action to improve the therapy of high-grade glioma to overcome drug resistance.

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神经胶质瘤中的异常Notch信号:联合治疗方法中可操作的会聚靶点的潜在景观。
目前胶质瘤的治疗方案和预后仍取决于临床病理和影像学特征。对于高级别胶质瘤,标准治疗是切除后放疗加替莫唑胺化疗。然而,耐药的产生有不同的机制,其中包括肿瘤与其微环境之间的动态相互作用。不同的信号通路导致所谓的胶质瘤干细胞的增殖,胶质瘤干细胞是一种具有干细胞样特征和侵袭性表型的小型癌细胞群。在过去的几十年里,大量的研究表明Notch是维持耐药胶质瘤干细胞特征的关键通路。从临床前模型获得的数据表明,Notch通路的下调可诱导多方面的药物敏感性,影响药物转运蛋白的表达,诱导上皮-间质转化,塑造肿瘤微环境。本综述简要概述了支持Notch在耐药中的作用的已发表数据,并展示了靶向Notch的潜在新策略如何成为改善高级别胶质瘤治疗以克服耐药的有效措施。
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