Radiotherapy as a tool to elicit clinically actionable signalling pathways in cancer

被引:130
作者
Petroni, Giulia [1 ]
Cantley, Lewis C. [2 ,3 ]
Santambrogio, Laura [1 ,3 ,4 ]
Formenti, Silvia C. [1 ,2 ,3 ]
Galluzzi, Lorenzo [1 ,3 ,4 ]
机构
[1] Weill Cornell Med Coll, Dept Radiat Oncol, New York, NY 10021 USA
[2] Weill Cornell Med Coll, Dept Med, New York, NY USA
[3] Sandra & Edward Meyer Canc Ctr, New York, NY 10065 USA
[4] Caryl & Israel Englander Inst Precis Med, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; DNA-DAMAGE RESPONSE; RADIATION-INDUCED CYTOTOXICITY; GLIOBLASTOMA-INITIATING CELLS; CHECKPOINT KINASE INHIBITOR; DUAL PI3K/MTOR INHIBITOR; INCREASED LOCAL FAILURE; RANDOMIZED PHASE-II; HUMAN TUMOR-CELLS;
D O I
10.1038/s41571-021-00579-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A variety of targeted anticancer agents have been successfully introduced into clinical practice, largely reflecting their ability to inhibit specific molecular alterations that are required for disease progression. However, not all malignant cells rely on such alterations to survive, proliferate, disseminate and/or evade anticancer immunity, implying that many tumours are intrinsically resistant to targeted therapies. Radiotherapy is well known for its ability to activate cytotoxic signalling pathways that ultimately promote the death of cancer cells, as well as numerous cytoprotective mechanisms that are elicited by cellular damage. Importantly, many cytoprotective mechanisms elicited by radiotherapy can be abrogated by targeted anticancer agents, suggesting that radiotherapy could be harnessed to enhance the clinical efficacy of these drugs. In this Review, we discuss preclinical and clinical data that introduce radiotherapy as a tool to elicit or amplify clinically actionable signalling pathways in patients with cancer. Targeted therapies have improved the outcomes of many patients with cancer, although many more lack targetable alterations or do not derive clinical benefit for other reasons. Radiotherapy can also provide benefit to many patients, although radioresistance often limits the effectiveness of this intervention. Here, the authors describe the potential for radiotherapy to promote non-oncogene dependence on targetable signalling pathways, thus extending the benefits of both targeted therapy and radiotherapy to greater numbers of patients.
引用
收藏
页码:114 / 131
页数:18
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