Radiotherapy targeting cancer stem cells “awakens” them to induce tumour relapse and metastasis in oral cancer

被引:0
作者
Yangfan Liu
Miao Yang
Jingjing Luo
Hongmei Zhou
机构
[1] West China Hospital of Stomatology,State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Oral Medicine
[2] Sichuan University,State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Preventive Dentistry
[3] West China Hospital of Stomatology,undefined
[4] Sichuan University,undefined
来源
International Journal of Oral Science | 2020年 / 12卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Radiotherapy is one of the most common treatments for oral cancer. However, in the clinic, recurrence and metastasis of oral cancer occur after radiotherapy, and the underlying mechanism remains unclear. Cancer stem cells (CSCs), considered the “seeds” of cancer, have been confirmed to be in a quiescent state in most established tumours, with their innate radioresistance helping them survive more easily when exposed to radiation than differentiated cancer cells. There is increasing evidence that CSCs play an important role in recurrence and metastasis post-radiotherapy in many cancers. However, little is known about how oral CSCs cause tumour recurrence and metastasis post-radiotherapy. In this review article, we will first summarise methods for the identification of oral CSCs and then focus on the characteristics of a CSC subpopulation induced by radiation, hereafter referred to as “awakened” CSCs, to highlight their response to radiotherapy and potential role in tumour recurrence and metastasis post-radiotherapy as well as potential therapeutics targeting CSCs. In addition, we explore potential therapeutic strategies targeting these “awakened” CSCs to solve the serious clinical challenges of recurrence and metastasis in oral cancer after radiotherapy.
引用
收藏
相关论文
共 298 条
[1]  
Bray F(2018)Global cancer statistics 2018: globocan estimates of incidence and mortality worldwide for 36 cancers in 185 countries CA Cancer J. Clin. 68 394-424
[2]  
Shahinas J(2018)Methods and risk of bias in molecular marker prognosis studies in oral squamous cell carcinoma Oral Dis. 24 115-119
[3]  
Hysi D(2014)Ionizing radiation-induced DNA damage, response, and repair Antioxid. Redox Signal. 21 251-259
[4]  
Santivasi WL(2002)Reactive oxygen species in cell responses to toxic agents Hum. Exp. Toxicol. 21 85-90
[5]  
Xia F(2013)Various modes of cell death induced by DNA damage Oncogene 32 3789-3797
[6]  
Feinendegen LE(2016)Ionizing radiation promotes advanced malignant traits in nasopharyngeal carcinoma via activation of epithelial-mesenchymal transition and the cancer stem cell phenotype Oncol. Rep. 36 72-78
[7]  
Surova O(2018)Radiotherapeutic studies of head and neck cancer-highlights of the 2018 asco annual meeting HNO 66 901-906
[8]  
Zhivotovsky B(1993)Head and neck-cancer N. Engl. J. Med. 328 1783-1784
[9]  
Su Z(2009)Incidence of isolated regional recurrence after definitive (chemo-) radiotherapy for head and neck squamous cell carcinoma Radiother. Oncol. 93 498-502
[10]  
Ott S(2010)Protein biomarker discovery for head and neck cancer J. Proteom. 73 1790-1803