Role of DNA-dependent protein kinase catalytic subunit in cancer development and treatment

被引:93
作者
Hsu, Feng-Ming [1 ]
Zhang, Shichuan [2 ]
Chen, Benjamin P. C. [3 ]
机构
[1] Natl Taiwan Univ, Coll Med, Natl Taiwan Univ Hosp, Dept Oncol, Taipei 10764, Taiwan
[2] Sichuan Tumor Hosp, Dept Radiat Oncol, Chengdu 610041, Peoples R China
[3] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, 2201 Inwood Rd,Rm NC7-502, Dallas, TX 75390 USA
基金
美国国家航空航天局; 美国国家卫生研究院;
关键词
DNA damage; carcinogenesis; anti-DNA-PKcs strategies; GROWTH-FACTOR RECEPTOR; DOUBLE-STRAND BREAKS; UP-REGULATION; IN-VITRO; PKCS PHOSPHORYLATIONS; ESOPHAGEAL CANCER; STEM-CELLS; B-CELLS; RADIATION; REPAIR;
D O I
10.3978/j.issn.2218-676X.2012.04.01
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a key component of the non-homologous end-joining (NHEJ) pathway, is involved in DNA double-strand break repair, immunocompetence, genomic integrity, and epidermal growth factor receptor signaling. Clinical studies indicate that expression and activity of DNA-PKcs is correlated with cancer progression and response to treatment. Various anti-DNA-PKcs strategies have been developed and tested in preclinical studies to exploit the benefit of DNA-PKcs inhibition in sensitization of radiotherapy and in combined modality therapy with other antitumor agents. In this article, we review the association between DNA-PKcs and cancer development and discuss current approaches and mechanisms for inhibition of DNA-PKcs. The future challenges are to understand how DNA-PKcs activity is correlated with cancer susceptibility and to identify those patients who would most benefit from DNA-PKcs inhibition.
引用
收藏
页码:22 / 34
页数:13
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