Abstract
AbstractIncreasing evidence indicates that DNA damage-induced apoptosis suppressor (DDIAS) is an oncogenic protein that is highly expressed in a variety of cancers, including colorectal cancer, lung cancer, breast cancer, and hepatocellular carcinoma (HCC). The discovery of DDIAS as a novel therapeutic target and its role in human cancer biology is fascinating and noteworthy. Recent studies have shown that DDIAS is involved in tumorigenesis, metastasis, DNA repair and synthesis, and drug resistance and that it plays multiple roles with distinct binding partners in several human cancers. This review focuses on the function of DDIAS and its regulatory proteins in human cancer as potential targets for cancer therapy, as well as the development and future prospects of DDIAS inhibitors.
Funder
National Research Foundation of Korea
Korea Research Institute of Bioscience and Biotechnology
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry,Molecular Biology,Molecular Medicine,Biochemistry
Reference56 articles.
1. Nakaya, N. et al. noxin, a novel stress-induced gene involved in cell cycle and apoptosis. Mol. Cell. Biol. 27, 5430–5444 (2007).
2. Won, K. J. et al. Human Noxin is an anti-apoptotic protein in response to DNA damage of A549 non-small cell lung carcinoma. Int. J. Cancer 134, 2595–2604 (2014).
3. Zhang, X. et al. Noxin promotes proliferation of breast cancer cells via P38-ATF2 signaling pathway. Tumour Biol. 39, 1010428317705515 (2017).
4. Liu, N. et al. DDIAS promotes invasion and proliferation of non-small cell lung cancer and predicts poor survival of lung cancer patients. Int. J. Clin. Exp. Pathol. 10, 11506–11515 (2017).
5. Zhang, Z. Z., Huang, J., Wang, Y. P., Cai, B. & Han, Z. G. NOXIN as a cofactor of DNA polymerase-primase complex could promote hepatocellular carcinoma. Int. J. Cancer 137, 765–775 (2015).
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献