Author： Sarni Dan Kerem Batsheva
Publisher： MDPI
E-ISSN： 1422-0067|18|7|1339-1339
ISSN： 1422-0067
Source： International Journal of Molecular Sciences, Vol.18, Iss.7, 2017-06, pp. : 1339-1339
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Genomic instability plays a key role in driving cancer development. It is already found in precancerous lesions and allows the acquisition of additional cancerous features. A major source of genomic instability in early stages of tumorigenesis is DNA replication stress. Normally, origin licensing and activation, as well as replication fork progression, are tightly regulated to allow faithful duplication of the genome. Aberrant origin usage and/or perturbed replication fork progression leads to DNA damage and genomic instability. Oncogene activation is an endogenous source of replication stress, disrupting replication regulation and inducing DNA damage. Oncogene-induced replication stress and its role in cancer development have been studied comprehensively, however its molecular basis is still unclear. Here, we review the current understanding of replication regulation, its potential disruption and how oncogenes perturb the replication and induce DNA damage leading to genomic instability in cancer.
Related content
Access to resources
Recommend
By Villanueva Cleva Kross Robert D.
International Journal of Molecular Sciences, Vol. 13, Iss. 2, 2012-02 ,pp. :
By Zhang Xiao-Lin Yu Hao Xiong You-Yi Ma Shi-Tang Zhao Lei She Shi-Feng
International Journal of Molecular Sciences, Vol. 14, Iss. 1, 2013-01 ,pp. :