| Literature DB >> 29254745 |
Raymond Che1, Jun Zhang2, Manoj Nepal1, Bing Han3, Peiwen Fei4.
Abstract
In 1927 Guido Fanconi described a hereditary condition presenting panmyelopathy accompanied by short stature and hyperpigmentation, now better known as Fanconi anemia (FA). With this discovery the genetic and molecular basis underlying FA has emerged as a field of great interest. FA signaling is crucial in the DNA damage response (DDR) to mediate the repair of damaged DNA. This has attracted a diverse range of investigators, especially those interested in aging and cancer. However, recent evidence suggests FA signaling also regulates functions outside the DDR, with implications for many other frontiers of research. We discuss here the characteristics of FA functions and expand upon current perspectives regarding the genetics of FA, indicating that FA plays a role in a myriad of molecular and cellular processes.Entities:
Keywords: DNA damage response; Fanconi anemia; aging; cancer; developmental defects; replication
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Year: 2017 PMID: 29254745 PMCID: PMC5858900 DOI: 10.1016/j.tig.2017.11.006
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639