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Multifaceted Fanconi Anemia Signaling.

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.

SUBMITTER: Che R

PROVIDER: S-EPMC5858900 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature

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Multifaceted Fanconi Anemia Signaling.

Che Raymond R Zhang Jun J Nepal Manoj M Han Bing B Fei Peiwen P

Trends in genetics : TIG 20171216 3

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 eviden ...[more]

PMID: 29254745

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