| Literature DB >> 30930412 |
Takafumi Ishida1, Mari Ishida2, Satoshi Tashiro3, Yasuchika Takeishi1.
Abstract
DNA suffers various types of damage even in a normal condition, although they are rapidly repaired by mechanisms called DNA repair. Most progeroid syndromes are caused by genetic defects in specific molecules involved in the DNA repair. DNA damage activates a broad range of signaling pathway that leads to repair, cell cycle arrest, apoptosis and so on, which is called DNA damage response. Recent studies revealed that persistent DNA damage response triggers induction of cell senescence and senescence-associated secretory phenotype (SASP). Here, we review recent advances in the understanding of the molecular mechanisms by which SASP components are regulated, and discuss the possible roles of DNA damage and the DNA damage response, and SASP in the pathogenesis of cardiovascular disease.Entities:
Keywords: DNA repair; inflammation; progeria; senescence
Mesh:
Year: 2019 PMID: 30930412 DOI: 10.1248/bpb.b18-00865
Source DB: PubMed Journal: Biol Pharm Bull ISSN: 0918-6158 Impact factor: 2.233