| Literature DB >> 30097231 |
Hoang Quy Nguyen1, Nhu Hanh To2, Patricia Zadigue3, Stéphane Kerbrat4, Alexandre De La Taille5, Sabine Le Gouvello6, Yazid Belkacemi7.
Abstract
Ionizing radiation-exposure induces a variety of cellular reactions, such as senescence and apoptosis. Senescence is a permanent arrest state of the cell division, which can be beneficial or detrimental for normal tissue via an inflammatory response and senescence-associated secretion phenotype. Damage to healthy cells and their microenvironment is considered as an important source of early and late complications with an increased risk of morbidity in patients after radiotherapy (RT). In addition, the benefit/risk ratio may depend on the radiation technique/dose used for cancer eradication and the irradiated volume of healthy tissues. For radiation-induced fibrosis risk, the knowledge of mechanisms and potential prevention has become a crucial point to determining radiation parameters and patients' intrinsic radiosensitivity. This review summarizes our understanding of ionizing radiation-induced senescent cell in fibrogenesis. This mechanism may provide new insights for therapeutic modalities for better risk/benefit ratios after RT in the new era of personalized treatments.Entities:
Keywords: Fibrotic tissue; Radiosensitivity; Senescence; Senescence-associated secretion phenotype
Mesh:
Year: 2018 PMID: 30097231 DOI: 10.1016/j.critrevonc.2018.06.012
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312