Cell Death and Survival Pathways Involving ATM Protein Kinase

被引:19
作者
Aki, Toshihiko [1 ]
Uemura, Koichi [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Forens Med, Tokyo 1138519, Japan
关键词
ATM; apoptosis; necroptosis; ferroptosis; autophagy; DNA-DAMAGE RESPONSE; DOUBLE-STRAND BREAKS; CYTOCHROME-C; ACTIVATION; APOPTOSIS; P53; AIF; PHOSPHORYLATION; MECHANISMS; AUTOPHAGY;
D O I
10.3390/genes12101581
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cell death is the ultimate form of cellular dysfunction, and is induced by a wide range of stresses including genotoxic stresses. During genotoxic stress, two opposite cellular reactions, cellular protection through DNA repair and elimination of damaged cells by the induction of cell death, can occur in both separate and simultaneous manners. ATM (ataxia telangiectasia mutated) kinase (hereafter referred to as ATM) is a protein kinase that plays central roles in the induction of cell death during genotoxic stresses. It has long been considered that ATM mediates DNA damage-induced cell death through inducing apoptosis. However, recent research progress in cell death modality is now revealing ATM-dependent cell death pathways that consist of not only apoptosis but also necroptosis, ferroptosis, and dysfunction of autophagy, a cellular survival mechanism. In this short review, we intend to provide a brief outline of cell death mechanisms in which ATM is involved, with emphasis on pathways other than apoptosis.</p>
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Differential regulation of extrinsic and intrinsic cell death pathways by protein kinase C
    Basu, A
    Miura, A
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2002, 10 (05) : 541 - 545
  • [32] Research progress on multiple cell death pathways of podocytes in diabetic kidney disease
    Can Yang
    Zhen Zhang
    Jieting Liu
    Peijian Chen
    Jialing Li
    Haiying Shu
    Yanhui Chu
    Luxin Li
    Molecular Medicine, 29
  • [33] Targeting regulated cell death pathways in cancers for effective treatment: a comprehensive review
    Saxena, Ruchi
    Welsh, Craig M.
    He, You-Wen
    FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2024, 12
  • [34] ATM-associated signalling triggers the unfolded protein response and cell death in response to stress
    Hotokezaka, Yuka
    Katayama, Ikuo
    Nakamura, Takashi
    COMMUNICATIONS BIOLOGY, 2020, 3 (01)
  • [35] Stress/cell death pathways, neuroinflammation, and neuropathic pain
    Li, Lu
    Li, Tian
    Qu, Xinyu
    Sun, Guangwei
    Fu, Qi
    Han, Guang
    IMMUNOLOGICAL REVIEWS, 2024, 321 (01) : 33 - 51
  • [36] Disruptive multiple cell death pathways of bisphenol-A
    S., Yukta
    Milan, K. L.
    Harithpriya, Kannan
    Zong, Cai
    Sahabudeen, S.
    Ichihara, Gaku
    Ramkumar, K. M.
    TOXICOLOGY MECHANISMS AND METHODS, 2025,
  • [37] A multiplicity of cell death pathways - Symposium on apoptotic and non-apoptotic cell death pathways
    Golstein, Pierre
    Kroemer, Guido
    EMBO REPORTS, 2007, 8 (09) : 829 - 833
  • [38] The induction of the p53 tumor suppressor protein bridges the apoptotic and autophagic signaling pathways to regulate cell death in prostate cancer cells
    Ringer, Lymor
    Sirajuddin, Paul
    Tricoli, Lucas
    Waye, Sarah
    Choudhry, Muhammad Umer
    Parasido, Erika
    Sivakumar, Angiela
    Heckler, Mary
    Naeem, Aisha
    Abdelgawad, Iman
    Liu, Xuefeng
    Feldman, Adam S.
    Lee, Richard J.
    Wu, Chin-Lee
    Yenugonda, Venkata
    Kallakury, Bhaskar
    Dritschilo, Anatoly
    Lynch, John
    Schlegel, Richard
    Rodriguez, Olga
    Pestell, Richard G.
    Avantaggiati, Maria Laura
    Albanese, Chris
    ONCOTARGET, 2014, 5 (21) : 10678 - 10691
  • [39] Mechanisms of programmed cell death: structural and functional pathways. A narrative review.
    Fernandez-Lazaro, Diego
    Sanz, Begona
    Seco-Calvo, Jesus
    INVESTIGACION CLINICA, 2024, 65 (02):
  • [40] Timing the multiple cell death pathways initiated by Rose Bengal acetate photodynamic therapy
    Panzarini, E.
    Inguscio, V.
    Dini, L.
    CELL DEATH & DISEASE, 2011, 2 : e169 - e169