The p38-mediated stress-activated checkpoint - A rapid response system for delaying progression through antephase and entry into mitosis

被引:79
|
作者
Mikhailov, A
Shinohara, M
Rieder, CL
机构
[1] New York State Dept Hlth, Wadsworth Ctr, Lab Cell Regulat, Div Mol Med, Albany, NY 12201 USA
[2] SUNY Albany, Sch Publ Hlth, Dept Biomed Sci, Albany, NY USA
关键词
topoisomerase II; p38; antephase; stress reponse; checkpoint; mitosis;
D O I
10.4161/cc.4.1.1357
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells have evolved a number of control pathways that delay or prevent them from entering mitosis under conditions that can compromise genome integrity. One recently appreciated and versatile control pathway involves the p38 stress activated protein kinase. During late G(2) p38 is rapidly activated by diverse stresses ( topoisomerase II ( topo II)) and histone deacetylase inhibitors, osmotic shock, microtubule disassembly, UV light, etc) via a number of different pathways. Once activated p38 appears to delay entry into mitosis by inhibiting cdc25B phosphatase that, in turn, down-regulates cyclin A/CDK2 activity. Depending on the agent and degree of stress, this delay may be transient, or it may last until transcription mediated checkpoint pathways can take over.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 37 条
  • [1] The G2 P38-mediated stress-activated checkpoint pathway becomes attenuated in transformed cells
    Mikhailov, Alexei
    Patel, Daksha
    McCance, Dennis J.
    Rieder, Conly L.
    [J]. CURRENT BIOLOGY, 2007, 17 (24) : 2162 - 2168
  • [2] Carnosol Induces p38-Mediated ER Stress Response and Autophagy in Human Breast Cancer Cells
    Alsamri, Halima
    Alneyadi, Aysha
    Muhammad, Khalid
    Ayoub, Mohammed Akli
    Eid, Ali
    Iratni, Rabah
    [J]. FRONTIERS IN ONCOLOGY, 2022, 12
  • [3] Suppression of ATAD2 inhibits hepatocellular carcinoma progression through activation of p53-and p38-mediated apoptotic signaling
    Lu, Wen-Jing
    Chua, Mei-Sze
    So, Samuel K.
    [J]. ONCOTARGET, 2015, 6 (39) : 41722 - 41735
  • [4] Activation of the stress-activated JNK and p38 MAP kinases in human cells by Photofrin-mediated photodynamic therapy
    Tong, ZM
    Singh, G
    Valerie, K
    Rainbow, AJ
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2003, 71 (1-3) : 77 - 85
  • [5] Nuclear export of the stress-activated protein kinase p38 mediated by its substrate MAPKAP kinase-2
    Ben-Levy, R
    Hooper, S
    Wilson, R
    Paterson, HF
    Marshall, CJ
    [J]. CURRENT BIOLOGY, 1998, 8 (19) : 1049 - 1057
  • [6] Signaling through stress-activated ASK1JNK/p38 pathways and their therapeutic implications for human diseases
    Ichijo, Hidenori
    [J]. ACTA PHARMACOLOGICA SINICA, 2006, 27 : 25 - 25
  • [7] Entry of influenza A virus into host cells is mediated by p38 MAPK-dependent stress response
    Miyamoto, D
    Deguchi, H
    Suzuki, T
    Hidari, KIPJ
    Suzuki, Y
    [J]. OPTIONS FOR THE CONTROL OF INFLUENZA V, 2004, 1263 : 466 - 467
  • [8] Signaling pathways involved in the physiological response of mussel hemocytes to bacterial challenge: the role of stress-activated p38 MAP kinases
    Canesi, L
    Betti, M
    Ciacci, C
    Scarpato, A
    Citterio, B
    Pruzzo, C
    Gallo, G
    [J]. DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2002, 26 (04): : 325 - 334
  • [9] The BH3-only protein BID impairs the p38-mediated stress response and promotes hepatocarcinogenesis during chronic liver injury in mice
    Orlik, Johanna
    Schuengel, Sven
    Buitrago-Molina, Laura Elisa
    Marhenke, Silke
    Geffers, Robert
    Endig, Jessica
    Lobschat, Katharina
    Roessler, Stephanie
    Goeppert, Benjamin
    Manns, Michael P.
    Gross, Atan
    Vogel, Arndt
    [J]. HEPATOLOGY, 2015, 62 (03) : 816 - 828
  • [10] p38 stress-activated protein kinase inhibitor reverses bradykinin B1 receptor-mediated component of inflammatory hyperalgesia
    Ganju, P
    Davis, A
    Patel, S
    Núñez, X
    Fox, A
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 421 (03) : 191 - 199