The transforming oncoproteins determine the mechanism by which p53 suppresses cell transformation: pRb-mediated growth arrest or apoptosis

被引:0
|
作者
Hansen, R [1 ]
Reddel, R [1 ]
Braithwaite, A [1 ]
机构
[1] CHILDRENS MED RES INST,SYDNEY,NSW 2145,AUSTRALIA
关键词
p53; retinoblastoma protein; SV40 large T antigen; transformation; cell cycle; apoptosis;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate the mechanisms by which p53 suppresses cell transformation, we used the simian virus 40 (SV40) large T antigen (LTag), the adenovirus Ela proteins, and an activated ras protein (EJ-ras), to examine different pathways of transformation for their susceptibility to suppression by p53, While p53 can suppress transformation by various oncoproteins, we have shown that it is unable to suppress the transformation of rat embryo fibroblasts (REFs) by LTag, Interestingly, the function of LTag which enables it to overcome the proliferative effects of p53 is not the binding inactivation of p53, but the binding and inactivation of the pRb family of proteins, This observation indicates that pRb mediates a suppressive effect of p53 on cell transformation, We have also observed that in contrast to LTag, both Ela and EJ-ras cause transformation-related events which are susceptible to suppression by p53, Further studies have revealed that cells expressing Ela are susceptible to p53-mediated apoptosis, while cells expressing EJ-ras are susceptible to p53-induced growth inhibition, We therefore propose that p53 suppresses transformation either by arresting cell growth (mediated by pRb in late G1) or by inducing apoptosis, with the mechanism being determined by the transforming oncoprotein(s).
引用
收藏
页码:2535 / 2545
页数:11
相关论文
共 50 条
  • [1] The polyproline region of p53 is required to activate apoptosis but not growth arrest
    Daitoku Sakamuro
    Peter Sabbatini
    Eileen White
    George C Prendergast
    Oncogene, 1997, 15 : 887 - 898
  • [2] The polyproline region of p53 is required to activate apoptosis but not growth arrest
    Sakamuro, D
    Sabbatini, P
    White, E
    Prendergast, GC
    ONCOGENE, 1997, 15 (08) : 887 - 898
  • [3] A threshold mechanism mediates p53 cell fate decision between growth arrest and apoptosis
    Kracikova, M.
    Akiri, G.
    George, A.
    Sachidanandam, R.
    Aaronson, S. A.
    CELL DEATH AND DIFFERENTIATION, 2013, 20 (04): : 576 - 588
  • [4] A threshold mechanism mediates p53 cell fate decision between growth arrest and apoptosis
    M Kracikova
    G Akiri
    A George
    R Sachidanandam
    S A Aaronson
    Cell Death & Differentiation, 2013, 20 : 576 - 588
  • [5] Selenomethionine induces p53 mediated cell cycle arrest and apoptosis in human colon cancer cells
    Goel, Ajay
    Fuerst, Florentine
    Hotchkiss, Erin
    Boland, Richard
    Boland, C. Richard
    CANCER BIOLOGY & THERAPY, 2006, 5 (05) : 529 - 535
  • [6] p53 oligomerization status modulates cell fate decisions between growth, arrest and apoptosis
    Fischer, Nicholas W.
    Prodeus, Aaron
    Malkin, David
    Gariepy, Jean
    CELL CYCLE, 2016, 15 (23) : 3210 - 3219
  • [7] Vaccinia virus-mediated expression of wild-type p53 suppresses glioma cell growth and induces apoptosis
    Timiryasova, TM
    Chen, B
    Haghighat, P
    Fodor, I
    INTERNATIONAL JOURNAL OF ONCOLOGY, 1999, 14 (05) : 845 - 854
  • [8] Growth arrest-specific gene 2 suppresses hepatocarcinogenesis by intervention of cell cycle and p53-dependent apoptosis
    Zhu, Ran-Xu
    Cheng, Alfred Sze Lok
    Chan, Henry Lik Yuen
    Yang, Dong-Ye
    Seto, Wai-Kay
    WORLD JOURNAL OF GASTROENTEROLOGY, 2019, 25 (32) : 4715 - 4726
  • [9] Apoptosis or growth arrest: modulation of the cellular response to p53 by proliferative signals
    Heinrichs, S
    Deppert, W
    ONCOGENE, 2003, 22 (04) : 555 - 571
  • [10] Apoptosis or growth arrest: modulation of the cellular response to p53 by proliferative signals
    Stefan Heinrichs
    Wolfgang Deppert
    Oncogene, 2003, 22 : 555 - 571