The power of chemotherapeutic engineering Arresting cell cycle and suppressing senescence to protect from mitotic inhibitors

被引:18
作者
Blagosklonny, Mikhail V. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA
关键词
cellular senescence; rapamycin; arrest; apoptosis; p53; p21; DNA-DAMAGING AGENTS; P53; MTOR; ACTIVATION; GROWTH; DRUGS; PROLIFERATION; QUIESCENCE; MECHANISM; LEADS;
D O I
10.4161/cc.10.14.16819
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Suppose one drug causes lethal mitotic arrest, another treatment causes irreversible senescence and a third drug inhibits cellular mass growth. Could cells treated with a combination of all three agents magically emerge alive and proliferating? The result of this experiment is presented here. By knowing the mechanisms of cell cycle arrest, death and senescence, we can design 'rainbow combinations' that obediently kill or spare desired cells. Knowledge is power.
引用
收藏
页码:2295 / 2298
页数:4
相关论文
共 53 条
  • [41] DNA damaging agents and p53 do not cause senescence in quiescent cells, while consecutive re-activation of mTOR is associated with conversion to senescence
    Leontieva, Olga V.
    Blagosklonny, Mikhail V.
    [J]. AGING-US, 2010, 2 (12): : 924 - U55
  • [42] Weak p53 permits senescence during cell cycle arrest
    Leontieva, Olga V.
    Gudkov, Andrei V.
    Blagosklonny, Mikhail V.
    [J]. CELL CYCLE, 2010, 9 (21) : 4323 - 4327
  • [43] Microtubule Active Agents: Beyond the Taxane Frontier
    Morris, Patrick G.
    Fornier, Monica N.
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (22) : 7167 - 7172
  • [44] Microtubule inhibitors: Differentiating tubulin-inhibiting agents based on mechanisms of action, clinical activity, and resistance
    Perez, Edith A.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2009, 8 (08) : 2086 - 2095
  • [45] Rao B, 2010, ONCOTARGET, V1, P639
  • [46] Novel agents that target tublin and related elements
    Rowinsky, Eric K.
    Calvo, Emiliano
    [J]. SEMINARS IN ONCOLOGY, 2006, 33 (04) : 421 - 435
  • [47] Growing roles for the mTOR pathway
    Sarbassov, DD
    Ali, SM
    Sabatini, DM
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (06) : 596 - 603
  • [48] TOR, a central controller of cell growth
    Schmelzle, T
    Hall, MN
    [J]. CELL, 2000, 103 (02) : 253 - 262
  • [49] Steelman LS, 2011, ONCOTARGET, V2, P109
  • [50] A panel of isogenic human cancer cells suggests a therapeutic approach for cancers with inactivated p53
    Sur, Surojit
    Pagliarini, Raymond
    Bunz, Fred
    Rago, Carlo
    Diaz, Luis A., Jr.
    Kinzler, Kenneth W.
    Vogelstein, Bert
    Papadopoulos, Nickolas
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (10) : 3964 - 3969