4.5 Article

Synthetic lethality by co-targeting mitochondrial apoptosis and PI3K/Akt/mTOR signaling

期刊

MITOCHONDRION
卷 19, 期 -, 页码 85-87

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.mito.2014.04.011

关键词

Apoptosis; Mitochondria; Cell death; PI3K/Akt/mTOR; BH3 mimetics

资金

  1. Deutsche Forschungsgemeinschaft
  2. Ministerium fur Bildung und Forschung [01GM1104C]
  3. IUAP
  4. Deutsche Krebshilfe

向作者/读者索取更多资源

Small-molecule inhibitors that antagonize anti-apoptotic BcI-2 proteins such as BH3 mimetics are currently considered as promising cancer therapeutics to engage the mitochondrial pathway of apoptosis in cancer cells. However, BH3 mimetics may be effective as monotherapy only in cancers that critically depend on anti-apoptotic Bc1-2 proteins for their survival. Since most cancers have evolved multiple strategies to evade programmed cell death, concomitant targeting of several signaling transduction pathways becomes more and more relevant. The current review highlights the potential of combined inhibition of anti-apoptotic BcI-2 proteins together with the PI3K/Akt/mTOR signaling cascade to trigger apoptosis in cancer cells. (C) 2014 Elsevier B.V. and Mitochondria Research Society. All rights reserved.

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