4.7 Review

Regulation of apoptosis pathways in cancer stem cells

Journal

CANCER LETTERS
Volume 338, Issue 1, Pages 168-173

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2012.03.014

Keywords

Cancer stem cells; Apoptosis; Death receptors; BcI-2; IAP proteins

Categories

Funding

  1. Deutsche Forschungsgemeinschaft
  2. Deutsche Krebshilfe
  3. Bundesministerium far Forschung und Technologie
  4. Else-Kroner-Fresenius Stiftung
  5. Wilhelm-Sander Stiftung
  6. Novartis Stiftung far therapeutische Forschung
  7. European Community (ApopTrain, APO-SYS)

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Cancer stem cell are considered to represent a population within the bulk tumor that share many similarities to normal stem cells as far as their capacities to self-renew, differentiate, proliferate and to reconstitute the entire tumor upon serial transplantation are concerned. Since cancer stem cells have been shown to be critical for maintaining tumor growth and have been implicated in treatment resistance and tumor progression, they constitute relevant targets for therapeutic intervention. Indeed, it has been postulated that eradication of cancer stem cells will be pivotal in order to achieve long-term relapse-free survival. However, one of the hallmarks of cancer stem cells is their high resistance to undergo cell death including apoptosis in response to environmental cues or cytotoxic stimuli. Since activation of apoptosis programs in tumor cells underlies the antitumor activity of most currently used cancer therapeutics, it will be critical to develop strategies to overcome the intrinsic resistance to apoptosis of cancer stem cells. Thus, a better understanding of the molecular mechanisms that are responsible for the ability of cancer stem cells to evade apoptosis will likely open new avenues to target this critical pool of cells within the tumor in order to develop more efficient treatment options for patients suffering from cancer. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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