Redox-Related Mechanisms to Rebalance Cancer-Deregulated Cell Growth

  • An-Sofie Stevens
  • , Nicky Pirotte
  • , Annelies Wouters
  • , Andromeda Van Roten
  • , Frank Van Belleghem
  • , Maxime Willems
  • , Ann Cuypers
  • , Tom Artois
  • , Karen Smeets*
  • *Corresponding author for this work

Research output: Contribution to journal(Systematic) Review articlepeer-review

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Abstract

A delicate balance exists between the process of carcinogenesis and tissue regeneration. A number of malignant tumours are considered the outcome of an impaired or incomplete regeneration process, resulting in persistently dividing cells. Regeneration-competent tissues and animals are able to prevent and counteract growth abnormalities and seem to have a low vulnerability to chemical carcinogenesis. Cancer cell survival depends, among other things, on various redox-related mechanisms, which are targets of currently developed therapies. Disadvantages of these therapies are a lack of specificity and drug resistance. As the majority of these redox-related mechanisms also play an important role in successful and coordinated cell functioning and reproduction, the regeneration process offers a unique parallel context for modern cancer research. This review focuses on the interconnections between regeneration and carcinogenesis and how an understanding of regenerative forces and redox-controlled mechanisms could contribute to the identification of new therapeutic targets to block the growth and survival of cancer cells.

Original languageEnglish
Pages (from-to)1414-1437
Number of pages24
JournalCurrent Drug Targets
Volume17
Issue number12
DOIs
Publication statusPublished - 2016

Keywords

  • Anticarcinogenic therapies
  • carcinogenesis
  • redox-related mechanisms
  • regeneration
  • stem cells
  • NF-KAPPA-B
  • EPITHELIAL-MESENCHYMAL TRANSITION
  • OXYGEN SPECIES ACCUMULATION
  • AXON REGENERATION REQUIRES
  • INDUCIBLE FACTOR 1-ALPHA
  • INHIBITS TUMOR-GROWTH
  • OXIDATIVE STRESS
  • BREAST-CANCER
  • STEM-CELLS
  • PLANARIAN REGENERATION

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