4.7 Review

Redox biology of regulated cell death in cancer: A focus on necroptosis and ferroptosis

Journal

FREE RADICAL BIOLOGY AND MEDICINE
Volume 134, Issue -, Pages 177-189

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2019.01.008

Keywords

ROS; Redox changes; Regulated cell death; Necroptosis; Ferroptosis; Cancer; Anticancer therapy

Funding

  1. Televie Luxemburg
  2. Recherche Cancer et Sang foundation
  3. Recherches Scientifiques Luxembourg association
  4. Een Haerz fir Kriibskrank Kanner association
  5. Action Lions Vaincre le Cancer
  6. Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Korea
  7. Tumor Microenvironment GCRC from the National Research Foundation - Ministry of Science and ICT of Korea [2011-0030001]
  8. Creative-Pioneering Researchers Program through Seoul National University (SNU) [370C-20160062]

Ask authors/readers for more resources

Redox changes and generation of reactive oxygen species (ROS) are part of normal cell metabolism. While low ROS levels are implicated in cellular signaling pathways necessary for survival, higher levels play major roles in cancer development as well as cell death signaling and execution. A role for redox changes in apoptosis has been long established; however, several new modalities of regulated cell death have been brought to light, for which the importance of ROS production as well as ROS source and targets are being actively investigated. In this review, we summarize recent findings on the role of ROS and redox changes in the activation and execution of two major forms of regulated cell death, necroptosis and ferroptosis. We also discuss the potential of using modulators of these two forms of cell death to exacerbate ROS as a promising anticancer therapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available