Together we stand, apart we fall: how cell-to-cell contact/interplay provides resistance to ferroptosis

Cell Death Dis. 2020 Sep 23;11(9):789. doi: 10.1038/s41419-020-02994-w.

Abstract

Contextualisation of the new type of cell death called "ferroptosis" opened a completely new avenue for the development of anti-cancer therapies. Cumulative fundamental research dating back to the mid-20th century, crowned by the extraordinary work of the group led by Dr. Stockwell from Columbia University in 2012, finally got its candidature to be applied in the clinical settings. Although the potential for clinical importance is undoubtedly growing every day, as showed by the increasing number of papers dealing with ferroptosis and its applications, long experience of cancer research and treatment taught us that caution is still necessary. The plasticity of the tumour cells, particularly acute, along with its involvement in the resistance mechanisms, that have been seen, to greater or lesser extent, for almost all currently used therapies, represents the biggest fascinations in biomedical research field and also the biggest challenge to achieving cures in cancer patients. Accordingly, the main features of fundamental research have to be vigilance and anticipation. In this review, we tried to summarize the literature data, accumulated in the past couple of years, which point out the pitfalls in which "ferroptosis inducers" can fall if used prematurely in the clinical settings, but at the same time can provide a great advantage in the exhausting battle with cancer resistance. This is the first comprehensive review focusing on the effects of the cell-to-cell contact/interplay in the development of resistance to ferroptosis, while the contribution of cell-born factors has been summarized previously so here we just listed them.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Communication / physiology*
  • Cell Death / drug effects
  • Cell Death / physiology*
  • Drug Resistance / physiology
  • Ferroptosis* / drug effects
  • Ferroptosis* / physiology
  • Humans
  • Iron* / metabolism
  • Iron* / pharmacology
  • Neoplasms / metabolism
  • Neoplasms / pathology*

Substances

  • Iron