Crosstalk between noncoding RNAs and ferroptosis: new dawn for overcoming cancer progression

Cell Death Dis. 2020 Jul 24;11(7):580. doi: 10.1038/s41419-020-02772-8.

Abstract

Cancer progression including proliferation, metastasis, and chemoresistance has become a serious hindrance to cancer therapy. This phenomenon mainly derives from the innate insensitive or acquired resistance of cancer cells to apoptosis. Ferroptosis is a newly discovered mechanism of programmed cell death characterized by peroxidation of the lipid membrane induced by reactive oxygen species. Ferroptosis has been confirmed to eliminate cancer cells in an apoptosis-independent manner, however, the specific regulatory mechanism of ferroptosis is still unknown. The use of ferroptosis for overcoming cancer progression is limited. Noncoding RNAs have been found to play an important roles in cancer. They regulate gene expression to affect biological processes of cancer cells such as proliferation, cell cycle, and cell death. Thus far, the functions of ncRNAs in ferroptosis of cancer cells have been examined, and the specific mechanisms by which noncoding RNAs regulate ferroptosis have been partially discovered. However, there is no summary of ferroptosis associated noncoding RNAs and their functions in different cancer types. In this review, we discuss the roles of ferroptosis-associated noncoding RNAs in detail. Moreover, future work regarding the interaction between noncoding RNAs and ferroptosis is proposed, the possible obstacles are predicted and associated solutions are put forward. This review will deepen our understanding of the relationship between noncoding RNAs and ferroptosis, and provide new insights in targeting noncoding RNAs in ferroptosis associated therapeutic strategies.

Publication types

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

MeSH terms

  • Disease Progression*
  • Ferroptosis / genetics*
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Neoplasms / genetics*
  • Neoplasms / pathology*
  • RNA, Untranslated / genetics*
  • RNA, Untranslated / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • MicroRNAs
  • RNA, Untranslated
  • Reactive Oxygen Species