Ferroptosis: An emerging approach for targeting cancer stem cells and drug resistance
•Cancer stem cells play a crucial role in cancer drug resistance and tumor relapse.•Complete tumor eradication could be achieved by targeting cancer stem cells.•The induction of ferroptosis in CSCs is a promising target for cancer treatment.•Cancer stem cells possess unique features that render them...
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Veröffentlicht in: | Critical reviews in oncology/hematology 2020-11, Vol.155, p.103095-103095, Article 103095 |
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Sprache: | eng |
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Zusammenfassung: | •Cancer stem cells play a crucial role in cancer drug resistance and tumor relapse.•Complete tumor eradication could be achieved by targeting cancer stem cells.•The induction of ferroptosis in CSCs is a promising target for cancer treatment.•Cancer stem cells possess unique features that render them sensitive to ferroptosis.•Ferroptosis inducing agents show great potential in eliminating cancer stem cells.
Resistance to chemotherapeutic agents remains a major challenge in the fierce battle against cancer. Cancer stem cells (CSCs) are a small population of cells in tumors that possesses the ability to self-renew, initiate tumors, and cause resistance to conventional anticancer agents. Targeting this population of cells was proven as a promising approach to eliminate cancer recurrence and improve the clinical outcome. CSCs are less susceptible to death by classical anticancer agents inducing apoptosis. CSCs can be eradicated by ferroptosis, which is a non-apoptotic-regulated mechanism of cell death. The induction of ferroptosis is an attractive strategy to eliminate tumors due to its ability to selectively target aggressive CSCs. The current review critically explored the crosstalk and regulatory pathways controlling ferroptosis, which can selectively induce CSCs death. In addition, successful chemotherapeutic agents that achieve better therapeutic outcomes through the induction of ferroptosis in CSCs were discussed to highlight their promising clinical impact. |
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ISSN: | 1040-8428 1879-0461 |
DOI: | 10.1016/j.critrevonc.2020.103095 |