Ferroptosis as a Novel Therapeutic Strategy to Overcome Multidrug Resistance in Colorectal Cancer
Dina Mahemuti, Lanfei Ma, Waqas Siddiqe, Ziyue Tang, Yuxin Kong, Wenfang Li, Zhiwei Zhang, Zhengding Su, Ayitila Maimaitijiang

TL;DR
This review explores how triggering ferroptosis, a unique form of cell death, could help overcome drug resistance in colorectal cancer.
Contribution
The paper introduces ferroptosis as a novel strategy to bypass multidrug resistance in colon cancer.
Findings
MDR cancer cells suppress ferroptosis through antioxidant upregulation and iron sequestration.
Ferroptosis inducers like erastin and RSL3 can overcome apoptotic resistance and avoid efflux pathways.
Stimulating iron accumulation may reverse multidrug resistance in colon cancer.
Abstract
Colon cancer (CC) remains a leading cause of cancer-related mortality worldwide, with multidrug resistance (MDR) presenting a formidable barrier to successful chemotherapy. Ferroptosis—an iron-dependent, lipid peroxidation-driven form of cell death—offers a novel therapeutic avenue to bypass MDR by exploiting metabolic vulnerabilities distinct from traditional apoptosis pathways. Emerging evidence reveals a dynamic interplay between MDR and ferroptosis: MDR cancer cells suppress ferroptosis through NRF2/GPX4-mediated antioxidant upregulation, iron sequestration by ferritin, and lipid metabolism reprogramming, including SREBP1-driven monounsaturated fatty acid accumulation, while ABC transporters actively efflux ferroptosis inducers. On the other hand, ferroptosis inducers such as erastin and RSL3 have the potential to overcome apoptotic resistance and avoid efflux pathways, which…
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Taxonomy
TopicsFerroptosis and cancer prognosis · Drug Transport and Resistance Mechanisms · Cancer, Lipids, and Metabolism
