From synergy to resistance: Navigating the complex relationship between sorafenib and ferroptosis in hepatocellular carcinoma DOI Creative Commons
Zijian Wang, Chunyang Zhou, Yiming Zhang

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2023, Volume and Issue: 170, P. 116074 - 116074

Published: Dec. 25, 2023

Hepatocellular carcinoma (HCC) remains a major global health burden, and sorafenib, multi-kinase inhibitor, has shown effectiveness in the treatment of HCC is considered as first-line therapy for advanced HCC. However, response to sorafenib varies among patients, development drug resistance poses prevalent obstacle. Ferroptosis, newly characterized form cell death featured by iron-dependent lipid peroxidation, emerged critical player reaction The induction ferroptosis been augment anticancer benefits sorafenib. it also observed contribute resistance. This review presents comprehensive thorough analysis that elucidates intricate relationship between over recent years, aiming formulate effective therapeutic approaches liver cancer. Based on this exploration, we propose innovative strategies intended overcome via targeted modulation ferroptosis.

Language: Английский

Cross-talks of GSH, mitochondria, RNA m6A modification, NRF2, and p53 between ferroptosis and cuproptosis in HCC: A review DOI

Leihan Wang,

Zhenni ChenLiu,

Daorong Wang

et al.

International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: 302, P. 140523 - 140523

Published: Feb. 1, 2025

Language: Английский

Citations

2

Exceedingly Small Magnetic Iron Oxide Nanoparticles for T1‐Weighted Magnetic Resonance Imaging and Imaging‐Guided Therapy of Tumors DOI Open Access
Jing Yang, Jie Feng, Su‐Geun Yang

et al.

Small, Journal Year: 2023, Volume and Issue: 19(49)

Published: Aug. 18, 2023

Abstract Magnetic iron oxide nanoparticles (MIONs) based T 2 ‐weighted magnetic resonance imaging (MRI) contrast agents (CAs) are liver‐specific with good biocompatibility, but have been withdrawn from the market and replaced Eovist (Gd‐EOB‐DTPA) due to their inherent limitations (e.g., susceptibility artifacts, high moment, dark signals, long processing time of imaging, waiting for patients after administration). Without disadvantages Gd‐chelates MIONs, recently emerging exceedingly small MIONs (ES‐MIONs) (<5 nm) promising 1 CAs MRI. However, there rare review articles focusing on ES‐MIONs Herein, recent progress ES‐MIONs, including synthesis methods (the current basic improved methods), surface modifications (artificial polymers, natural zwitterions, functional protein), ‐MRI visual strategies (structural remodeling, reversible self‐assemblies, metal ions doped, / dual modes, PET/MRI strategy), imaging‐guided cancer therapy (chemotherapy, gene therapy, ferroptosis photothermal photodymatic radiotherapy, immuotherapy, sonodynamic multimode therapy), is summarized. The detailed description applications in this anticipated attract extensive interest researchers different fields promote participation establishment nanoplatforms tumor theranostics.

Language: Английский

Citations

36

Integrated chemical and genetic screens unveil FSP1 mechanisms of ferroptosis regulation DOI Creative Commons
Toshitaka Nakamura, Eikan Mishima, Naoya Yamada

et al.

Nature Structural & Molecular Biology, Journal Year: 2023, Volume and Issue: 30(11), P. 1806 - 1815

Published: Nov. 1, 2023

Ferroptosis, marked by iron-dependent lipid peroxidation, may present an Achilles heel for the treatment of cancers. Ferroptosis suppressor protein-1 (FSP1), as second ferroptosis mainstay, efficiently prevents peroxidation via NAD(P)H-dependent reduction quinones. Because its molecular mechanisms have remained obscure, we studied numerous FSP1 mutations in cancer or identified untargeted random mutagenesis. This mutational analysis elucidates FAD/NAD(P)H-binding site and proton-transfer function FSP1, which emerged to be evolutionarily conserved among different NADH quinone reductases. Using mutagenesis screens, uncover mechanism action next-generation inhibitors. Our studies identify binding pocket first inhibitor, iFSP1, introduce species-independent targeting NAD(P)H-binding pocket. Conclusively, our study provides new insights into functions enables rational design inhibitors cells.

Language: Английский

Citations

33

Emerging significance and therapeutic targets of ferroptosis: a potential avenue for human kidney diseases DOI Creative Commons
Jinghan Li,

Sujuan Zheng,

Yumei Fan

et al.

Cell Death and Disease, Journal Year: 2023, Volume and Issue: 14(9)

Published: Sept. 22, 2023

Abstract Kidney diseases remain one of the leading causes human death and have placed a heavy burden on medical system. Regulated cell contributes to pathology plethora renal diseases. Recently, with in-depth studies into kidney death, new iron-dependent modality, known as ferroptosis, has been identified attracted considerable attention among researchers in pathogenesis therapeutics treat them. The majority suggest that ferroptosis plays an important role pathologies multiple diseases, such acute injury (AKI), chronic disease, carcinoma. In this review, we summarize recently regulatory molecular mechanisms discuss pathways action various describe protective effect inhibitors against especially AKI. By summarizing prominent roles different progress made studying provide directions strategies for future research summary, ferroptotic factors are potential targets therapeutic intervention alleviate targeting them may lead treatments patients

Language: Английский

Citations

27

From synergy to resistance: Navigating the complex relationship between sorafenib and ferroptosis in hepatocellular carcinoma DOI Creative Commons
Zijian Wang, Chunyang Zhou, Yiming Zhang

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2023, Volume and Issue: 170, P. 116074 - 116074

Published: Dec. 25, 2023

Hepatocellular carcinoma (HCC) remains a major global health burden, and sorafenib, multi-kinase inhibitor, has shown effectiveness in the treatment of HCC is considered as first-line therapy for advanced HCC. However, response to sorafenib varies among patients, development drug resistance poses prevalent obstacle. Ferroptosis, newly characterized form cell death featured by iron-dependent lipid peroxidation, emerged critical player reaction The induction ferroptosis been augment anticancer benefits sorafenib. it also observed contribute resistance. This review presents comprehensive thorough analysis that elucidates intricate relationship between over recent years, aiming formulate effective therapeutic approaches liver cancer. Based on this exploration, we propose innovative strategies intended overcome via targeted modulation ferroptosis.

Language: Английский

Citations

22