Related Experiment Video
Updated: Jul 23, 2025

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics
Published on: March 15, 2024
Understanding sorafenib-induced ferroptosis and resistance mechanisms: Implications for cancer therapy
Qiuhong Li1, Kexin Chen1, Tianyi Zhang1
1School of Basic Medical Sciences, Southwest Medical University, Luzhou, 646000, Sichuan, China.
Abstract:
Sorafenib is an important first-line treatment option for liver cancer due to its well-characterized safety profile. While novel first-line drugs may have better efficacy than Sorafenib, they also have limitations such as worse safety and cost-effectiveness. In addition to inducing apoptosis, Sorafenib can also trigger ferroptosis, which has recently been recognized as an immunogenic cell death, unleashing new possibilities for cancer treatment. However, resistance to Sorafenib-induced ferroptosis remains a major challenge. To overcome this resistance and augment the efficacy of Sorafenib, a wide range of nanomedicines has been developed to amplify its pro-ferroptotic effects. This review highlights the mechanisms underlying Sorafenib-triggered ferroptosis and its resistance, and outlines innovative strategies, particularly nanomedicines, to overcome ferroptosis resistance. Moreover, we summarize molecular biomarkers that signify resistance to Sorafenib-mediated ferroptosis, which can assist in predicting therapeutic outcomes.
Insights
Sorafenib triggers ferroptosis, a cell death process, in liver cancer treatment. Nanomedicines are being developed to overcome resistance to this therapy and improve outcomes.
Area of Science:
- Oncology
- Nanomedicine
- Cell Death Mechanisms
Background:
- Sorafenib is a first-line liver cancer treatment with a known safety profile.
- Novel therapies may offer better efficacy but present safety and cost challenges.
- Sorafenib induces apoptosis and ferroptosis, a recognized form of immunogenic cell death.
Purpose of the Study:
- To review mechanisms of Sorafenib-induced ferroptosis and resistance.
- To outline nanomedicine strategies for overcoming ferroptosis resistance.
- To summarize biomarkers for predicting Sorafenib resistance.
Main Methods:
- Literature review of Sorafenib mechanisms, resistance pathways, and nanomedicine applications.
- Analysis of studies on ferroptosis induction and immunogenic cell death.
- Compilation of data on molecular biomarkers associated with Sorafenib resistance.
Main Results:
- Sorafenib's dual action includes apoptosis and ferroptosis induction.
- Resistance to Sorafenib-induced ferroptosis is a significant clinical challenge.
- Nanomedicines show promise in enhancing Sorafenib efficacy by overcoming resistance.
Conclusions:
- Understanding Sorafenib-induced ferroptosis and resistance is crucial for optimizing liver cancer therapy.
- Nanomedicine offers innovative approaches to potentiate Sorafenib's anti-cancer effects.
- Biomarker identification can guide personalized treatment strategies for Sorafenib therapy.
More Related Videos
00:06An Oncogenic Hepatocyte-Induced Orthotopic Mouse Model of Hepatocellular Cancer Arising in the Setting of Hepatic Inflammation and Fibrosis
Published on: September 12, 2019
08:02Isolation of Primary Cancer-Associated Fibroblasts from a Syngeneic Murine Model of Breast Cancer for the Study of Targeted Nanoparticles
Published on: May 14, 2021
Related Concept Videos
Treatment Resistant Cancers
Targeted Cancer Therapies
There are several types of targeted therapies against...
Necrosis
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Electron Transport Chain: Complex I and II
ROS generation is regulated and maintained at moderate levels necessary...