TY - JOUR
T1 - Intracellular magnetic hyperthermia reverses sorafenib resistance in hepatocellular carcinoma through its action on signaling pathways
AU - Li, Hugang
AU - Ye, Zirui
AU - Wang, Xun
AU - Yuan, Jianlan
AU - Guo, Jingyi
AU - Liu, Chen
AU - Yan, Bin
AU - Fan, Haiming
AU - Lyu, Yi
AU - Liu, Xiaoli
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/6/21
Y1 - 2024/6/21
N2 - Sorafenib, a first-line drug for advanced hepatocellular carcinoma (HCC), unfortunately encounters resistance in most patients, leading to disease progression. Traditional approaches to counteract this resistance, particularly those targeting the RAF-MEK-ERK pathway, often face clinical feasibility limitations. Magnetic hyperthermia (MH), unlike conventional thermal therapies, emerges as a promising alternative. It uniquely combines magnetothermal effects with an increase in reactive oxygen species (ROS). This study found the potential of intracellular MH enhanced the efficacy of sorafenib, increased cellular sensitivity to sorafenib, and reversed sorafenib resistance by inhibiting the RAF-MEK-ERK pathway in an ROS-dependent manner in a sorafenib-resistant HCC cell. Further, in a sorafenib-resistant HCC mouse model, MH significantly sensitized tumors to sorafenib therapy, resulting in inhibited tumor growth and improved survival rates. This presents a promising strategy to overcome sorafenib resistance in HCC, potentially enhancing therapeutic outcomes for patients with this challenging condition.
AB - Sorafenib, a first-line drug for advanced hepatocellular carcinoma (HCC), unfortunately encounters resistance in most patients, leading to disease progression. Traditional approaches to counteract this resistance, particularly those targeting the RAF-MEK-ERK pathway, often face clinical feasibility limitations. Magnetic hyperthermia (MH), unlike conventional thermal therapies, emerges as a promising alternative. It uniquely combines magnetothermal effects with an increase in reactive oxygen species (ROS). This study found the potential of intracellular MH enhanced the efficacy of sorafenib, increased cellular sensitivity to sorafenib, and reversed sorafenib resistance by inhibiting the RAF-MEK-ERK pathway in an ROS-dependent manner in a sorafenib-resistant HCC cell. Further, in a sorafenib-resistant HCC mouse model, MH significantly sensitized tumors to sorafenib therapy, resulting in inhibited tumor growth and improved survival rates. This presents a promising strategy to overcome sorafenib resistance in HCC, potentially enhancing therapeutic outcomes for patients with this challenging condition.
KW - Biomaterials
KW - Biomedical Engineering
KW - Molecular biology
KW - Nanomedicine
UR - https://www.scopus.com/pages/publications/85194549739
U2 - 10.1016/j.isci.2024.110029
DO - 10.1016/j.isci.2024.110029
M3 - 文章
AN - SCOPUS:85194549739
SN - 2589-0042
VL - 27
JO - iScience
JF - iScience
IS - 6
M1 - 110029
ER -