Targeting cell death mechanisms: the potential of autophagy and ferroptosis in hepatocellular carcinoma therapy

被引:8
作者
Liu, Beibei [1 ,2 ]
Liu, Ling [3 ]
Liu, Yang [4 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Radiol, Funct & Mol Imaging Key Lab Sichuan Prov, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Huaxi MR Res Ctr HMRRC, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Gen Surg, Div Biliary Surg, Chengdu, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Day Surg Ctr, Gen Practice Med Ctr, Chengdu, Sichuan, Peoples R China
关键词
autophagy; ferroptosis; cancer progression; drug resistance; cell death; tumor; SORAFENIB-INDUCED FERROPTOSIS; ENDOPLASMIC-RETICULUM STRESS; DOWN-REGULATION; DRUG-RESISTANCE; CANCER-CELL; INHIBITS AUTOPHAGY; SIGNALING PATHWAY; ACTIVATING AUTOPHAGY; LIPID-PEROXIDATION; METABOLIC STRESS;
D O I
10.3389/fimmu.2024.1450487
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ferroptosis is a type of cell death that plays a remarkable role in the growth and advancement of malignancies including hepatocellular carcinoma (HCC). Non-coding RNAs (ncRNAs) have a considerable impact on HCC by functioning as either oncogenes or suppressors. Recent research has demonstrated that non-coding RNAs (ncRNAs) have the ability to control ferroptosis in HCC cells, hence impacting the advancement of tumors and the resistance of these cells to drugs. Autophagy is a mechanism that is conserved throughout evolution and plays a role in maintaining balance in the body under normal settings. Nevertheless, the occurrence of dysregulation of autophagy is evident in the progression of various human disorders, specifically cancer. Autophagy plays dual roles in cancer, potentially influencing both cell survival and cell death. HCC is a prevalent kind of liver cancer, and genetic mutations and changes in molecular pathways might worsen its advancement. The role of autophagy in HCC is a subject of debate, as it has the capacity to both repress and promote tumor growth. Autophagy activation can impact apoptosis, control proliferation and glucose metabolism, and facilitate tumor spread through EMT. Inhibiting autophagy can hinder the growth and spread of HCC and enhance the ability of tumor cells to respond to treatment. Autophagy in HCC is regulated by several signaling pathways, such as STAT3, Wnt, miRNAs, lncRNAs, and circRNAs. Utilizing anticancer drugs to target autophagy may have advantageous implications for the efficacy of cancer treatment.
引用
收藏
页数:28
相关论文
共 337 条
[1]   Deregulation of RB1 expression by loss of imprinting in human hepatocellular carcinoma [J].
Anwar, Sumadi Lukman ;
Krech, Till ;
Hasemeier, Britta ;
Schipper, Elisa ;
Schweitzer, Nora ;
Vogel, Arndt ;
Kreipe, Hans ;
Lehmann, Ulrich .
JOURNAL OF PATHOLOGY, 2014, 233 (04) :392-401
[2]   Manipulation of autophagy in cancer cells: an innovative strategy to fight drug resistance [J].
Aredia, Francesca ;
Scovassi, A. Ivana .
FUTURE MEDICINAL CHEMISTRY, 2013, 5 (09) :1009-1021
[3]   A bioinformatics analysis, pre-clinical and clinical conception of autophagy in pancreatic cancer: Complexity and simplicity in crosstalk [J].
Ashrafizadeh, Milad ;
Zhang, Wei ;
Zou, Rongjun ;
Sethi, Gautam ;
Klionsky, Daniel J. ;
Zhang, Xianbin .
PHARMACOLOGICAL RESEARCH, 2023, 194
[4]   Targeting autophagy in prostate cancer: preclinical and clinical evidence for therapeutic response [J].
Ashrafizadeh, Milad ;
Paskeh, Mahshid Deldar Abad ;
Mirzaei, Sepideh ;
Gholami, Mohammad Hossein ;
Zarrabi, Ali ;
Hashemi, Farid ;
Hushmandi, Kiavash ;
Hashemi, Mehrdad ;
Nabavi, Noushin ;
Crea, Francesco ;
Ren, Jun ;
Klionsky, Daniel J. ;
Kumar, Alan Prem ;
Wang, Yuzhuo .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2022, 41 (01)
[5]   New Insight into Triple-Negative Breast Cancer Therapy: The Potential Roles of Endoplasmic Reticulum Stress and Autophagy Mechanisms [J].
Ashrafizadeh, Milad ;
Mohammadinejad, Reza ;
Tavakol, Shima ;
Ahmadi, Zahra ;
Sahebkar, Amirhossein .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2021, 21 (06) :679-691
[6]   MicroRNA-214-3p enhances erastin-induced ferroptosis by targeting ATF4 in hepatoma cells [J].
Bai, Tao ;
Liang, Ruopeng ;
Zhu, Rongtao ;
Wang, Weijie ;
Zhou, Lin ;
Sun, Yuling .
JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (7-8) :5637-5648
[7]   Sigma-1 receptor protects against ferroptosis in hepatocellular carcinoma cells [J].
Bai, Tao ;
Lei, Pengxu ;
Zhou, Hao ;
Liang, Ruopeng ;
Zhu, Rongtao ;
Wang, Weijie ;
Zhou, Lin ;
Sun, Yuling .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2019, 23 (11) :7349-7359
[8]   PIAS3 promotes ferroptosis by regulating TXNIP via TGF-β signaling pathway in hepatocellular carcinoma [J].
Bao, Wenfang ;
Wang, Jialin ;
Fan, Kailing ;
Gao, Yong ;
Chen, Jingde .
PHARMACOLOGICAL RESEARCH, 2023, 196
[9]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[10]   PI3Kγ promotes obesity-associated hepatocellular carcinoma by regulating metabolism and inflammation [J].
Becattini, Barbara ;
Breasson, Ludovic ;
Sardi, Claudia ;
Zani, Fabio ;
Solinas, Giovanni .
JHEP REPORTS, 2021, 3 (06)