FBXW7 attenuates tumor drug resistance and enhances the efficacy of immunotherapy

被引:7
|
作者
Chen, Shimin [1 ,2 ,3 ]
Lin, Jichun [1 ,2 ,3 ]
Zhao, Jiaojiao [1 ,2 ,3 ]
Lin, Qian [1 ]
Liu, Jia [4 ]
Wang, Qiang [5 ]
Mui, Ryan [6 ]
Ma, Leina [1 ,2 ]
机构
[1] Qingdao Univ, Canc Inst, Dept Oncol, Affiliated Hosp, Qingdao, Peoples R China
[2] Qingdao Canc Inst, Qingdao, Peoples R China
[3] Qingdao Univ, Sch Basic Med, Qingdao, Peoples R China
[4] Qingdao Univ, Sch Pharm, Dept Pharmacol, Qingdao, Peoples R China
[5] Shandong Second Prov Gen Hosp, Oncol Dept, Jinan, Peoples R China
[6] Sparrow Hosp, Dept Gastroenterol, Lansing, MI USA
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
基金
中国国家自然科学基金;
关键词
FBXW7; drug resistance; E3; ligase; cancer; immunotherapy; F-BOX PROTEINS; GASTRIC-CANCER; MESENCHYMAL TRANSITION; PROMOTES PROLIFERATION; CHEMO-RESISTANCE; CYCLIN-E; C-MYC; FBW7; DEGRADATION; EXPRESSION;
D O I
10.3389/fonc.2023.1147239
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
FBXW7 (F-box and WD repeat domain containing 7) is a critical subunit of the Skp1-Cullin1-F-box protein (SCF), acting as an E3 ubiquitin ligase by ubiquitinating targeted protein. Through degradation of its substrates, FBXW7 plays a pivotal role in drug resistance in tumor cells and shows the potential to rescue the sensitivity of cancer cells to drug treatment. This explains why patients with higher FBXW7 levels exhibit higher survival times and more favorable prognosis. Furthermore, FBXW7 has been demonstrated to enhance the efficacy of immunotherapy by targeting the degradation of specific proteins, as compared to the inactivated form of FBXW7. Additionally, other F-box proteins have also shown the ability to conquer drug resistance in certain cancers. Overall, this review aims to explore the function of FBXW7 and its specific effects on drug resistance in cancer cells.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] FBXW7 and human tumors: mechanisms of drug resistance and potential therapeutic strategies
    Wang, Wanqing
    Jiang, Kaipeng
    Liu, Xue
    Li, Ju
    Zhou, Wenshuo
    Wang, Chang
    Cui, Jiuwei
    Liang, Tingting
    FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [2] Recent Insight on Regulations of FBXW7 and Its Role in Immunotherapy
    Xing, Liangliang
    Xu, Leidi
    Zhang, Yong
    Che, Yinggang
    Wang, Min
    Shao, Yongxiang
    Qiu, Dan
    Yu, Honglian
    Zhao, Feng
    Zhang, Jian
    FRONTIERS IN ONCOLOGY, 2022, 12
  • [3] The role of FBXW7 as a predictor of imatinib resistance for GIST
    Wu, Xiyu
    Iwatsuki, Masaaki
    Baba, Hideo
    Lou, Meiyue
    Ishimoto, Takatsugu
    Baba, Yoshifumi
    Miyamoto, Yuji
    CANCER SCIENCE, 2023, 114 : 1847 - 1847
  • [4] FBXW7: a critical tumor suppressor of human cancers
    Yeh, Chien-Hung
    Bellon, Marcia
    Nicot, Christophe
    MOLECULAR CANCER, 2018, 17
  • [5] FBXW7γ is a tumor-suppressive and prognosis-related FBXW7 transcript isoform in ovarian serous cystadenocarcinoma
    Xu, Zhou
    Zhuang, Lin
    Wang, Xiaoyin
    Li, Qianrong
    Sang, Yan
    Xu, Jiao
    FUTURE ONCOLOGY, 2020, 16 (25) : 1921 - 1930
  • [6] Recent insight into the role of FBXW7 as a tumor suppressor
    Yumimoto, Kanae
    Nakayama, Keiichi I.
    SEMINARS IN CANCER BIOLOGY, 2020, 67 : 1 - 15
  • [7] FBXW7: a critical tumor suppressor of human cancers
    Chien-Hung Yeh
    Marcia Bellon
    Christophe Nicot
    Molecular Cancer, 17
  • [8] FBXW7 deletion contributes to lung tumor development and confers resistance to gefitinib therapy
    Xiao, Yi
    Yin, Chunli
    Wang, Yuli
    Lv, Hanlin
    Wang, Wenqing
    Huang, Yurong
    Perez-Losada, Jesus
    Snijders, Antoine M.
    Mao, Jian-Hua
    Zhang, Pengju
    MOLECULAR ONCOLOGY, 2018, 12 (06) : 883 - 895
  • [9] Role of FBXW7 in imatinib primary and secondary resistance to GIST
    Iwatsuki, Masaaki
    Wu, Xiyu
    Baba, Hideo
    CANCER SCIENCE, 2024, 115 : 1900 - 1900
  • [10] Mutation in the FBXW7 Tumor Suppressor Gene of a childlike Melanoma
    Pfoehler, C.
    Ugurel, S.
    Sucker, A.
    Krecke, N.
    Becker, S.
    Vogt, T.
    Mueller, C.
    JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2017, 15 : 21 - 21