Progress in the studies on the molecular mechanisms associated with multidrug resistance in cancers

被引:49
|
作者
Zhang, Lei [1 ,2 ,3 ]
Ye, Biwei [1 ,3 ]
Chen, Zhuo [1 ,2 ,3 ]
Chen, Zhe-Sheng [4 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Fujian Agr & Forestry Univ, Fuzhou 350002, Peoples R China
[4] St Johns Univ, Coll Pharm & Hlth Sci, Dept Pharmaceut Sci, New York, NY 11439 USA
基金
中国国家自然科学基金;
关键词
Multidrug resistance (MDR); ABC transporter family; Signaling pathway; Alternative splicing (AS); Gene mutation; None-coding RNA (ncRNA); Tumor microenvironment; CELL LUNG-CANCER; MULTIPLE-DRUG RESISTANCE; NEGATIVE BREAST-CANCER; HEAT-SHOCK PROTEINS; P-GLYCOPROTEIN; OVARIAN-CANCER; IN-VITRO; ENHANCES CHEMOSENSITIVITY; MESENCHYMAL TRANSITION; TUMOR-SUPPRESSOR;
D O I
10.1016/j.apsb.2022.10.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemotherapy is one of the important methods to treat cancer, and the emergence of multi-drug resistance (MDR) is one major cause for the failure of cancer chemotherapy. Almost all anti-tumor drugs develop drug resistance over a period of time of application in cancer patients, reducing their ef-fects on killing cancer cells. Chemoresistance can lead to a rapid recurrence of cancers and ultimately patient death. MDR may be induced by multiple mechanisms, which are associated with a complex pro-cess of multiple genes, factors, pathways, and multiple steps, and today the MDR-associated mechanisms are largely unknown. In this paper, from the aspects of protein-protein interactions, alternative splicing (AS) in pre-mRNA, non-coding RNA (ncRNA) mediation, genome mutations, variance in cell functions, and influence from the tumor microenvironment, we summarize the molecular mechanisms associated with MDR in cancers. In the end, prospects for the exploration of antitumor drugs that can reverse MDR are briefly discussed from the angle of drug systems with improved targeting properties, biocom-patibility, availability, and other advantages.(c) 2023 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:982 / 997
页数:16
相关论文
共 50 条
  • [1] Progress in the studies on the molecular mechanisms associated with multidrug resistance in cancers
    Lei Zhang
    Biwei Ye
    Zhuo Chen
    Zhe-Sheng Chen
    Acta Pharmaceutica Sinica B, 2023, (03) : 982 - 997
  • [2] New insights into the mechanisms of multidrug resistance in cancers
    Montazami, N.
    Aghapour, M.
    Farajnia, S.
    Baradaran, B.
    CELLULAR AND MOLECULAR BIOLOGY, 2015, 61 (07) : 70 - 80
  • [3] Molecular mechanisms of antibacterial multidrug resistance
    Alekshun, Michael N.
    Levy, Stuart B.
    CELL, 2007, 128 (06) : 1037 - 1050
  • [4] Recent Advances in the Studies of Molecular Mechanisms Regulating Multidrug Resistance in Cancer Cells
    Stavrovskaya, A. A.
    Rybalkina, E. Yu.
    BIOCHEMISTRY-MOSCOW, 2018, 83 (07) : 779 - 786
  • [5] Recent Advances in the Studies of Molecular Mechanisms Regulating Multidrug Resistance in Cancer Cells
    A. A. Stavrovskaya
    E. Yu. Rybalkina
    Biochemistry (Moscow), 2018, 83 : 779 - 786
  • [6] Multidrug resistance: molecular mechanisms and clinical relevance
    Victor Ling
    Cancer Chemotherapy and Pharmacology, 1997, 40 : S3 - S8
  • [7] Multiple molecular mechanisms for multidrug resistance transporters
    Higgins, Christopher F.
    NATURE, 2007, 446 (7137) : 749 - 757
  • [8] Multiple molecular mechanisms for multidrug resistance transporters
    Christopher F. Higgins
    Nature, 2007, 446 : 749 - 757
  • [9] Multidrug resistance: Molecular mechanisms and clinical relevance
    Ling, V
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (Suppl 1) : S3 - S8
  • [10] Molecular mechanisms of multidrug resistance in cancer chemotherapy
    Nooter, K
    Stoter, G
    PATHOLOGY RESEARCH AND PRACTICE, 1996, 192 (07) : 768 - 780