Single and dual target inhibitors based on Bcl-2: Promising anti-tumor agents for cancer therapy

被引:29
作者
Liu, Tingting [1 ]
Wu, Zhongyu [2 ]
He, Yujing [1 ]
Xiao, Yuliang [1 ]
Xia, Chengcai [1 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Sch Pharm, Dept Med Chem, Tai An 271016, Shandong, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Inst Mat Med, Jinan 250062, Shandong, Peoples R China
关键词
Bcl-2; Apoptosis; Inhibitor; Anti-Tumor; Structure-activity relationships; Interplay; BH3 MIMETIC ABT-737; EFFICIENTLY INDUCES APOPTOSIS; CHRONIC LYMPHOCYTIC-LEUKEMIA; POTENTIAL ANTICANCER AGENTS; SMALL-MOLECULE INHIBITORS; OVERCOME DRUG-RESISTANCE; G-QUADRUPLEX DNA; CELL-DEATH; FAMILY PROTEINS; IN-VITRO;
D O I
10.1016/j.ejmech.2020.112446
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
B-cell lymphoma-2 (Bcl-2) proteins family is an essential checkpoint in apoptosis. Extensive evidences suggested that overexpression of anti-apoptotic Bcl-2 proteins can be observed in multiple cancer cell lines and primary tumor biopsy samples, which is an important reason for tumor cells to evade apoptosis and further acquire drug resistance for chemotherapy. Hence, down-regulation of anti-apoptotic Bcl-2 proteins is effective for the treatment of cancers. In view that Bcl-2 inhibitors and some other anti-tumor agents, such as HDAC inhibitors and Mdm2 inhibitors, exert synergy effects in tumor cells, it is pointed out that dual-targeting therapies based on these targets are regarded as rational strategies to enhance the effectiveness of single target agents for cancer treatment. This review briefly introduces the apoptosis, the structure of Bcl-2 family proteins, and focuses on the current status and recent advances of Bcl-2 inhibitors and the corresponding SARs of them. Moreover, we discuss the synergisms between Bcl2 and other anti-tumor targets, and summarize the current dual-target agents. (C) 2020 Elsevier Masson SAS. All rights reserved.
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页数:18
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共 141 条
  • [1] Abou-Nassar K, 2010, CLIN ADV HEMATOL ONC, V8, P886
  • [2] The Bcl-2 apoptotic switch in cancer development and therapy
    Adams, J. M.
    Cory, S.
    [J]. ONCOGENE, 2007, 26 (09) : 1324 - 1337
  • [3] Dual targeting of Bcl-2 and VEGF: A potential strategy to improve therapy for prostate cancer
    Anai, Satoshi
    Sakamoto, Noboru
    Sakai, Yoshihisa
    Tanaka, Motoyoshi
    Porvasnik, Stacy
    Urbanek, Cydney
    Cao, Wengang
    Goodison, Steve
    Rosser, Charles J.
    [J]. UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2011, 29 (04) : 421 - 429
  • [4] [Anonymous], 2006, J MED CHEM, DOI DOI 10.1021/JM060968R
  • [5] [Anonymous], 2007, DRUG RESIST UPDATE, DOI DOI 10.1016/J.DRUP.2007.08.002
  • [6] [Anonymous], 1992, NATURE
  • [7] [Anonymous], 2018, BIOORG MED CHEM LETT, DOI DOI 10.1016/J.BMCL.2017.08.049
  • [8] [Anonymous], 2007, INT J CANCER, DOI DOI 10.1002/IJC.22977
  • [9] [Anonymous], 2017, BIOORGAN MED CHEM, DOI DOI 10.1016/J.BMC.2017.08.024
  • [10] [Anonymous], 2007, CANCER RES, DOI DOI 10.1158/0008-5472.CAN-06-3964