Utilization of macrocyclic peptides to target protein-protein interactions in cancer

被引:10
作者
Yang, Jiawen [1 ,2 ,3 ]
Zhu, Qiaoliang [1 ]
Wu, Yifan [2 ,4 ,5 ]
Qu, Xiaojuan [2 ,4 ,5 ]
Liu, Haixia [2 ,5 ,6 ]
Jiang, Biao [2 ,7 ]
Ge, Di [1 ]
Song, Xiaoling [2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Thorac Surg, Shanghai, Peoples R China
[2] ShanghaiTech Univ, Shanghai Inst Adv Immunochem Studies, Shanghai, Peoples R China
[3] Shanghai Clin Res & Trial Ctr, Shanghai, Peoples R China
[4] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai, Peoples R China
[5] Univ Chinese Acad Sci, Beijing, Peoples R China
[6] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai, Peoples R China
[7] Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Synthet Chem Nat Subst, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
protein-protein interactions; macrocyclic peptide; cancer; treatment; drug; CXCR4 ANTAGONIST BKT140; HUMAN CD34(+) CELLS; IN-VITRO SELECTION; OPEN-LABEL; PHASE-II; MONTHLY PASIREOTIDE; UBIQUITIN LIGASES; CYCLIC-PEPTIDES; SOMATOSTATIN; INHIBITOR;
D O I
10.3389/fonc.2022.992171
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protein-protein interactions (PPIs) play vital roles in normal cellular processes. Dysregulated PPIs are involved in the process of various diseases, including cancer. Thus, these PPIs may serve as potential therapeutic targets in cancer treatment. However, despite rapid advances in small-molecule drugs and biologics, it is still hard to target PPIs, especially for those intracellular PPIs. Macrocyclic peptides have gained growing attention for their therapeutic properties in targeting dysregulated PPIs. Macrocyclic peptides have some unique features, such as moderate sizes, high selectivity, and high binding affinities, which make them good drug candidates. In addition, some oncology macrocyclic peptide drugs have been approved by the US Food and Drug Administration (FDA) for clinical use. Here, we reviewed the recent development of macrocyclic peptides in cancer treatment. The opportunities and challenges were also discussed to inspire new perspectives.
引用
收藏
页数:21
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共 175 条
[81]   Targeting autophagy in cancer [J].
Levy, Jean M. Mulcahy ;
Towers, Christina G. ;
Thorburn, Andrew .
NATURE REVIEWS CANCER, 2017, 17 (09) :528-542
[82]   A novel somatostatin mimic with broad somatotropin release inhibitory factor receptor binding and superior therapeutic potential [J].
Lewis, I ;
Bauer, W ;
Albert, R ;
Chandramouli, N ;
Pless, J ;
Weckbecker, G ;
Bruns, C .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (12) :2334-2344
[83]   Stapled Helical Peptides Bearing Different Anchoring Residues [J].
Li, Xiang ;
Chen, Si ;
Zhang, Wei-Dong ;
Hu, Hong-Gang .
CHEMICAL REVIEWS, 2020, 120 (18) :10079-10144
[84]   Dithiocarbamate-inspired side chain stapling chemistry for peptide drug design [J].
Li, Xiang ;
Tolbert, W. David ;
Hu, Hong-Gang ;
Gohain, Neelakshi ;
Zou, Yan ;
Niu, Fan ;
He, Wang-Xiao ;
Yuan, Weirong ;
Su, Jia-Can ;
Pazgier, Marzena ;
Lu, Wuyuan .
CHEMICAL SCIENCE, 2019, 10 (05) :1522-1530
[85]   Autophagy and autophagy-related proteins in cancer [J].
Li, Xiaohua ;
He, Shikun ;
Ma, Binyun .
MOLECULAR CANCER, 2020, 19 (01)
[86]   Discovery of cell active macrocyclic peptides with on-target inhibition of KRAS signaling [J].
Lim, Shuhui ;
Boyer, Nicolas ;
Boo, Nicole ;
Huang, Chunhui ;
Venkatachalam, Gireedhar ;
Juang, Yu-Chi Angela ;
Garrigou, Michael ;
Kaan, Kristal ;
Duggal, Ruchia ;
Peh, Khong Ming ;
Sadruddin, Ahmad ;
Gopal, Pooja ;
Yuen, Tsz Ying ;
Ng, Simon ;
Kannan, Srinivasaraghavan ;
Brown, Christopher J. ;
Verma, Chandra ;
Orth, Peter ;
Peier, Andrea ;
Ge, Lan ;
Yu, Xiang ;
Bhatt, Bhavana ;
Chen, Feifei ;
Wang, Erjia ;
Li, Nianyu Jason ;
Gonzales, Raymond J. ;
Stoeck, Alexander ;
Henry, Brian ;
Sawyer, Tomi K. ;
Lane, David ;
Johannes, Charles W. ;
Biswas, Kaustav ;
Partridge, Anthony W. .
CHEMICAL SCIENCE, 2021, 12 (48) :15975-15987
[87]   Progress in PD-1/PD-L1 pathway inhibitors: From biomacromolecules to small molecules [J].
Lin, Xin ;
Lu, Xiang ;
Luo, Guoshun ;
Xiang, Hua .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2020, 186
[88]   Identification of a peptide antagonist of the FGF1-FGFR1 signaling axis by phage display selection [J].
Lipok, Magdalena ;
Szlachcic, Anna ;
Kindela, Kinga ;
Czyrek, Aleksandra ;
Otlewski, Jacek .
FEBS OPEN BIO, 2019, 9 (05) :914-924
[89]   Recent advances in the development of protein-protein interactions modulators: mechanisms and clinical trials [J].
Lu, Haiying ;
Zhou, Qiaodan ;
He, Jun ;
Jiang, Zhongliang ;
Peng, Cheng ;
Tong, Rongsheng ;
Shi, Jianyou .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2020, 5 (01)
[90]   Bioactive Macrocyclic Inhibitors of the PD-1/PD-L1 Immune Checkpoint [J].
Magiera-Mularz, Katarzyna ;
Skalniak, Lukasz ;
Zak, Krzysztof M. ;
Musielak, Bogdan ;
Rudzinska-Szostak, Ewa ;
Berlicki, Lukasz ;
Kocik, Justyna ;
Grudnik, Przemyslaw ;
Sala, Dominik ;
Zarganes-Tzitzikas, Tryfon ;
Shaabani, Shabnam ;
Doemling, Alexander ;
Dubin, Grzegorz ;
Holak, Tad A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2017, 56 (44) :13732-13735