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

被引:6
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
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
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
相关论文
共 175 条
[31]   Advances in therapeutic peptides targeting G protein-coupled receptors [J].
Davenport, Anthony P. ;
Scully, Conor C. G. ;
de Graaf, Chris ;
Brown, Alastair J. H. ;
Maguire, Janet J. .
NATURE REVIEWS DRUG DISCOVERY, 2020, 19 (06) :389-413
[32]   CXCR4 Inhibitors: Tumor Vasculature and Therapeutic Challenges [J].
de Nigris, Filomena ;
Schiano, Concetta ;
Infante, Teresa ;
Napoli, Claudio .
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY, 2012, 7 (03) :251-264
[33]   Structure-Activity Relationships and Biological Characterization of a Novel, Potent, and Serum Stable C-X-C Chemokine Receptor Type 4 (CXCR4) Antagonist [J].
Di Maro, Salvatore ;
Di Leva, Francesco Saverio ;
Trotta, Anna Maria ;
Brancaccio, Diego ;
Portella, Luigi ;
Aurilio, Michela ;
Tomassi, Stefano ;
Messere, Anna ;
Sementa, Deborah ;
Lastoria, Secondo ;
Carotenuto, Alfonso ;
Novellino, Ettore ;
Scala, Stefania ;
Marinelli, Luciana .
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (23) :9641-9652
[34]   Exploring the N-Terminal Region of C-X-C Motif Chemokine 12 (CXCL12): Identification of Plasma-Stable Cyclic Peptides As Novel, Potent C-X-C Chemokine Receptor Type 4 (CXCR4) Antagonists [J].
Di Maro, Salvatore ;
Trotta, Anna Maria ;
Brancaccio, Diego ;
Di Leva, Francesco Saverio ;
La Pietra, Valeria ;
Ierano, Caterina ;
Napolitano, Maria ;
Portella, Luigi ;
D'Alterio, Crescenzo ;
Siciliano, Rosa Anna ;
Sementa, Deborah ;
Tomassi, Stefano ;
Carotenuto, Alfonso ;
Novellino, Ettore ;
Scala, Stefania ;
Marinelli, Luciana .
JOURNAL OF MEDICINAL CHEMISTRY, 2016, 59 (18) :8369-8380
[35]   A review on CXCR4/CXCL12 axis in oncology: No place to hide [J].
Domanska, Urszula M. ;
Kruizinga, Roeliene C. ;
Nagengast, Wouter B. ;
Timmer-Bosscha, Hetty ;
Huls, Gerwin ;
de Vries, Elisabeth G. E. ;
Walenkamp, Annemiek M. E. .
EUROPEAN JOURNAL OF CANCER, 2013, 49 (01) :219-230
[36]   Understanding Cell Penetration of Cyclic Peptides [J].
Dougherty, Patrick G. ;
Sahni, Ashweta ;
Pei, Dehua .
CHEMICAL REVIEWS, 2019, 119 (17) :10241-10287
[37]   Macrocycles as protein-protein interaction inhibitors [J].
Dougherty, Patrick G. ;
Qian, Ziqing ;
Pei, Dehua .
BIOCHEMICAL JOURNAL, 2017, 474 (07) :1109-1125
[38]   Pharmacology, ADME and selectivity profile of the next generation CXCR4 antagonist balixafortide. [J].
Douglas, Garry ;
Gambino, Giorgio ;
Lemercier, Guillaume ;
Longuet, Sandrine ;
Remus, Tobias ;
Zimmermann, Johann .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
[39]   Mechanisms of receptor tyrosine kinase activation in cancer [J].
Du, Zhenfang ;
Lovly, Christine M. .
MOLECULAR CANCER, 2018, 17
[40]   The CXCL12-CXCR4 chemotactic pathway as a target of adjuvant breast cancer therapies [J].
Epstein, RJ .
NATURE REVIEWS CANCER, 2004, 4 (11) :901-909