Fabrication of a Polymeric Inhibitor of Proximal Metabolic Enzymes in Hypoxia for Synergistic Inhibition of Cancer Cell Proliferation, Survival, and Migration

被引:4
作者
Koba, Yuki [1 ]
Nakamoto, Masahiko [1 ]
Matsusaki, Michiya [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Div Appl Chem, Osaka 5650871, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
polymer inhibitor; enzyme inhibition; cancer therapy; proximal enzymes; multivalent interaction; CARBONIC-ANHYDRASE-IX; DRUG-COMBINATIONS; NANOPARTICLE; INTERNALIZATION; STRATEGY; DELIVERY; DESIGN; DOMAIN; EGFR;
D O I
10.1021/acsami.2c16454
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Since conventional molecular targeted drugs often result in side effects, the development of novel molecular targeted drugs with both high efficacy and selectivity is desired. Simultaneous inhibition of metabolically and spatiotemporally related proteins/enzymes is a promising strategy for improving therapeutic interventions in cancer treatment. Herein, we report a poly-alpha-L-glutamate-based polymer inhibitor that simultaneously targets proximal transmembrane enzymes under hypoxia, namely, carbonic anhydrase IX (CAIX) and zinc-dependent metal-loproteinases. A polymer incorporating two types of inhibitors more effectively inhibited the proliferation and migration of human breast cancer cells than a combination of two polymers functionalized exclusively with either inhibitor. Synergistic inhibition of cancer cells would occur owing to the hetero-multivalent interactions of the polymer with proximate enzymes on the cancer cell membrane. Our results highlight the potential of polymer-based cancer therapeutics.
引用
收藏
页码:51790 / 51797
页数:8
相关论文
共 59 条
[51]   Apoptosis-induced ectodomain shedding of hypoxia-regulated carbonic anhydrase IX from tumor cells: a double-edged response to chemotherapy [J].
Vidlickova, Ivana ;
Dequiedt, Franck ;
Jelenska, Lenka ;
Sedlakova, Olga ;
Pastorek, Michal ;
Stuchlik, Stanislav ;
Pastorek, Jaromir ;
Zatovicova, Miriam ;
Pastorekova, Silvia .
BMC CANCER, 2016, 16
[52]   A Disintegrin and Metalloproteinase Domain 17 Regulates Colorectal Cancer Stem Cells and Chemosensitivity Via Notch1 Signaling [J].
Wang, Rui ;
Ye, Xiangcang ;
Bhattacharya, Rajat ;
Boulbes, Delphine R. ;
Fan, Fan ;
Xia, Ling ;
Ellis, Lee M. .
STEM CELLS TRANSLATIONAL MEDICINE, 2016, 5 (03) :331-338
[53]   The metabolism of tumors in the body. [J].
Warburg, O ;
Wind, F ;
Negelein, E .
JOURNAL OF GENERAL PHYSIOLOGY, 1927, 8 (06) :519-530
[54]   Review: Side effects of approved molecular targeted therapies in solid cancers [J].
Widakowich, Christian ;
De Castro, Gilberto, Jr. ;
De Azambuja, Evandro ;
Dinh, Phuong ;
Awada, Ahmad .
ONCOLOGIST, 2007, 12 (12) :1443-1455
[55]   Targeting hypoxia in cancer therapy [J].
Wilson, William R. ;
Hay, Michael P. .
NATURE REVIEWS CANCER, 2011, 11 (06) :393-410
[56]   Biorecognition: A key to drug-free macromolecular therapeutics [J].
Yang, Jiyuan ;
Li, Lian ;
Kopecek, Jindrich .
BIOMATERIALS, 2019, 190 :11-23
[57]   Ectodomain shedding of the hypoxia-induced carbonic anhydrase IX is a metalloprotease-dependent process regulated by TACE/ADAM17 [J].
Zatovicova, M ;
Sedlakova, O ;
Svastova, E ;
Ohradanova, A ;
Ciampor, F ;
Arribas, J ;
Pastorek, J ;
Pastorekova, S .
BRITISH JOURNAL OF CANCER, 2005, 93 (11) :1267-1276
[58]   Monoclonal antibody G250 targeting CA IX: Binding specificity, internalization and therapeutic effects in a non-renal cancer model [J].
Zatovicova, Miriam ;
Jelenska, Lenka ;
Hulikova, Alzbeta ;
Ditte, Peter ;
Ditte, Zuzana ;
Csaderova, Lucia ;
Svastova, Eliska ;
Schmalix, Wolfgang ;
Boettger, Volker ;
Bevan, Paul ;
Pastorek, Jaromir ;
Pastorekova, Silvia .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2014, 45 (06) :2455-2467
[59]   The shedding protease ADAM17: Physiology and pathophysiology [J].
Zunke, Friederike ;
Rose-John, Stefan .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2017, 1864 (11) :2059-2070