Self-assembled peptide and protein nanostructures for anti-cancer therapy: Targeted delivery, stimuli-responsive devices and immunotherapy
Status PubMed-not-MEDLINE Language English Country England, Great Britain Media print-electronic
Document type Journal Article
Grant support
18TPA34230113
American Heart Association-American Stroke Association - United States
R01 CA244491
NCI NIH HHS - United States
PubMed
34267794
PubMed Central
PMC8276870
DOI
10.1016/j.nantod.2021.101119
PII: 101119
Knihovny.cz E-resources
- Keywords
- Cancer therapy, Drug delivery, Immunotherapy, Self-assembled peptides and proteins, Stimuli-responsive, Virus-like particles,
- Publication type
- Journal Article MeSH
Self-assembled peptides and proteins possess tremendous potential as targeted drug delivery systems and key applications of these well-defined nanostructures reside in anti-cancer therapy. Peptides and proteins can self-assemble into nanostructures of diverse sizes and shapes in response to changing environmental conditions such as pH, temperature, ionic strength, as well as host and guest molecular interactions; their countless benefits include good biocompatibility and high loading capacity for hydrophobic and hydrophilic drugs. These self-assembled nanomaterials can be adorned with functional moieties to specifically target tumor cells. Stimuli-responsive features can also be incorporated with respect to the tumor microenvironment. This review sheds light on the growing interest in self-assembled peptides and proteins and their burgeoning applications in cancer treatment and immunotherapy.
Department of Radiology and the Molecular Imaging Program Stanford University Stanford CA 94305 USA
Institute of Biochemistry and Cell Biology Naples 80131 Italy
Sabanci University Nanotechnology Research and Application Center Tuzla 34956 Istanbul Turkey
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