Back to Search
Start Over
Integration of Dual Targeting and Dual Therapeutic Modules Endows Self-Assembled Nanoparticles with Anti-Tumor Growth and Metastasis Functions
- Source :
- International Journal of Nanomedicine
- Publication Year :
- 2021
- Publisher :
- Informa UK Limited, 2021.
-
Abstract
- Object High targeting and efficient cytotoxicity toward tumor cells endow NPs excellent anti-tumor activity. Herein, a peptide polymer possessing dual-targeting ability and double therapeutic activity was developed and named TGMF, which can form NPs through self-assembly. It is composed of four functional modules: 1) Active targeting peptide TMTP1 (T) deliver NPs to tumors specifically; 2) Therapeutic peptide GO-203 (G), which can significantly inhibit tumor growth by disrupting the redox balance in cells; 3) A passively targeted enzyme-responsive peptide PLGLGA (M), which can be cleaved specifically by metalloproteinase-2 (MMP-2) highly expressed in the tumor microenvironment (TME); and 4) Hexadecyl (F), which has strong hydrophobicity, can promote the self-assembly of TGMF NPs. Methods Five modular peptide probes, namely, TGF, TMF, TGM, GMF, and TGMF were synthesized and self-assembled into NPs in solution. The characterization, enzyme reactivity, and cytotoxicity of NPs were evaluated in vitro, and the pharmacokinetics, bio-distribution, anti-tumor activity of NPs were investigated in vivo. In addition, transcriptome sequencing identified the intracellular signaling pathway-related genes involved in the anti-tumor effect of TGMF. Results Upon enzyme cleavage, two types of nanostructure, NPs and nanofibers (NFs), were detected under TEM. Moreover, the cytotoxicity and anti-invasion activity of TGMF against tumor cells used were strongest among the five modular probes examined in vitro. TGMF increased reactive oxygen species (ROS) levels in cytoplasm and produced numerous NFs in extracellular interval and intracellular space. Transcriptome sequencing revealed that TGMF caused 446 genes' down-regulation and 270 genes' up-regulation in HeLa cells. In vivo, TGMF has a good anti-tumor effect, effectively prolonging the survival time of HeLa-tumor-bearing mice without systemic side effects. Conclusion Integration of multiple functional modules into NPs could be a promising strategy for the future of nanomedicine design towards tumor treatment.
- Subjects :
- Polymers
Nanofibers
Pharmaceutical Science
Peptide
02 engineering and technology
01 natural sciences
HeLa
Neoplasms
Drug Discovery
Tumor Microenvironment
modular peptide
Neoplasm Metastasis
Cytotoxicity
Original Research
chemistry.chemical_classification
Mice, Inbred BALB C
Principal Component Analysis
biology
Chemistry
General Medicine
021001 nanoscience & nanotechnology
Cell biology
Matrix Metalloproteinase 2
Nanomedicine
Female
0210 nano-technology
Intracellular
anti-metastasis
Cell Survival
Biophysics
Mice, Nude
Antineoplastic Agents
Bioengineering
transcriptome sequencing
010402 general chemistry
Biomaterials
In vivo
Cell Line, Tumor
Animals
Humans
Neoplasm Invasiveness
nanofiber
anti-tumor
Cell Proliferation
Tumor microenvironment
Organic Chemistry
biology.organism_classification
In vitro
0104 chemical sciences
Nanoparticles
Peptides
Reactive Oxygen Species
Transcriptome
HeLa Cells
Subjects
Details
- ISSN :
- 11782013
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- International Journal of Nanomedicine
- Accession number :
- edsair.doi.dedup.....e9ee474cac433bb21ce656190bb9d0fd