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Table 2 Applications of GBNs in gene-based therapy

From: Graphene-based nanomaterials for breast cancer treatment: promising therapeutic strategies

References

Type of GBN

Targeting ligands

Modification

Gene

Properties

Cell line

Results

[151]

GO

_

PEI

siRNA

_

MDA-MB-231

Suppressed the gene expression and metastatic potential of breast cancer cells

[152]

GO

_

CPPs, PL-PEG

siRNA

_

MCF-7

Showed significant cell death

[153]

GO

P-L-Arg

Au

miRNA-101

Gene release was improved by NIR thermal therapy

MCF-7, MDA

Reduced the viability of MCF-7 cell lines

[154]

GO

P-L-Arg

PEG

miR-101

Higher miRNA payload, selective transfection

MCF-7, MDA-MB-231

Autophagy was downregulated, and the apoptosis cascade was activated

[155]

GO

_

Hap, ganciclovir

HSV-TK

Tumor-specific promoters

MCF-7, MDA-MB-231, MCF-10A

Induced the apoptosis of breast cancer cells and inhibited their growth

[156]

GO

_

PEG-diamine, R8

siRNA and pDNA

Superior internalization

efficacy of 85%

MCF-7, MDA-MB-231

Protected siRNA and pDNA against enzyme degradation

[139]

GO

_

_

MDR1 beacon, ETS1 beacon

_

MCF-7/Adr

Reversed MDR

[150]

GO

_

PAMAM, PEG

siRNA

pH-triggered release of siRNA

MDA-MB-231

Effectively silenced genes with high transfection efficiency

  1. PEI, polyethylenimine; siRNA, small interfering RNA; CPPs, cell penetrating peptide; PL-PEG, a phospholipid-based amphiphilic polymer; Au, gold; P-L-Arg, poly-L-arginine; miR-101, microRNA-101; PEG, polyethylene glycol; HSV-TK, herpes simplex virus thymidine kinase gene; Hap, hydroxyapatite; PEG-diamine, aminated-polyethylene glycol; R8, octaarginine; MDR1, multidrug resistance 1; ETS1, erythroblastosis virus E26 oncogene homolog 1; PAMAM, polyamidoamine; GPD, hybrid vector consisting of GO, PAMAM and PEG