Agonist & Antagonist |
CD28Apt |
Either reducing the T-cell tolerance by blocking the interaction with B7 or enhancing the vaccine-induced immune response |
[94] |
OX40 aptamer |
Stimulating the T cell proliferation and cytokine production |
[70,95] |
PSMA-4-1BB aptamer |
Promoting the survival and expansion of activated CD8+ T cells |
[69] |
PEG-MP7 |
Inhibiting the PD-L1-mediated suppression of IL-2 secretion in T cells |
[68] |
NX1838 aptamer |
Binding to VEGF165 with high affinity and preventing blood vessel growth and arresting the progression |
[98] |
Cot-pega oligobody |
Inhibiting the Akt pathway that induces the cell survival, angiogenesis, differentiation, cell growth, proliferation |
[99] |
Aptamer-drug conjugates |
A10-Plk1 |
Suppressing the expression of polo-like kinase 1 that pro-survival genes |
[100] |
BAFF-R-STAT3 siRNA |
Blocking the BAFF-mediated proliferation of B-cell malignancies and suppressing the transcription factor STAT3 to inhibit the cell cycle progression, angiogenesis and tumor cell evasion of immune system |
[101] |
GL21.T-222 |
Inhibiting the receptor tyrosine kinases Axl and PDGFR β and reducing the level of miR-222 or miR-10b |
[102] |
CD40-SMG1-shRNA chimera |
Inhibiting SMG1 kinase that is essential for nonsense mRNA mediated decay initiation in tumor cells |
[103] |
3WJ-EGFRapt/anti-miR-21 |
Inhibiting of tumor progression, invasion, and metastasis by suppressing of miR-21 |
[104] |
AS1411-Dox |
Inhibiting of tumor cell proliferation by inducing G2/M arrest |
[105] |
Sgc8c-Dox |
Recognizing the protein tyrosine kinase 7 and delivering Dox to the target CCRF-CEM (T-cell Acute Lymphoblastic Leukemia) cells |
[106] |
ApDCs |
Recognizing target cancer cells and release the Fluorouracil in a photocontrollable manner |
[108] |
MA3 Apt-Dox |
Selectively delivering the cytotoxic agent doxorubicin to MUC1-positivie adenocarcinomas cancer cells |
[111] |
ApDC |
Delivering the Dox to CD38-positive m1ultiple myeloma tumor cells and intracellular release of a high drug payload under a pH-controlled mechanism |
[112] |
ApS&Dox |
Targeting nucleolin molecule and circumventing Dox resistance by cell cycle arrest in S phase, effectively increased cell uptake |
[113] |
Poly-Aptamer-Drug |
Targeting and killing leukemia cells due to enhanced binding affinity and cell internalization via multivalent effects |
[114] |
aptNTrs |
Targeting human T-cell acute lymphocytic leukemia with high payload of drugs |
[115] |
Aptamer-conjugated nano-vehicles |
DAG-NX213-L |
Inhibiting the VEGF-induced endothelial cell proliferation and vascular permeability increase and angiogenesis |
[90] |
Aptamosome |
Selectively delivering the drug to PSMA-positive prostate cancer cells by Dox-encapsulating liposome conjugated with aptamers |
[81] |
TDO5-micelle |
Efficient delivering the drug to target cancer cells by aptamer-micelle assembly with high sensitivity and specificity in flow channel system |
[118] |
QD-Apt |
Delivering Dox to the prostate cancer cells and imaging the cancer cells by quantum dot |
[120] |
NP-Apt |
Suppressing the metastatic cancer progression and inducing the apoptosis of cancer cells |
[79] |
MUC-1 Origami-Dox-AuNRs |
Chemotherapeutically and photothermally killing the MUC1-overexpressed multidrug resistant breast cancer cells |
[126] |