Table 2.
Peptide | Cargo | Results | Reference |
---|---|---|---|
p28 | p28 | This shows that p28 can be tolerated by the body and did not result in any cytotoxic reactions. Shown to prevent p53 ubiquitination, thereby inhibiting cancer cell proliferation. | [148,149,150] |
pVEC | Cyclic homing peptides CREKA CREKAD AREKA Anti-cancer therapeutics Imaging/diagnostic tag |
General CPPs (including pVEC and others in the above table) have low cancer-targeting abilities, but when combined with novel targeting sequences such as CREKA or AREKA, they can deliver therapeutics to the tumor. | [25,46,151] |
ACCPs Activatable cell penetrating peptides |
Fluorescence acceptors Fluorescence donors |
When the ACCP comes in contact with matrix metalloproteinases (MMP-2 MMP-9) which are involved in metastasis and proliferation pathways, the fluorescing agent is activated, allowing for more accurate diagnostics. | [126,128] |
RI-TAT | p53C’ | Mice treated with the peptide complex showed a significant decrease in tumor numbers, and the proliferation of cancer cells is inhibited by the reactivation of p53 | [152] |
caPCNA | p21cip | caPCNA is a highly specific antigen that can interact with proteins along the DNA repair pathway inside cancer cells. Combined with the ability of p21 to induce apoptosis, the caPCNA-p21 complex is a promising treatment for breast cancer. | [153,154] |
PepFect14 and 28 | siRNAs | When combined with glioma-targeting peptides, PepFect showed highly efficient gene slicing of U87 GBM cells | [155] |
SCPP-PS | Methotrexate disodium (MTX) | When mice with A549 lung tumors, MTX-SCCP-PS inhibits tumor growth and progression and improves survival time by an average of 37 days compared to free MTX | [139] |
DTS-108 | SN38 | When compared to traditional chemotherapeutic agents such as irinotecan, DTS-108 introduced significantly higher levels of topoisomerase 1 inhibitor SN38 | [156] |
Listed are CPPs that have been involved in preclinical and/ or clinical trials and their respective results.