Table 1.
Drug | Action | Consequence | Tissue/Cells | Ref. |
---|---|---|---|---|
RETRA | Inhibit mutant p53-p73 interaction | Restore TAp73 function | Various cancer cells | [84] |
Peptide aptamers | Inhibit mutant p53-p73 interaction | Restore TAp73 function | Tumour cells | [85] |
SIMPs * | Inhibit mutant p53-p73 interaction | Restore TAp73 function | Various cancer cells | [86] |
Benzyl isothiocyanate | Inhibit mutant p53-p73 interaction | Upregulate and restore function of TAp73, induce LKB1 | Breast cancer cells | [87] |
LEM2 | Inhibit mutant p53-p73 interaction | Restore TAp73 function and prevent MDM2 mediated degradation | Neuroblastoma cancer cells | [88] |
Prodigiosin | Inhibit mutant p53-p73 interaction | Restore TAp73 function | Various cancer cell lines | [89] |
NSC59984 | Inhibit mutant p53-p73 interaction | Restore TAp73 function | Colorectal cancer cells | [90] |
PDGFR-β inhibition | Downstream of mutant p53-p73-NF-Y | Prevent PDGFR-β signalling | Pancreatic cancer | [91] |
Curcumol | Upregulation p73 + target genes | Enhance TAp73 function | Triple negative breast cancer | [92] |
miR-3158 | Downstream of mutant p53/p73 | Reactivate the miR-3158 signalling pathway | Breast cancer cells | [93] |
Pramlintine | Downstream of mutant p53/p63 | Inhibit the function of amylin | Lymphomas | [30] |
Tamoxifen/inhibition ER β1 | Downstream of mutant p53-p63/ER β1 | Prevent transcription of GOF associated genes | Triple negative breast cancer cells | [94] |
miR-130b | Downstream of mutant p53-p63 | Reactivate the miR-130b signalling pathway | Ovarian cancer cells | [95] |
Let7i | Downstream of mutant p53-p63 | Reactivate the let7i signalling pathway | Breast cancer cells | [96] |
Inhibition of TGF β or RAS signaling | Prevent TGF β-induced mutantp53-p63-pSMAD interaction | Reactivate TAp63 function | Various cancer cells | [59] |
Inhibition of EGFR, c-MET, ROCK | Downstream of mutant p53-p63 | Prevent invasion induced by loss of TAp63 function | Various cancer cells | [47,97] |
* Short Interfering Mutant p53 Peptides.