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. 2020 Nov 12;11(48):12888–12917. doi: 10.1039/d0sc04082g

Examples of metallodrugs investigated by multi-omics techniques.

M Complex Method Mechanism of action Ref.
As ZIO-101 (As2) Metalloproteomics by GE-ICP-MS Binds to and disrupts dimerisation of H3.3 248
Ru NAMI-A (Ru4) Proteomics by MALDI-TOF or LC-ESI/MS–MS NAMI-A and RAPTA-T similar mechanism; NIT2, TMK, HINT1 and PFD3 up-regulated, POLE3 down-regulated 250
Ru Plecstatin-1 (Ru15†) Proteomics by LC-MS/MS Targets plectin 251
Ru RAPTA-C (Ru12) Proteomics by shotgun and pull-down Influences cytokines midkine, pleiotrophin, fibroblast growth factor-binding protein 3, FAM32A 252
Os FY26 (Os4) RNA transcriptomics and proteomics by reverse-phase protein arrays Shifts cellular metabolism to oxidative phosphorylation, up-regulates ATM, p53 and p21 220
Pt Cisplatin (Pt1) Genomics by damage-seq, XR-seq, RNA-seq Per1 upregulated. Transcription-coupled repair and global repair high in liver 253
Proteomics by nanoLC-MS/MS HMGB1 binds to cisplatin cross-linked ODN specifically 254
Metabolomics by GC-MS, LC-MS 27 potential biomarkers defined related to cisplatin-induced nephrotoxicity 255
Au [Au(TPP)]Cl (Au4†) Proteomics by MALDI-TOF-MS Targets Hsp60 256
Affinity-based proteome profiling SILAC 246