Recent Progresses in Conjugation with Bioactive Ligands to Improve the Anticancer Activity of Platinum Compounds

Curr Med Chem. 2022;29(15):2566-2601. doi: 10.2174/0929867328666210806110857.

Abstract

Platinum (Pt) drugs, including cisplatin, are widely used for the treatment of solid tumors. Despite the clinical success, side effects and occurrence of resistance represent major limitations to the use of clinically available Pt drugs. To overcome these problems, a variety of derivatives have been designed and synthetized. Here, we summarize the recent progress in the development of Pt(II) and Pt(IV) complexes with bioactive ligands. The development of Pt(II) and Pt(IV) complexes with targeting molecules, clinically available agents, and other bioactive molecules is an active field of research. Even if none of the reported Pt derivatives has been yet approved for clinical use, many of these compounds exhibit promising anticancer activities with an improved pharmacological profile. Thus, planning hybrid compounds can be considered as a promising approach to improve the available Pt-based anticancer agents and to obtain new molecular tools to deepen the knowledge of cancer progression and drug resistance mechanisms.

Keywords: Platinum compounds; cisplatin; conjugates; drug resistance; hybrid anticancer agents; tumor targeting.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Antineoplastic Agents, Alkylating / therapeutic use
  • Cell Line, Tumor
  • Cisplatin / therapeutic use
  • Humans
  • Ligands
  • Neoplasms* / drug therapy
  • Platinum / therapeutic use
  • Platinum Compounds / pharmacology
  • Platinum Compounds / therapeutic use
  • Radiation-Sensitizing Agents* / therapeutic use

Substances

  • Antineoplastic Agents
  • Antineoplastic Agents, Alkylating
  • Ligands
  • Platinum Compounds
  • Radiation-Sensitizing Agents
  • Platinum
  • Cisplatin