Cisplatin: The first metal based anticancer drug

2019 Bioorganic Chemistry 1,601 citations

Abstract

Cisplatin or (SP-4-2)-diamminedichloridoplatinum(II) is one of the most potential and widely used drugs for the treatment of various solid cancers such as testicular, ovarian, head and neck, bladder, lung, cervical cancer, melanoma, lymphomas and several others. Cisplatin exerts anticancer activity via multiple mechanisms but its most acceptable mechanism involves generation of DNA lesions by interacting with purine bases on DNA followed by activation of several signal transduction pathways which finally lead to apoptosis. However, side effects and drug resistance are the two inherent challenges of cisplatin which limit its application and effectiveness. Reduction of drug accumulation inside cancer cells, inactivation of drug by reacting with glutathione and metallothioneins and faster repairing of DNA lesions are responsible for cisplatin resistance. To minimize cisplatin side effects and resistance, combination therapies are used and have proven more effective to defect cancers. This article highlights a systematic description on cisplatin which includes a brief history, synthesis, action mechanism, resistance, uses, side effects and modulation of side effects. It also briefly describes development of platinum drugs from very small cisplatin complex to very large next generation nanocarriers conjugated platinum complexes.

Keywords

CisplatinChemistryPharmacologyDrug resistanceCancer researchDrugChemotherapyMedicineInternal medicineBiology

MeSH Terms

Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCisplatinCoordination ComplexesDNADrug ResistanceNeoplasmHumansMetal NanoparticlesNeoplasmsPlatinum

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Publication Info

Year
2019
Type
review
Volume
88
Pages
102925-102925
Citations
1601
Access
Closed

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1601
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29
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1453
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Cite This

Sumit Ghosh (2019). Cisplatin: The first metal based anticancer drug. Bioorganic Chemistry , 88 , 102925-102925. https://doi.org/10.1016/j.bioorg.2019.102925

Identifiers

DOI
10.1016/j.bioorg.2019.102925
PMID
31003078

Data Quality

Data completeness: 81%