2020
DOI: 10.1016/j.jinorgbio.2020.111070
|View full text |Cite
|
Sign up to set email alerts
|

Recent advances in platinum-based chemotherapeutics that exhibit inhibitory and targeted mechanisms of action

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
37
0
2

Year Published

2020
2020
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 72 publications
(39 citation statements)
references
References 109 publications
0
37
0
2
Order By: Relevance
“…[1][2][3] In view of this, platinum-based drugs such as cisplatin, carboplatin, and oxaliplatin are used worldwide to treat patients. [4][5][6] However, adverse side effects and increased drug resistance results in lack of specicity towards cancer targets. 7 As a result, nanoformulations that involve inorganic platinum nanoparticles have not yet entered clinical studies so far.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3] In view of this, platinum-based drugs such as cisplatin, carboplatin, and oxaliplatin are used worldwide to treat patients. [4][5][6] However, adverse side effects and increased drug resistance results in lack of specicity towards cancer targets. 7 As a result, nanoformulations that involve inorganic platinum nanoparticles have not yet entered clinical studies so far.…”
Section: Introductionmentioning
confidence: 99%
“…Simultaneous modulation of additional biological targets, or synergistic/additive activity against the same target, can be beneficial for treating malignancies that develop resistance to a particular group of drugs. Cisplatin and platinum(II)-based analogs are approved for the treatment of many solid tumors [ 62 , 63 , 64 ]. Unfortunately, these DNA-damaging drugs exhibit severe toxicity due to a lack of selectivity.…”
Section: Hybrid Drugs As An Answer To the Anticancer Drug Resistance Problem?mentioning
confidence: 99%
“…Alkylating agents (including nitrogen mustard, ethyleneimine, nitrosourea, methylxanthate, and epoxy compounds) can produce intra-chain or inter-chain cross links or transfer alkyl groups to guanine residues of DNA, leading to the formation of DNA base mispairs and preventing strand separation during DNA synthesis [47]. Although platinum drugs are also alkylating agents, they do not interact with biological macromolecules, but form a complex with the N7 position of guanine, thereby inhibiting DNA replication and transcription, and inducing apoptosis [48]. Topo inhibitors, which are divided into [49], irinotecan [50], belotecan [51] and camptothecin (CPT) [52]) and topoisomerase II inhibitors (e.g., etoposide, teniposide), can inhibit the activity of Topo involved in DNA replication and transcription, causing DNA singlestrand or double-strand breaks.…”
Section: The Action Mechanism Of the Commonly Used Chemotherapeutic Drugsmentioning
confidence: 99%