Evidence map›Paper›PMID 38398498›Full record

ReviewMolecules (Basel, Switzerland)2024

Current Status of Novel Multifunctional Targeted Pt(IV) Compounds and Their Reductive Release Properties.

Lingwen Xu, Xiangyu Kong, Xinzhi Li, Bin Zhang, Yuxiao Deng, Jinhu Wang, Chonggang Duan, Daizhou Zhang, Wentao Liu

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Lingwen XuInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Xiangyu KongInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Xinzhi LiInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Bin ZhangInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Yuxiao DengInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Jinhu WangInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Chonggang DuanInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Daizhou ZhangInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Wentao LiuInstitute of Chemical Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.
Shandong Academy of Pharmaceutical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platinum-based drugs are widely used in chemotherapy for various types of cancer and are considered crucial. Tetravalent platinum (Pt(IV)) compounds have gained significant attention and have been extensively researched among these drugs. Traditionally, Pt(IV) compounds are reduced to divalent platinum (Pt(II)) after entering cells, causing DNA lesions and exhibiting their anti-tumor effect. However, the available evidence indicates that some Pt(IV) derivatives may differ from the traditional mechanism and exert their anti-tumor effect through their overall structure. This review primarily focuses on the existing literature regarding targeted Pt(II) and Pt(IV) compounds, with a specific emphasis on their in vivo mode of action and the properties of reduction release in multifunctional Pt(IV) compounds. This review provides a comprehensive summary of the design and synthesis strategies employed for Pt(II) derivatives that selectively target various enzymes (glucose receptor, folate, telomerase, etc.) or substances (mitochondria, oleic acid, etc.). Furthermore, it thoroughly examines and summarizes the rational design, anti-tumor mechanism of action, and reductive release capacity of novel multifunctional Pt(IV) compounds, such as those targeting p53-MDM2, COX-2, lipid metabolism, dual drugs, and drug delivery systems. Finally, this review aims to provide theoretical support for the rational design and development of new targeted Pt(IV) compounds.

Indexed as

Antineoplastic AgentsNeoplasmsProdrugsCell Line, TumorDrug Delivery SystemsHumansPlatinumAntineoplastic AgentsPlatinumProdrugsanti-tumordivalent platinummultifunctional targetedreductive releasetetravalent platinum

Identifiers

PMID38398498
PMCPMC10892972
OpenAlexW4391576119

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.