Evidence map›Paper›PMID 33479681›Full record

ReviewRSC medicinal chemistry2020

TPP-based mitocans: a potent strategy for anticancer drug design.

Jiayao Wang, Jiaqi Li, Yumei Xiao, Bin Fu, Zhaohai Qin

Abstract readReview
In one paragraph

Review in RSC medicinal chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
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

31 citing papers in PubMed.

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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

5 authors.

Jiayao WangCollege of science , China Agriculture University , Haidian District 100089 , China . Email: qinzhaohai@263.net ; Tel: +86 130 0199 1198.ORCID 0000-0003-4128-8541
Jiaqi LiCollege of science , China Agriculture University , Haidian District 100089 , China . Email: qinzhaohai@263.net ; Tel: +86 130 0199 1198.ORCID 0000-0002-3716-2543
Yumei XiaoCollege of science , China Agriculture University , Haidian District 100089 , China . Email: qinzhaohai@263.net ; Tel: +86 130 0199 1198.
Bin FuCollege of science , China Agriculture University , Haidian District 100089 , China . Email: qinzhaohai@263.net ; Tel: +86 130 0199 1198.
Zhaohai QinCollege of science , China Agriculture University , Haidian District 100089 , China . Email: qinzhaohai@263.net ; Tel: +86 130 0199 1198.ORCID 0000-0001-7516-2432

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is one of the most important problems that endanger human health. The number of cancer patients is increasing rapidly worldwide. Compared with normal cells, cancer cells exhibit abnormal metabolism (abnormal glycolysis and oxidative phosphorylation, high levels of reactive oxygen species, anti-apoptosis, high mitochondrial membrane potential, and so on), and specific targeting of these metabolic abnormalities would be a promising drug design direction. These physiological characteristics are closely related to tumorigenesis and development, which are mainly regulated by mitochondria. Therefore, mitochondria have become important anticancer drug targets, attracting much attention in recent years. In this review, we systematically summarize various mitochondrial anticancer drugs developed, especially mitocans based on triphenylphosphonium (TPP), and discuss the advantages of TPP in endowing mitochondrial targeting function.

Identifiers

PMID33479681
PMCPMC7489259

What OpenQuestion holds

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Registered trials

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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.