Evidence map›Paper›PMID 31861339›Full record

ReviewCancers2019

Recent Progress in Mitochondria-Targeted Drug and Drug-Free Agents for Cancer Therapy.

M T Jeena, Sangpil Kim, Seongeon Jin, Ja-Hyoung Ryu

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 150 citations in OpenAlex.

  1. Article
  2. Mitochondria-Targeting Moieties Based on N-Tethered Pyridinium Cations.Angewandte Chemie (International ed. in English) · 2026
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4 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

M T JeenaDepartment of Chemistry, Ulsan National Institute of Science and Technology, Ulsan 44919, Korea.
Sangpil KimDepartment of Chemistry, Ulsan National Institute of Science and Technology, Ulsan 44919, Korea.
Seongeon JinDepartment of Chemistry, Ulsan National Institute of Science and Technology, Ulsan 44919, Korea.
Ja-Hyoung RyuDepartment of Chemistry, Ulsan National Institute of Science and Technology, Ulsan 44919, Korea.
Ulsan National Institute of Science and Technology · KR

Funding

National Research Foundation of Korea 2017R1A2B4003617, 2016R1A5A1009405, 2017K1A3A1A19071083, 2018R1E1A2A02058946, and 2019R1I1A1A01062414
6 · The paper itself

Abstract

The mitochondrion is a dynamic eukaryotic organelle that controls lethal and vital functions of the cell. Being a critical center of metabolic activities and involved in many diseases, mitochondria have been attracting attention as a potential target for therapeutics, especially for cancer treatment. Structural and functional differences between healthy and cancerous mitochondria, such as membrane potential, respiratory rate, energy production pathway, and gene mutations, could be employed for the design of selective targeting systems for cancer mitochondria. A number of mitochondria-targeting compounds, including mitochondria-directed conventional drugs, mitochondrial proteins/metabolism-inhibiting agents, and mitochondria-targeted photosensitizers, have been discussed. Recently, certain drug-free approaches have been introduced as an alternative to induce selective cancer mitochondria dysfunction, such as intramitochondrial aggregation, self-assembly, and biomineralization. In this review, we discuss the recent progress in mitochondria-targeted cancer therapy from the conventional approach of drug/cytotoxic agent conjugates to advanced drug-free approaches.

Indexed as

cancerdrug conjugatesdrug-free approachmitochondria

Identifiers

PMID31861339
PMCPMC7016936
OpenAlexW2996231268

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.