Evidence map›Paper›PMID 25367773›Full record

ReviewJournal of proteome research2015

Mitochondrial targets for pharmacological intervention in human disease.

Ramy H Malty, Matthew Jessulat, Ke Jin, Gabriel Musso, James Vlasblom, Sadhna Phanse, Zhaolei Zhang, Mohan Babu

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of proteome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
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  13. Article
  14. Non-Peptidic Cell-Penetrating Motifs for Mitochondrion-Specific Cargo Delivery.Angewandte Chemie (International ed. in English) · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Review
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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

8 authors at 3 institutions in 2 countries.

Ramy H MaltyDepartment of Biochemistry, Research and Innovation Centre, University of Regina , Regina, Saskatchewan S4S 0A2, Canada.
Matthew Jessulat
Ke Jin
Gabriel Musso
James Vlasblom
Sadhna Phanse
Zhaolei Zhang
Mohan Babu
University of Regina · CAUniversity of Toronto · CAHarvard University · US

Funding

Supplement to: PHYSICAL AND FUNCTIONAL SYSTEMS ANALYSIS OF MAMMALIAN MITOCHONDRIAR01GM106019 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BABU, MOHAN, NUNNARI, JODI M. · 2013 to 2016
$954k
Canadian Institutes of Health Research MOP125952Canadian Institutes of Health Research MOP132191NIGMS NIH HHS R01 GM106019NIGMS NIH HHS R01GM106019
6 · The paper itself

Abstract

Over the past several years, mitochondrial dysfunction has been linked to an increasing number of human illnesses, making mitochondrial proteins (MPs) an ever more appealing target for therapeutic intervention. With 20% of the mitochondrial proteome (312 of an estimated 1500 MPs) having known interactions with small molecules, MPs appear to be highly targetable. Yet, despite these targeted proteins functioning in a range of biological processes (including induction of apoptosis, calcium homeostasis, and metabolism), very few of the compounds targeting MPs find clinical use. Recent work has greatly expanded the number of proteins known to localize to the mitochondria and has generated a considerable increase in MP 3D structures available in public databases, allowing experimental screening and in silico prediction of mitochondrial drug targets on an unprecedented scale. Here, we summarize the current literature on clinically active drugs that target MPs, with a focus on how existing drug targets are distributed across biochemical pathways and organelle substructures. Also, we examine current strategies for mitochondrial drug discovery, focusing on genetic, proteomic, and chemogenomic assays, and relevant model systems. As cell models and screening techniques improve, MPs appear poised to emerge as relevant targets for a wide range of complex human diseases, an eventuality that can be expedited through systematic analysis of MP function.

Indexed as

Molecular Targeted TherapyAnimalsDrug Evaluation, PreclinicalHumansMitochondriaMitochondrial ProteinsProteomeMitochondrial ProteinsProteomeDrug−protein interactionshuman diseasemitochondriamodel systemnetworkpathwayspharmacological targetprotein complexsmall moleculessystems biology

Identifiers

PMID25367773
PMCPMC4286170
OpenAlexW2000160686

What OpenQuestion holds

Textmetadata
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.