Evidence map›Paper›PMID 31819039›Full record

ArticleCell death & disease2019

Intramitochondrial Src kinase links mitochondrial dysfunctions and aggressiveness of breast cancer cells.

Marie-Ange Djeungoue-Petga, Olivier Lurette, Stéphanie Jean, Geneviève Hamel-Côté, Rebeca Martín-Jiménez, Marine Bou, Astrid Cannich, Patrick Roy, Etienne Hebert-Chatelain

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 38 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 2 institutions in 2 countries.

Marie-Ange Djeungoue-PetgaCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Olivier LuretteCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Stéphanie JeanCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Geneviève Hamel-CôtéCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Rebeca Martín-JiménezCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Marine BouCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada.
Astrid CannichEndocannabinoids and NeuroAdaptation, NeuroCentre, INSERM U1215, Bordeaux, France.
Patrick RoyDepartment of Chemistry and Biochemistry, Université de Moncton, Moncton, NB, Canada.
Etienne Hebert-ChatelainCanada Research Chair in Mitochondrial Signaling and Physiopathology, Moncton, NB, Canada. etienne.hebert.chatelain@umoncton.ca.
Université de Moncton · CAInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High levels and activity of Src kinase are common among breast cancer subtypes, and several inhibitors of the kinase are currently tested in clinical trials. Alterations in mitochondrial activity is also observed among the different types of breast cancer. Src kinase is localized in several subcellular compartments, including mitochondria where it targets several proteins to modulate the activity of the organelle. Although the subcellular localization of other oncogenes modulates the potency of known treatments, nothing is known about the specific role of intra-mitochondrial Src (mtSrc) in breast cancer. The aim of this work was to determine whether mtSrc kinase has specific impact on breast cancer cells. We first observed that activity of mtSrc is higher in breast cancer cells of the triple negative subtype. Over-expression of Src specifically targeted to mitochondria reduced mtDNA levels, mitochondrial membrane potential and cellular respiration. These alterations of mitochondrial functions led to lower cellular viability, shorter cell cycle and increased invasive capacity. Proteomic analyses revealed that mtSrc targets the mitochondrial single-stranded DNA-binding protein, a regulator of mtDNA replication. Our findings suggest that mtSrc promotes aggressiveness of breast cancer cells via phosphorylation of mitochondrial single-stranded DNA-binding protein leading to reduced mtDNA levels and mitochondrial activity. This study highlights the importance of considering the subcellular localization of Src kinase in the development of potent therapy for breast cancer.

Indexed as

Adenosine TriphosphateApoptosisBreast NeoplasmsCell MovementCell ProliferationCell RespirationDNA-Binding ProteinsDNA, MitochondrialFemaleHumansMCF-7 CellsMembrane Potential, MitochondrialMitochondriaPhosphorylationReactive Oxygen Speciessrc-Family KinasesAdenosine TriphosphateDNA-Binding ProteinsDNA, MitochondrialReactive Oxygen Speciessrc-Family Kinases

Identifiers

PMID31819039
PMCPMC6901437
OpenAlexW2992856652

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.