Evidence map›Paper›PMID 33549532›Full record

ArticleBiochimica et biophysica acta. Bioenergetics2021

Structural and functional remodeling of mitochondria as an adaptive response to energy deprivation.

Andrey V Kuznetsov, Sabzali Javadov, Raimund Margreiter, Michael Grimm, Judith Hagenbuchner, Michael J Ausserlechner

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Bioenergetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 22 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

6 authors at 2 institutions in 2 countries.

Andrey V KuznetsovCardiac Surgery Research Laboratory, Department of Cardiac Surgery, Innsbruck Medical University, Innsbruck, Austria; Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: andrey.kuznetsov@tirol-kliniken.at.
Sabzali JavadovDepartment of Physiology, School of Medicine, University of Puerto Rico, San Juan, PR, USA. Electronic address: sabzali.javadov@upr.edu.
Raimund MargreiterDepartment of Visceral, Transplant and Thoracic Surgery, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: raimund.margreiter@tirol-kliniken.at.
Michael GrimmCardiac Surgery Research Laboratory, Department of Cardiac Surgery, Innsbruck Medical University, Innsbruck, Austria. Electronic address: michael.grimm@tirol-kliniken.at.
Judith HagenbuchnerDepartment of Pediatrics II, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: judith.hagenbuchner@i-med.ac.at.
Michael J AusserlechnerDepartment of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: michael.j.ausserlechner@i-med.ac.at.
Innsbruck Medical University · ATUniversity of Puerto Rico System · PR

Funding

Crosstalk between mitochondrial permeability transition and ETC supercomplexes in myocardial infarctionSC1GM128210 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI JAVADOV, SABZALI · 2017 to 2019
$1.1M
Austrian Science Fund FWF I 3089NIGMS NIH HHS SC1 GM128210
6 · The paper itself

Abstract

Cancer cells bioenergetics is more dependent on glycolysis than mitochondrial oxidative phosphorylation, a phenomenon known as the Warburg Effect. It has been proposed that inhibition of glycolysis may selectively affect cancer cells. However, the effects of glycolysis inhibition on mitochondrial function and structure in cancer cells are not completely understood. Here, we investigated the comparative effects of 2-deoxy-d-glucose (2-DG, a glucose analogue, which suppresses cellular glycolysis) on cellular bioenergetics in human colon cancer DLD-1 cells, smooth muscle cells, human umbilical vein endothelial cells and HL-1 cardiomyocytes. In all cells, 2-DG treatment resulted in significant ATP depletion, however, the cell viability remained unchanged. Also, we did not observe the synergistic effects of 2-DG with anticancer drugs doxorubicin and 5-fluorouracil. Instead, after 2-DG treatment and ATP depletion, mitochondrial respiration and membrane potential were significantly enhanced and mitochondrial morphology changed in the direction of more network organization. Analysis of protein expression demonstrated that 2-DG treatment induced an activation of AMPK (elevated pAMPK/AMPK ratio), increased mitochondrial fusion (mitofusins 1 and 2) and decreased fission (Drp1) proteins. In conclusion, this study suggests a strong link between respiratory function and structural organization of mitochondria in the cell. We propose that the functionality of the mitochondrial network is enhanced compared to disconnected mitochondria.

Indexed as

Energy MetabolismOxidative PhosphorylationAdenosine TriphosphateAntineoplastic AgentsCell ProliferationColonic NeoplasmsDeoxyglucoseGlycolysisHumansHuman Umbilical Vein Endothelial CellsMitochondriaMitochondrial DynamicsAdenosine TriphosphateAntineoplastic AgentsDeoxyglucose2-deoxy-d-glucoseCancer cellsCellular ATPEnergy stressGlucose metabolismMitochondriaMitochondrial dynamics/networkMitochondrial functionMitochondrial membrane potential

Identifiers

PMID33549532
PMCPMC9022200
OpenAlexW3128502371

What OpenQuestion holds

Textmetadata
LicenceTDM
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.