Evidence map›Paper›PMID 27080907›Full record

ArticleScientific reports2016

Unique fractal evaluation and therapeutic implications of mitochondrial morphology in malignant mesothelioma.

Frances E Lennon, Gianguido C Cianci, Rajani Kanteti, Jacob J Riehm, Qudsia Arif, Valeriy A Poroyko, Eitan Lupovitch, Wickii Vigneswaran, Aliya Husain, Phetcharat Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

  1. Dysregulation of Mitochondrial Function in Cancer Cells.International journal of molecular sciences · 2025
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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

14 authors at 5 institutions in 1 country.

Frances E LennonDepartment of Medicine, Section of Hematology/Oncology and the Comprehensive Cancer Center, University of Chicago, Chicago, IL, 60637, USA.
Gianguido C CianciDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Rajani KantetiDepartment of Medicine, Section of Hematology/Oncology and the Comprehensive Cancer Center, University of Chicago, Chicago, IL, 60637, USA.
Jacob J RiehmDepartment of Medicine, Section of Hematology/Oncology and the Comprehensive Cancer Center, University of Chicago, Chicago, IL, 60637, USA.
Qudsia ArifDepartment of Pathology, University of Chicago, Chicago, IL, 60637, USA.
Valeriy A PoroykoDepartment of Medical Oncology and Therapeutics Research, City of Hope, Duarte, CA 91010, USA.
Eitan LupovitchUniversity of Maryland, College Park, MD, 20742, USA.
Wickii VigneswaranDepartment of Surgery, University of Chicago, Chicago, IL, 60637, USA.
Aliya HusainDepartment of Pathology, University of Chicago, Chicago, IL, 60637, USA.
Phetcharat ChenDepartment of Medicine, Section of Cardiology, University of Chicago, Chicago, IL, 60637, USA.
James K LiaoDepartment of Medicine, Section of Cardiology, University of Chicago, Chicago, IL, 60637, USA.
Martin SattlerDepartment of Medicine, Hematology/Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Hedy L KindlerDepartment of Medicine, Section of Hematology/Oncology and the Comprehensive Cancer Center, University of Chicago, Chicago, IL, 60637, USA.
Ravi SalgiaDepartment of Medicine, Section of Hematology/Oncology and the Comprehensive Cancer Center, University of Chicago, Chicago, IL, 60637, USA.
University of Chicago · USCity of Hope · USDana-Farber Cancer Institute · USNorthwestern University · USUniversity of Maryland, College Park · US

Funding

LIPOPROTEINS EFFECTS ON G PROTEIN FUNCTIONR01HL052233 · NHLBI · UNIVERSITY OF CHICAGO · PI LIAO, JAMES KUANG-JAN · 1995 to 2016
$5.3M
Novel Signaling Pathways in Ischemic StrokeR01NS070001 · NINDS · UNIVERSITY OF CHICAGO · PI LIAO, JAMES KUANG-JAN · 2010 to 2014
$1.8M
ROCK and ObesityR01DK085006 · NIDDK · UNIVERSITY OF CHICAGO · PI LIAO, JAMES KUANG-JAN · 2010 to 2014
$1.7M
NHLBI NIH HHS HL052233NHLBI NIH HHS R01 HL052233NIDDK NIH HHS DK085006NIDDK NIH HHS R01 DK085006NINDS NIH HHS R01 NS070001
6 · The paper itself

Abstract

Malignant mesothelioma (MM), is an intractable disease with limited therapeutic options and grim survival rates. Altered metabolic and mitochondrial functions are hallmarks of MM and most other cancers. Mitochondria exist as a dynamic network, playing a central role in cellular metabolism. MM cell lines display a spectrum of altered mitochondrial morphologies and function compared to control mesothelial cells. Fractal dimension and lacunarity measurements are a sensitive and objective method to quantify mitochondrial morphology and most importantly are a promising predictor of response to mitochondrial inhibition. Control cells have high fractal dimension and low lacunarity and are relatively insensitive to mitochondrial inhibition. MM cells exhibit a spectrum of sensitivities to mitochondrial inhibitors. Low mitochondrial fractal dimension and high lacunarity correlates with increased sensitivity to the mitochondrial inhibitor metformin. Lacunarity also correlates with sensitivity to Mdivi-1, a mitochondrial fission inhibitor. MM and control cells have similar sensitivities to cisplatin, a chemotherapeutic agent used in the treatment of MM. Neither oxidative phosphorylation nor glycolytic activity, correlated with sensitivity to either metformin or mdivi-1. Our results suggest that mitochondrial inhibition may be an effective and selective therapeutic strategy in mesothelioma, and identifies mitochondrial morphology as a possible predictor of response to targeted mitochondrial inhibition.

Indexed as

FractalsCell Line, TumorCisplatinGlycolysisHumansLung NeoplasmsMesotheliomaMesothelioma, MalignantMetforminMitochondriaMitochondrial ProteinsCisplatinMetforminMitochondrial Proteins

Identifiers

PMID27080907
PMCPMC4832330
OpenAlexW2335851379

What OpenQuestion holds

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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.