Evidence map›Paper›PMID 31542392›Full record

ArticleEBioMedicine2019

Mitochondrial fission factor is a novel Myc-dependent regulator of mitochondrial permeability in cancer.

Jae Ho Seo, Ekta Agarwal, Young Chan Chae, Yu Geon Lee, David S Garlick, Alessandra Maria Storaci, Stefano Ferrero, Gabriella Gaudioso, Umberto Gianelli, Valentina Vaira and 1 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 52 citations in OpenAlex.

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  12. The bioenergetic landscape of cancer.Molecular metabolism · 2024
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  18. Mitochondrial fragmentation is crucial for c-Myc-driven hepatoblastoma-like liver tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
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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

11 authors at 4 institutions in 3 countries.

Jae Ho SeoProstate Cancer Discovery and Development Program, USA; Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Ekta AgarwalProstate Cancer Discovery and Development Program, USA; Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA.
Young Chan ChaeProstate Cancer Discovery and Development Program, USA; Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA; School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea. Electronic address: ychae@unist.ac.kr.
Yu Geon LeeSchool of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.
David S GarlickHisto-Scientific Research Laboratories, Mount Jackson, VA 22842, USA.
Alessandra Maria StoraciDivision of Pathology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan 20122, Italy; Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy.
Stefano FerreroDivision of Pathology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan 20122, Italy; Department of Biomedical Surgical and Dental Sciences, University of Milan, Milan 20122, Italy.
Gabriella GaudiosoDivision of Pathology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan 20122, Italy.
Umberto GianelliDivision of Pathology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan 20122, Italy; Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy.
Valentina VairaDivision of Pathology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan 20122, Italy; Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy.
Dario C AltieriProstate Cancer Discovery and Development Program, USA; Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, PA 19104, USA. Electronic address: daltieri@wistar.org.
The Wistar Institute · USUniversity of Milan · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUlsan National Institute of Science and Technology · KR

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Role of Runx2 in prostate tumorigenesis and metastasisP01CA140043 · NCI · WISTAR INSTITUTE · PI ALTIERI, DARIO C · 2010 to 2021
$12.2M
Tumor PlasticityR35CA220446 · NCI · WISTAR INSTITUTE · PI ALTIERI, DARIO C · 2017 to 2023
$7.7M
Advancing Cancer Research through Comprehensive Proteomics and Metabolomics AnalysesR50CA221838 · NCI · WISTAR INSTITUTE · PI Hsin-Yao Tang · 2017 to 2026
$2.1M
Purchase of a Seahorse Bioscience XF AnalyzerS10OD023658 · OD · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2017 to 2017
$188k
NCI NIH HHS P01 CA140043NCI NIH HHS P30 CA010815NCI NIH HHS R35 CA220446NCI NIH HHS R50 CA221838NIH HHS S10 OD023658
6 · The paper itself

Abstract

backgroundMitochondrial functions are exploited in cancer and provide a validated therapeutic target. However, how this process is regulated has remained mostly elusive and the identification of new pathways that control mitochondrial integrity in cancer is an urgent priority.

methodsWe studied clinically-annotated patient series of primary and metastatic prostate cancer, representative cases of multiple myeloma (MM) and publicly available genetic databases. Gene regulation studies involved chromatin immunoprecipitation, PCR amplification and Western blotting of conditional Myc-expressing cell lines. Transient or stable gene silencing was used to quantify mitochondrial functions in bioenergetics, outer membrane permeability, Ca

findingsWe identified Mitochondrial Fission Factor (MFF) as a novel transcriptional target of oncogenic Myc overexpressed in primary and metastatic cancer, compared to normal tissues. Biochemically, MFF isoforms, MFF1 and MFF2 associate with the Voltage-Dependent Anion Channel-1 (VDAC1) at the mitochondrial outer membrane, in vivo. Disruption of this complex by MFF silencing induces general collapse of mitochondrial functions with increased outer membrane permeability, loss of inner membrane potential, Ca

interpretationAn MFF-VDAC1 complex is a novel regulator of mitochondrial integrity and actionable therapeutic target in cancer.

Indexed as

Cell Line, TumorCell Membrane PermeabilityCell ProliferationHumansMembrane Potential, MitochondrialMitochondriaMitochondrial DynamicsMitochondrial ProteinsNeoplasmsPermeabilityProto-Oncogene Proteins c-mycMitochondrial ProteinsProto-Oncogene Proteins c-mycCancer therapyCell deathMFFMitochondriaTumour metabolismVDAC1

Identifiers

PMID31542392
PMCPMC6838406
OpenAlexW2974819163

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.