Evidence map›Paper›PMID 37248394›Full record

ArticleNature cancer2023

Limiting mitochondrial plasticity by targeting DRP1 induces metabolic reprogramming and reduces breast cancer brain metastases.

Pravat Kumar Parida, Mauricio Marquez-Palencia, Suvranil Ghosh, Nitin Khandelwal, Kangsan Kim, Vidhya Nair, Xiao-Zheng Liu, Hieu S Vu, Lauren G Zacharias, Paula I Gonzalez-Ericsson and 12 more

Open access · greenAbstract read
In one paragraph

Article in Nature cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
12.8field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  8. Strategies for Targeting Mitochondria in the Treatment of Breast Cancer.ACS pharmacology & translational science · 2026
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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 5 institutions in 2 countries.

Pravat Kumar ParidaDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mauricio Marquez-PalenciaDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Suvranil GhoshDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Nitin KhandelwalDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Kangsan KimDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Vidhya NairDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Xiao-Zheng LiuDepartment of Biomedicine, University of Bergen, Bergen, Norway.
Hieu S VuChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lauren G ZachariasChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Paula I Gonzalez-EricssonBreast Cancer Research Program, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-6292-6963
Melinda E SandersDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Bret C MobleyDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Jeffrey G McDonaldCenter for Human Nutrition and Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-1570-4142
Andrew LemoffDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yan PengDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Cheryl LewisDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Gonçalo ValeCenter for Human Nutrition and Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-1104-0289
Nils HalbergDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0002-2943-3147
Carlos L ArteagaHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-0870-9586
Ariella B HankerHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-8655-8341
Ralph J DeBerardinisHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-2705-7432
Srinivas MalladiDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Srinivas.malladi@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-0829-2365
The University of Texas Southwestern Medical Center · USVanderbilt University Medical Center · USUniversity of Bergen · NOHoward Hughes Medical Institute · USSouthwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Kathryn Ann O'Donnell · 2010 to 2026
$53.7M
Metabolic Regulators of Tumor Growth and ProgressionR35CA220449 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI RALPH J DEBERARDINIS · 2017 to 2026
$9.4M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA142543NCI NIH HHS R35 CA220449NIDDK NIH HHS P30 DK127984
6 · The paper itself

Abstract

Disseminated tumor cells with metabolic flexibility to utilize available nutrients in distal organs persist, but the precise mechanisms that facilitate metabolic adaptations remain unclear. Here we show fragmented mitochondrial puncta in latent brain metastatic (Lat) cells enable fatty acid oxidation (FAO) to sustain cellular bioenergetics and maintain redox homeostasis. Depleting the enriched dynamin-related protein 1 (DRP1) and limiting mitochondrial plasticity in Lat cells results in increased lipid droplet accumulation, impaired FAO and attenuated metastasis. Likewise, pharmacological inhibition of DRP1 using a small-molecule brain-permeable inhibitor attenuated metastatic burden in preclinical models. In agreement with these findings, increased phospho-DRP1 expression was observed in metachronous brain metastasis compared with patient-matched primary tumors. Overall, our findings reveal the pivotal role of mitochondrial plasticity in supporting the survival of Lat cells and highlight the therapeutic potential of targeting cellular plasticity programs in combination with tumor-specific alterations to prevent metastatic recurrences.

Indexed as

Brain NeoplasmsBreast NeoplasmsCell Line, TumorDynaminsFemaleHumansMitochondriaDynamins

Identifiers

PMID37248394
PMCPMC11290463
OpenAlexW4378648504

What Socratic 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 Socratic graph.