Evidence map›Paper›PMID 29700304›Full record

ArticleNature communications2018

Dysregulation of mitochondrial dynamics proteins are a targetable feature of human tumors.

Gray R Anderson, Suzanne E Wardell, Merve Cakir, Catherine Yip, Yeong-Ran Ahn, Moiez Ali, Alexander P Yllanes, Christina A Chao, Donald P McDonnell, Kris C Wood

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
–field-weighted citation impact
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

89 citing papers in PubMed.

  1. Article
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  11. Dysregulation of Mitochondrial Function in Cancer Cells.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

29 more citing papers are in PubMed but not listed here.

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

10 authors.

Gray R AndersonDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Suzanne E WardellDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Merve CakirProgram in Computational Biology and Bioinformatics, Duke University, Durham, NC, 27710, USA.
Catherine YipDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Yeong-Ran AhnDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Moiez AliDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Alexander P YllanesDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Christina A ChaoDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Donald P McDonnellDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Kris C WoodDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA. kris.wood@duke.edu.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Interdisciplinary Research Careers in Women's HealthK12HD043446 · NICHD · DUKE UNIVERSITY · PI AMUNDSEN, CINDY · 2002 to 2023
$9.6M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Selectively targeting apoptosis in PIK3CA mutant colorectal cancersR01CA207083 · NCI · DUKE UNIVERSITY · PI WOOD, KRIS C. · 2016 to 2020
$1.8M
Unmasking targetable dependencies in cancer with intrinsic or acquired resistance to anti-cancer therapiesF99CA222728 · NCI · DUKE UNIVERSITY · PI ANDERSON, GRACE R · 2017 to 2018
$72k
Unmasking targetable dependencies in cancer with intrinsic or acquired resistance to anti-cancer therapiesK00CA222728 · NCI · STANFORD UNIVERSITY · PI ANDERSON, GRACE R · 2019 to 2019
$72k
NCI NIH HHS F99 CA222728NCI NIH HHS K00 CA222728NCI NIH HHS R01 CA207083NICHD NIH HHS K12 HD043446NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Altered mitochondrial dynamics can broadly impact tumor cell physiology. Using genetic and pharmacological profiling of cancer cell lines and human tumors, we here establish that perturbations to the mitochondrial dynamics network also result in specific therapeutic vulnerabilities. In particular, through distinct mechanisms, tumors with increased mitochondrial fragmentation or connectivity are hypersensitive to SMAC mimetics, a class of compounds that induce apoptosis through inhibition of IAPs and for which robust sensitivity biomarkers remain to be identified. Further, because driver oncogenes exert dominant control over mitochondrial dynamics, oncogene-targeted therapies can be used to sensitize tumors to SMAC mimetics via their effects on fission/fusion dynamics. Collectively, these data demonstrate that perturbations to the mitochondrial dynamics network induce targetable vulnerabilities across diverse human tumors and, more broadly, suggest that the altered structures, activities, and trafficking of cellular organelles may facilitate additional cancer therapeutic opportunities.

Indexed as

Mitochondrial DynamicsAnimalsAntineoplastic AgentsCell Line, TumorFemaleHumansMiceMice, NudeMitochondriaMitochondrial ProteinsNeoplasmsAntineoplastic AgentsMitochondrial Proteins

Identifiers

PMID29700304
PMCPMC5919970

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.