Evidence map›Paper›PMID 27129239›Full record

ArticleThe Journal of biological chemistry2016

RhoC GTPase Is a Potent Regulator of Glutamine Metabolism and N-Acetylaspartate Production in Inflammatory Breast Cancer Cells.

Michelle L Wynn, Joel A Yates, Charles R Evans, Lauren D Van Wassenhove, Zhi Fen Wu, Sydney Bridges, Liwei Bao, Chelsea Fournier, Sepideh Ashrafzadeh, Matthew J Merrins and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

  1. The Emerging Role of N-Acetylaspartate in Cancer.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Reprogramming the Immune Landscape of Inflammatory Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  5. Review
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  19. Ex VivoScientific reports · 2019
    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

14 authors at 5 institutions in 3 countries.

Michelle L WynnFrom the Departments of Internal Medicine, Molecular and Integrative Physiology, and.
Joel A YatesFrom the Departments of Internal Medicine.
Charles R EvansFrom the Departments of Internal Medicine.ORCID 0000-0001-6698-5330
Lauren D Van Wassenhovethe Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305.
Zhi Fen WuFrom the Departments of Internal Medicine.
Sydney BridgesFrom the Departments of Internal Medicine.
Liwei BaoFrom the Departments of Internal Medicine.
Chelsea FournierFrom the Departments of Internal Medicine.
Sepideh AshrafzadehFrom the Departments of Internal Medicine.
Matthew J Merrinsthe Department of Medicine, University of Wisconsin, Madison, Wisconsin 53705, and the William S. Middleton Memorial Veterans Hospital, Madison, Wisconsin 53705.ORCID 0000-0003-1599-9227
Leslie S SatinPharmacology, University of Michigan, Ann Arbor, Michigan 48109.
Santiago SchnellMolecular and Integrative Physiology, and.ORCID 0000-0002-9477-3914
Charles F BurantFrom the Departments of Internal Medicine.ORCID 0000-0001-9189-5003
Sofia D MerajverFrom the Departments of Internal Medicine, smerajve@umich.edu.
Laboratoire d’immunologie intégrative du cancer · FRSingapore Maritime Institute · SGStanford University · USUniversity of Michigan · USUniversity of Wisconsin–Madison · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Statistics and Bioinformatics Core - WangU24DK097153 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2012 to 2017
$10.1M
Cellular Biotechnology Training Program (CBTP)T32GM008353 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWENDEMAN, ANNA · 1991 to 2021
$9.3M
METABOLICALLY-COUPLED ION CHANNEL INTERACTIONS IN ISLETSR01DK046409 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SATIN, LESLIE S. · 1994 to 2023
$9.1M
Proteogenomics of Cancer Training ProgramT32CA140044 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAO, ARVIND, SARTOR, MAUREEN AGNES · 2010 to 2024
$3.9M
Metabolic flux in a model of reduced oxidative capacityK25DK092558 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EVANS, CHARLES ROBERT · 2011 to 2015
$700k
NCI NIH HHS P30 CA046592NCI NIH HHS T32 CA140044NIDDK NIH HHS K25 DK092558NIDDK NIH HHS R01 DK046409NIDDK NIH HHS U24 DK097153NIGMS NIH HHS T32 GM008353
6 · The paper itself

Abstract

Inflammatory breast cancer (IBC) is an extremely lethal cancer that rapidly metastasizes. Although the molecular attributes of IBC have been described, little is known about the underlying metabolic features of the disease. Using a variety of metabolic assays, including (13)C tracer experiments, we found that SUM149 cells, the primary in vitro model of IBC, exhibit metabolic abnormalities that distinguish them from other breast cancer cells, including elevated levels of N-acetylaspartate, a metabolite primarily associated with neuronal disorders and gliomas. Here we provide the first evidence of N-acetylaspartate in breast cancer. We also report that the oncogene RhoC, a driver of metastatic potential, modulates glutamine and N-acetylaspartate metabolism in IBC cells in vitro, revealing a novel role for RhoC as a regulator of tumor cell metabolism that extends beyond its well known role in cytoskeletal rearrangement.

Indexed as

Aspartic AcidCell Line, TumorFemaleGlutamineHumansInflammatory Breast NeoplasmsNeoplasm ProteinsrhoC GTP-Binding Proteinrho GTP-Binding ProteinsAspartic AcidGlutamineN-acetylaspartateNeoplasm ProteinsrhoC GTP-Binding ProteinRHOC protein, humanrho GTP-Binding Proteinsbreast cancerglutaminehypoxia-inducible factor (HIF)N-acetylaspartateRho (Rho GTPase)tumor metabolism

Identifiers

PMID27129239
PMCPMC4919454
OpenAlexW2343668821

What OpenQuestion holds

Textmetadata
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.