Evidence map›Paper›PMID 27743905›Full record

ArticleEBioMedicine2016

Collagen Matrix Density Drives the Metabolic Shift in Breast Cancer Cells.

Brett A Morris, Brian Burkel, Suzanne M Ponik, Jing Fan, John S Condeelis, Julio A Aguirre-Ghiso, James Castracane, John M Denu, Patricia J Keely

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

83 citing papers in PubMed, 2 syntheses or guidelines pooled it, 126 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  6. Article
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  10. Article
  11. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
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  13. Article
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23 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

9 authors at 6 institutions in 1 country.

Brett A MorrisDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, United States.
Brian BurkelDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, United States; Department of Biomedical Engineering, University of Wisconsin-Madison, United States.
Suzanne M PonikDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, United States. Electronic address: ponik@wisc.edu.
Jing FanWisconsin Institute for Discovery and Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin-Madison, United States; Morgridge Institute for Research, Madison, WI, United States.
John S CondeelisDept. of Anatomy & Structural Biology, Albert Einstein College of Medicine, United States.
Julio A Aguirre-GhisoDivision of Hematology and Oncology, Department of Medicine, Tisch Cancer Institute, Mount Sinai School of Medicine, United States; Department of Otolaryngology, Tisch Cancer Institute, Mount Sinai School of Medicine, United States; Department of Oncological Sciences, Tisch Cancer Institute, Mount Sinai School of Medicine, United States; Black Family Stem Cell Institute, Mount Sinai School of Medicine, United States.
James CastracaneColleges of Nanoscale Science and Engineering (CNSE), SUNY Polytechnic Institute, United States.
John M DenuWisconsin Institute for Discovery and Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin-Madison, United States; Morgridge Institute for Research, Madison, WI, United States.
Patricia J KeelyDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, United States; Paul C. Carbone Cancer Center, University of Wisconsin-Madison, United States.
California Institute for Regenerative Medicine · USMorgridge Institute for Research · USAlbert Einstein College of Medicine · USIcahn School of Medicine at Mount Sinai · USSUNY Polytechnic Institute · USUniversity of Wisconsin–Madison · US

Funding

Tumor Progression and MetastasisP01CA100324 · NCI · YESHIVA UNIVERSITY · PI CONDEELIS, JOHN S · 2003 to 2018
$30.0M
INTEGRATED TRAINING FOR PHYSICIAN-SCIENTISTST32GM008692 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BURKARD, MARK E · 1998 to 2020
$10.3M
Biology of Aging and Age-Related Diseases Training GrantT32AG000213 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Rozalyn M. Anderson, Sanjay Asthana · 1991 to 2026
$9.9M
Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
Tumor microenvironments determing migration, dissemination and dormancyU54CA163131 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AGUIRRE-GHISO, JULIO A., CASTRACANE, JAMES · 2011 to 2015
$3.9M
Molecular mechanisms of histone modification - Alzheimer’s supplement NOT-AG-18-008R37GM059785 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI DENU, JOHN M · 2013 to 2022
$3.7M
NCI NIH HHS P01 CA100324NCI NIH HHS R01 CA109182NCI NIH HHS U54 CA163131NIA NIH HHS T32 AG000213NIGMS NIH HHS R37 GM059785NIGMS NIH HHS T32 GM008692
6 · The paper itself

Abstract

Increased breast density attributed to collagen I deposition is associated with a 4-6 fold increased risk of developing breast cancer. Here, we assessed cellular metabolic reprogramming of mammary carcinoma cells in response to increased collagen matrix density using an in vitro 3D model. Our initial observations demonstrated changes in functional metabolism in both normal mammary epithelial cells and mammary carcinoma cells in response to changes in matrix density. Further, mammary carcinoma cells grown in high density collagen matrices displayed decreased oxygen consumption and glucose metabolism via the tricarboxylic acid (TCA) cycle compared to cells cultured in low density matrices. Despite decreased glucose entry into the TCA cycle, levels of glucose uptake, cell viability, and ROS were not different between high and low density matrices. Interestingly, under high density conditions the contribution of glutamine as a fuel source to drive the TCA cycle was significantly enhanced. These alterations in functional metabolism mirrored significant changes in the expression of metabolic genes involved in glycolysis, oxidative phosphorylation, and the serine synthesis pathway. This study highlights the broad importance of the collagen microenvironment to cellular expression profiles, and shows that changes in density of the collagen microenvironment can modulate metabolic shifts of cancer cells.

Indexed as

Energy MetabolismBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalCitric Acid CycleCollagenExtracellular MatrixFemaleGene Expression Regulation, NeoplasticGlucoseGlutamineHumansMitochondriaModels, BiologicalOxygenCollagenGlucoseGlutamineOxygenReactive Oxygen SpeciesBreast cancerCollagenMatrix densityMetabolism

Identifiers

PMID27743905
PMCPMC5264313
OpenAlexW2530608816

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.