Evidence map›Paper›PMID 34255770›Full record

ArticlePloS one2021

An experimental-mathematical approach to predict tumor cell growth as a function of glucose availability in breast cancer cell lines.

Jianchen Yang, Jack Virostko, David A Hormuth, Junyan Liu, Amy Brock, Jeanne Kowalski, Thomas E Yankeelov

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Stochastic pharmacodynamics of a heterogeneous tumour-cell population.Journal of pharmacokinetics and pharmacodynamics · 2025
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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

7 authors at 2 institutions in 1 country.

Jianchen YangDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, United States of America.
Jack VirostkoDepartment of Diagnostic Medicine, The University of Texas at Austin, Austin, Texas, United States of America.ORCID 0000-0003-3413-8801
David A HormuthLivestrong Cancer Institutes, The University of Texas at Austin, Austin, Texas, United States of America.ORCID 0000-0002-9643-1694
Junyan LiuDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, United States of America.
Amy BrockDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, United States of America.
Jeanne KowalskiDepartment of Oncology, The University of Texas at Austin, Austin, Texas, United States of America.ORCID 0000-0003-3458-3024
Thomas E YankeelovDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, United States of America.
Livestrong Foundation · USThe University of Texas at Austin · US

Funding

Quantitative MRI for Predicting Response of Breast Cancer to Neoadjuvant TherapyU01CA142565 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KARCZMAR, GREGORY S., NANDA, RITA · 2010 to 2019
$4.5M
Quantitative Multiscale Imaging to Optimize Cancer Treatment StrategiesR01CA186193 · NCI · VANDERBILT UNIVERSITY · PI QUARANTA, VITO, RERICHA, ERIN C · 2014 to 2019
$3.1M
Image Driven Multi-Scale Modeling to Predict Treatment Response in Breast CancerU01CA174706 · NCI · VANDERBILT UNIVERSITY · PI QUARANTA, VITO, YANKEELOV, THOMAS E · 2013 to 2018
$2.5M
Using label-free Raman microscopy to predict therapeutic resistance of TNBC cellsU01CA253540 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI BROCK, AMY, YANKEELOV, THOMAS E · 2020 to 2024
$2.1M
NCI NIH HHS R01 CA186193NCI NIH HHS U01 CA142565NCI NIH HHS U01 CA174706NCI NIH HHS U01 CA253540
6 · The paper itself

Abstract

We present the development and validation of a mathematical model that predicts how glucose dynamics influence metabolism and therefore tumor cell growth. Glucose, the starting material for glycolysis, has a fundamental influence on tumor cell growth. We employed time-resolved microscopy to track the temporal change of the number of live and dead tumor cells under different initial glucose concentrations and seeding densities. We then constructed a family of mathematical models (where cell death was accounted for differently in each member of the family) to describe overall tumor cell growth in response to the initial glucose and confluence conditions. The Akaikie Information Criteria was then employed to identify the most parsimonious model. The selected model was then trained on 75% of the data to calibrate the system and identify trends in model parameters as a function of initial glucose concentration and confluence. The calibrated parameters were applied to the remaining 25% of the data to predict the temporal dynamics given the known initial glucose concentration and confluence, and tested against the corresponding experimental measurements. With the selected model, we achieved an accuracy (defined as the fraction of measured data that fell within the 95% confidence intervals of the predicted growth curves) of 77.2 ± 6.3% and 87.2 ± 5.1% for live BT-474 and MDA-MB-231 cells, respectively.

Indexed as

Breast NeoplasmsCell ProliferationGlucoseCell Line, TumorFemaleGlycolysisHumansModels, BiologicalModels, TheoreticalGlucose

Identifiers

PMID34255770
PMCPMC8277046
OpenAlexW3179421927

What OpenQuestion 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 OpenQuestion graph.