Evidence map›Paper›PMID 25057922›Full record

ArticlePLoS computational biology2014

Network analysis of breast cancer progression and reversal using a tree-evolving network algorithm.

Ankur P Parikh, Ross E Curtis, Irene Kuhn, Sabine Becker-Weimann, Mina Bissell, Eric P Xing, Wei Wu

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 96% 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

4 citing papers in PubMed, 0 citations in OpenAlex.

  1. The Good, the Bad and the Tick.Frontiers in cell and developmental biology · 2019
    Article
  2. Article
  3. Article
  4. Article
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.

Ankur P ParikhMachine Learning Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America.
Ross E CurtisLane Center for Computational Biology, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America.
Irene KuhnLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Sabine Becker-WeimannLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Mina BissellLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Eric P XingMachine Learning Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America; Lane Center for Computational Biology, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America; Joint Carnegie Mellon University-University of Pittsburgh PhD Program in Computational Biology, Pittsburgh, Pennsylvania, United States of America.
Wei WuLane Center for Computational Biology, School of Computer Science, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America.
Carnegie Mellon University · USLawrence Berkeley National Laboratory · US

Funding

Time/Space-Varying Networks of Molecular Interactions: A New Paradigm for StudyinR01GM093156 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI XING, ERIC P · 2010 to 2014
$2.2M
Definition of Microenvironment in Breast CancerR37CA064786 · NCI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BISSELL, MINA · 2009 to 2013
$2.0M
NCI NIH HHS R37 CA064786NIGMS NIH HHS R01 GM093156NIGMS NIH HHS R01 GM093156-01
6 · The paper itself

Abstract

The HMT3522 progression series of human breast cells have been used to discover how tissue architecture, microenvironment and signaling molecules affect breast cell growth and behaviors. However, much remains to be elucidated about malignant and phenotypic reversion behaviors of the HMT3522-T4-2 cells of this series. We employed a "pan-cell-state" strategy, and analyzed jointly microarray profiles obtained from different state-specific cell populations from this progression and reversion model of the breast cells using a tree-lineage multi-network inference algorithm, Treegl. We found that different breast cell states contain distinct gene networks. The network specific to non-malignant HMT3522-S1 cells is dominated by genes involved in normal processes, whereas the T4-2-specific network is enriched with cancer-related genes. The networks specific to various conditions of the reverted T4-2 cells are enriched with pathways suggestive of compensatory effects, consistent with clinical data showing patient resistance to anticancer drugs. We validated the findings using an external dataset, and showed that aberrant expression values of certain hubs in the identified networks are associated with poor clinical outcomes. Thus, analysis of various reversion conditions (including non-reverted) of HMT3522 cells using Treegl can be a good model system to study drug effects on breast cancer.

Indexed as

AlgorithmsBreast NeoplasmsCell Line, TumorComputational BiologyComputer SimulationDatabases, FactualDisease ProgressionFemaleGene Regulatory NetworksHumansKaplan-Meier EstimateMarkov ChainsOligonucleotide Array Sequence Analysis

Identifiers

PMID25057922
PMCPMC4109850
OpenAlexW1536179049

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.