Evidence map›Paper›PMID 28266149›Full record

ReviewCPT: pharmacometrics & systems pharmacology2017

IODNE: An integrated optimization method for identifying the deregulated subnetwork for precision medicine in cancer.

S Mounika Inavolu, J Renbarger, M Radovich, V Vasudevaraja, G H Kinnebrew, S Zhang, L Cheng

Open access · goldAbstract readReview
In one paragraph

Review in CPT: pharmacometrics & systems pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Network-based approaches for modeling disease regulation and progression.Computational and structural biotechnology journal · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Precision Medicine in Pharmacometrics and Systems Pharmacology.CPT: pharmacometrics & systems pharmacology · 2017
    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.

S Mounika InavoluCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
J RenbargerDepartment of Pediatrics, Hematology/Oncology, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
M RadovichCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
V VasudevarajaCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
G H KinnebrewCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
S ZhangCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
L ChengCenter for Computational Biology and Bioinformatics, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
Indiana University – Purdue University Indianapolis · USUrology of Indiana · US

Funding

Project 2: Biomarkers of endothelial dysfunction in pediatric patients receiving high intensity chemotherapy/irradiationU54HD090215 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI PACZESNY, SOPHIE · 2016 to 2018
$2.3M
NICHD NIH HHS U54 HD090215
6 · The paper itself

Abstract

Subnetwork analysis can explore complex patterns of entire molecular pathways for the purpose of drug target identification. In this article, the gene expression profiles of a cohort of patients with breast cancer are integrated with protein-protein interaction (PPI) networks using, simultaneously, both edge scoring and node scoring. A novel optimization algorithm, integrated optimization method to identify deregulated subnetwork (IODNE), is developed to search for the optimal dysregulated subnetwork of the merged gene and protein network. IODNE is applied to select subnetworks for Luminal-A breast cancer from The Cancer Genome Atlas (TCGA) data. A large fraction of cancer-related genes and the well-known clinical targets, ER1/PR and HER2, are found by IODNE. This validates the utility of IODNE. When applying IODNE to the triple-negative breast cancer (TNBC) subtype data, we identified subnetworks that contain genes such as ERBB2, HRAS, PGR, CAD, POLE, and SLC2A1.

Indexed as

Breast NeoplasmsCohort StudiesFemaleGene Regulatory NetworksGenetic TherapyHumansPrecision MedicineProtein Interaction Domains and MotifsTranscriptome

Identifiers

PMID28266149
PMCPMC5351413
OpenAlexW2591869837

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.