Evidence map›Paper›PMID 30760313›Full record

ArticleBiology direct2019

Integrative analysis based on survival associated co-expression gene modules for predicting Neuroblastoma patients' survival time.

Yatong Han, Xiufen Ye, Jun Cheng, Siyuan Zhang, Weixing Feng, Zhi Han, Jie Zhang, Kun Huang

Abstract read
In one paragraph

Article in Biology direct, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Liquid biopsies and cancer omics.Cell death discovery · 2020
    Review
  17. Review
  18. Article
  19. 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

8 authors.

Yatong HanDepartment of Automation, Harbin Engineering University, Harbin, China.
Xiufen YeDepartment of Automation, Harbin Engineering University, Harbin, China.
Jun ChengDepartment of Medicine, Indiana University School of Medicine, Indianapolis, USA.
Siyuan ZhangDepartment of Automation, Harbin Engineering University, Harbin, China.
Weixing FengDepartment of Automation, Harbin Engineering University, Harbin, China.
Zhi HanDepartment of Medicine, Indiana University School of Medicine, Indianapolis, USA.
Jie ZhangDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, USA.
Kun HuangDepartment of Medicine, Indiana University School of Medicine, Indianapolis, USA. kunhuang@iu.edu.ORCID 0000-0002-8530-370X

Funding

Informatics Links Between Histological Features and Genetics in CancerU01CA188547 · NCI · OHIO STATE UNIVERSITY · PI HUANG, KUN · 2015 to 2017
$1.2M
NCI NIH HHS U01 CA188547
6 · The paper itself

Abstract

backgroundMore than 90% of neuroblastoma patients are cured in the low-risk group while only less than 50% for those with high-risk disease can be cured. Since the high-risk patients still have poor outcomes, we need more accurate stratification to establish an individualized precise treatment plan for the patients to improve the long-term survival rate.

resultsWe focus on extracting features and providing a workflow to improve survival prediction for neuroblastoma patients. With a workflow for gene co-expression network (GCN) mining in microarray and RNA-Seq datasets, we extracted molecular features from each co-expressed module and summarized them into eigengenes. Then we adopted the lasso-regularized Cox proportional hazards model to select the most informative eigengene features regarding association to the risk of metastasis. Nine eigengenes were selected which show strong association with patient survival prognosis. All of the nine corresponding gene modules also have highly enriched biological functions or cytoband locations. Three of them are unique modules to RNA-Seq data, which complement the modules from microarray data in terms of survival prognosis. We then merged all eigengenes from these unique modules and used an integrative method called Similarity Network Fusion to test the prognostic power of these eigengenes for prognosis. The prognostic accuracies are significantly improved as compared to using all eigengenes, and a subgroup of patients with very poor survival rate was identified.

conclusionsWe first compared GCNs mined from microarray and RNA-seq data. We discovered that each data modality yields unique GCNs, which are enriched with clear biological functions. Then we do module unique analysis and use lasso-cox model to select survival-associated eigengenes. Integration of unique and survival-associated eigengenes from both data types provides complementary information that leads to more accurate survival prognosis. REVIEWERS: Reviewed by Susmita Datta, Marco Chierici and Dimitar Vassilev.

Indexed as

Gene Regulatory NetworksTranscriptomeAdolescentChildChild, PreschoolHumansInfantInfant, NewbornLongevityNeuroblastomaPrognosisProportional Hazards ModelsProtein Array AnalysisSequence Analysis, RNASurvival AnalysisYoung AdultGene co-expression networkIntegrative clusterNeuroblastoma survival time predict

Identifiers

PMID30760313
PMCPMC6375203

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.