Evidence map›Paper›PMID 34112093›Full record

ArticleBMC genomics2021

A novel method to identify gene interaction patterns.

Xinguo Lu, Fang Liu, Qiumai Miao, Ping Liu, Yan Gao, Keren He

Abstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

6 authors.

Xinguo LuCollege of Computer Science and Electronic Engineering, Hunan University, Lushan Nan Road, Changsha, 410082, China. hnluxinguo@126.com.ORCID http://orcid.org/0000-0001-8607-8121
Fang LiuCollege of Computer Science and Electronic Engineering, Hunan University, Lushan Nan Road, Changsha, 410082, China.
Qiumai MiaoCollege of Computer Science and Electronic Engineering, Hunan University, Lushan Nan Road, Changsha, 410082, China.
Ping LiuHunan Want Want Hospital, Renmin Zhong Road, Changsha, 410006, China.
Yan GaoCollege of Computer Science and Electronic Engineering, Hunan University, Lushan Nan Road, Changsha, 410082, China.
Keren HeCollege of Computer Science and Electronic Engineering, Hunan University, Lushan Nan Road, Changsha, 410082, China.

Funding

National Natural Science Foundation of China Grant No. 61972141Natural Science Foundation of?Hunan Province Grant No. 2018JJ2053
6 · The paper itself

Abstract

backgroundGene interaction patterns, including modules and motifs, can be used to identify cancer specific biomarkers and to reveal the mechanism of tumorigenesis. Most of the existing module network inferencing methods focus on gene independent functional patterns, while the studies of overlapping characteristics between modules are lacking. The objective of this study was to reveal the functional overlapping patterns in gene modules, helping elucidate the regulatory relationship between overlapping genes and communities, as well as to explore cancer formation and progression.

resultsWe analyzed six cancer datasets from The Cancer Genome Atlas and obtained three kinds of gene functional modules for each cancer, including Independent-Community, Dependent-Community and Merged-Community. In the six cancers, 59(3.5%) Independent-Communities were identified, while 1631(96.5%) Dependent-Communities were acquired. Compared with Lemon-Tree and K-Means, the gene communities identified by our method were enriched in more known GO categories with lower p-values. Meanwhile, those identified distinguishing communities can significantly distinguish the survival prognostic of patients by Kaplan-Meier analysis. Furthermore, identified driver genes in the gene communities can be considered as biomarkers which can accurately distinguish the tumour or normal samples for each cancer type.

conclusionsIn all identified communities, Dependent-Communities are the majority. Our method is more effective than the other two methods which do not consider the overlapping characteristics of modules. This indicates that overlapping genes are located in different specific functional groups, and a communication bridge is established between the communities to construct a comprehensive carcinogenesis.

Indexed as

Gene Regulatory NetworksNeoplasmsCarcinogenesisGene Expression ProfilingHumansKaplan-Meier EstimatePrognosisGene communitiesModule networkProtein-protein interaction

Identifiers

PMID34112093
PMCPMC8194229

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.