Evidence map›Paper›PMID 27625019›Full record

ArticleScientific reports2016

Subpathway-CorSP: Identification of metabolic subpathways via integrating expression correlations and topological features between metabolites and genes of interest within pathways.

Chenchen Feng, Jian Zhang, Xuecang Li, Bo Ai, Junwei Han, Qiuyu Wang, Taiming Wei, Yong Xu, Meng Li, Shang Li and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

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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

12 authors.

Chenchen FengSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Jian ZhangSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Xuecang LiSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Bo AiSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Junwei HanCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081,China.
Qiuyu WangSchool of Nursing, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Taiming WeiSchool of Pharmacy, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Yong XuThe fifth Affiliated Hospital of Harbin Medical University, Daqing 163319, China.
Meng LiSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Shang LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081,China.
Chao SongDepartment of Pharmacology, Daqing Campus, Harbin Medical University, Daqing 163319, China.
Chunquan LiSchool of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic pathway analysis is a popular strategy for comprehensively researching metabolites and genes of interest associated with specific diseases. However, the traditional pathway identification methods do not accurately consider the combined effect of these interesting molecules and neglects expression correlations or topological features embedded in the pathways. In this study, we propose a powerful method, Subpathway-CorSP, for identifying metabolic subpathway regions. This method improved on original pathway identification methods by using a subpathway identification strategy and emphasizing expression correlations between metabolites and genes of interest based on topological features within the metabolic pathways. We analyzed a prostate cancer data set and its metastatic sub-group data set with detailed comparison of Subpathway-CorSP with four traditional pathway identification methods. Subpathway-CorSP was able to identify multiple subpathway regions whose entire corresponding pathways were not detected by traditional pathway identification methods. Further evidences indicated that Subpathway-CorSP provided a robust and efficient way of reliably recalling cancer-related subpathways and locating novel subpathways by the combined effect of metabolites and genes. This was a novel subpathway strategy based on systematically considering expression correlations and topological features between metabolites and genes of interest within given pathways.

Indexed as

Biochemical PhenomenaGene Expression RegulationHumansMetabolic Networks and PathwaysNeoplasm MetastasisNeoplasm ProteinsNeoplasmsNeoplasm Proteins

Identifiers

PMID27625019
PMCPMC5021946

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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.