Evidence map›Paper›PMID 31528097›Full record

ArticleWorld journal of gastroenterology2019

Integrative analysis of the inverse expression patterns in pancreas development and cancer progression.

Hong-Liang Zang, Guo-Min Huang, Hai-Ying Ju, Xiao-Feng Tian

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2019. 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
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1 · What the graph read from it

What it found

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2 · The registry

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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

3 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

4 authors.

Hong-Liang ZangDepartment of Hepatobiliary and Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, Jilin Province, China.
Guo-Min HuangDepartment of Hepatobiliary and Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, Jilin Province, China.
Hai-Ying JuDepartment of Hematology, Jilin Province Blood Center, Changchun 130000, Jilin Province, China.
Xiao-Feng TianDepartment of Hepatobiliary and Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, Jilin Province, China. chuie03755@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs the malignant tumor, pancreatic cancer with a meager 5-years survival rate has been widely concerning. However, the molecular mechanisms that result in malignant transformation of pancreatic cells remain elusive.

aimTo investigate the gene expression profiles in normal or malignant transformed pancreas development.

methodsMaSigPro and ANOVA were performed on two pancreas development datasets downloaded from the Gene Expression Omnibus database. Six pancreatic cancer datasets collected from TCGA database were used to establish differentially expressed genes related to pancreas development and pancreatic cancer. Moreover, gene clusters with highly similar interpretation patterns between pancreas development and pancreatic cancer progression were established by self-organizing map and singular value decomposition. Additionally, the hypergeometric test was performed to compare the corresponding interpretation patterns. Abnormal regions of metabolic pathway were analyzed using the Sub-pathway-GM method.

resultsThis study established the continuously upregulated and downregulated genes at different stages in pancreas development and progression of pancreatic cancer. Through analysis of the differentially expressed genes, we established the inverse and consistent direction development-cancer pattern associations. Based on the application of the Subpathway-GM analysis, we established 17 significant metabolic sub-pathways that were closely associated with pancreatic cancer. Of note, the most significant metabolites sub-pathway was related to glycerophospholipid metabolism.

conclusionThe inverse and consistent direction development-cancer pattern associations were established. There was a significant correlation in the inverse patterns, but not consistent direction patterns.

Indexed as

Gene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticCell Transformation, NeoplasticDatasets as TopicDisease ProgressionFemaleGene Expression ProfilingHomeodomain ProteinsHumansMaleMetabolic Networks and PathwaysOligonucleotide Array Sequence AnalysisPancreasPancreatic NeoplasmsTrans-ActivatorsHomeodomain Proteinspancreatic and duodenal homeobox 1 proteinTrans-ActivatorsInverse patternMetabolites subpathwayPancreas developmentPancreatic cancer

Identifiers

PMID31528097
PMCPMC6718033

What Socratic holds

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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 Socratic graph.