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pmid:30774815

SRC and TP53 play critical role in low-grade dysplasia colorectal mucosa transformation into cancer.

Hamid Asadzadeh-Aghdaei · Mona Zamanian Azodi · Reza Vafaee · Hamideh Moravvej Farshi · Nosratollah Naderi

Gastroenterology and hepatology from bed to bench · 2018

Paper

partial

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
SRC and TP53 play critical role in low-grade dysplasia colorectal mucosa transformation into cancer.
doi
null
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30774815
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[0]
Hamid Asadzadeh-Aghdaei
[1]
Mona Zamanian Azodi
[2]
Reza Vafaee
[3]
Hamideh Moravvej Farshi
[4]
Nosratollah Naderi
journal
Gastroenterology and hepatology from bed to bench
year
2018
abstract
AIM: Determination of crucial genes that are involved in onset and progress of dysplasia of colorectal mucosa is the aim of this study. BACKGROUND: Management of dysplasia as one of the risk factors of colon cancer is very challenging. Molecular studies could be helpful in this matter. Here, the transcriptome profile of low-grade dysplasia in colon tissue in comparison with normal one is studied by protein-protein interaction (PPI) network analysis. METHODS: For detecting differentially expressed genes (DEGs) of dysplasia lesion, the data was downloaded from the gene chip GSE31106, platform GPL1261, GSM770092-94 as normal colorectal mucosa group and GSM770098-100 as low-grade dysplasia colorectal mucosa from the Gene Expression Omnibus database (GEO). The expression profile is evaluated by GEO2R and a network of DEGs is constructed and analyzed by Cytoscape algorithms. RESULTS: The findings indicate that a PPI network analysis of 113 DEGs is consist of 8 nodes that 6 of them are common with inflammation state. Only SRC and TP53 were recognized as the specific makers for dysplasia. In this respect, a subnetwork of these two genes introduce a panel of 8 nodes consist of HRAS, MYC, PIK3CA, PIK3CB, PIK3CD, PIK3CG, SRC, and TP53. CONCLUSION: It can be concluded that SRC and TP53 may play prominent role in dysplasia pathogenicity after running validation tests.
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Gene expression profiles were matched via boxplot analysis and p-value <0.05 was considered for significant findings.
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Expression data for the different phases of ulcerative colitis-associated carcinogenesis in a mouse model
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Molecular studies could be helpful in this matter. Here, the transcriptome profile of low-grade dysplasia in colon tissue in comparison with normal one is studied by protein-protein interaction (PPI) network analysis.\nMETHODS: For detecting differentially expressed genes (DEGs) of dysplasia lesion, the data was downloaded from the gene chip GSE31106, platform GPL1261, GSM770092-94 as normal colorectal mucosa group and GSM770098-100 as low-grade dysplasia colorectal mucosa from the Gene Expression Omnibus database (GEO). The expression profile is evaluated by GEO2R and a network of DEGs is constructed and analyzed by Cytoscape algorithms.\nRESULTS: The findings indicate that a PPI network analysis of 113 DEGs is consist of 8 nodes that 6 of them are common with inflammation state. Only SRC and TP53 were recognized as the specific makers for dysplasia. In this respect, a subnetwork of these two genes introduce a panel of 8 nodes consist of HRAS, MYC, PIK3CA, PIK3CB, PIK3CD, PIK3CG, SRC, and TP53.\nCONCLUSION: It can be concluded that SRC and TP53 may play prominent role in dysplasia pathogenicity after running validation tests.", "claims": [{"id": "claim-method", "statement": "Gene expression profiles were matched via boxplot analysis and p-value <0.05 was considered for significant findings.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30774815", "locator": "sections[2] \"Methods\" paragraph 7", "quote": "Gene expression profiles were matched via boxplot analysis and p-value <0.05 was considered for significant findings."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Series GSE31106, platform GPL1261, GSM770092-94 as normal colorectal mucosa group and GSM770098-100 as low-grade dysplasia colorectal mucosa group were downloaded from GEO database.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:30774815", "locator": "sections[2] \"Methods\" paragraph 3", "quote": "Series GSE31106, platform GPL1261, GSM770092-94 as normal colorectal mucosa group and GSM770098-100 as low-grade dysplasia colorectal mucosa group were downloaded from GEO database."}], "state": "complete"}], "gaps": ["doi"]}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:30774815"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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