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TM4SF5-CTD-2354A18.1-miR-4697-3P may play a key role in the pathogenesis of gastric cancer.
Bratisl Lek Listy ; 116(10): 608-15, 2015.
Article in En | MEDLINE | ID: mdl-26531872
ABSTRACT

AIMS:

Our aim is to identify important lncRNAs and mRNAs which may play a key role in contributing to pathogenesis of gastric cancer.

METHODS:

Different LncRNAs and mRNAs are identified by microarray in gastric cancer tissue and corresponding normal tissues. The function and relationship of different LncRNAs and mRNAs is performed by GO analysis and Pathway analysis and made code-non-code network (CNC) by Pearson correlation coefficients (PCC). Then mRNA-miRNA relationship is predicted through mRNA-miRNA relationship software (http//www.targetscan.org). Lastly, mRNA-miRNA-LncRNA network is established for further research.

RESULTS:

The expression profiles of 3732 lncRNAs showed different expression (fold change (FC)≥2.0, p<0.05) in gastric cancer tissue and normal tissue and expression profiles of 3994 mRNAs also showed different expression (FC≥2.0, p<0.05) in gastric cancer and corresponding normal tissue.

CONCLUSION:

The expression of TM4SF5, CTD-2354A18.1 and miR-4697-3P is in balance at physiological conditions, however, the balance is disrupted by some situations, which may contribute to gastric cancer. GO analysis and Pathway analysis also showed TM4SF5 played an important role in proliferation, differentiation and apoptosis. Therefore, TM4SF5-miR-4697-3P- CTD-2354A18.1 may play a key role in the pathogenesis of gastric cancer (Tab. 2, Fig. 4, Ref. 30).
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Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / RNA, Neoplasm / Gene Expression Regulation, Neoplastic / Apoptosis / RNA, Long Noncoding / Membrane Proteins Type of study: Etiology_studies Limits: Humans Language: En Journal: Bratisl Lek Listy Year: 2015 Document type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / RNA, Neoplasm / Gene Expression Regulation, Neoplastic / Apoptosis / RNA, Long Noncoding / Membrane Proteins Type of study: Etiology_studies Limits: Humans Language: En Journal: Bratisl Lek Listy Year: 2015 Document type: Article
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