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Identification of Potential Biomarkers with Diagnostic Value in Pituitary Adenomas Using Prediction Analysis for Microarrays Method

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Abstract

Pituitary adenomas are the most common intrasellar tumors. Patients should be identified at an early stage so that effective treatment can be implemented. The study aims at detecting the potential biomarkers with diagnostic value of pituitary adenomas. Using a total of seven gene expression profiles (GEPs) of the datasets from the Gene Expression Omnibus (GEO) database, we first screened 1980 significant differentially expressed genes (DEGs). Then, we employed the prediction analysis for microarray (PAM) algorithm to identify 340 significant DEGs able to differ pituitary tumor from normal samples, which include 208 upregulated DEGs and 132 downregulated DEGs. DAVID database was used to carry out the enrichment analysis on Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) pathways. We found that upregulated candidates were enriched in protein folding and metabolic pathways. Downregulated DEGs saw a significant enrichment in insulin receptor signaling pathway and hedgehog signaling pathway. Based on the protein-protein interaction (PPI) network as well as module analysis, we determined ten hub genes including PHLPP, ENO2, ACTR1A, EHHADH, EHMT2, FOXO1, DLD, CCT2, CSNK1D, and CETN2 that could be potential biomarkers with diagnostic value in pituitary adenomas. In conclusion, the study contributes to reliable and potential molecular biomarkers with diagnostic value. Moreover, these potential biomarkers may be used for prognosis and new therapeutic targets for the pituitary adenomas.

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Availability of Data and Materials

The datasets generated during this study are available in the online GEO database (https://www.ncbi.nlm.nih.gov/geo/).

Abbreviations

BP:

Biological process

CC:

Cellular constituent

DEGs:

Differentially expressed genes

EHHADH:

Enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase

ENO2:

Enolase 2

FC:

Fold change

FDR:

False discovery rate

FOXO1:

Forkhead box O1

GEO:

Gene Expression Omnibus

GEPs:

Gene expression profiles

GO:

Gene Ontology

HCC:

Hepatocellular carcinoma cell

KEGG:

Kyoto Encyclopedia of Genes and Genomes

MF:

Molecular function

PAM:

Prediction analysis for microarray

PHLPP:

PH domain leucine-rich repeat protein phosphatase

PPI:

Protein-protein interaction

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Funding

This work was supported by the National Natural Science Foundation of China (Grant No. 81702643, 81770980, 81570906), China Postdoctoral Science Foundation (Grant No. 2017M611586), Science Project of Shanghai (Grant No. 14DZ2260300), Science Project of Shanghai Municipal Commission of Health and Family Planning (Grant No. 201540173), Shanghai sailing program (Grant No.16YF1403400), and The Second Military Medical University Project (Grant No. 2017JS18).

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Correspondence to Jianchun Liao or Hao Wu.

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The authors declare that they have no competing interests.

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Peng, H., Deng, Y., Wang, L. et al. Identification of Potential Biomarkers with Diagnostic Value in Pituitary Adenomas Using Prediction Analysis for Microarrays Method. J Mol Neurosci 69, 399–410 (2019). https://doi.org/10.1007/s12031-019-01369-x

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  • DOI: https://doi.org/10.1007/s12031-019-01369-x

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