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. 2019 Dec 17;2019:1372571. doi: 10.1155/2019/1372571

Table 1.

Functional and pathway enrichment analyses of the DEGs in trastuzumab-resistant gastric cancer.

Category Description Count P value
GO function BP Type I interferon signaling pathway 13 1.04E − 09
BP Negative regulation of viral genome replication 10 2.46E − 08
BP Cell proliferation 23 5.99E − 07
BP Positive regulation of apoptotic process 18 2.51E − 05
BP Extracellular matrix organization 13 1.92E − 04
CC Extracellular exosome 90 1.28E − 09
CC Intermediate filament 11 2.26E − 05
CC Cytoplasm 122 3.98E − 05
CC Proteinaceous extracellular matrix 16 5.65E − 05
CC Basolateral plasma membrane 13 5.98E − 05
MF Structural molecule activity 17 8.93E − 06
MF Calcium ion binding 27 4.52E − 04
MF Protein homodimerization activity 26 1.31E − 03
MF 2′-5′-oligoadenylate synthetase activity 3 1.83E − 03
MF Fibronectin binding 4 1.06E − 02

KEGG pathway
hsa05200 Pathways in cancer 18 5.47E − 04
hsa04550 Signaling pathways regulating pluripotency of stem cells 8 1.22E − 02
hsa05166 HTLV-I infection 11 1.56E − 02
hsa04512 ECM-receptor interaction 6 1.91E − 02
hsa05230 Central carbon metabolism in cancer 5 2.68E − 02

Note: top five terms were selected according to P value. Abbreviation: DEGs: differentially expressed genes; GO: gene ontology; BP: biological process; CC: cellular component; MF: molecular function; HTLV-I: human T lymphocyte virus-I; ECM: extracellular matrix.