Abstract |
Fascin-1 (FSCN1) is an actin-bundling protein that induces cell membrane protrusions, increases cell motility, and is overexpressed in various human epithelial cancers, including esophageal squamous cell carcinoma (ESCC). We analyzed various protein- protein interactions (PPI) of differentially-expressed genes (DEGs), in fascin knockdown ESCC cells, to explore the role of fascin overexpression. The node-degree distributions indicated these PPI sub-networks to be characterized as scale-free. Subcellular localization analysis revealed DEGs to interact with other proteins directly or indirectly, distributed in multiple layers of extracellular membrane-cytoskeleton/ cytoplasm-nucleus. The functional annotation map revealed hundreds of significant gene ontology (GO) terms, especially those associated with cytoskeleton organization of FSCN1. The Random Walk with Restart algorithm was applied to identify the prioritizations of these DEGs when considering their relationship with FSCN1. These analyses based on PPI network have greatly expanded our comprehension of the mRNA expression profile following fascin knockdown to future examine the roles and mechanisms of fascin action.
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Authors | Ze-Peng Du, Bing-Li Wu, Jian-Jun Xie, Xuan-Hao Lin, Xiao-Yang Qiu, Xiao-Fen Zhan, Shao-Hong Wang, Jin-Hui Shen, En-Min Li, Li-Yan Xu |
Journal | Asian Pacific journal of cancer prevention : APJCP
(Asian Pac J Cancer Prev)
Vol. 16
Issue 13
Pg. 5445-51
( 2015)
ISSN: 2476-762X [Electronic] Thailand |
PMID | 26225692
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers, Tumor
- Carrier Proteins
- FSCN1 protein, human
- Microfilament Proteins
- RNA, Small Interfering
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Topics |
- Biomarkers, Tumor
(genetics, metabolism)
- Carcinoma, Squamous Cell
(genetics, metabolism)
- Carrier Proteins
(antagonists & inhibitors, genetics)
- Esophageal Neoplasms
(genetics, metabolism)
- Gene Expression Profiling
- Gene Expression Regulation, Neoplastic
- Gene Regulatory Networks
- Humans
- Microfilament Proteins
(antagonists & inhibitors, genetics)
- Protein Interaction Maps
- RNA, Small Interfering
(genetics)
- Tumor Cells, Cultured
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