| Literature DB >> 28529078 |
Qiongye Dong1, Hongqing Han1, Xuehui Liu1, Lei Wei1, Wei Zhang1, Zhen Zhao1, Michael Q Zhang2, Xiaowo Wang3.
Abstract
Cellular senescence is an irreversible cell cycle arrest program in response to various exogenous and endogenous stimuli like telomere dysfunction and DNA damage. It has been widely accepted as an anti-tumor program and is also found closely related to embryo development, tissue repair, organismal aging and age-related degenerative diseases. In the past decades, numerous efforts have been made to uncover the gene regulatory mechanisms of cellular senescence. There is a strong demand to integrate these data from various resources into one open platform. To facilitate researchers on cellular senescence, we have developed Human Cellular Senescence Gene Database (HCSGD) by integrating multiple online published data sources into a comprehensive senescence gene annotation platform (http://bioinfo.au.tsinghua.edu.cn/member/xwwang/HCSGD). Potential Human Cellular Senescence Genes (HCSGS) were collected by combining information from published literatures, gene expression profiling data and Protein-Protein Interaction networks. Additionally, genes are annotated with gene ontology annotation and microRNA/drug/compound target information. HCSGD provides a valuable resource to visualize cellular senescence gene networks, browse annotated functional information, and retrieve senescence-associated genes with a user-friendly web interface.Entities:
Keywords: Cellular senescence; Meta-analysis; Text-mining
Mesh:
Year: 2017 PMID: 28529078 DOI: 10.1016/j.jgg.2017.04.001
Source DB: PubMed Journal: J Genet Genomics ISSN: 1673-8527 Impact factor: 4.275