| Literature DB >> 27235449 |
Chunyan Luo1, Fan Wang2, Subo Qin1, Qiuyun Chen3, Qing K Wang4.
Abstract
The ADTRP gene encodes the androgen-dependent TFPI-regulating protein and is a susceptibility gene for contrary artery disease (CAD). We performed global gene expression profiling for ADTRP knock-down using microarrays in human HepG2 cells. Follow-up real-time RT-PCR analysis demonstrated that ADTRP knock-down regulates a diverse set of genes, including upregulation of seven histone genes, downregulation of multiple cell cycle genes (CCND1, CDK4, and CDKN1A), and upregulation of apoptosis genes (CASP7 and PDCD2) in HepG2 cells and endothelial cells. Consistently, ADTRP increases the number of S phase cells during cell cycle, promotes cell proliferation, and inhibits apoptosis. Our study provides novel insights into the function of ADTRP and biological pathways involving ADTRP, which may be involved in the pathogenesis of CAD.Entities:
Keywords: ADTRP; CDK4; caspase 7; coronary artery disease (CAD); cyclin D1; global gene expression microarray; histone; p21CIP
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Year: 2016 PMID: 27235449 PMCID: PMC5005456 DOI: 10.1152/physiolgenomics.00028.2016
Source DB: PubMed Journal: Physiol Genomics ISSN: 1094-8341 Impact factor: 3.107