Chromosomal localization of human GRIM-19, a novel IFN-beta and retinoic acid-activated regulator of cell death

Citation
Nv. Chidambaram et al., Chromosomal localization of human GRIM-19, a novel IFN-beta and retinoic acid-activated regulator of cell death, J INTERF CY, 20(7), 2000, pp. 661-665
Citations number
22
Categorie Soggetti
Immunology
Journal title
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH
ISSN journal
10799907 → ACNP
Volume
20
Issue
7
Year of publication
2000
Pages
661 - 665
Database
ISI
SICI code
1079-9907(200007)20:7<661:CLOHGA>2.0.ZU;2-Q
Abstract
Apoptosis is a tightly regulated mechanism that controls the proliferation of cells in metazoans, In mammals, multiple genes are required to regulate cell death, We have employed a gene expression knockout technique to isolat e cell death-related genes, One such gene, gene associated with retinoid-in terferon-induced mortality-19 (GRIM-19), is essential for tumor cell death induced by interferon-beta (IFN-beta) and retinoic acid (RA), Here, we desc ribe the localization of GRIM-19 to human chromosome 19p13.2. This region i s essential for prostate tumor suppression. Together with its death-inducti ve role in the IFN-retinoid-regulated pathways and the tumor-suppressive fu nction of this locus, the data suggest that GRIM-19 may be a novel tumor su ppressor.