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OGFOD1 is required for breast cancer cell proliferation and is associated with poor prognosis in breast cancer
- Source :
- Oncotarget
- Publication Year :
- 2015
- Publisher :
- Impact Journals LLC, 2015.
-
Abstract
- 2-oxogluatrate and Fe(II)-dependent oxygenase domain-containing protein 1 (OGFOD1) was recently revealed to be a proline hydroxylase of RPS23 for translational termination. However, OGFOD1 is nuclear, whereas translational termination occurs in the cytoplasm, raising the possibility of another function of OGFOD1 in the nucleus. In this study, we demonstrate that OGFOD1 is involved in cell cycle regulation. OGFOD1 knockdown in MDA-MB-231 breast cancer cells significantly impeded cell proliferation and resulted in the accumulation of G1 and G2/M cells by decreasing the mRNA levels of G1/S transition- and G2/M-related transcription factors and their target genes. We also confirmed that OGFOD1 is highly expressed in breast cancer tissues by bioinformatic analysis and immunohistochemistry. Thus, we propose that OGFOD1 is required for breast cancer cell proliferation and is associated with poor prognosis in breast cancer.
- Subjects :
- Gerontology
Time Factors
Translational termination
Breast Neoplasms
Cell Cycle Proteins
Kaplan-Meier Estimate
Transfection
Breast cancer
breast cancer
Databases, Genetic
medicine
Humans
RNA, Messenger
Nuclear protein
Transcription factor
In Situ Hybridization
Cell Proliferation
Gene knockdown
Cell growth
business.industry
Computational Biology
Nuclear Proteins
G2/M phase
Cell cycle
medicine.disease
Chromatin Assembly and Disassembly
Prognosis
G1 Phase Cell Cycle Checkpoints
Immunohistochemistry
G2 Phase Cell Cycle Checkpoints
Gene Expression Regulation, Neoplastic
HEK293 Cells
Oncology
Cytoplasm
Gene Knockdown Techniques
Cancer research
MCF-7 Cells
OGFOD1
cell cycle
Female
RNA Interference
business
Carrier Proteins
Research Paper
HeLa Cells
Signal Transduction
Transcription Factors
Subjects
Details
- Language :
- English
- ISSN :
- 19492553
- Volume :
- 6
- Issue :
- 23
- Database :
- OpenAIRE
- Journal :
- Oncotarget
- Accession number :
- edsair.doi.dedup.....110ede9c53030e3254a064c537792280