Back to Search
Start Over
A siRNA-based method for efficient silencing of PYROXD1 gene expression in the colon cancer cell line HCT116.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 2019 Dec; Vol. 120 (12), pp. 19310-19317. Date of Electronic Publication: 2019 Sep 10. - Publication Year :
- 2019
-
Abstract
- Purpose: The aim of this study was to determine the biological function of pyridine nucleotide-disulfide oxidoreductase domain 1 (PYROXD1), a recently discovered protein, in colon cancer cell line HCT116.<br />Methods: The small interfering RNA (siRNA) was designed rationally on the basis of the target sequence against PYROXD1. Relative PYROXD1 mRNA levels were measured by a quantitative real-time polymerase chain reaction. Flow cytometry was performed to monitor tumor cells proliferation and apoptosis after siRNA transfection.<br />Results: Knockdown of PYROXD1 arrested the cell cycle, and induced late apoptosis in colon cancer cell line HCT116 DISCUSSION: Taken together, these results revealed the critical roles of PYROXD1 in regulating cell cycle and apoptosis and possibly will signify its therapeutic potential for targeting colorectal cancer models.<br /> (© 2019 Wiley Periodicals, Inc.)
- Subjects :
- Annexin A6 genetics
Annexin A6 metabolism
Apoptosis genetics
Apoptosis physiology
Cell Cycle genetics
Cell Cycle physiology
Cell Cycle Checkpoints genetics
Cell Cycle Checkpoints physiology
Colonic Neoplasms genetics
Flow Cytometry
HCT116 Cells
Humans
Oxidoreductases Acting on Sulfur Group Donors genetics
RNA, Small Interfering genetics
Real-Time Polymerase Chain Reaction
Reverse Transcriptase Polymerase Chain Reaction
Colonic Neoplasms metabolism
Oxidoreductases Acting on Sulfur Group Donors metabolism
RNA, Small Interfering metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4644
- Volume :
- 120
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 31502705
- Full Text :
- https://doi.org/10.1002/jcb.26858