Regulation of Ferroptosis by the p53/CDK/Rb Axis.

NIH RePORTER · NIH · R15 · $12,888 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract: Many types of cancer are still detected to late to be effectively treated. Therefore, new systemic therapies for cancer are required. In our parent application we proposed to investigate the cell death mechanism called ferroptosis as a potential means to kill cancer cells. Our studies were focused on understanding important cellular pathways that modulate ferroptosis to uncover better mechansism to specifically target cancer cells. While our work was underway, damage to the HVAC system in our building resulted in flooding of a neighboring labortory. As a result, that lab will relocate to another location in the building and will remove an ultralow (-80°C) freezer that my lab was using to store samples. This freezer is essential to store bacterial stocks, cell lysates, protein samples among other important reagents. The purpose of this administrative supplement is to seeks funds to purchase an ultralow -80°C freezer so that our research may continue without major disruption.

Key facts

NIH application ID
10632830
Project number
3R15GM141712-01S1
Recipient
UNIVERSITY OF TOLEDO
Principal Investigator
William R. Taylor
Activity code
R15
Funding institute
NIH
Fiscal year
2022
Award amount
$12,888
Award type
3
Project period
2021-06-01 → 2025-05-31