Year: 2015
Type: article
Abstract: Oncogenic oxidative stress is an intrinsic part of the transformation process and needs to be mitigated for optimal malignancy in the transformed cancer cells. The source of oncogenic reactive oxygen species (ROS) likely differs depending on the stage of transformation and can be, separately or collectively, the result of hyperactivated oncogenic signaling, inflammation, aberrant mitochondrial metabolism, and instigation of invasion-promoting pathways[1]. In RAS-driven tumor cells, we have found that MTH1, the mammalian Nudix hydrolase that degrades oxidized purine nucleotides, effectively counteracts the resistance to transformation and malignancy from this inherent oxidative stress. Our work was the first to show that MTH1 is required to facilitate the formation, proliferation and tumorigenic capability of
Source: Oncoscience
Authors: Dominick G.A. Burton, Priyamvada Rai
Institution: University of Miami
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: diamond
Funder: National Cancer Institute
OpenAlex ID: W2409723809
