Life-long reduction in MnSOD activity results in increased DNA damage and higher incidence of cancer but does not accelerate aging
The University of Texas at San Antonio Health Science Center · Geriatric Research Education and Clinical Center · +5 more institutions
Abstract
Mice heterozygous for the Sod2 gene (Sod2+/- mice) have been used to study the phenotype of life-long reduced Mn-superoxide dismutase (MnSOD) activity. The Sod2+/- mice have reduced MnSOD activity (50%) in all tissues throughout life. The Sod2+/- mice have increased oxidative damage as demonstrated by significantly elevated levels of 8-oxo-2-deoxyguanosine (8oxodG) in nuclear DNA in all tissues of Sod2+/- mice studied. The levels of 8oxodG in nuclear DNA increased with age in all tissues of Sod2+/- and wild-type (WT) mice, and at 26 mo of age, the levels of 8oxodG in nuclear DNA were significantly higher (from 15% in heart to over 60% in liver) in the Sod2+/- mice compared with WT mice. The level of 8oxodG was…
Citation impact
- FWCI
- 13.06
- Percentile
- 100%
- References
- 52
Authors
13- HVHolly Van RemmenCorresponding
The University of Texas at San Antonio Health Science Center, Geriatric Research Education and Clinical Center, South Texas Veterans Health Care System
- YIYuji Ikeno
The University of Texas at San Antonio Health Science Center, Geriatric Research Education and Clinical Center, South Texas Veterans Health Care System
- MMMichelle M. Hamilton
The University of Texas at San Antonio Health Science Center
- MAMohammad A. Pahlavani
The University of Texas at San Antonio Health Science Center
- NSNorman S. Wolf
University of Washington
Topics & keywords
- SOD2
- DNA damage
- Biology
- Superoxide dismutase
- Oxidative stress
- Senescence
- Endocrinology
- Cockayne syndrome