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CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life
Abstract
Mice deficient in CuZn superoxide dismutase (CuZnSOD) showed no overt abnormalities during development and early adulthood, but had a reduced lifespan and increased incidence of neoplastic changes in the liver. Greater than 70% of Sod1-/- mice developed liver nodules that were either nodular hyperplasia or hepatocellular carcinoma (HCC). Cross-sectional studies with livers collected from Sod1-/- and age-matched +/+ controls revealed extensive oxidative damage in the cytoplasm and, to a lesser extent, in the nucleus and mitochondria from as early as 3 months of age. A marked reduction in cytosolic aconitase, increased levels of 8-oxo dG and F2-isoprostanes, and a moderate reduction in glutathione peroxidase activities and porin levels were observed in all age groups of Sod1-/- mice examined. There were also age-related reductions in Mn superoxide dismutase activities and carbonic anhydrase III. Parallel to the biochemical changes, there were progressive increases in the DNA repair enzyme APEX1, the cell cycle control proteins cyclin D1 and D3, and the hepatocyte growth factor receptor Met. Increased cell proliferation in the presence of persistent oxidative damage to macromolecules likely contributes to hepatocarcinogenesis later in life.
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“For example, mice deficient in either Cu-ZnSOD or MnSOD have widespread oxidative damage and hepatocarcinogenesis or neurodegeneration with reduced lifespan (Elchuri et al., 2005; Lebovitz et al., 1996).”
From Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases (2017) · cites this paper as Elchuri et al., 2005
Citations
Cites
Aebi, H. (1984) · Methods in Enzymology · doi:10.1016/s0076-6879(84)05016-3 · Cited by 25,696
Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study
Murray, C. J., & Lopez, A. D. (1997) · The Lancet · doi:10.1016/s0140-6736(96)07495-8 · Cited by 4,492 · cited 2×
“Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide (Murray and Lopez, 1997; Levy et al., 2002) and accounts for approximately 84% of all liver cancers.”
BackgroundSuperoxide radical and superoxide dismutases
Fridovich, I. (1995) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.64.070195.000525 · Cited by 3,455
[37] Carbonyl assays for determination of oxidatively modified proteins
Levine, R. L., Williams, J. A., Stadtman, E. R., & Shacter, E. B. (1994) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(94)33040-9 · Cited by 2,707
Jaeschke, H. (2002) · Toxicological Sciences · doi:10.1093/toxsci/65.2.166 · Cited by 1,308
Cytochromes P450 and metabolism of xenobiotics
Anzenbacher, P., & Anzenbacherová, E. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000897 · Cited by 890
Pigeolet, E., Corbisier, P., Houbion, A., Lambert, D., Michiels, C., Raes, M. J., Zachary, M.-D., & Remacle, J. (1990) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(90)90078-t · Cited by 747
Sturtz, L. A., Diekert, K., Jensen, L. T., Lill, R., & Culotta, V. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105296200 · Cited by 735
Molecular pathogenesis of hepatocellular carcinoma in hepatitis B virus transgenic mice
Chisari, F. V., Klopchin, K., Moriyama, T., Pasquinelli, C., Dunsford, H. A., Sell, S., Pinkert, C. A., Brinster, R. L., & Palmiter, R. D. (1989) · Cell · doi:10.1016/0092-8674(89)90770-8 · Cited by 696
Levine, R. L. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00765-7 · Cited by 675
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Deschênes‐Simard, X., Lessard, F., Gaumont‐Leclerc, M., Bardeesy, N. M., & Ferbeyre, G. (2014) · Cell Cycle · doi:10.4161/cc.29335 · Cited by 66
Beyond Diabetes: Does Obesity-Induced Oxidative Stress Drive the Aging Process?
Salmon, A. B. (2016) · Antioxidants · doi:10.3390/antiox5030024 · Cited by 62
Vasilaki, A., van der Meulen, J. H., Larkin, L. M., Harrison, D. C., Pearson, T., Remmen, H. V., Richardson, A., Brooks, S. V., Jackson, M. J., & McArdle, A. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00635.x · Cited by 60
The paradoxical role of thioredoxin on oxidative stress and aging
Cunningham, G. M., Roman, M. G., Flores, L. C., Hubbard, G. B., Salmon, A. B., Zhang, Y., Gelfond, J., & Ikeno, Y. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.02.025 · Cited by 61
Chapter 9 Oxidative Stress in Malignant Progression
Trougakos, I. P., & Gonos, E. S. (2009) · Advances in cancer research · doi:10.1016/s0065-230x(09)04009-3 · Cited by 60
Page, M. M., Richardson, J. M. L., Wiens, B. E., Tiedtke, E., Peters, C. W., Faure, P. A., Burness, G., & Stuart, J. A. (2010) · AGE · doi:10.1007/s11357-010-9131-2 · Cited by 58
Genetic Disruption of SOD1 Gene Causes Glucose Intolerance and Impairs β-Cell Function
Muscogiuri, G., Salmon, A. B., Aguayo‐Mazzucato, C., Li, M., Balas, B., Guardado‐Mendoza, R., Giaccari, A., Reddick, R. L., Reyna, S. M., Weir, G. C., et al. (2013) · Diabetes · doi:10.2337/db13-0314 · Cited by 60
Oxidative Stress in Poultry and the Therapeutic Role of Herbal Medicine in Intestinal Health
Li, Y., Wang, K., & Li, C. (2024) · Antioxidants · doi:10.3390/antiox13111375 · Cited by 57
Mele, J., Remmen, H. V., Vijg, J., & Richardson, A. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.628 · Cited by 57
Rodrigues, M. S., Reddy, M. M., & Sattler, M. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2071 · Cited by 58
Rodriguez, K. A., Wywiał, E., Pérez, V., Lambert, A. J., Edrey, Y. H., Lewis, K. N., Grimes, K. M., Lindsey, M. L., Brand, M. D., & Buffenstein, R. (2011) · Current Pharmaceutical Design · doi:10.2174/138161211797052457 · Cited by 58
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Brown, J. L., Lawrence, M. M., Ahn, B., Kneis, P., Piekarz, K. M., Qaisar, R., Ranjit, R., Bian, J., Pharaoh, G. A., Brown, C. A., et al. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12615 · Cited by 56
Liao, C., & Kennedy, B. K. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00003-2 · Cited by 59
Li, X., Chen, Y., Zhao, J., Shi, J., Wang, M., Qiu, S., Hu, Y., Xu, Y., Cui, Y., Liu, C., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/9706792 · Cited by 65
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Long, Y. C., Tan, T. M. C., Inoue, T., & Tang, B. L. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00665.2013 · Cited by 57
Garratt, M., Pichaud, N., King, E. D. A., & Brooks, R. C. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.082669 · Cited by 55
Chung, W. (2017) · The Journal of Microbiology · doi:10.1007/s12275-017-6647-5 · Cited by 55
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Logan, S., Royce, G. H., Owen, D. B., Farley, J. A., Ranjo‐Bishop, M., Sonntag, W. E., & Deepa, S. S. (2019) · GeroScience · doi:10.1007/s11357-019-00105-y · Cited by 56
Perrone, M. A., Gualtieri, P., Gratteri, S., Ali, W., Sergi, D., Muscoli, S., Cammarano, A., Bernardini, S., Renzo, L. D., & Romeo, F. (2019) · Journal of Cardiovascular Medicine · doi:10.2459/jcm.0000000000000816 · Cited by 55
Shi, Y., Ivannikov, M. V., Walsh, M. E., Liu, Y., Zhang, Y., Jaramillo, C. A., Macleod, G. T., & Remmen, H. V. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100834 · Cited by 54
Mouse Models of Oxidative Stress Indicate a Role for Modulating Healthy Aging
Hamilton, R. T. (2012) · Journal of Clinical & Experimental Pathology · doi:10.4172/2161-0681.s4-005 · Cited by 53
Chu, V. C., Bhattacharya, S., Nomoto, A. M., Lin, J., Zaidi, S. K., Oberley, T. D., Weinman, S. A., Azhar, S., & Huang, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028551 · Cited by 52
van de Wetering, C. I., Coleman, M. C., Spitz, D. R., Smith, B. J., & Knudson, C. M. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.01.022 · Cited by 52
Sakellariou, G. K., McDonagh, B., Porter, H., Giakoumaki, I. I., Earl, K. E., Nye, G., Vasilaki, A., Brooks, S. V., Richardson, A. G., Remmen, H. V., et al. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7249 · Cited by 52
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Olofsson, E. M., Marklund, S. L., & Behndig, A. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-3510 · Cited by 51
Role of Dietary and Endogenous Antioxidants in Diabetes
Marrazzo, G., Barbagallo, I. A., Galvano, F., Malaguarnera, M., Gazzolo, D., Frigiola, A., D’Orazio, N., & Volti, G. L. (2013) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2011.644874 · Cited by 51
Cu–Zn super oxide dismutase as a potential antifibrotic drug for hepatitis C related fibrosis
Emerit, J., Samuel, D., & Pavio, N. (2005) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2005.09.002 · Cited by 51
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Usman, M., & Volpi, E. V. (2018) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2018.08.002 · Cited by 52
Elchuri, S. V., Naeemuddin, M., Sharpe, O., Robinson, W. H., & Huang, T. (2007) · PROTEOMICS · doi:10.1002/pmic.200601011 · Cited by 49
Kim, C., Han, S., Lee, S.-Y.-O., Youk, H. S., Moon, J., Duong, H.-Q., Park, M. J., Joo, Y., Park, H., Kim, Y.-J., et al. (2007) · Journal of Cellular Physiology · doi:10.1002/jcp.20941 · Cited by 48
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Bhusari, S. S., Dobosy, J. R., Fu, V., Almassi, N., Oberley, T., & Jarrard, D. F. (2010) · Epigenetics · doi:10.4161/epi.5.5.11853 · Cited by 50
Zhan, X., Li, J., & Zhou, T. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.565748 · Cited by 51
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Bougen-Zhukov, N. M., Steiner, M., Pertziger, M., Banerjee, A., Brunet-Dunand, S. E., Zhu, T., Lobie, P. E., & Perry, J. K. (2012) · Endocrine Related Cancer · doi:10.1530/erc-12-0042 · Cited by 49
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Chen, F., Zhang, L., Qiang, L., Yang, Z., Wu, T., Zou, M., Tao, L., You, Q., Li, Z., Yang, Y., et al. (2010) · Cancer Letters · doi:10.1016/j.canlet.2010.04.004 · Cited by 50
Sun, X., Komatsu, T., Lim, J., Laslo, M., Yolitz, J., Wang, C., Poirier, L., Alberico, T., & Zou, S. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00842.x · Cited by 50
Zhang, Y., Zhang, H., Shi, Y., Lustgarten, M. S., Li, Y., Qi, W., Zhang, B.-X., & Remmen, H. V. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.07.006 · Cited by 48
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Hamilton, R. T., Bhattacharya, A., Walsh, M. E., Shi, Y., Wei, R., Zhang, Y., Rodriguez, K. A., Buffenstein, R., Chaudhuri, A. R., & Remmen, H. V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065725 · Cited by 48
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Wu, Z., Lv, G., Xing, F., Xiang, W., Ma, Y., Feng, Q., Yang, W. K., & Wang, H. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216348 · Cited by 48
Na, B., Huang, Z., Wang, Q., Qi, Z., Tian, Y., Lu, C., Yu, J., Hanes, M. A., Kakar, S., Huang, E. J., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026240 · Cited by 47
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Yamanobe, T., Okada, F., Iuchi, Y., Onuma, K., Tomita, Y., & Fujii, J. (2006) · Free Radical Research · doi:10.1080/10715760601038791 · Cited by 46
Fischer, L. R., & Glass, J. D. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0631-z · Cited by 46
Chughtai, M. F. J., Pasha, I., Zahoor, T., Khaliq, A., Ahsan, S., Zheng-zhong, W., Nadeem, M., Mehmood, T., Amir, R. M., Yasmin, I., et al. (2020) · CyTA - Journal of Food · doi:10.1080/19476337.2020.1721562 · Cited by 46
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Shan, D., Jinling, S., Ren, Y., Zhang, Y., Ba, Y., Luo, P., Cheng, Q., Xu, H., Weng, S., Zuo, A., et al. (2025) · 癌症:英文版 · doi:10.1002/cac2.70005 · Cited by 53
Jayakumar, J. K., Nirmala, P., Kumar, B. A. P., & Kumar, A. P. (2014) · South Asian Journal of Cancer · doi:10.4103/2278-330x.130443 · Cited by 45
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Henkel, C., Roderfeld, M., Weiskirchen, R., Berres, M., Hillebrandt, S., Lammert, F., Meyer, H. E., Stühler, K., Graf, J., & Roeb, E. (2006) · PROTEOMICS · doi:10.1002/pmic.200600580 · Cited by 42
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Klöppel, C., Michels, C., Zimmer, J., Herrmann, J. M., & Riemer, J. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.10.129 · Cited by 42
Chen, B., Caballero, S., Seo, S., Grant, M. B., & Lewin, A. S. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-3633 · Cited by 40
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Hecht, F., Cazarin, J., Lima, C., de Faria, C. C., Leitão, Á. C., Ferreira, A. C. F., de Carvalho, D. P., & Fortunato, R. S. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.06.016 · Cited by 41
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Kondo, Y., Masutomi, H., Noda, Y., Ozawa, Y., Takahashi, K., Handa, S., Maruyama, N., Shimizu, T., & Ishigami, A. (2014) · FEBS Open Bio · doi:10.1016/j.fob.2014.05.003 · Cited by 42
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Zafar, N., & Khan, M. A. (2019) · Aquaculture · doi:10.1016/j.aquaculture.2019.05.022 · Cited by 39
Chen, F., Su, R., Ni, S., Liu, Y., Huang, J., Li, G., Wang, Q., Zhang, X., & Yang, Y. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101835 · Cited by 38
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Gałgańska, H., Karachitos, A., Wojtkowska, M., Stobienia, O., Budzińska, M., & Kmita, H. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.02.004 · Cited by 40
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Lukić, I., Mitić, M., Djordjevic, J., Tatalović, N., Bozovic, N., Soldatović, I., Mihaljevic, M. M., Pavlović, Z., Radojcic, M. B., Marić, N. P., et al. (2014) · Neuropsychobiology · doi:10.1159/000362841 · Cited by 37
El‐Bab, M. F., Zaki, N. S., Mojaddidi, M. A., Albarry, M. A., & El-Beshbishy, H. A. (2013) · International Journal of General Medicine · doi:10.2147/ijgm.s40665 · Cited by 35
Age-Related Hearing Loss in Mn-SOD Heterozygous Knockout Mice
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Metadata
- Authors
- Elchuri, S., Oberley, T. D., Qi, W., Eisenstein, R. S., Jackson Roberts, L., Van Remmen, H., Epstein, C. J., & Huang, T.-T.
- Affiliations
- Stanford University (US)
- University of Wisconsin–Madison (US)
- The University of Texas at San Antonio Health Science Center (US)
- University of California, San Francisco (US)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Huang, Ting-Ting
- Venue
- Oncogene
- Published
- 2004-11-08
- Volume
- 24
- Issue
- 3
- Pages
- 367-380
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W2042637324
- Cited by
- 667
- References
- 72
- Citations by year
- 2026: 11 · 2025: 22 · 2024: 24 · 2023: 27 · 2022: 32 · 2021: 25 · 2020: 24 · 2019: 24 · 2018: 25 · 2017: 31 · 2016: 29 · 2015: 35 · 2014: 48 · 2013: 48 · 2012: 45
- FWCI
- 5.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (AG16998, R01AG016998, R01AG016633, AG16633)
- National Institute of General Medical Sciences (GM 15431, GM 42056)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK-26657, DK47219, P30DK026657)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer and biochemical research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- Cu/Zn superoxide dismutase, Sod1 knockout mice, hepatocarcinogenesis, oxidative damage, liver nodules, hepatocellular carcinoma, nodular hyperplasia, aconitase, 8-oxoguanine, F2-isoprostanes, glutathione peroxidase, Mn superoxide dismutase, carbonic anhydrase III, APEX1, DNA repair, cyclin D1, cyclin D3, c-Met, hepatocyte proliferation, aging
- MeSH terms
- Aging, Animals, Cell Nucleus, Liver, Liver Neoplasms, Mitochondria, Superoxide Dismutase, Mice, Knockout, Oxidative Stress, Mice
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