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. 2025 Aug 5;15(8):1130. doi: 10.3390/biom15081130

Table 1.

A summary of different studies emphasizing the implications of SOD in various diseases.

Disease Type of SOD Subjects Conclusion of the Study Reference
Breast cancer Cu/Zn-SOD and Mn-SOD 70 Patients with breast cancer may have elevated SOD expression in response to the buildup of free radicals.
The improvement in the expression of activated SODs may be attributed to anastrozole treatment.
[63]
Breast cancer SOD2 80 A poor prognosis was associated with increased SOD2 expression. [64]
Glioblastomas Mn-SOD 30 Using this SOD protein as a marker could aid in developing treatment plans for glioblastoma patients. [65]
Glioblastomas SOD 100 Following treatment, SOD and CAT levels increased and the hydrogen inhalation group’s overall impact was noticeably superior to that of the conventional group. [66]
Colorectal cancer Serum SOD 176 The total cohort’s risk of colorectal cancer (CRC) decreased as SOD increased, with the lowest risk being seen in the fourth quartile of SOD levels relative to the first. [67]
Pancreatic cancer SOD1 50 In pancreatic cancer and chronic pancreatitis, oxidative stress indicators were elevated and antioxidant defense system capacity was decreased. [68]
Gastric cancer Serum SOD 34 A poor prognosis for individuals with far-advanced (stage IV) stomach cancer may come from a decrease in serum SOD activity in older patients, which could be caused by a weakened host antioxidant defense. [69]
Oral cancer NA 87 The amount of SOD falls and the amount of NO activity rises during carcinogenesis and tumor growth. These NO and SOD levels may also be used as prognostic indicators and treatment goals for patients with this type of illness. [70]
Lung cancer Cu-Zn SOD 32 Patients with NSCLC and SCLC had overall higher levels of NOradical dot, MDA, and TGHS as well as activity of XO, CAT, CuZn SOD, and unaltered GSH-Px GST as compared to the control group. [71]
Brain cancer (Intracranial neoplasm) Erythrocyte SOD 30 Significant oxidative stress in brain tumors may be triggered by a considerable decline in antioxidant levels. Furthermore, the degree of aggressiveness in brain tumors may be indicated by the drop in antioxidant levels. [72]
Brain Tumor Total SOD (Both Mn-SOD and Cu,Zn-SOD) 32 CAT activity was 106.3% greater and SOD activity was much lower in brain tumor tissue compared to controls. [73]
Inflammatory disease (Periprosthetic joint infection) Serum SOD 50 Serum SOD demonstrated significant promise in periprosthetic joint infection diagnosis. [74]
HEV-induced liver failure Serum SOD 30 SOD levels were higher in patients with HEV-induced liver failure than in HEV-AVH patients and healthy controls. [75]
Cardiovascular disease SOD 50 Patients with ST elevated myocardial infarction (STEMI) and non-ST elevated myocardial infarction (NSTEMI) had considerably lower levels of SOD and catalase, which may indicate that they are experiencing elevated oxidative stress. [76]
Coronary artery disease SOD2 150 One marker gene for CAD susceptibility is the SOD2 locus. [77]
Aging SOD3 1100 EC-SOD has positive effects on diabetes mellitus in the elderly and works in tandem with adiponectin. [78]
Aging Plasma SOD 78 Smoking and low superoxide dismutase (SOD) levels are risk factors for early aging in women between the ages of 20 and 35. [79]
Rheumatoid arthritis Cu,Zn-SOD 28 The study documented a negative correlation between CRP levels and Cu,Zn-SOD activities. [80]
Rheumatoid arthritis SOD 54 Serum albumin levels and SOD concentrations in the peripheral antioxidant status were better after multigrain supplementation than in the control group. [81]
Amyotrophic lateral sclerosis (ALS) SOD 24 The cerebrospinal fluid SOD and NO level might serve as useful biomarkers for functional disorder and progression of the disease. [82]
Huntington’s disease SOD 375 Triglycerides, high-density lipoproteins, low-density lipoproteins, cholesterol, and blood SOD did not significantly differ between patients and controls. [83]
Parkinson’s disease Erythrocyte SOD 29 There may be distinct clinical subgroups of Parkinson’s disease (PD) that can be distinguished by a biological marker, as suggested by the variation in SOD activity in clinically diverse subgroups. [84]
Alzheimer’s disease Cu,Zn-SOD 44 Compared to the controls, the patients’ red blood cells had substantially less SOD activity. [85]