- Research article
- Open Access
Association between manganese superoxide dismutase promoter gene polymorphism and breast cancer survival
Breast Cancer Research volume 8, Article number: R45 (2006)
Manganese superoxide dismutase (MnSOD) plays a critical role in the detoxification of mitochondrial reactive oxygen species, constituting a major cellular defense mechanism against agents that induce oxidative stress. A genetic polymorphism in the mitochondrial targeting sequence of this gene has been associated with increased cancer risk and survival in breast cancer. This base pair transition (-9 T > C) leads to a valine to alanine amino acid change in the mitochondrial targeting sequence. A polymorphism has also been identified in the proximal region of the promoter (-102 C>T) that alters the recognition sequence of the AP-2 transcription factor, leading to a reduction in transcriptional activity. The aim of our study was to investigate possible associations of the -102 C>T polymorphism with overall and relapse-free breast cancer survival in a hospital-based case-only study.
Materials and methods
The relationship between the MnSOD -102 C>T polymorphism and survival was examined in a cohort of 291 women who received chemotherapy and/or radiotherapy for incident breast cancer. The MnSOD -102 C>T genotype was determined using a TaqMan allele discrimination assay. Patient survival was evaluated according to the MnSOD genotype using Kaplan–Meier survival functions. Hazard ratios were calculated from adjusted Cox proportional hazards modeling. All statistical tests were two-sided.
In an evaluation of all women, there was a borderline significant reduction in recurrence-free survival with either one or both variant alleles (CT + TT) when compared with patients with wild-type alleles (CC) (odds ratio, 0.65; 95% confidence interval, 0.42–1.01). When the analysis was restricted to patients receiving radiation therapy, there was a significant reduction in relapse-free survival in women who were heterozygous for the MnSOD -102 genotype (relative risk, 0.40; 95% confidence interval, 0.18–0.86). Similarly, when the homozygous and heterozygous variant genotypes were combined, there remained a significant reduction in relapse-free survival in this group (hazard ratio, 0.42; 95% confidence interval, 0.20–0.87).
The MnSOD -102 variant allele appears to be associated with an improved recurrence-free survival in all patients, and more dramatically in subjects who received adjuvant radiation therapy.
Breast cancer represents one of the most common cancers among women residing in the United States and worldwide [1, 2]. In 2005, 145,920 US residents will be diagnosed with breast cancer . The etiological risk factors common to breast cancer include age, personal or family history, obesity, and lifetime exposure to exogenous and endogenous estrogens.
Genetic risk factors have also been identified, such as the high-penetrance cancer susceptibility genes, BRCA1 and BRCA2, but these genes only account for 5% of all breast cancer cases [4, 5]. It has therefore been established that relatively common genes acting together with endogenous/lifestyle risk factors (low-penetrance genes) are likely to account for a much higher portion of the breast cancer cases together with as yet unidentified high-penetrance genes .
The development of breast cancer has been linked to the degree of oxidative stress, particularly with perturbations in the delicate balance between reactive oxygen species (ROS) and oxidative defenses . ROS are generated through the metabolism of estradiol, polyunsaturated fats, ethanol and calories, all which have been considered potential risk factors for breast cancer . Antioxidant enzymes such as superoxide dismutase have been demonstrated to protect cells from oxidative stress. Generation of ROS has been implicated in the etiology of a diversity of human diseases, including cancer . Oxidative stress has been demonstrated to induce cell death as a result of excessive cellular damage associated with lipid peroxidation and alterations of nucleic acids and proteins, triggering apoptosis through the mitochondria .
Superoxide dismutase catalyzes the dismutation of the superoxide radical (O2 -) to hydrogen peroxide (H2O2) and oxygen (O2). Three distinct types of superoxide dismutases have been identified in human cells: a homodimeric cytosolic CuZnSOD , an extracellular homotetrameric glycosylated superoxide dismutase , and a mitochondrial matrix homotetrameric manganese superoxide dismutase (MnSOD) .
A specific region of the MnSOD protein is essential for the correct transport and processing of MnSOD by mitochondria. There have been conflicting reports of the association of the polymorphism within the MnSOD mitochondrial targeting sequence (-9 T>C; Val to Ala) and the risk of cancer. A significant gene dose-response relationship has been observed in breast cancer [14, 15]; however, more recent reports did not find an association between -9 T>C MnSODand breast cancer [16–18].
Since radiation therapy remains an integral part of the multimodality therapy in the treatment of breast cancer, determining maximal efficacy among patients remains of the utmost importance. Radiation therapy exerts its antitumor effects through the increased formation of ROS, including hydroxyl radicals (OH), hydrogen peroxide (H2O2) and superoxide anions (O2 -), and its efficacy may be related to the ability to neutralize these effects. Because mitochondrial MnSOD is responsible for catalyzing the conversion of superoxide radicals, there has been a growing belief that gene variants could impact the efficacy of radiation therapy for breast cancer. Similarly, the chemotherapeutic agents most commonly utilized in the treatment of breast cancer, adriamycin and cyclophosphamide, generate ROS that may be effected by MnSOD activity. We recently found that the combination of the MnSOD -9 genotype and the myeloperoxidase genotype led to a threefold decrease in the hazard of death among women treated for breast cancer . This association has further strengthened the need to evaluate other possible gene variants that may play a role in therapeutic efficacy.
The polymorphism in the signal sequence, a mutation in the MnSOD promoter sequence (MnSOD -102 C>T) has been shown to change the binding pattern of AP-2, leading to a reduction in transcriptional activity . We recently reported that this polymorphism is relatively frequent in human populations [21, 22]. A relationship between this polymorphism in the MnSOD promoter and breast cancer treatment outcomes has not, however, been reported. Similarly, there have been no published reports of the effects the MnSOD -102 C>T polymorphism on protein function.
The aim of our study was therefore to investigate the possible associations of the MnSOD -102 C>T polymorphism within a case-only study of breast cancer patients to evaluate possible associations with overall and relapse-free survival in relation to the patients' adjuvant therapy.
As previously described [19, 23], patients who received their first course of adjuvant treatment for primary invasive breast cancer at the Arkansas Cancer Research Center, University of Arkansas for Medical Sciences from 1985 to 1996 were identified from hospital tumor registry records. Patients with a prior history of cancer were excluded. Hospital tumor registry records were used to obtain information concerning age, stage at diagnosis, tumor size, tumor grade, hormone receptor status, race, and date and type of therapy received (chemotherapy, radiotherapy, surgery, and hormonal treatment). The hospital tumor registry was also the source of follow-up information; the registry conducts active follow-up for each patient, contacting the physician or the patient annually and recording the date last contacted and the vital status. The study protocol was approved by the Institutional Review Board of University of Arkansas for Medical Sciences.
Archived normal lymph nodes or skin, stored in paraffin blocks in the Pathology Department, were used as a source of DNA for genotyping as described previously [19, 23]. Hospital tumor registry records identified 815 patients with invasive breast cancer who had been treated at University of Arkansas for Medical Sciences from 1985 to 1996. One hundred and twenty-four (15%) of these patients had received no adjuvant therapy (chemotherapy, radiation therapy, or tamoxifen)and were excluded from the study, as were five (1%) patients with missing adjuvant therapy information. Most of the excluded patients who did not receive adjuvant therapy had lymph node-negative disease.
DNA extraction and genotyping
Sections (50 μm thick) were cut from archived paraffin normal tissue blocks, the tissue was deparaffinized, and DNA was extracted using a commercially available kit (Qiagen Inc., Valencia, CA, US), as previously described [19, 23].
The MnSOD -102 C>T polymorphism was determined using a technique developed in our laboratory . Single nucleotide polymorphism-specific PCR primers and fluorogenic probes were designed using Primer Express (version 1.5; Applied Biosystems, Foster City, CA, USA). The fluorogenic probes were labeled with a reporter dye (either FAM or VIC) and are specific for one of the two possible bases (-102 C or -102 T) in the MnSOD promoter region. TaqMan Universal PCR Master Mix (Applied Biosystems) was used to prepare the PCR. The two-times mix was optimized for TaqMan reactions and contained AmpliTaq-Gold DNA polymerase, AmpErase, deoxyribonucleotide triphosphate with uracil triphosphate, and a passive reference. Primers, probes, and genomic DNA were added to final concentrations of 300 nM, 100 nM, and 0.5–2.5 ng/μl, respectively.
Controls (no DNA template) were run to ensure there was no amplification of contaminating DNA. The amplification reactions were carried out in an ABI Prism 7700 Sequence Detection System (Applied Biosystems) with two initial hold steps (50°C for 2 min, followed by 95°C for 10 min) and 50 cycles of a two-step PCR (95°C for 15 s, 60°C for 1 min).
The fluorescence intensity of each sample was measured at each temperature change to monitor amplification of the 278-base-pair MnSOD promoter region. The -102 nucleotide was determined by the fluorescence ratio of the two single nucleotide polymorphism-specific fluorogenic probes. The fluorescence signal increases when the probe with the exact sequence match binds to the single-stranded template DNA and is digested by the 5'-3' exonuclease activity of AmpliTaq-Gold DNA polymerase (Applied Biosystems). Digestion of the probe releases the fluorescent reporter dye (either FAM or VIC) from the quencher dye.
Crude associations between genotypes for MnSOD and overall survival were evaluated using the Kaplan–Meier survival function. The survival time was calculated as the time from diagnosis to death or to the last contact date for living subjects. Both heterozygotes and homozygotes were assessed separately in relation to the referent. Cox proportional hazard models were constructed to assess potential confounding effects of other breast cancer prognostic factors, including age, stage with nodal status, and estrogen and progesterone receptor status. The final multivariate-adjusted models shown include those factors that either changed the estimated effect by 10% or more in a best-fitting model, which was developed by starting with a full model and then excluding covariates that did not improve the overall fit. Survival analysis according to MnSOD genotype was conducted separately by treatment group (i.e. chemotherapy or radiation therapy). All analyses were conducted using SAS software (version 8.2; SAS Institute, Inc., Cary, NC, USA). All statistical tests were two sided.
Acceptable tissue samples and complete baseline information were obtained for 291 cases (Table 1). A slight majority of patients were older than 50 years of age (53%), with a small percentage being of African-American decent (18%). There was an even distribution of patients who were stage 1 (28%), patients who were stage 2 lymph node negative (20%), patients who were stage 2 lymph node positive (30%), patients who were stage 3 (16%), and a smaller percentage who were stage 4 (6%). Fifty-nine percent of estrogen receptor-positive patients received tamoxifen therapy. A large percentage of patients received chemotherapy alone (33%), when compared with those who received radiation alone (9%), with those who received chemotherapy/radiation therapy (19%), and with those who received other combinations (Table 1).
In patients with one or two copies of the variant MnSOD -102 (CT or TT), there was a nonsignificant impact of genotype on overall survival (Table 2). Similarly, combining patients with one or both variant alleles did not result in a significant change in overall survival when compared with the reference genotype (CC) (Figure 1a). In an evaluation of recurrence-free survival, there was a trend towards significant improvement in recurrence-free survival in patients with one or two variant alleles when compared with women homozygous for the common allele (CC) (odds ratio, 0.65; 95% confidence interval, 0.42–1.01) (Table 2). There was a trend towards an improvement in recurrence-free survival with both homozygous (TT) and heterozygous (CT) variant genotypes (Figure 1b).
Of the study population, there were 160 women who received radiation therapy. Twenty-five patients received radiation alone, 54 patients received radiation and chemotherapy, 46 patients received radiation and tamoxifen, and 35 patients received radiation, chemotherapy, and tamoxifen.
In an evaluation of relapse-free survival in subjects receiving radiation therapy there was a significant reduction in relapse-free survival among women who were heterozygous for the MnSOD -102 genotype (relative risk, 0.40; 95% confidence interval, 0.18–0.86) (Table 3). When the homozygous and heterozygous variant alleles were combined, there remained a significant reduction in relapse-free survival in this group (Figure 2).
There were 230 patients in the study population who received chemotherapy. Among these women, there was an association of borderline significance between MnSOD genotypes and relapse-free survival (adjusted hazard ratio for CT + TT genotype, 0.65; 95% confidence interval, 0.40–1.05) (Table 4). There were, however, no significant associations with overall survival.
In this evaluation of the effects of the MnSOD -102 polymorphism on survival after treatment for breast cancer, we found that women with genotypes that would result in less MnSOD expression, and thus higher levels of ROS, had a significant decrease in relapse-free survival among breast cancer subjects who received adjuvant radiation therapy as well as chemotherapy. There was also a trend toward decreased overall relapse-free survival in all subjects with breast cancer. This study further indicates that genetic variants that may result in decreased function, and thus increased oxidative stress, may enhance the efficacy of radiation therapy and thus translate into better disease control. This is the first study to examine the relationship between the MnSOD -102 genotype and the survival of breast cancer patients treated with adjuvant therapy.
These results support the our previous findings that demonstrated a decrease in the hazard of death with the MnSOD -9 CC and MPO GG genotypes . In that analysis, genotypes associated with higher levels of ROS for women with breast cancer treated with adjuvant therapy led to improved overall survival when compared with women with lower levels of ROS.
Our results also add to the already large volume of literature on the role of the mitochondrial MnSOD in cancer cell survival. Evaluation of MnSOD suggests that it is critically important in maintenance of mitochondrial function. Mice with deficiency of this enzyme exhibit progressive cardiomyopathy, neurodegeneration, and perinatal death . These studies also confirmed that transgenic mice that express human MnSOD in the mitochondria are protected from environmental oxygen-induced lung injury  and adriamycin-induced cardiac toxicity . In contrast, disruption of the other two superoxide dismutases yielded viable mice that were normal in nonstressful conditions . The mitochondrial MnSOD therefore represents a major cellular defense against oxidative stress.
Additional clinical studies have evaluated MnSOD expression with conflicting results. Janssen and colleagues  evaluated 81 gastric adenocarcinomas and found a significantly higher MnSOD expression within the tumor when compared with the normal mucosa. This higher expression did not correlate to a worse outcome; however, the ratio of MnSOD expression of tumor compared with the normal tissue was correlated with a worse overall survival. The significance of this upregulation and worse outcome was felt to be related to chemoresistance but was not elucidated in this study.
A study by Malafa and colleagues  reported the difference in MnSOD expression in gastric carcinoma for metastatic and nonmetastatic cancers. Although the nonmetastatic gastric cancers showed no increase in expression versus normal gastric epithelial cells, 93% of primary tumor cells of metastatic gastric cancer cells showed an upregulation of MnSOD enzymatic activity. This correlation of increased MnSOD expression and increased metastatic prevalence correlates with the theory that MnSOD's role changes during the transformation of a cell from normal to dysplasia to cancer. MnSOD initially appears to acts as a tumor suppressor by inhibiting the ROS and preventing cellular damage; however, once the transformation to malignant cells has taken place, the results of several studies infer that the MnSOD acts to protect the malignant cell both from chemotherapy [28, 30] and from radiation therapy [31, 32] to allow for its progression, replication, and metastasis. This can be explained by the fact that the defenses against malignant cells, whether the body's host defenses or exogenous treatments such as radiation or chemotherapy, often use ROS as a mechanism for cellular destruction. Malignant cells that have an increased expression of MnSOD would therefore be more resistant to cellular destruction and would therefore more probably be resistant to treatment. This increase in MnSOD expression would lead to an increase in the probability of proliferation and metastasis.
The theory has been strengthened by Izutani and colleagues'  demonstration of the role of MnSOD after progression to cancer. An upregulation of MnSOD mRNA in gastric carcinoma was demonstrated, which provided a protective mechanism from the cell toxicity of tumor necrosis factor alpha from ROS. Izutani and colleagues'  later report confirmed these findings by demonstrating an upregulation of MnSOD mRNA in squamous esophageal carcinoma. This upregulation of MnSOD mRNA in active malignant cells not only acts to protect from the body's host defensive mechanisms, but a recent report by Hur and colleagues  demonstrated that MnSOD upregulation also gives gastric cancers protection against current chemotherapy agents. Further research by Izutani and colleagues  indicated that MnSOD expression inhibited the tumor sensitivity of adriamycin in esophageal and gastric cancers. Furthermore, use of transforming growth factor beta to inhibit MnSOD showed an increase in the effectiveness of adriamycin as a suppressor of these tumors . Not only does this research solidify the theory that MnSOD protects the tumor cells after their transformation, but it leads us to believe that, by inhibiting MnSOD, chemotherapy may be made more effective.
Our results are in contrast to a smaller study (n = 80) of women receiving radiation therapy for breast cancer, who found no effects of the MnSOD -9 polymorphisms on clinically detectable skin reactions to therapy . These discrepant results may be due to more dominant effects that the MnSOD -102 polymorphism plays in MnSOD function, or could be due to differential effects of MnSOD variability on normal and tumor tissue or, finally, could be due to the small number of subjects (n = 80) in the study. Since the MnSOD -9 polymorphism leads to partial inner mitochondrial membrane transport arrest , there have been conflicting reports as to which polymorphism (c allele = alanine or t allele = valine) leads to the greater risk of cancer. Since the MnSOD -102 polymorphism affects the AP-2 binding and thus reduces transcriptional activity, however, there may be a greater effect from this polymorphism than from other polymorphisms that have been reported.
Even with this report indicating the efficacy effects of ROS producing therapies and the relationship to MnSOD polymorphisms, this initial evaluation needs to be replicated in a larger study, with greater homogeneity of the subject population. Since very little is know about the clinical effects of the MnSOD -102 polymorphism in carcinogenesis, tumor cell resistance and chemotherapy/radiation therapy efficacy, further evaluation is needed. Because this study involved women who received various adjuvant treatments (radiation, chemotherapy and/or hormonal therapy), we are unable to establish the effects that each individual therapy had on overall survival and on relapse-free survival. Since there is a similarity in the effects that chemotherapy in breast cancer treatment and radiation therapy induce (generation of ROS), however, it is less likely that individual treatment evaluation will lead to different results. Radiation therapy and the chemotherapeutic agents most commonly utilized in the treatment of breast cancer, adriamycin and cyclophosphamide, exert their antitumor effects through the increased formation of ROS, including hydroxyl radicals (OH), hydrogen peroxide (H2O2), and superoxide anions (O2 -), and the efficacy may be related to the ability of the patients'/tumors' ability to neutralize these effects. Since MnSOD is not involved in the metabolism of any specific chemotherapeutic agent we believe these results will remain consistent, but they need to be evaluated in a larger study.
In summary, this reports demonstrates the first evaluation that decreases in MnSOD by the variant genotype are associated with improved relapse-free survival in women treated for breast cancer.
manganese superoxide dismutase
polymerase chain reaction
reactive oxygen species.
Jemal A, Murray T, Ward E, Samuels A, Tiwari RC, Ghafoor A, Feuer EJ, Thun MJ: Cancer statistics, 2005. CA Cancer J Clin. 2005, 55: 10-30.
World Health Organization: The World Health Report. 1997, Geneva: World Health Organization
American Cancer Society I: Cancer Facts and Figures 2005. 2005, Chicago, IL
Easton D, Ford D, Peto J: Inherited susceptibility to breast cancer. Cancer Surv. 1993, 18: 95-113.
Oesterreich S, Fuqua SA: Tumor suppressor genes in breast cancer. Endocr Relat Cancer. 1999, 6: 405-419. 10.1677/erc.0.0060405.
Johnson-Thompson MC, Guthrie J: Ongoing research to identify environmental risk factors in breast carcinoma. Cancer. 2000, 88: 1224-1229. 10.1002/(SICI)1097-0142(20000301)88:5+<1224::AID-CNCR8>3.0.CO;2-H.
Ambrosone CB: Oxidants and antioxidants in breast cancer. Antioxid Redox Signal. 2000, 2: 903-917.
Ambrosone CB, Freudenheim JL, Thompson PA, Bowman E, Vena JE, Marshall JR, Graham S, Laughlin R, Nemoto T, Shields PG: Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer. Cancer Res. 1999, 59: 602-606.
St Clair DK, Wan XS, Kuroda M, Vichitbandha S, Tsuchida E, Urano M: Suppression of tumor metastasis by maganese superoxide dismutase is associated with reduced tumorigenicity and elevated fibronectin. Oncol Rep. 1997, 4: 753-757.
Mignotte B, Vayssiere JL: Mitochondria and apoptosis. Eur J Biochem. 1998, 252: 1-15. 10.1046/j.1432-1327.1998.2520001.x.
McCord JM, Fridovich I: Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J Biol Chem. 1969, 244: 6049-6055.
Marklund SL: Human copper-containing superoxide dismutase of high molecular weight. Proc Natl Acad Sci USA. 1982, 79: 7634-7638. 10.1073/pnas.79.24.7634.
Weisiger RA, Fridovich I: Mitochondrial superoxide simutase. Site of synthesis and intramitochondrial localization. J Biol Chem. 1973, 248: 4793-4796.
Ambrosone CB, Freudenheim JL, Thompson PA, Bowman E, Vena JE, Marshall JR, Graham S, Laughlin R, Nemoto T, Shields PG: Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer. Cancer Res. 1999, 59: 602-606.
Mitrunen K, Sillanpaa P, Kataja V, Eskelinen M, Kosma VM, Benhamou S, Uusitupa M, Hirvonen A: Association between manganese superoxide dismutase (MnSOD) gene polymorphism and breast cancer risk. Carcinogenesis. 2001, 22: 827-829. 10.1093/carcin/22.5.827.
Knight JA, Onay UV, Wells S, Li H, Shi EJ, Andrulis IL, Ozcelik H: Genetic variants of GPX1 and SOD2 and breast cancer risk at the Ontario site of the Breast Cancer Family Registry. Cancer Epidemiol Biomarkers Prev. 2004, 13: 146-149. 10.1158/1055-9965.EPI-03-0164.
Egan KM, Thompson PA, Titus-Ernstoff L, Moore JH, Ambrosone CB: MnSOD polymorphism and breast cancer in a population-based case-control study. Cancer Lett. 2003, 199: 27-33. 10.1016/S0304-3835(03)00349-5.
Tamimi RM, Hankinson SE, Spiegelman D, Colditz GA, Hunter DJ: Manganese superoxide dismutase polymorphism, plasma antioxidants, cigarette smoking, and risk of breast cancer. Cancer Epidemiol Biomarkers Prev. 2004, 13: 989-996.
Ambrosone CB, Ahn J, Singh KK, Rezaishiraz H, Furberg H, Sweeney C, Coles B, Trovato A: Polymorphisms in genes related to oxidative stress (MPO, MnSOD, CAT) and survival after treatment for breast cancer. Cancer Res. 2005, 65: 1105-1111.
Zhao Y, Xue Y, Oberley TD, Kiningham KK, Lin SM, Yen HC, Majima H, Hines J, St Clair D: Overexpression of manganese superoxide dismutase suppresses tumor formation by modulation of activator protein-1 signaling in a multistage skin carcinogenesis model. Cancer Res. 2001, 61: 6082-6088.
Martin RC, Hughes K, Doll MA, Lan Q, Martini BD, Lissowska J, Rothman N, Hein DW: Method for determination of (-102 C>T) single nucleotide polymorphism in the human manganese superoxide dismutase promoter. BMC Genet. 2004, 5: 33-38. 10.1186/1471-2156-5-33.
Martin RC, Lan Q, Hughes K, Doll MA, Martini BD, Lissowska J, Zatonski W, Rothman N, Hein DW: No apparent association between genetic polymorphisms (-102 C>T) and (-9 T>C) in the human manganese superoxide dismutase gene and gastric cancer (1). J Surg Res. 2005, 124: 92-97. 10.1016/j.jss.2004.09.009.
Nowell S, Sweeney C, Winters M, Stone A, Lang NP, Hutchins LF, Kadlubar FF, Ambrosone CB: Association between sulfotransferase 1A1 genotype and survival of breast cancer patients receiving tamoxifen therapy. J Natl Cancer Inst. 2002, 94: 1635-1640.
Li Y, Huang TT, Carlson EJ, Melov S, Ursell PC, Olson JL, Noble LJ, Yoshimura MP, Berger C, Chan PH: Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat Genet. 1995, 11: 376-381. 10.1038/ng1295-376.
Wispe JR, Warner BB, Clark JC, Dey CR, Neuman J, Glasser SW, Crapo JD, Chang LY, Whitsett JA: Human Mn-superoxide dismutase in pulmonary epithelial cells of transgenic mice confers protection from oxygen injury. J Biol Chem. 1992, 267: 23937-23941.
Yen HC, Oberley TD, Vichitbandha S, Ho YS, St Clair DK: The protective role of manganese superoxide dismutase against adriamycin-induced acute cardiac toxicity in transgenic mice. J Clin Invest. 1996, 98: 1253-1260.
Yen HC, Oberley TD, Gairola CG, Szweda LI, St Clair DK: Manganese superoxide dismutase protects mitochondrial complex I against adriamycin-induced cardiomyopathy in transgenic mice. Arch Biochem Biophys. 1999, 362: 59-66. 10.1006/abbi.1998.1011.
Janssen AM, Bosman CB, van Duijn W, Oostendorp-van de Ruit MM, Kubben FJ, Griffioen G, Lamers CB, van Krieken JH, van de Velde CJ, Verspaget HW: Superoxide dismutases in gastric and esophageal cancer and the prognostic impact in gastric cancer. Clin Cancer Res. 2000, 6: 3183-3192.
Malafa M, Margenthaler J, Webb B, Neitzel L, Christophersen M: MnSOD expression is increased in metastatic gastric cancer. J Surg Res. 2000, 88: 130-134. 10.1006/jsre.1999.5773.
Hur GC, Cho SJ, Kim CH, Kim MK, Bae SI, Nam SY, Park JW, Kim WH, Lee BL: Manganese superoxide dismutase expression correlates with chemosensitivity in human gastric cancer cell lines. Clin Cancer Res. 2003, 9: 5768-5775.
Izutani R, Katoh M, Asano S, Ohyanagi H, Hirose K: Enhanced expression of manganese superoxide dismutase mRNA and increased TNFalpha mRNA expression by gastric mucosa in gastric cancer. World J Surg. 1996, 20: 228-233. 10.1007/s002689900035.
Izutani R, Asano S, Imano M, Kuroda D, Kato M, Ohyanagi H: Expression of manganese superoxide dismutase in esophageal and gastric cancers. J Gastroenterol. 1998, 33: 816-822. 10.1007/s005350050181.
Izutani R, Kato M, Asano S, Imano M, Ohyanagi H: Expression of manganese superoxide disumutase influences chemosensitivity in esophageal and gastric cancers. Cancer Detect Prev. 2002, 26: 213-221. 10.1016/S0361-090X(02)00059-4.
Green H, Ross G, Peacock J, Owen R, Yarnold J, Houlston R: Variation in the manganese superoxide dismutase gene (SOD2) is not a major cause of radiotherapy complications in breast cancer patients. Radiother Oncol. 2002, 63: 213-216. 10.1016/S0167-8140(02)00079-8.
Sutton A, Khoury H, Prip-Buus C, Cepanec C, Pessayre D, Degoul F: The Ala16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria. Pharmacogenetics. 2003, 13: 145-157. 10.1097/00008571-200303000-00004.
A pilot grant was received from the James Graham Brown Cancer Center and USPHS grant CA34627 was received from the National Cancer Institute.
The authors declare that they have no competing interests.
RM participated in design of the study and manuscript preparation. JA participated in the statistical analysis. SN contributed to the study design and to the analysis and interpretation of the data. DH participated in design of the study and manuscript preparation. MD and BM participated in the design of the assay methods. CA contributed to the study design, analysis, and interpretation of the data, and to manuscript preparation.
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Martin, R.C., Ahn, J., Nowell, S.A. et al. Association between manganese superoxide dismutase promoter gene polymorphism and breast cancer survival. Breast Cancer Res 8, R45 (2006). https://doi.org/10.1186/bcr1532
- Breast Cancer
- Receive Radiation Therapy
- Manganese Superoxide Dismutase
- Mitochondrial Target Sequence
- Fluorogenic Probe