ETMExperimental and Therapeutic Medicine1792-09811792-1015D.A. Spandidos10.3892/etm_00000092etm-01-04-0585ArticlesAlteration of extracellular superoxide dismutase expression is associated with an aggressive phenotype of oral squamous-cell carcinomaYOKOEHIDETAKA1*NOMURAHITOMI2*YAMANOYUKIO2FUSHIMIKAZUAKI2SAKAMOTOYOSUKE1OGAWARAKATSUNORI2SHIIBAMASASHI2BUKAWAHIROKI2UZAWAKATSUHIRO12TAKIGUCHIYUICHI3TANZAWAHIDEKI12
Division of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital;
Departments of Clinical Molecular Biology, and
Respirology, Graduate School of Medicine, Chiba University, Chiba 260-8670,
Japan
Oxidative stress results in damage to cellular structures and has been linked to numerous diseases, including cancer. Extracellular superoxide dismutase (EC-SOD) is a principal enzymatic antioxidant in extracellular space. The purpose of this study was to determine whether the expression of EC-SOD protein is altered in the carcinogenetic process of oral squamous-cell carcinoma (OSCC). Immunohistochemical analysis was carried out in matched normal and tumour specimens collected from 58 OSCCs and 20 oral premalignant lesions (OPLs). Correlations between the EC-SOD expression levels and clinicopathological features of OSCC patients were evaluated by Fisher’s exact test. Although EC-SOD protein was consistently expressed on the plasma membrane of cells in normal tissues, plasma membranous EC-SOD expression was lost in almost all the OSCC specimens examined (98%). Instead, positive EC-SOD expression was detected in the cytoplasmic compartments of cancerous cells in both OPLs (65%) and OSCCs (52%), together with a high incidence of lymph node metastasis (p=0.0397). These results suggest that the dysregulation of EC-SOD protein expression is a frequently occuring and early event in oral carcinogenesis, and that cytoplasmic EC-SOD may contribute to the increased aggressiveness of OSCC.
Oral squamous-cell carcinoma (OSCC) is a major cause of morbidity and mortality worldwide, accounting for 275,000 new cases and more than 120,000 deaths annually (1). Despite therapeutic and diagnostic advances, patients are often diagnosed at advanced stages, and mortality rates are still increasing (2). This highlights the need for continued efforts to discover suitable biomarkers for early disease diagnosis and for the improved understanding of disease pathogenesis as a first step towards improving treatment. Considering these issues, it is imperative to study OSCC at the genetic level and to characterize the genetic changes responsible for carcinogenesis and tumour behavior.
Since cancer has the specific potential of rapid and unlimited growth, oxidative stress, which is characterized by an imbalance between the presence of relatively high levels of toxic reactive species principally consisting of reactive oxygen species (ROS) and antioxidative defense mechanisms, is a common feature in a wide range of solid tumors, including OSCC (3,4). Some studies have found that cells undergoing neoplastic transformation show marked changes in metabolism, resulting in an increase in oxidative stress in cancerous cells (5,6). Enhanced oxidizing status in transforming cells is thought to induce DNA damage, leading to genetic lesions that initiate tumorigenicity and facilitate immortalization, enhance cell proliferation and sustain subsequent local and systemic tumor progression (7–9). Additionally, recent studies revealed that oxidative stress is not merely toxic due to ROS production by metabolism, but also serves an important regulatory role in numerous oncogenic signaling pathways in cancerous cells (10,11).
Superoxide dismutase (SOD) is generally regarded as one of the first lines of antioxidant defense in aerobic cells (12). This enzyme is highly efficient in protecting cells and tissues against oxidative stress based on the potency of the cellular defense mechanism against ROS, including true free radicals, superoxide anion (O2−) and hydroxyl radical (OH−), as well as non-radical compounds, such as hydrogen peroxide (H2O2) (13). Substantial studies have reported that the effects of SOD in human malignancies are associated with tumor growth and drug resistance in vitro and in vivo (14,15). To date, three distinct isoforms of SOD and their distribution have been characterized in mammals (16). Of these, extracellular superoxide dismutase (EC-SOD) is the only isoform that is mainly expressed in the extracellular space via binding with heparin sulfate proteoglycans (17). Since the extracellular space is known to have many potential sources of ROS and to be a relatively more oxidized state than the interior of cells, dysregulation of extracellular oxidant-moderating proteins, including EC-SOD, is considered more important in cancer (18–20). However, in contrast to the intracellular SODs, little is known regarding EC-SOD in human tumors, including OSCC. The purpose of the present study was therefore to determine EC-SOD protein expression in a series of human primary OSCCs and oral premalignant lesions (OPLs), and to correlate the expression with its clinical relevance in patients with OSCC.
Materials and methodsTissue specimens
Fifty-eight pairs of primary OSCC samples and corresponding normal oral epithelium tissues were obtained at the time of surgery, performed at Chiba University Hospital between 1998 and 2007. All patients provided their informed consent according to the study protocol, which was reviewed and approved by the institutional review board of Chiba University before any procedures were performed. In addition, 20 samples from cases of advanced OPLs pathologically diagnosed as leukoplakia with epithelial dysplasia, i.e., mild (n=2), moderate (n=11) and severe (n=7), in a high-risk oral site, such as the ventral-lateral tongue or gingiva, were obtained as described above.
Histopathological diagnosis of each tumor specimen was performed according to the International Histological Classification of Tumors by the Department of Pathology, Chiba University Hospital. Clinicopathological staging was determined by the TNM classification of the International Union against Cancer.
Immunohistochemistry
Immunohistochemical (IHC) staining was carried out on 4-μm sections of paraffin-embedded specimens. The clinicopathological characteristics of the OSCCs in this series are summarized in Table I. Briefly, after deparaffinization and hydration, the slides were pre-treated in 10 mM sodium citrate buffer (pH 6.0) in a microwave oven for 5 min at 95°C. Endogenous peroxidase activity was quenched by a 30-min incubation in a mixture of 0.3% hydrogen peroxide solution in 100% methanol. After being washed with PBS buffer, the sections were incubated with primary antibody affinity-purified goat antihuman EC-SOD polyclonal antibody (1:100 dilution; Santa Cruz Biotechnology) at room temperature in a moist chamber for 2 h. After being washed with PBS buffer, the slides were treated with peroxidase-labeled secondary antibody for 1 h followed by color development in 3,3′-diaminobenzidine tetrahydrochloride (Dako Japan Inc.). Finally, the slides were lightly counterstained with hematoxylin. As negative controls, the slides were incubated with PBS instead of primary antibodies. To quantitate the state of EC-SOD protein expression in these of components, we used previously described Histo (H)-score systems (21,22). In brief, the mean percentage of the epithelial cells that showed a persistent EC-SOD signal was respectively determined in at least five distinct fields in each section at a magnification of x400. The intensity of the immunoreaction was scored as follows: 1+, weak; 2+, moderate; 3+, intense. Three target cell types, normal, pre-malignant and malignant epithelial cells, were identified for scoring. The percentage of EC-SOD-positive cells and the staining intensity were then multiplied to produce an EC-SOD H-score. Cases with a cytoplasmic EC-SOD H-score exceeding 50.15 (maximum score of normal tissues) were considered positive. Specimens were evaluated by two independent pathologists, neither of whom had knowledge of patient clinical status.
Statistical analysis
Statistical analysis of the OSCC tissue and corresponding normal tissue was performed using Wilcoxon’s signed rank sum test. The comparison OPLs and other tissue including normal samples and OSCCs or the Mn-SOD-positive and Mn-SOD-negative cases of OSCC were analyzed using the Mann-Whitney U-test. Correlations between Mn-SOD H-score and clinicopathological features were evaluated by Fisher’s exact test. Data are expressed as the median values. p<0.05 was considered statistically significant.
ResultsEC-SOD expression in OSCCs and OPLs
IHC staining was performed using a series of OSCC specimens, including 58 OSCCs with corresponding normal tissues and 20 OPLs that were histopathologically diagnosed as leukoplakia with epithelial dysplasia. Considering that the evidence indicated that the malignant transformation rate of oral leukoplakia with dysplasia was apparently higher than that of oral leukoplakia without dysplasia (23), patients with advanced OPLs, defined as leukoplakia exhibiting epithelial dysplasia, were eligible for the trial. Representative results for EC-SOD protein expression in normal oral tissues, OPLs and primary OSCCs are shown in Fig. 1.
Normal oral mucosal specimens exhibited consistently strong EC-SOD immunoreaction on the plasma membrane of cells. In OPLs, a loss of plasma membranous EC-SOD immunostaining was observed in some cases, but many of the specimens revealed positive immunoreactivity for EC-SOD on the plasma membrane of cells. Notably, positive staining of the protein was also detected on the cytoplasm of OPL cells in 65% of the specimens examined. Regarding OSCCs, plasma membranous EC-SOD immunoreaction was largely lost in the specimens examined (98%), whereas strong immunoreactivity of the protein was observed on the cytoplasm of cancerous cells in 52% of the specimens (cytoplasmic EC-SOD-positive). According to the H-scores, the expression levels of plasma membrane EC-SOD were significantly reduced in OSCCs compared to their normal counterparts (Wilcoxon’s signed rank sum test, p<0.001; Fig. 2A), whereas cytoplasmic EC-SOD expression levels were considerably higher not only in OSCCs (Wilcoxon’s signed rank sum test, p<0.001; Fig. 2B), but also in OPLs (Mann-Whitney U-test, p<0.001) compared to normal tissues.
Correlation of EC-SOD expression with clinicopathological parameters
In the present study, 52% of the OSCC patients were characterized as EC-SOD-positive in the cytoplasmic compartments of cancerous cells. The correlation between the clinicopathological characteristics of the patients with OSCC and the status of cytoplasmic EC-SOD expression is summarized in Table I. Positive EC-SOD expression of cytoplasm was significantly associated with regional lymph node metastasis (Fisher’s exact test, p=0.0397). The cytoplasmic EC-SOD H-scores for tumors with lymph node metastasis and for those without ranged from 0 to 210.55 (median 100.03) and from 0 to 160.02 (median 30.47), respectively. Cytoplasmic EC-SOD expression levels were significantly higher in patients with OSCC who were pN-positive, compared to those who were pN-negative (Mann-Whitney U-test, p=0.002; Fig. 3).
Disscussion
In the present study, we initially characterized EC-SOD protein expression in cancerous and pre-cancerous lesions of the oral cavity using IHC analysis. Of particular interest is that, although normal oral epithelium tissues consistently exhibited positive expression of EC-SOD on the plasma membrane of cells in all specimens, plasma membranous EC-SOD expression was significantly down-regulated in almost all the OSCC specimens examined (98%), indicating that EC-SOD may be critical for normal functioning, and that the loss of the protein resultsan increased risk of cancer development in cells. This notion is supported by a number of previous studies in vitro and in vivo. Kim et al demonstrated that EC-SOD transgenic mice showed reduced incidence of tumors induced by dimethylbenzanthracene/12-O-tetradecanoylphorbol-13-acetate compared to controls (24). EC-SOD overexpression significantly inhibited the growth of B16 melanomas with high growth potential and decreased the metastatic behavior of lung cancer cells in mice (25). Moreover, a recent study revealed that EC-SOD inhibited the invasive capacity of human prostate cancer cells. This was correlated with reduced metalloproteinase activities (26), suggesting that EC-SOD may have the potential to suppress aggressive tumor behavior.
Conversely, our study also identified altered localization of EC-SOD protein at a high level of expression on the cytoplasm of cancerous cells in 52% of the OSCC specimens examined (p<0.001). Additionally, cytoplasmic EC-SOD overexpression was associated with an aggressive phenotype of OSCC, including lymph node metastasis (p=0.0397). The exact cause of the heterogeneous distribution of EC-SOD in cancerous cells is not as yet clear; however, the most likely cause is the polymorphic variant of the EC-SOD gene, which involves a single nucleotide substitution (G to C) and results in an amino acid change from arginine (Arg) to glycine (Gly) at 213. This amino acid substitution decreases the anchoring of EC-SOD to negatively charged polysaccharides, including heparin (27). Considering that EC-SOD localizes in extracellular spaces via binding with heparin sulfate proteoglycans, this could be linked to the EC-SOD heterogeneous localization in OSCC cells.
Subcellular localization of a protein often provides important clues to its function (28), and the transition from the benign state to the fully malignant one may involve a change in subcellular presence. Some insight into the cytoplasmic mechanism of EC-SOD associated with tumor aggressiveness can be gained from the recent findings that manganese SOD, an intracellular SOD isoform, enhances the invasive and migratory activity of tumor cells though H2O2 production (29), and that overexpression of the protein has been identified in various cancers together with an association with poor prognosis (30,31). Recently, we also found that manganese SOD up-regulation was correlated with a high incidence of lymph node metastasis in OSCC patients (32). Together, it is possible that EC-SOD may function independently in cellular components in cancer cells, acting as a tumor-suppressor on the plasma membrane, but as a tumor-activator in the cytoplasm. Changes in cytoplasmic EC-SOD protein expression were even detected in the OPLs examined (65%), suggesting that the dysregulation of the protein expression is a frequent and early event during oral carcinogenesis.
In conclusion, our study provides the first documentation that EC-SOD protein expression and subcellular distribution is altered in both OPLs and OSCCs, and that positive cytoplasmic EC-SOD expression is associated with an aggressive tumor phenotype in OSCCs. The molecular mechanisms linked to the aberrant expression of EC-SOD in OSCC cells remain unclear, and further studies are warranted to elucidate the molecular alterations involved in EC-SOD dysregulation in oral carcinogenesis.
This study was partly supported by a Grant-in-Aid for Scientific Research (No. 20791492) from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and the Global COE Program (Global Center for Education and Research in Immune System Regulation and Treatment), MEXT, Japan.
ReferencesFerlayJBrayPPisaniPParkinDMGLOBOCAN 2002: Cancer Incidence, Mortalityand Prevalence WorldwideIARC Cancer Base No. 5, version 2.0IARC PressLyon2004La VecchiaCLucchiniFNegriELeviFTrends in oral cancer mortality in EuropeOral Oncol404334392004ValkoMRhodesCJMoncolJIzakovicMMazurMFree radicals, metals and antioxidants in oxidative stress-induced cancerChem Biol Interact1601402006KlaunigJEKamendulisLMThe role of oxidative stress in carcinogenesisAnnu Rev Pharmacol Toxicol442392672004OberleyLWOberleyTDBuettnerGRCell division in normal and transformed cells: the possible role of superoxide and hydrogen peroxideMed Hypoth721421981SpitzDSSimJERidnourLAGaloforoSSLeeYJGlucose deprivation-induced oxidative stress in human tumor cells: a fundamental defect in metabolism?Ann NY Acad Sci8993493622000ValkoMIzakovicMMazurMRhodesCJTelserJRole of oxygen radicals in DNA damage and cancer incidenceMol Cell Biochem26637562004FrancoRSchoneveldOGeorgakilasAGPanayiotidisMIOxidative stress, DNA methylation and carcinogenesisCancer Lett2666112008GromadzińskaJWasowiczWThe role of reactive oxygen species in the development of malignanciesInt J Occup Med Environ Health132332452000KuznetsovAVSmigelskaiteJDoblanderCSurvival signaling by C-RAF: mitochondrial reactive oxygen species and Ca2+ are critical targetsMol Cell Biol28230423132008ChoHJJeongHGLeeJSOncogenic H-Ras enhances DNA repair through the Ras/phosphatidylinositol 3-kinase/Rac1 pathway in NIH3T3 cells. Evidence for association with reactive oxygen speciesJ Biol Chem27719358193662002BlokhinaOVirolainenEFagerstedtKVAntioxidants, oxidative damage and oxygen deprivation stress: a reviewAnn Bot911791942003LiochevSIFridovichIThe effects of superoxide dismutase on H2O2 formationFree Radic Biol Med42146514692007HilemanEAAchantaGHuangPSuperoxide dismutase: an emerging target for cancer therapeuticsExpert Opin Ther Targets56977102001KinnulaVLCrapoJDSuperoxide dismutases in malignant cells and human tumorsFree Radic Biol Med367187442004ZelkoINMarianiTJFolzRJSuperoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution and expressionFree Radic Biol Med333373492002SandströmJKarlssonKEdlundTMarklundSLHeparin-affinity patterns and composition of extracellular superoxide dismutase in human plasma and tissuesBiochem J2948538571993Moriarty-CraigeSEJonesDPExtracellular thiols and thiol/disulfide redox in metabolismAnnu Rev Nutr244815092004NakamuraHMasutaniHYodoiJExtracellular thioredoxin and thioredoxin-binding protein 2 in control of cancerSemin Cancer Biol164444512006ReesMDKennettECWhitelockJMDaviesMJOxidative damage to extracellular matrix and its role in human pathologiesFree Radic Biol Med44197320012008BilalovicNSandstadBGolouhRCD10 protein expression in tumor and stromal cells of malignant melanoma is associated with tumor progressionMod Pathol17125112582004McCartyKSJrSzaboEFlowersJLUse of monoclonal anti-estrogen receptor antibody in the immunohistochemical evaluation of human tumorsCancer Res46424442481986AmagasaTYamashiroMIshikawaHOral leukoplakia related to malignant transformationOral Sci Int345552006KimSHKimMOGaoPOverexpression of extracellular superoxide dismutase (EC-SOD) in mouse skin plays a protective role in DMBA/TPA-induced tumor formationOncol Res153333412005WheelerMDSmutneyOMSamulskiRJSecretion of extracellular superoxide dismutase from muscle transduced with recombinant adenovirus inhibits the growth of B16 melanomas in miceMol Cancer Res18718812003ChaiswingLZhongWCullenJJOberleyLWOberleyTDExtracellular redox state regulates features associated with prostate cancer cell invasionCancer Res68582058262008SandströmJNilssonPKarlssonKMarklundSL10-fold increase in human plasma extracellular superoxide dismutase content caused by a mutation in heparin-binding domainJ Biol Chem26919163191661994HortonPParkKJObayashiTWoLF PSORT: protein localization predictorNucleic Acids Res355855872007ConnorKMHempelNNelsonKKManganese super-oxide dismutase enhances the invasive and migratory activity of tumor cellsCancer Res6710260102672007KimJJChaeSWHurGCManganese superoxide dismutase expression correlates with a poor prognosis in gastric cancerPathobiology703533602003JanssenAMBosmanCBSierCFSuperoxide dismutases in relation to the overall survival of colorectal cancer patientsBr J Cancer78105110571998YokoeHNomuraHYamanoYCharacterization of intra-cellular superoxide dismutase alterations in premalignant and malignant lesions of the oral cavity: correlation with lymph node metastasisJ Cancer Res Clin Oncol135162516332009Figures and Table
Representative results of immunohistochemical staining of EC-SOD in normal tissues, OPLs and primary OSCCs. (A) Normal oral tissue exhibited marked EC-SOD immunoreactivity on the plasma membrane of cells. (B) EC-SOD immunoreactivity was detected heterogeneously on the plasma membrane and cytoplasm of OPL cells. (C) EC-SOD-negative case of OSCCs. (D) Cytoplasmic EC-SOD-positive case of OSCC. (E) Lymph node metastasis disease specimens also exhibited positive cytoplasmic immunostaining for EC-SOD. Original magnification ×100 (A and B), ×200 (C–E).
The state of EC-SOD protein expression in normal tissues (n=58), OPLs (n=20) and primary OSCCs (n=58). (A) H-scores for plasma membranous EC-SOD protein expression. Plasma membranous EC-SOD protein expression was significantly down-regulated in OSCCs compared to normal oral tissue (p<0.001, Wilcoxon’s signed rank sum test) and OPLs (p<0.001, Mann-Whitney U-test). (B) H-scores for cytoplasmic EC-SOD protein expression. The protein expression levels of cytoplasmic EC-SOD in OSCCs (p<0.001, Wilcoxon’s signed rank sum test) and OPLs (p<0.001, Mann-Whitney U-test) were significantly elevated compared to those in normal compartments. Results are expressed as the mean ± SD. H-score, histo-score; *p<0.05.
H-scores for node-negative (n=31) vs. node-positive cases (n=27) compared. EC-SOD protein expression levels were significantly higher in pN-positive OSCC tissue compared to those in pN-negative tissue (p=0.002, Mann-Whitney U-test). Results are expressed as the mean ± SD. H-score, histo-score; *p<0.05.
Correlation between cytoplasmic EC-SOD protein expression and clinical calssification in OSCCs (n=58) and OPLs (n=20).