Maspin staining in TCC. (A) A strong Maspin protein expression with cytoplasmic and nuclear staining in non-recurrent and non-progressive pTa tumor. (B) Faint Maspin protein expression without nuclear staining in a progressive pTa tumor. 

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... of 3 years. In case of tumor recurrence or progression, tumor specimens were included regardless of the time when either recurrence or progression occurred. Recurrence was defined as the reap - pearance of tumors of the same stage. Progression was defined as tumor development from non-muscle to muscle invasive disease. For classification, the tumor, node and metastasis (TNM) staging system was used. The tumors were initially graded by pathologists according to the 1973 World Helath Organization grading system (18). Tumor specimens were fixed in formalin, dehydrated and embedded in paraffin. The paraffin blocks were cut into 4-μm sections. Hematoxylin and eosin staining was performed for each tumor specimen to validate tumor stage and grade. Tissue microarrays (TMAs) were constructed and stained as previously described (17,19-21). A commercially available Maspin antibody (monoclonal mouse antibody; NCL-Maspin, Novocastra Laboratories Ltd.) in a dilution of 1:500 was used. For the negative control, the primary anti-human Maspin anti- body was replaced by non-immune mouse serum. The TMA slides were reviewed and classified by two independent investigators (M.W.K. and A.S.M) in a blinded manner. For statistical analysis, the immunohistochemical staining reaction was classified according to a semiquantita - tive reference scale ranging from ʻ0̓ to ʻ3+̓, depending on the intensity of the Maspin protein expression. The rela- tive amount of tumor cells stained positively for Maspin (0-100%) in conjunction with the rating of the staining inten- sity, resulted in a staining score ranging from 0 to 300 as previously described (19). The same evaluation method was validated in previous studies (17,21). The concordance rate of the investigators was 90%. Statistical analysis. The JMP program was used for statis- tical evaluations. A D’Augostino and Pearson omnibus normality test was performed to determine whether all data sets were parametric or non-parametric. One-way ANOVA and the Student's t-test were applied to correlate the Maspin expression with various tumor characteristics. Time-to-event probabilities were estimated by the univariate Kaplan-Meier method. The Cox proportional hazard model was applied for the multivariate analysis. P<0.05 was considered to indicate statistically significant differences. Clinicopathological data. Specimens of 162 patients [119 (73%) male and 43 (27%) female] with non-muscle invasive TCC as detected using cystoscopy were included in the present study. Tumor stages according to the TNM system were determined as follows: pTa, n=91 (56%) and pT1, n=71 (44%). Since exclusively non-muscle invasive tumors were investigated, no information on lymph node invasion and distant metastasis was recorded. Of the 162 specimens, 59 (36%) were graded as G1, 90 (56%) as G2 and 13 (8%) as G3. Follow-up data were available for patients with a median follow-up of 58.5 months. Tumor recurrence was observed in 84 (52%) patients, and tumor progression in 28 (17%) patients. The average time interval between initial treatment and time of recurrence was 14 (3-72) and 23 (3-79) months for tumor progression (Table I). Maspin expression. Maspin protein was detected in the nucleus and cytoplasm of the TCC specimens. A clear shift from high to faint staining within the nucleus was observed with more aggressive forms of non-muscle invasive TCC specimens in terms of risk of recurrence and progression. In 12 muscle-invasive tumor tissues used as comparative samples, no nuclear staining was observed (unpublished data). Statistical analysis of Maspin protein expression in the TMAs is shown in Table II. Urothelium-defined (pTa) and minimally invasive TCC (pT1) were not distinguished by immunohistochemically detected Maspin protein expression (p=0.42). TCCs with low and high tumor grades (G1 and G3) showed a lower Maspin expression compared to grade 2 tumors. CIS was noted in 8 patients. While the presence of CIS correlated with Maspin staining scores (p<0.05), multi - focal tumors at the time of diagnosis showed no significant correlation (p=0.41). We evaluated whether the Maspin protein expression in non- muscle invasive bladder cancer specimens predicts tumor recurrence and/or muscle invasion. Results are shown in Table II. Table II. Decreased staining levels in pTa, as well as in combi- nation with pT1 tumors showed a higher incidence of tumor relapse (p<0.05, Student's t-test) as confirmed by Chi-square analyses (Table II, Fig. 1). However, the Kaplan-Meier analysis did not indicate any significant prognostic value in respect to tumor recurrence. As shown in Table III, sensitivity and speci- ficity were low, at 52 and 67%, respectively. The univariate analysis of the prognostic significance of the staining score in relation to the likelihood of tumor progression showed that a strong Maspin expression and nuclear staining were associated with better survival in terms of tumor progression (Table II, (Table II, Fig. Fig. 3). Significant lower staining scores were noted in pTa and pT1 tumors and a reduction in nuclear staining in tissue samples of patients who showed tumor progression within the follow-up time period (p<0.001; Student's t-test). Subsequently, a Kaplan-Meier analysis was performed to further stratify the prognostic value of Maspin. Therefore, we classified the analyzed cohort into groups (A vs. B) according to a receiver operating curve. The cut-off limit (Group A ≥ 175 vs. B < 175) was based on the highest area under the curve and selected using the JMP statistical program (JMP 6 software, SAS Institute, Cary, NC, USA). Sensitivity and specificity were then calculated as 95 and 70%, respectively (Table III). As illustrated in Fig. 2, low Maspin protein expression levels were highly associated with a shorter progression-free survival (46 vs. 18 months; p<0.0001, Log-rank test). To determine which of the studied parameters and/or Maspin staining are independent prognostic indicators of tumor progression to muscle invasion, we used the Cox proportional hazard model. The statistical analysis affirmed only Maspin as an indepen - dent prognostic predictor for the likelihood of progression (p<0.0001; Table II). Further parameters, such as tumor stage and grade, presence of concomitant CIS, multifocality, age and gender, were included. None of these parameters were statistically significant. Maspin is a 42-kDa protein associated with various tumor- related processes such as the inhibition of cell migration, cell invasion, angiogenesis, as well as improvement in cell adhesion and the induction of programmed cell death, thus classifying it as a tumor suppressor (8-12). Maspin expression has been observed in multiple tissues, e.g., epithelium of the breast, prostate, epidermis and lung (10,22-24). Localization within the cell appears to define its function. Loss of nuclear expression in ovarian, breast and lung cancer coincides with more aggressive phenotypes and decreased survival (25-27). We found a shift from nuclear to a predominantly cytoplasmic staining in 12 muscle-invasive tissue samples and, notably, in highly aggressive forms of non-muscle invasive bladder cancer. Tissues from patients that showed progression to muscle-invasive disease detected by subsequent cytoscopies following initial diagnosis showed less nuclear staining in the primary tissue. This observation stresses the assumption that cytoplasmic Maspin in the early steps of tumor progres- sion may signal an imperfect suppressive effect. Currently, only four studies evaluating Maspin expression in bladder cancer have been published. Of these, only Blandamura et al described the possible role of nuclear vs. cytoplasmic staining (16). These authors found a correlation between nuclear Maspin expression and lower histological grades (PUNLMP and low grade). This stresses the prognostic value of Maspin since low-grade and PUNLMP tumors are less likely to progress to muscle-invasive tumor stages (pT≥2). By exclusively including pTa and pT1 tissues in this inves- tigation, we were unable to show significance in respect to tumor stage and grade of the 162 examined samples. Similar results were published by Friedrich et al who found a predom- inantly weak Maspin protein expression in pTa and pT1 tumors without any correlation in respect to stage and grade (15). The two studies must be analyzed in contrast to that of Blandamura and colleagues who reported a statistical associa- tion between the Maspin staining pattern and stage and grade. It appears that a strong Maspin expression was associated with high-grade tumors whereas low-grade tumors and PUNLMP expressed less Maspin (16). When comparing Maspin protein expression in non-muscle invasive to muscle-invasive bladder cancer, Sugimoto et al were the first to describe an increased expression in higher tumor stages (pT≥2 > pTa/pT1) (14). However, in concordance to our results, no statistical differ - ence was found when comparing pTa and pT1 tumors as 23 of the 27 specimens showed no Maspin expression at any rate. Following loss of the Maspin protein expression in muscle-invasive tumor samples which suggested prognostic significance, Beecken and colleagues further examined Maspin mRNA expression in different bladder cell lines (13). Highly aggressive tumor cell lines (MGHU1, UMUC3) showed no Maspin mRNA expression. A subsequent investigation of the in vivo tumor growth rate found a close inverse correlation to the Maspin expression, highly emphasizing its prognostic value. However, apart from the previous promising results, no statistically significant correlation between Maspin staining and tumor relapse of pTa tumors was observed. Notably, the cohort of 24 patients for follow-up information in that study was small. In the present study, follow-up information was collected from 162 patients with a minimum follow-up time of 36 months (median 58.5). A Chi-square analysis indicated Maspin to be a ...