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Cancer Research and Treatment > Volume 42(3); 2010 > Article
Cho, Chung, Cho, Kim, Joung, Seo, Chung, Park, Hong, and Lee: Bcl-2 as a Predictive Factor for Biochemical Recurrence after Radical Prostatectomy: An Interim Analysis



The objective of this study was to determine Bcl-2 expression in localized prostate cancer and its potential role as a predictive factor for biochemical recurrence (BCR).

Materials and Methods

This study included 171 Korean patients with newly diagnosed adenocarcinoma of the prostate who underwent radical prostatectomy (RP) without neoadjuvant therapy at a single center between February 2005 and May 2009. RP specimens obtained from these patients were analyzed for the expression of Bcl-2 using tissue microarray. The values of Bcl-2 and other clinicopathologic factors were evaluated. Statistical analysis was performed with contingency table analysis, chi-square tests, and a Cox proportional hazard model.


Bcl-2 expression was immunohistologically-confirmed in 42 patients (24.6%). Bcl-2 expression was not associated with conventional clinicopathologic factors. Bcl-2 negative patients had a significantly longer mean BCR-free survival than Bcl-2-positive patients (p=0.036). Among several variables, a high Gleason score in the RP specimen (≥8), extraprostatic extension, seminal vesicle invasion (SVI), lymphovascular invasion (LVI), and Bcl-2 expression were significant predictors of BCR based on univariate analysis. Multivariate Cox proportional hazards analysis revealed that BCR was significantly associated with a high prostate specific antigen level (p=0.047), SVI (p<0.001), a positive surgical margin (p=0.004) and Bcl-2 expression (p=0.012).


Bcl-2 expression in RP specimens is associated with a significantly worse outcome, suggesting a potential clinical role for Bcl-2. Post-operative Bcl-2 could be a significant predictor of outcome after RP.


The early detection of prostate cancer with prostate specific antigen (PSA) testing allows many patients the option of radical treatment with curative intent. However, approximately 25% of patients will develop a post-operative biochemical recurrence (BCR) (1). The prognosis after radical prostatectomy (RP) is usually based on clinical findings, such as the pre-operative PSA level and PSA doubling time, pathologic findings, such as the Gleason score, surgical margin status (SMS), extraprostatic extension, and seminal vesicle invasion (SVI) (1-5). Furthermore, several investigators have reported the usefulness of nomograms in calculating survival after definitive therapy for localized prostate cancer, which were developed based on multiple clinical parameters. To date, numerous attempts have been made to use tissue biomarkers to enhance the prediction of outcome after RP. However, no molecular markers have been identified that contribute independent prognostic information on prostate specimens to enable prediction of treatment failure after RP. Many potentially prognostic markers have been studied, and some have been incorporated into prognostic models or therapeutic decision making. The oncoprotein encoded by the Bcl-2 gene is well-accepted for its involvement in the development of human follicular B-cell lymphomas (6). Likewise, this gene is suspected of participating in the development of other types of human malignancies (lymphomas, and breast and prostate cancer) (7-9). Unlike in breast cancer and lymphoma, a report by Berges et al. (10) suggests that p53 gene expression is not required to mediate programmed cell death in androgen-deprived prostatic glandular epithelial cells in prostate cancer. Furthermore in clinical specimens, it is not clear that p53 and bcl-2 necessarily interact in apoptosis mechanisms. Bauer et al. (11) reported that only 3 of 40 (7.5 percent) adenocarcinoma specimens of the prostate exhibited combined p53 and bcl-2 positivity. Bcl-2 overexpression is a relatively low-frequency event in clinically localized prostate cancer. In addition, bcl-2 showed higher specificity and positive predictive value than that of p53. Thus, in prostate cancer, we think that bcl-2 could be an independent biomarker.
In this study, we analyzed the expression of Bcl-2 in a group of Korean patients to ascertain the clinical significance of Bcl-2 expression in relation to BCR after RP.

Materials and Methods

1. Study population

One hundred and seventy-one Korean men, 49-80 years of age, with clinically localized adenocarcinoma of the prostate were included in this study. The patients underwent RP at the Korean National Cancer Center (NCC) between February 2005 and May 2009. None of the patients received androgen deprivation therapy before RP. All patients had a pre-treatment serum PSA, which ranged from 0.8 to 79 ng/mL (mean, 9.8 ng/mL). TNM (primary tumor, regional nodes, metastasis) classification was performed according to the 2002 American Joint Committee on Cancer. The margin was considered positive when cancer cells were detected in ≥1 surgical margins.
In accordance with the requirements of our institutional review board, informed consent to the prospective study was obtained from each patient, and the study design was approved by the Research Ethics Committee of our institution. The mean duration of follow-up after RP was 23.3 months (range, 2 to 51 months). After RP, patients were followed up by measurements of serum PSA levels at ≤3 month intervals for the first 2 years and every 6 months thereafter. A BCR was defined as a post-operative serum PSA of at least 0.4 ng/mL. Irrespective of pathologic findings, suggesting a poor prognosis, none of the patients received any adjuvant therapy until BCR was detected.

2. Immunohistochemical technique

RP specimens obtained from these patients were analyzed for the expression of Bcl-2 using tissue microarray (TMA). Paraffin-embedded formalin-fixed prostatectomy tissue blocks were cut in 3 µm thicknesses onto silane-coated slides and heated for 30 minutes in an 57℃ oven. The tissue was then deparaffinized in xylene, rinsed well over several ethanol washes (95%), and finally with distilled water. The slides were then microwaved in EDTA buffer (pH 8.0) for 60 minutes for antigen retrieval. Following a rinse with water, 3% hydrogen peroxide was applied to the slides for 4 minutes at room temperature. Another rinse with Tris buffer was performed before the primary Bcl-2 antibody (Dako co., Carpinteria, CA) was overlaid for 32 minutes at 42℃. The slides were again rinsed in Tris buffer twice, then incubated with Biotin (iVIEW DAB detection kit, Ventana, Tucson, AZ) for 10 minutes, rinsed again as before, and incubated with streptavidin for 8 minutes. After a final rinse with Tris buffer, chromogen (dimethylaminoazobenzene, Ventana) was applied for 8 minutes, followed by copper solution for 4 minutes. Counterstaining was then performed with commercially prepared hematoxylin for 4 minutes. After post-counterstaining was performed with bluing solution, the slides were dehydrated and coverslipped with Permount. BenchMark XT (Ventana) was used for all staining. Two independent uropathologists (WSP and EKH) viewed and interpreted the stained slides without knowledge of patient outcome. As shown in Fig. 1, the intensity of immunostaining for Bcl-2 was visually scored, and stratified into four groups (negative, weak, moderate, and strong); each group was defined as having no tumor cells, <10% the tumor cells, 10% to 50% tumor cells, and >50% tumor cells, respectively. Any cytoplasmic staining with Bcl-2 was considered positive, indicating expression. Staining in the basal epithelial cells of normal prostate epithelium served as an internal control.

3. End points and statistical analysis

Because there were too few patients with Bcl-2 weak, moderate, and strong staining, it was necessary to combine the groups which stained weak, moderate, and strong for this analysis. Contingency table analysis and chi-square tests were used to determine the relationship between the expression of Bcl-2 and other clinicopathologic features. In addition, we determined the impact of Bcl-2 on BCR. Recurrence-free survival curves were plotted according to the Kaplan-Meier method. A log-rank test was applied to determine the relationship between prognostic markers and BCR. A Cox proportional hazard model with stepwise selection of the co-variates was used to determine the parameters with the greatest influence on the risk of BCR. The level of statistical significance was set at p<0.05 (two-sided), and the SPSS ver. 12.0 (SPSS Inc., Chicago, IL) was used for the statistical analysis.


1. Patients

Data on all 171 patients were available. The mean age was 64.4 years (49 to 80 years). The patient characteristics are listed in Table 1. The pre-treatment serum PSA 4~10 group was most common in our study. Pre- and post-operative Gleason scores ranged from 5 to 10. One hundred and sixty-seven patients had pre- and post-operative Gleason scores. The post-operative Gleason scores were higher than the pre-operative scores (p<0.001). SVI, perineural invasion (PNI), and lymphovascular invasion (LVI) were detected in 13 (7.8%), 104 (61.2%), and 16 (9.4%) patients, respectively. The surgical margin positive rate was 34.7%.

2. Bcl-2 expression and clinicopathologic factors

Bcl-2 expression was immunohistologically confirmed in 42 patients (24.6%). The association between several clinicopathologic factors and Bcl-2 expression in RP specimens was analyzed. Bcl-2 staining was not associated with PSA level, pre-operative Gleason score, post-operative Gleason score, clinical stage, SVI, LVI and SMS.

3. The impact of Bcl-2 on BCR

During the present observation period, BCR developed in 15 of 171 patients (8.8%); there were BCRs in 6 of 41 patients (14.6%) with Bcl-2-positive RP specimens and in 9 of 126 patients (7.1%) with Bcl-2-negative RP specimens. The Kaplan-Meier survival estimates by Bcl-2 status are shown in Fig. 2. BCR-free survival in patients with Bcl-2 positive specimens was significantly lower than in patients with Bcl-2 negative specimens (p=0.036). At the time of mean follow-up, 23.3 months, BCR-free survivals of Bcl-2 positive and negative patients were 87.8% and 94.4% respectively. However, these findings were not significant statistically. Furthermore, we evaluated the predictive value of several clinicopathologic factors for BCR. Eight variables recorded at the time of prostatectomy were considered potential prognostic factors for BCR. By univariate Cox proportional hazards analysis, the post-operative Gleason score ≥8 (p=0.002), extraprostatic extension (p=0.006), SVI (p<0.001), LVI (p=0.008), and Bcl-2 expression (p=0.039) significantly influenced the time to BCR. Furthermore, the pre-operative Gleason score (p=0.060) influenced BCR with borderline significance. Multivariate Cox proportional hazards analysis revealed that BCR was significantly associated with a high PSA level (hazard ratio [HR], 10.147; p=0.047), SVI (HR, 42.613; p<0.001), a positive surgical margin (HR, 6.294; p=0.004), and Bcl-2 expression (HR, 4.503; p=0.012) (Table 2).


Carcinoma of the prostate varies greatly in biological behavior, ranging from slowly progressive to highly aggressive metastasizing tumors. The advent of immunohistochemical staining has led to many studies using tumor biomarkers, but no marker has moved from the research setting into the routine assessment of prostate carcinoma. Several groups have studied Bcl-2 with conflicting results (12). Given the alleged role of Bcl-2 expression for hormone resistance in prostate cancer, such a result would be expected after anti-androgen treatment (13-15). However, none of our patients had undergone neoadjuvant or adjuvant anti-androgen therapy, thus our results cannot be explained by this mechanism. Bauer et al. (11) reported that increased expression of Bcl-2 correlates with higher rates of BCR in patients who have undergone a RP for clinically-localized prostate cancer. Further studies have also shown the ability of Bcl-2 to be of prognostic value for patients with organ-confined disease (16,17). However, other studies have shown that Bcl-2 does not have prognostic significance in prostate cancer patients (18).
In the current study, the routine clinical outcome predictors (preoperative PSA level, biopsy Gleason score, Gleason score in the RP specimen, pathologic stage, SVI, PNI, LVI, SMS) and the expression of Bcl-2 in specimens from 171 RPs performed during a 5-year period were compared. Based on the contingency table analysis and chi-square tests, we did not find a significant relationship between Bcl-2 expression and other parameters. Several previous studies showed that Bcl-2 expression was not significantly associated with Gleason score or stage. For example, in a report of patients with Stage B, C, or D disease, Amirghofran et al. (19) found that Bcl-2 expression had no relationship to prostate carcinoma stage or Gleason score.
Our analysis of conventional clinicopathologic parameters showed that the post-operative Gleason score, extraprostatic extension, SVI, and LVI were predictors of BCR by univariate analysis and that a high PSA level, SVI, and positive surgical margin were significant by multivariate analysis. A notable finding was that the expression of Bcl-2 was an independent prognostic factor in univariate and multivariate analyses. Furthermore, based on the Kaplan-Meier curve, Bcl-2 expression was associated with a shortened BCR-free survival in our series.
Several groups have studied Bcl-2, p53, and Ki-67 immunostaining, but the results have been variable (11,16,20-22). The reasons for the differences in these results include various definitions of BCR, differences in the sensitivity of the commercial antibodies, and carcinogenetic differences in marker expression. Marks et al. (23) reported that prostate cancer specimens from native Japanese and Japanese-American men were histologically-similar, but tissue biomarker expression suggested differing mechanisms of carcinogenesis. In our study, study populations were native Korean men. We concluded that racial, ethnicity, and environmental differences affect expression of biomarkers. Based on the results reported herein, Bcl-2 appears to be an independent prognostic factor for BCR. This result implies that Bcl-2 expression in a Korean population has unique clinical significance.
A number of factors may have contributed to the differences between the findings of the current study and earlier studies. First, this study was a planned prospective study. Second, unlike the previous studies, the current study used a well-defined and relatively homogeneous group of patients. In a number of the earlier studies, heterogeneous groups of patients with pathologic stages ranging from pT1-pT4 were used, with some studies including patients with anti-androgen therapy or multiple ethnic groups. As a result, substantial variation in the risk of BCR would have related to tumor stage and Gleason grade, and these biologic differences would have contributed to potentially non-linear changes in biomarker expression that may not have extrapolated to clinical subgroups. Third, in contrast to earlier studies, two uropathologists (WSP and EKH) viewed the stained slides without knowledge of patient outcome in our study. This fact strengthens the significance of our study. In similarity to previous studies, the total Bcl-2 positive rate of our study group was 24.6% (11). In contrast to previous studies, on the other hand, the weak positive rate for our study group was 17.5%. We, thus, feel that pathologist subjectivity may have affected the results of previous studies.
We would like to address several limitations of this study. First, a sample size of 171 patients in as common a disease as prostate cancer is not sufficiently large. Second, the average duration of follow-up of 23.3 months was relatively short. This reduces the clinical significance of our relatively low BCR rate. Third, it is possible that the high rate of positive surgical margins and the low BCR rate may have influenced the statistical analyses. Furthermore, although this study focused on patients who were diagnosed with organ-confined prostate cancer, the clinicopathologic features were relatively adverse compared with the large series performed in Western country (24). Nevertheless, the research focusing on Bcl-2 and other molecular markers is worthwhile. Therefore, in the future, studies with larger numbers of patients and longer-term follow-up will be required. Fourth, the TMA has some limitations compared with real-time PCR. The most important potential limitation is the small size of the tissue sample (tissue volume). Thus, strong heterogeneity of the tumor sample may not be reflective of the heterogeneity of the tumor as a whole (18).


The expression of Bcl-2 in RP specimens seems to be associated with a significantly worse outcome, highlighting a potential clinical role. Post-operative Bcl-2 could be a significant predictor of BCR in patients undergoing RP. In addition, Bcl-2 expression may influence the decision for adjuvant or salvage treatment.


This study was supported by a Korean National Cancer Center Grant, no. 0810220.


1. Kattan MW, Eastham JA, Stapleton AM, Wheeler TM, Scardino PT. A preoperative nomogram for disease recurrence following radical prostatectomy for prostate cancer. J Natl Cancer Inst. 1998;90:766–771. PMID: 9605647
crossref pmid
2. Kattan MW, Wheeler TM, Scardino PT. Postoperative nomogram for disease recurrence after radical prostatectomy for prostate cancer. J Clin Oncol. 1999;17:1499–1507. PMID: 10334537
crossref pmid
3. Epstein JI, Partin AW, Sauvageot J, Walsh PC. Prediction of progression following radical prostatectomy: a multivariate analysis of 721 men with long-term follow-up. Am J Surg Pathol. 1996;20:286–292. PMID: 8772781
crossref pmid
4. D'Amico AV, Chen MH, Roehl KA, Catalona WJ. Identifying patients at risk for significant versus clinically insignificant postoperative prostate-specific antigen failure. J Clin Oncol. 2005;23:4975–4979. PMID: 16051949
crossref pmid
5. Ross JS, Sheehan CE, Dolen EM, Kallakury BV. Morphologic and molecular prognostic markers in prostate cancer. Adv Anat Pathol. 2002;9:115–128. PMID: 11917165
crossref pmid
6. Korsmeyer SJ. Bcl-2: an antidote to programmed cell death. Cancer Surv. 1992;15:105–118. PMID: 1451107
7. Colombel M, Symmans F, Gil S, O'Toole KM, Chopin D, Benson M, et al. Detection of the apoptosis-suppressing oncoprotein bc1-2 in hormone-refractory human prostate cancers. Am J Pathol. 1993;143:390–400. PMID: 7688182
pmid pmc
8. Villuendas R, Piris MA, Orradre JL, Mollejo M, Rodriguez R, Morente M. Different bcl-2 protein expression in high-grade B-cell lymphomas derived from lymph node or mucosa-associated lymphoid tissue. Am J Pathol. 1991;139:989–993. PMID: 1951637
pmid pmc
9. Hur DS, Lee SW, Kim KH, Cho YS, Joo KJ, Park HJ, et al. Significance of expressions of bcl-2 and p53 protein as the prognostic factor in metastatic prostate adenocarcinoma. Korean J Urol. 2001;42:1265–1269.

10. Berges RR, Furuya Y, Remington L, English HF, Jacks T, Isaacs JT. Cell proliferation, DNA repair, and p53 function are not required for programmed death of prostatic glandular cells induced by androgen ablation. Proc Natl Acad Sci U S A. 1993;90:8910–8914. PMID: 8415631
crossref pmid pmc
11. Bauer JJ, Sesterhenn IA, Mostofi FK, McLeod DG, Srivastava S, Moul JW. Elevated levels of apoptosis regulator proteins p53 and bcl-2 are independent prognostic biomarkers in surgically treated clinically localized prostate cancer. J Urol. 1996;156:1511–1516. PMID: 8808919
crossref pmid
12. de la Taille A, Buttyan R, Benson MC, Katz AE. The role of tumor biomarkers as predictors of serum PSA recurrence after radical prostatectomy. Semin Urol Oncol. 1998;16:137–144. PMID: 9741418
13. McDonnell TJ, Troncoso P, Brisbay SM, Logothetis C, Chung LW, Hsieh JT, et al. Expression of the protooncogene bcl-2 in the prostate and its association with emergence of androgen-independent prostate cancer. Cancer Res. 1992;52:6940–6944. PMID: 1458483
14. Westin P, Stattin P, Damber JE, Bergh A. Castration therapy rapidly induces apoptosis in a minority and decreases cell proliferation in a majority of human prostatic tumors. Am J Pathol. 1995;146:1368–1375. PMID: 7778676
pmid pmc
15. Raffo AJ, Perlman H, Chen MW, Day ML, Streitman JS, Buttyan R. Overexpression of bcl-2 protects prostate cancer cells from apoptosis in vitro and confers resistance to androgen depletion in vivo. Cancer Res. 1995;55:4438–4445. PMID: 7671257
16. Wu TT, Hsu YS, Wang JS, Lee YH, Huang JK. The role of p53, bcl-2 and E-cadherin expression in predicting biochemical relapse for organ confined prostate cancer in Taiwan. J Urol. 2003;170:78–81. PMID: 12796649
crossref pmid
17. Stackhouse GB, Sesterhenn IA, Bauer JJ, Mostofi FK, Connelly RR, Srivastava SK, et al. p53 and bcl-2 immunohistochemistry in pretreatment prostate needle biopsies to predict recurrence of prostate cancer after radical prostatectomy. J Urol. 1999;162:2040–2045. PMID: 10569564
crossref pmid
18. Merseburger AS, Kuczyk MA, Serth J, Bokemeyer C, Young DY, Sun L, et al. Limitations of tissue microarrays in the evaluation of focal alterations of bcl-2and p53 in whole mount derived prostate tissues. Oncol Rep. 2003;10:223–228. PMID: 12469173
crossref pmid
19. Amirghofran Z, Monabati A, Gholijani N. Apoptosis in prostate cancer: bax correlation with stage. Int J Urol. 2005;12:340–345. PMID: 15948719
crossref pmid
20. Moul JW. Angiogenesis, p53, bcl-2 and Ki-67 in the progression of prostate cancer after radical prostatectomy. Eur Urol. 1999;35:399–407. PMID: 10325496
crossref pmid
21. Bubendorf L, Tapia C, Gasser TC, Casella R, Grunder B, Moch H, et al. Ki67 labeling index in core needle biopsies independently predicts tumor-specific survival in prostate cancer. Hum Pathol. 1998;29:949–954. PMID: 9744310
crossref pmid
22. Oxley JD, Winkler MH, Parry K, Brewster S, Abbott C, Gillatt DA. p53 and bcl-2 immunohistochemistry in preoperative biopsies as predictors of biochemical recurrence after radical prostatectomy. BJU Int. 2002;89:27–32. PMID: 11849156
crossref pmid
23. Marks LS, Kojima M, Demarzo A, Heber D, Bostwick DG, Qian J, et al. Prostate cancer in native Japanese and Japanese-American men: effects of dietary differences on prostatic tissue. Urology. 2004;64:765–771. PMID: 15491717
crossref pmid
24. Ramos CG, Roehl KA, Antenor JA, Humphrey PA, Catalona WJ. Percent carcinoma in prostatectomy specimen is associated with risk of recurrence after radical prostatectomy in patients with pathologically organ confined prostate cancer. J Urol. 2004;172:137–140. PMID: 15201754
crossref pmid
Fig. 1
Prostate prognostic tissue microarray (TMA) containing specimens from 171 tumors. (A) TMA section stained with hematoxylin and eosin (×100). (B) TMA section with Bcl-2 staining (×100). (a) Intensity of immunostaining for Bcl-2: negative group (×400). (b) Intensity of immunostaining for Bcl-2: weak group (×400). (c) Intensity of immunostaining for Bcl-2: moderate group (×400). (d) Intensity of immunostaining for Bcl-2: strong group (×400).
Fig. 2
Kaplan-Meier biochemical recurrence (BCR)-free survival curves according to the expression of Bcl-2.
Table 1
Patient characteristics

*prostate-specific antigen, gleason score.

Table 2
Univariate and multivariate analyses of prognostic factors for biochemical recurrence

*hazard ratio, confidence interval, prostate-specific antigen, §reference category, gleason score.

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