- Open Access
Evaluation of survivin expression in prostate specimens of patients with prostate adenocarcinoma and benign prostate hyperplasia underwent transurethral resection of the prostate or prostatectomy
© The Author(s). 2016
Received: 30 November 2015
Accepted: 5 May 2016
Published: 14 May 2016
Survivin is a newly found member of the inhibitors of apoptosis proteins, which plays a certain role in cancer. Survivin has a distinctly different expression in cancers, including prostate cancer. We are searching for the relationship between survivin levels in normal prostate tissue, benign prostate hyperplasia (BPH), and prostate adenocarcinoma in this study.
The study surveyed 282 prostate samples, 94 normal, 94 BPH, and 94 prostate adenocarcinoma samples. Survivin expression was absent in normal prostate tissues. In the BPH group, the survivin expression level was higher than that of the normal group. In the adenocarcinoma group, the survivin expression level was higher than that of the BPH group. There was a significant association between survivin expression level and the adenocarcinoma stage.
Although there is no expression of survivin in normal prostate tissue, its expression is slightly positive in BPH. High survivin expression is related to a higher Gleason score in the adenocarcinoma of the prostate.
The inhibitors of apoptosis (IAP) proteins are a group of proteins that mediate several pathways, including cell cycle, immunity, inflammation, and cell death (de Almagro and Vucic 2012). One of the recently discovered IAP proteins is survivin. It is the smallest member in the IAP family and is mainly expressed in the fetal tissue but has a known role in many cancers, such as bladder cancer, non-small cell lung cancer, esophageal cancer, breast carcinoma, gastric carcinoma, recurrent colorectal carcinoma, rectal cancer, neuroblastoma, and prostate cancer (Ambrosini et al. 1997; Kishi et al. 2004). Survivin is somehow unique in the IAP family, because of its structure and its definite difference of expression in cancer, including prostate cancer tissue as compared the normal tissue. Survivin is also associated with cancer prognosis and progression (Zhang et al. 2009). The absence of survivin in normal tissues and its over expression in tumors, and the correlation of survivin and poor prognosis of cancer, attracts many researchers to evaluate its potential therapeutic and diagnostic values (Lladser et al. 2011).
Since 1966, Gleason Grading is used in evaluation prostate cancer and it is the strongest prognostic factor in prostate cancer (Gleason 1966; Sauter et al. 2016). Its strong feature is that it is not influenced by cellular morphology and is based on the cancer features. Although tumor volume and PSA level increase may trigger treatment, the main treatment criteria is a Gleason score of 7 or more (Komisarenko et al. 2016). The Gleason grading system was updated in 2005 at a consensus conference of international experts in urological pathology (Epstein 2010) and they agreed that Gleason score between 2 and 4 should not be given on prostate biopsies. This update is currently recommended in international guidelines.
Studies have shown that the level of survivin expression gradually increases from normal prostate tissue and low risk prostate cancer to high risk prostate cancer and is highest in metastatic prostate cancer (Shariat et al. 2004). Some studies show that survivin has a higher expression in benign prostatic hypertrophy (BPH) and that it correlates with BPH parameters (Shariat et al. 2005). However, there are also some studies that confirm that the level of survivin in BPH is not higher than that in normal prostatic tissue (Yu et al. 2010). Although few studies have been conducted to clarify the relationship between survivin and the grading of prostate cancer, this relation appears contradictory. If this relationship is definite, we can use survivin as a prognostic factor and therapeutic target. In this study, we are searching for the relationship between survivin level in normal prostate tissue, BPH, and prostate adenocarcinoma.
The study sample size was calculated on the basis of the survivin level in BPH and the adenocarcinoma of the prostate in a previous study by Rodríguez-Berriguete et al. (Rodríguez-Berriguete et al. 2010). We assumed that there is no survivin expression in normal prostate samples. According to the 95 % confidence interval and power of 20 %, the sample size was calculated as 94 in each group (normal prostate, BPH, and adenocarcinoma of the prostate).
Samples obtained using prostatectomy or TURP and adenocarcinoma and BPH samples diagnosed on the basis of H&E staining. Samples from biopsies were not included in our study, because of the small size of the samples, that could negatively affect the accuracy of staining and Gleason grading. Normal prostate samples obtained from normal glands adjacent to adenocarcinoma or BPH tissue, are consistent with the method employed by Shariat et al. (Shariat et al. 2004).
These samples were obtained from patients admitted to Shahid Beheshty Hospital between 2002 and 2014. Normal prostate and BPH sampling was based on a table of random numbers from the patients admitted to the same hospital during the same period. All prostate samples archived in the pathology ward which had no history of urinary tract infection and prostatitis were included in the study. All of the cases with incomplete and damaged data, with improper staining, and results obtained via needle biopsy were excluded. There are some reports that suggest inflammation as a trigger of increased survivin expression in prostate cells (St. Sauver and Jacobsen 2008), therefore, samples with infiltration of inflammatory cells were also excluded from our study.
Samples were obtained with the usual method of sampling (Dabbs 2013): 5-µm paraffinated blocked sections were obtained from all prostate samples. HaematoxylinEosine (H&E) and Immunohistochemistry (IHC) methods used after sample preparation: (1) Samples were subjected to 60 °C for 2 h. (2) Rehydration was conducted with xylolose, alcohol, and distilled water for 15 min, 10 min, and 5 min, respectively. (3) Endogenous peroxidase activity removal: samples were put in 3 % hydrogen peroxidase for 20 min and washed with phosphate-buffered saline twice, for 5 min each time.
(4) Antigen retrieval: Samples are paled in a citrate puffer (pH 6) and in the autoclave of 134° and 1.5–2 bar pressure for 10 min. They are then let to cool at room temperature for 20 min and wash with distilled water thereafter. (5) Primary survivin antibody is added to the samples for 1 h. (6) They are washed with phosphate-buffered saline (PBS) three times for 5 min each time. (7) Secondary antibody is added and placed for 30 min at room temperature. (8) PBS washing. (9) 3,3′-diaminobenzidine (DAB) chromogen: samples are placed in the diluted solution for 10 min (1.9 DAB with DAB substance ratio). (10) Hematoxylin staining of the background for 1 min, followed by washing. (11) Dehydration of the slides with 96 % alcohol and 100 % xylol, every two sides, 10 min each side. (12) Mounting of the slides in preparation for viewing under the light microscope.
All collected data, including histopathological diagnosis, tumor grade, IHC results (positive or negative), and staining intensity were recorded, along with the patients’ age and serum PSA level.
All collected data were analyzed using SPSS version 17. We described survivin and other variables according to their distribution. We compared the survivin level between groups using the Chi squared test. Logistic regression analysis was used to remove the confounding factors. p was considered significant at the level of 0.05.
Demographic data of cases in different histopathological groups
Age (mean ± SD)
74 ± 9
72 ± 8
76 ± 8
Survivin expression levels in different histopathological groups of prostate samples
Survivin level (%)
These three groups were compared separately. It was found that survivin levels in the adenocarcinoma group were considerably greater than those in the normal group. Comparing the survivin levels of the BPH and adenocarcinoma groups with the normal group revealed a significant difference (p < 0.001).
Gleason staging of adenocarcinoma and survivin expression
Survivin expression (%)
Comparing survivin expression and Gleason grading of >7
Less than 3+ (%)
Comparing the Gleason grading of >7 with survivin expression
Odds Ratio (95 % CI)
Survivin expression up to 30 % (negative and 1+ degree in our staging) is associated with a slight increase in adenocarcinoma staging; however, this association is more apparent in the upper percentages of survivin expression. This correlation is considerable overall.
Serum PSA level and survivin expression correlation
This study evaluates the expression of survivin protein in prostate samples with the IHC method. According to our results, the expression of survivin was negative in the nucleus of normal prostate samples cells, slightly positive in the BPH sample cells, and associated with Gleason staging in the adenocarcinoma group. There is a significant correlation between nuclear and cytoplasmic survivin staining (Zhang et al. 2009), which is comparable with the results of studies evaluating the cytoplasmic and nuclear survivin levels.
Some studies used normal prostate tissues biopsies (Rodríguez-Berriguete et al. 2010). Normal autopsies could not be used in this study, however, owing to methodological limitations. We could not obtain autopsies because the families did not consent.
The results of absence of survivin expression in normal prostate tissues are consistent with other studies (Shariat et al. 2004; Rodríguez-Berriguete et al. 2010). There was a similar negative expression of survivin in these studies in the normal epithelial prostate glands.
In our study, in prostate adenocarcinoma, the survivin expression was higher than BPH and this result is in accordance with the results of Rodríguez-Berriguete et al. (Rodríguez-Berriguete et al. 2010), but the study by Yu et al. (2010) suggests that survivin expression in BPH does not differ significantly from normal prostate tissue. However according to our study we cannot efficiently use 3+ surviving staining for differentiating adenocarcinoma and BPH samples. Using other markers such as alpha-methylacyl CoA racemase and myoepithelial markers such as 34βE12 and P63 appears more functional to differentiate between these two anomalies (Carswell et al. 2006; Kalantari et al. 2014). Survivin is expressed in other tumor types (Shintani et al. 2013; Fukuda and Pelus 2006), and thus, cannot be used in locating the tumor’s origin in metastasis with an unknown origin.
The results of this study showed that malignant prostate carcinoma (based on the Gleason criteria) and survivin expression co-occur, as Shariat et al. suggested. However, our results are not in accordance with those of Rodríguez-Berriguete et al. (Rodríguez-Berriguete et al. 2010). Most patients (60.41 %) with a Gleason score of ≥7 were positive for survivin with a 3+ scale; thus, high survivin expression is related to a higher Gleason score. We found the chance of a Gleason grade of ≥7 in the patients with 3+ staining was 3.15 times in patients with staining <50 %. Although, we excluded the cases with UTI and inflammation to lower the confounding factors, however, the cases were not screened for other malignancies, which may in part, increase the survivin expression. Moreover, the effects of age has been considered, and after adjusting according to age, the results remained unchanged.
We used the IHC grading developed by Shariat et al. (Shariat et al. 2004). Other computer analytical and manual methods also exist (Shinde et al. 2014). For example Dabbs et al. (Dabbs 2013) uses the Histochemical score (H score) for hormonal receptors in breast tumors and counts the non-stained nucleases. This score ranges from 0 to 300. This method was used by Mazieres et al. for the expression of EGFR in lung tumors with IHC (Mazières et al. 2013).
Besides we can use survivin as a prognostic factor, there are therapeutic advantages of measuring it. Survivin can show chemotherapeutic resistance to cisplatin, bortezomib, vincristine, tamoxifen, TNF-a and TRAIL in tumor cells (Cheung et al. 2010; Liu et al. 2010; Zhang et al. 2006; Ling et al. 2010). There is also reports that survivin suppresses radiation-induced apoptosis (Soleimanpour and Babaei 2015), so, targeting survivin can increase the sensitivity to radiotherapy in cancer patients.
The retrospective nature of this study can be counted as a limitation, and a prospective study with other grading methods would further clarify the subject. We could not screen the patients for other tumor types as survivin has been suggested as a progression factor in some cancers, including bladder (Zhang et al. 2016), colon (Li et al. 2016) and breast (Liu et al. 2016). Prospective studies can lessen these confounding factors. Although studies on prostate cancer can reveal the prognostic and therapeutic importance of survivin, further studies on survivin level in different cancers would make a valuable therapeutic and prognostic target for treating patients with other cancers, as well.
We may conclude that there is no expression of survivin in normal prostate tissue but that its expression is slightly positive in the BPH and it is associated with Gleason staging. High survivin expression is related to a higher Gleason score in the adenocarcinoma of the prostate. Survivin detection with the IHC method is unhelpful for differentiating adenocarcinoma of the prostate and BPH.
All the authors participated in performing the study. Dr. Eslami analyzed the data and Dr. Alizargar drafted the paper. All authors read and approved the final manuscript.
We are very thankful of the pathology department and laboratories’ personnel of KAUMS for their contributions.
The authors declare that they have no competing interests.
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