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X-linked inhibitor of apoptosis positive nuclear labeling: a new independent prognostic biomarker of breast invasive ductal carcinoma

Yutao Zhang*, Jianhua Zhu, Yun Tang, Feng Li, Hongyuan Zhou, Bofang Peng, Chifeng Zhou and Rong Fu

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Department of Pathology, The First People' s Hospital of Zigong, Zigong, China

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Citation and License

Diagnostic Pathology 2011, 6:49  doi:10.1186/1746-1596-6-49

The electronic version of this article is the complete one and can be found online at: http://www.diagnosticpathology.org/content/6/1/49


Received:22 March 2011
Accepted:7 June 2011
Published:7 June 2011

© 2011 Zhang et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

It's well recognized that X-linked inhibitor of apoptosis (XIAP) was the most potent caspase inhibitor and second mitochondria-derived activator of caspase (Smac) was the antagonist of XIAP. Experiments in vitro identified that down regulation of XIAP expression or applying Smac mimics could sensitize breast cancer cells to chemotherapeutics and promote apoptosis. However, expression status and biologic or prognostic significance of XIAP/Smac in breast invasive ductal carcinoma (IDC) were not clear. The present study aimed to investigate relationship among expression status of XIAP/Smac, apoptosis index (AI), clinicopathologic parameters and prognosis in IDC.

Methods

Immunohistochemistry and TUNEL experiment were performed to detect expression of XIAP, Smac, ER, PR, HER2 and AI in 102 cases of paraffin-embedded IDC samples respectively. Expression of XIAP/Smac were also detected in limited 8 cases of fresh IDC specimens with Western blot.

Results

Positive ratio and immunoscore of XIAP was markedly higher than Smac in IDC (P < 0.0001). It was noteworthy that 44 cases of IDC were positive in nuclear for XIAP, but none was for Smac. Expression status of Smac was more prevalent in HER2 positive group than negative group (P < 0.0001) and AI was positively correlated with HER2 protein expression (rs = 0.265, P = 0.017). The present study first revealed that XIAP positive nuclear labeling (XIAP-N), but not cytoplasmic staining (XIAP-C), was the apoptotic marker correlated significantly with patients' shortened overall survival (P = 0.039). Survival analysis demonstrated that XIAP-N was a new independent prognostic factor except for patient age and lymph node status.

Conclusion

Disturbed balance of expression between XIAP and Smac probably contributed to carcinogenesis and XIAP positive nuclear labeling was a new independent prognostic biomarker of breast IDC.

Keywords:
XIAP nuclear labeling; Smac; apoptosis index; prognosis

Background

Disequilibration between cell proliferation and apoptosis has been identified for a momentous mechanism of tumorigenesis. Balance between expression status of anti-apoptotic and pro-apoptotic proteins determines cells to be alive or not. The key event of apoptosis occurrence is cascade activation of caspases, and inhibitor of apoptosis proteins (IAPs) play a important role in caspase inhibition. It is well recognized that XIAP is the most potent caspase inhibitor and Smac is one of the antagonists of XIAP. Unbalanced expression between XIAP and Smac probably contributes to progression of renal cell carcinomas and results in marked apoptosis resistance of this tumour[1]. Breast cancer is the most common malignant tumour of female and estimated new cases in America are 192,370 in 2010[2]. Previous experiments in vitro have identified that sustained overexpression of XIAP can cause acquired tumor necrosis factor-alpha related apoptosis-inducing ligand (TRAIL) resistance in MDA-231 human breast cancer cell[3]. Down regulation of XIAP expression or applying exogenous Smac mimics can sensitize tumor cells, especially for breast cancer cells, to chemotherapeutics and promote apoptosis[4-12]. IDC, not otherwise specified, is the most frequent histological subtype of breast cancer. However, expression status and biologic or prognostic significance of XIAP/Smac proteins in breast IDC are not clear. Immunohistochemistry and western blot are performed to detect expression of XIAP/Smac and terminal TdT-mediated dUTP nick-end labeling (TUNEL) method is performed to detect AI in IDC in the present study. And then, relationship among expression status of those proteins, AI, clinicopathologic parameters and prognosis is analyzed.

Materials and methods

Patients and Tissue samples

This study was done with IRB approval and all patients' consent. Formalin-fixed, paraffin-embedded 102 cases of consecutive IDC samples with different grades and stages (Table 1) were obtained from patients who had received modified radical mastectomy in the authors' institution. The haematoxylin-eosin staining sections had been checked by two experienced pathologists before experiment. All of the patients were not administered any treatment before operation and received postoperative chemotherapeutics (Paclitaxel + Adriamycin + Cyclophosphamide) for 15 consecutive weeks. And 9 out of the 102 patients still received radiotherapy in addition. Limited 8 cases of fresh IDC specimens were obtained from Laboratory of Pathology of West China Hospital.

Table 1. Pathological staging and grading of 102 cases of invasive ductal carcinoma

Antibodies

The following antibodies at indicated dilutions were used in our study: XIAP (rabbit polyclonal, ABZOOM, USA, 1:100 for IHC, and 1:1000 for immunoblotting), Smac (mouse monoclonal, Cell Signaling, USA, 1:100 for IHC, and 1:1000 for immunoblotting), ER and PR (rabbit monoclonal, MAIXIN, Fujian, China), HER2 (mouse monoclonal, MAIXIN, Fujian, China), GAPDH (mouse monoclonal, clone 6C5, Kangcheng, Shanghai, China, 1:10000 for immunoblotting).

Immunohistochemistry

Sections (4 μm) were immunostained by standard SP method protocol. H2O2 (0.3%) was employed to block endogenous peroxydase-binding activity. Antigen retrieval was by microwave boiling in citrate buffer (pH 6.0) for 12 min. Omission of primary antibodies was used as a blank control. Human normal skeletal muscle and adenocarcinoma of stomach tissue sections were immunostained as positive control for XIAP and Smac antibodies respectively. Immunostaining was evaluated and scored by two experienced pathologists independently. All the staining was scored in epithelial cells, but not in stromal cells or inflammatory cells. Cytoplasmic staining of XIAP/Smac and HER2 showed a diffuse staining pattern when positive and was scored by conventional four-tiered semiquantitative scoring system (scores 0-3 for negative, weak, moderate, and strong staining, respectively) based on staining intensity[13]. XIAP was detected in nucleus and cytoplasm, and these results were scored as XIAP-N and XIAP-C separately. The staining of hormone receptor markers ER and PR was exclusively in nucleus. It was assessed as positive that more than 10% tumor cells showed brown nucleus during ER, PR and XIAP-N immunostaining.

Western Blot Analysis

Fresh frozen tissue samples were minced and grinded down to powder with mortar and pestle on liquid nitrogen. Total proteins from powdered tissue samples were extracted in the presence of protease inhibitor cocktails (Roche Diagnostics, Mannheim, Germany), quantitated by using the BCA kit (Pierce Biotechnology Inc., Rockford, IL, USA) and resolved by 10% SDS polyacrylamide (Sigma, St Louis, MO, USA) gel electrophoresis. Proteins were electroblotted to PVDF membrane (Amersham Biosciences UK Ltd., Little Chalfont, UK) in CAPS buffer (pH 11.0) (Amresco, Solon, OH, USA), and then incubated with block solution (5% non-fat milk, 0.1% Tween 20, in 1×TBS, Sigma, St Louis, MO, USA) at room temperature for 2 h. Anti-GAPDH was used as internal control. Horseradish peroxidase-labeled secondary antibodies were from Zymed (San Francisco, CA, USA). Incubation with primary and secondary antibodies were at room temperature for 2 h and 1.5 h, respectively. Signals were detected by exposure to X-ray films after treatment with the Super Signal enhanced chemiluminescence kit (Pierce Biotechnology Inc., Rockford, IL, USA) after incubation with primary and secondary antibodies.

TUNEL assay

Apoptotic tumor cells were detected with TUNEL method, using an in situ cell death detection kit (Roche Diagnostics, Mannheim, Germany). The assay was performed according to the manufacturer's instructions. Briefly, after routine deparaffinization and treatment with H2O2 (3%), sections were digested with proteinase K (20 μg/ml, pH 7.4, 12 min) at 25°C and incubated with the reaction mixture (1:40, 60 min) at 37°C. Incorporated fluorescein was detected with horseradish peroxidase after a 30 min incubation at 37°C and subsequent dyed with DAB. Brown nucleus was assessed as positive apoptotic cell and counted for 1000 tumor cells, scoring as AI in one section for at least 10 high power fields.

Statistical Analysis

General statistical and survival analysis were carried out with the statistical software package SPSS 17.0 (SPSS, Chicago, USA). Intergroup differences were examined by using x2 test, independent example t-test and Mann-Whitney U-test. A P -value of less than 0.05 was considered to indicate the statistical significance.

Results

Relationship among expression status of XIAP/Smac detected by immunohistochemistry, clinicopathologic parameters and biomarkers

Both XIAP and Smac were positive in cytoplasm of tumor cells with strong or moderate intensity, respectively (Figure 1, 2). The positive ratio of XIAP (84.3%, 86/102) was more higher than that of Smac (33.3%, 34/102), and immunoscore of XIAP was higher than Smac in IDC too (P < 0.0001). It was noteworthy that 44 IDC samples were nuclear positive for XIAP (Figure 3), but none was for Smac. And cytoplasm positive status of XIAP nuclear positive group was stronger than the negative group (P = 0.030, 0.047) (Table 2, 3). Otherwise, Smac immunoscore was prevalent in HER2 positive group than negative group (P < 0.0001). Remaining data revealed that the expression status of XIAP/Smac was not correlated with patient age, tumor size, lymph node status, histologic grading, expression of ER and PR (Table 2, 3).

thumbnailFigure 1. Higher power view of representative cytoplasmic immunostaining of XIAP in IDC. Original magnification for this figure: ×400.

thumbnailFigure 2. Higher power view of representative cytoplasmic immunostaining of Smac in IDC. Original magnification for this figure: ×400.

thumbnailFigure 3. Higher power view of representative nuclear immunostaining of XIAP, in addition to cytoplasmic staining in IDC. Original magnification for this figure: ×400.

Table 2. Relationship analysis between positive rate of XIAP/Smac and clinicopathologic variables

Table 3. Relationship analysis among XIAP/Smac immunoscore, apoptosis index, and clinicopathologic variables

Western Blot detection of XIAP/Smac protein expression

In limited 8 cases of fresh IDC examples, we detected expression of both XIAP/Smac protein and GAPDH internal control (Figure 4). The semi-quantitation analysis data indicated that expression status of XIAP protein was more stronger than Smac in fresh IDC specimens with ImageQuant software (Data wasn't shown.).

thumbnailFigure 4. XIAP and Smac proteins in IDC (T1-T8) assessed by Western blot analysis. GAPDH served as internal control of protein loading. Expression of XIAP was more stronger than Smac in IDC with semi-quantitation analysis.

Relationship among apoptosis index, clinicopathologic parameters and biomarkers

The positive apoptotic tumor cells showed brown nucleus in TUNEL detection (Figure 5). AI of total 102 IDC examples variated from 0.212 to 6.044 (mean value 1.322 ± 1.052). The correlation analysis revealed that AI was positively correlated with HER2 protein expression (rs = 0.265, P = 0.017), but not correlated with patient age, tumor size, lymph node status, histologic grading and expression of XIAP, Smac, ER and PR (Data wasn't shown.).

thumbnailFigure 5. Representative positive apoptotic tumor cells in IDC by TUNEL detection. Original magnification for this figure: ×400.

Relationship among expression status of XIAP/Smac, apoptosis index, clinicopathologic parameters and prognosis in IDC

We further analyzed the prognostic value of XIAP-N, XIAP-C, Smac, HER2, ER, PR, AI, patient age, lymph node status and histologic grading in this cohort of 102 pathologically confirmed breast IDC patients, who received modified radical mastectomy, postoperative chemotherapeutics or radiotherapy. The median follow-up time for all patients was 60.0 months. In this cohort, 27 patients died of recurrence or metastases, and another three patients who had been pathologically confirmed recurrence were alive. Kaplan-Meier method and log rank test were used for univariate analysis of overall survival and Cox proportional hazard regression was used for multivariate analysis. Univariate analyses revealed that XIAP-N (positive vs negative), patient age (<50 years vs ≥50 years), tumor size (<5 cm vs ≥5 cm) and lymph node status (N0 vs N1-3) had prognostic significance (Figure 6, 7, 8 and 9). However, in multivariate analysis incorporating these parameters, only XIAP-N, patient age and lymph node status retained independent prognostic power, with approximately 3.0-, 9.2- to 14.8-fold increase of risk for disease-specific death respectively (Table 4).

thumbnailFigure 6. Kaplan-Meier comparison result showed that XIAP-N was correlated significantly with IDC patients' shortened overall survival. Log rank test P-value (two sided) was listed in the figure.

thumbnailFigure 7. Kaplan-Meier comparison result showed that patient age (≥50 years) was correlated significantly with IDC patients' shortened overall survival. Log rank test P-value (two sided) was listed in the figure.

thumbnailFigure 8. Kaplan-Meier comparison result showed that tumor size (>5 cm) was correlated significantly with IDC patients' shortened overall survival. Log rank test P-value (two sided) was listed in the figure.

thumbnailFigure 9. Kaplan-Meier comparison result showed that lymph node status was correlated significantly with IDC patients' shortened overall survival. Log rank test P-value (two sided) was listed in the figure.

Table 4. Relationship analysis among XIAP/Smac expression, apoptosis index, clinicopathologic parameters and prognosis

Discussion

XIAP was the most potent caspase inhibitor, whose molecular structure was known best in IAP family[14]. There were three important components in XIAP gene structure, including BIR domain, Linker domain and Ring-figure domain which possesed the activity as ubiquitin ligase E3, and XIAP could bind to caspase-3, 7, 9 directly to inhibit their activity[15]. Expression of XIAP protein had been detected in most of carcinoma cells, and overexpression of this protein was correlated with patients'sensitivity to anticancer drugs and prognosis[16]. For instance, overexpression of XIAP and Survivin, another member of IAP family, resulted in severe resistance to Adriamycin, Paclitaxel and Vincristine in several kinds of breast cancer cell[17,18]. In LNCaP prostate cancer cells, XIAP restrained apoptosis induced by Paclitaxel through cutting down activity of caspase-3 and inhibiting processing of pro-caspase-3 moreover[19]. On the contrary, patients of acute myeloid leukaemia with low expression level of XIAP could get more favorite prognosis[16].

Smac, which was named by direct IAP-binding protein with low pI (DIABLO) too, was one of the two known negative regulators of XIAP presently. Smac promoted apoptosis through several ways, including firstly interacting with cytochrome c/Apaf-1/pro-caspase-9 complex to activate caspase-9 or downstream effector molecule caspase-3[20,21], secondly binding to BIR domain of XIAP competively and blocking it's inhibitory effect on caspases[22], and lastly cooperating with Omi/HtrA2 to promote XIAP to degradation[23,24]. Previous study reported that total positive ratio of Smac was 62% in several carcinomas, and lack of Smac would lead to down regulation of apoptosis[25].

Preliminary research showed positive ratio of XIAP in breast cancer were 89.7%, but no related report about Smac[26]. Our data indicated not only positive ratio but also immunoscore of XIAP were more higher than Smac in breast IDC, and semi-quantitation analysis of western blot detection proved it too. But it just could be regarded as a attempt because the fresh samples were so limited in this study. Disturbed balance of expression between XIAP and Smac contributed to progression of renal cell carcinoma and XIAP was an independent prognostic biomarker of clear cell renal cell carcinoma[1,27]. Similarly, it also could be believed that disturbed balance of expression between XIAP and Smac contributed to carcinogenesis of IDC based on results of the present study. A set of data, consisting with other report, showed that expression status of XIAP/Smac was not correlated with patient age, tumor size, lymph node status, histologic grading, expression of ER and PR[26]. Whereas, Jaffer and his colleagues found a possible role of XIAP in the more aggressive clinical behavior of grade 3, compared with lower-grade ductal carcinomas[28]. These conflicting results need be confirmed in a following large sample study.

In previous reports, XIAP was only detected in cytoplasm[26,28]. However, we found 44 IDC samples were positive in nucleus and cytoplasm for XIAP simultaneously, but none was for Smac. This difference was maybe caused by using different primary antibodies and tissue specimens from different race. Tissue specimens in present study were all from Chinese female patients, but not from Europe or America. Something different from previous reports was that XIAP nuclear labeling (XIAP-N), but not cytoplasmic staining of XIAP (XIAP-C), was the apoptotic marker which correlated significantly with IDC patients' shortened overall survival. Univariate survival analysis disclosed that patient age, tumor size, lymph node status and XIAP-N had prognostic significance. Nevertheless, it was demonstrated by multivariate survival analysis that only patient age, lymph node status and XIAP-N were independent prognostic factors.

It had been introduced previously that XIAP and Survivin, two important caspase inhibitors of IAP family, were comitantly overexpressing in several kinds of breast cancer cell and oweing to elevated resistance to chemotherapeutics[17,18]. Even more, Survivin was an independent predictor of short-term survival in poor prognostic breast cancer patients[26]. All results stated above called attention to us that overexpression of XIAP and Survivin were significantly correlated with carcinogenesis, progression and prognosis of breast cancer, and the two molecules played similar role in several aspects in breast cancer. Therefore, we concluded XIAP, like Survivin, probably was a new independent prognostic biomarker of breast cancer although it was different that only XIAP nuclear labeling, but not cytoplasm staining, had prognostic significance. This condition was similar to previous reports that Survivin nuclear labeling was a prognostic biomarker of breast cancer and superficial urothelial carcinoma of urinary bladder[29,30].

There was another interesting result in our study that immunoscore of Smac was prevalent in HER2 positive group than negative group, and apoptosis index was positively correlated with HER2 protein expression. Someone believed that apoptosis was decreasing in malignant tumors. But in fact, increasing apoptotic tumor cells could usually be found in malignancies, especially for tumors with high proliferating rate. On the other hand, overexpression of oncogene HER2 contributed to breast carcinogenesis. So, it's not difficult for us to understand that apoptosis index was positively correlated with HER2 protein expression in our study. Our result also consisted with Hinnis' study that AI was not correlated with patient age, tumor size, lymph node status, histologic grading and expression of XIAP, Smac, ER and PR protein[26]. At the same time, our following up data revealed similar result with previous reports that AI was not correlated with IDC patients' prognosis[31,32]. However, why there was prevalent Smac in oncogene HER2 positive group? The relationship between the two parameters had not been reported before, and both mechanism and significance were not clear too. Maybe, this point would be a new target for us to perform a large sample study in the future.

As discussed above, XIAP was a potent protein for apoptosis inhibition and Smac was an important negative regulator of the former. Disturbed balance of expression between XIAP and Smac probably contributed to carcinogenesis and XIAP positive nuclear labeling was a sign of unfavourable prognosis in breast invasive ductal carcinoma. It was important for us to demonstrate the XIAP nuclear staining is genuine, and we were going to practice it in breast cancer cell lines in following study. Further more, Relationship among Smac, HER2 and apoptosis index would be explored in the following study too.

Conclusion

Disturbed balance of expression between XIAP and Smac probably contributed to carcinogenesis and XIAP-N was a new independent prognostic biomarker of breast invasive ductal carcinoma.

Competing interests

This paper has never been published and is not under simultaneous review by another journal. All authors have read and approved to submit it to your journal. There is no conflict of interest of any authors in relation to the submission.

Authors' contributions

YZ, YT and JZ participated in selecting cases, interpretation of results and writing of the manuscript. YZ, FL, BP and CZ carried out the immunohistochemistry, western blot and TUNEL experiment. HZ and RF collected the clinical details of the patients and carried out statistical analysis. All authors read and approved the final manuscript.

Acknowledgements

We thank Dr J Gong and Dr N Chen in the Laboratory of Pathology of West China Hospital for technical assistance. This study is supported by grants to Yutao Zhang from the Key Science and Technology Foundation of Zigong (No.08Y04). Written consent for publication is obtained from the patients or their relative.

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