CIAPIN1 nuclear accumulation predicts poor clinical outcome in epithelial ovarian cancer
© Cai et al.; licensee BioMed Central Ltd. 2012
Received: 17 February 2012
Accepted: 20 May 2012
Published: 19 June 2012
Epithelial ovarian cancer (EOC) is an aggressive disease with poor prognosis. The expression of cytokine-induced apoptosis inhibitor 1 (CIAPIN1) correlates with the malignant progression of several cancers. However, the relationship between the subcellular localization of CIAPIN1 and clinical characteristics in EOC remains unclear.
Immunohistochemistry was performed to detect CIAPIN1 expression in 108 EOC tissues. CIAPIN1 expressions in eight fresh EOC tissues were detected by Western blotting. The relationship between CIAPIN1 subcellular expression and patients’ clinicopathological features, including prognosis, was evaluated. Immunohistochemistry and immunofluorescence were employed to assess the CIAPIN1 subcellular localization in the EOC cell lines A2780 and HO8910. In addition, all patients were followed up to assess the prognostic value of CIAPIN1 in patients with EOC.
CIAPIN1 is highly expressed in EOC, but is present at low levels in paired non-cancerous ovarian epithelial tissues. The results of Western blotting were in accordance with the immunohistochemical results. Poor differentiation of the tumors and EOC cell lines correlated with higher levels of CIAPIN1 nuclear expression. CIAPIN1 nuclear expression significantly correlated with the Federation International of Gynecology and Obstetrics (FIGO) stage and histological differentiation (P = 0.034 and P < 0.0001, respectively). Moreover, nuclear localization of CIAPIN1 was selected as an unfavorable prognostic factor by both univariate and multivariate analyses ( P < 0.001). However, no significant correlations were observed between cytoplasmic localization of CIAPIN1 and clinicopathological parameters.
CIAPIN1 might play a crucial role in the differentiation of EOC cells. Elevated expression of nuclear CIAPIN1 negatively correlated with the survival of EOC patients, suggesting that nuclear CIAPIN1 might serve as a prognostic biomarker for EOC patients.
EOC is the fourth leading cause of cancer-related deaths among women worldwide[1, 2]. Despite considerable advances in surgical techniques and neoadjuvant chemotherapy, overall patient treatment outcomes have not substantially improved. EOC remains a clinical challenge, primarily because of the absence of effective methods for early diagnosis and lack of prognostic markers. Therefore, additional efforts are required to identify biomarkers for predicting poor outcome in EOC.
CIAPIN1, a novel anti-apoptotic molecule, has been identified to be a downstream effector of the receptor tyrosine kinase-Ras signaling pathway in the mouse Ba/F3 pro-B cell line. CIAPIN1 has been demonstrated to be ubiquitously distributed in normal fetal and tumor tissues, with high expression in actively metabolic tissues[5, 6]. Therefore, CIAPIN1 is likely involved in important physiological functions in tumors. Additionally, a previous study has shown that CIAPIN1 is localized not only in the cytoplasm, but also in the nucleus, and the authors suggest that subcellular localization of CIAPIN1 might be significant for its function. Moreover, CIAPIN1 has been demonstrated to be a critical molecule involved in tumor aggressiveness and may represent a prognostic marker for patient outcome in several types of cancer, such as hepatocellular cancer and leukemia. In recent studies, the significance of CIAPIN1 has been identified in tumors such as esophageal cancer and colorectal cancer; however, the correlations were detected between the expression level of CIAPIN1 in both the nucleus and cytoplasm, and tumor clinicopathological features. CIAPIN1 subcellular localization has not been examined in tumors. Therefore, improved knowledge of the subcellular localization of CIAPIN1 in tumors will be instrumental for the design of optimal strategies to selectively disrupt CIAPIN1 in human cancers.
The clinical significance of CIAPIN1 subcellular localization has not yet been examined in EOC. In this context, this study evaluated the expression of CIAPIN1 in EOC tissues and analyzed the clinical significance of the subcellular localization of CIAPIN1. Our data revealed that CIAPIN1 nuclear localization might provide additional information regarding EOC patient outcome, and represents a valuable biomarker for diagnosis and postoperative predictions of EOC.
A total of 108 EOC tissues and paired non-cancerous tissues from primary EOC patients were surgically obtained between 1998 and 2006 in Xijing Hospital, the Fourth Military Medical University, Xi’an, China. The median patient age was 53 years (range: 32–68 years). All patients agreed to the procedure and signed consent forms. This study was authorized by the Hospital’s Protection of Human Subjects Committee. No patient had received chemotherapy or radiation therapy prior to surgery. All of the patients died of EOC.
Correlation between CIAPIN1 nuclear expression and clinicopathological parameters ( P < 0.05 statistically significant)
I + II
III + IV
Lymph node status
Immunohistochemistry (IHC) staining was performed as previously described[10, 11]. The primary mouse monoclonal anti-CIAPIN1 antibody (dilution 1:800) was developed in our laboratory. Mouse anti-immunoglobulin G (Pierce, Rockford, IL, USA) was used as the negative control. An anti-APE1 mouse monoclonal antibody (1:5,000; Novus Biological, Littleton, CO) was used as the positive control. Each tissue specimen was de-waxed twice with xylene and gradually hydrated. After using a pressure cooker with 10 nM citrate buffer (PH 6.0) for 5 min, the immunostaining procedure was performed. Endogenous peroxidases were blocked with 3% H2O2-methanol for 10 min, and the samples were incubated with the primary monoclonal antibody overnight at 4 °C, rinsed three times for 5 min in phosphate-buffered saline (PBS) and incubated with a horseradish peroxidase-conjugated anti-IgG antibody (1:4,000; Santa Cruz) for 1 h. Finally, the sections were developed with diaminobenzidine solution for 2 min, washed briefly in running water, counterstained with hematoxylin, dehydrated through a graded series of alcohol to xylene and coverslipped. Three pathologists who did not know the clinical features or survival status of the patients then viewed the stained tissue slides separately.
To clarify the association between CIAPIN1 subcellular localization and clinicopathological characteristics, the nuclear and cytoplasmic expression of CIAPIN1 was examined and evaluated separately. An immunoreactivity score (IRS) system was applied using the following standards: (1) The nuclear expression of CIAPIN1 was scored by estimating the proportion of tumor cells with positive nuclear staining (0, none; 1, ≤10%; 2, 10 to ≤ 25%; 3, 26 to ≤ 50%; and 4, >50%). The proportion score was based on the proportion of tumor cells with positive cytoplasmic staining (0, none; 1, ≤10%; 2, 10 to ≤ 25%; 3, 26 to ≤ 50%; and 4, >50%). (2) The intensity score was assigned for the average intensity of positive tumor cells (colorless scored 0, pallid scored 1, yellow scored 2, and brown scored 3). The nuclear or cytoplasmic score for CIAPIN1 was the product of the proportion and intensity scores, ranging from 0 to 12. The immunoreactivity scoring was ranked as absent (−, score 0), weak (+, score 1–4), moderate (++, score 5–8) or strong (+++, score 9–12) according to the proportion and staining intensity. Images were obtained under a light microscope (Olympus BX51, Tokyo, Japan) equipped with a DP70 digital camera.
Western blotting analysis
Eight intraoperative fresh EOC specimens and paired non-cancerous ovarian epithelial specimens were sonicated with an ultrasonic tissue disrupter in lysis buffer for 30 min. The tissue debris was pelleted by centrifugation, and supernatants were collected. The total protein (30 ug was separated by 12% SDS-polyacrylamide gel electrophoresis for 45 min and electroblotted onto a nitrocellulose membrane for 30 min. Non-specific binding was blocked with 5% non-fat milk in TBS for 1 h at room temperature. Then, the membrane was hybridized using the primary antibodies Mab CIAPIN1 (1:2,000) or β-actin (1:4,000, Sigma) overnight at 4 °C. After three washes with TBS-T, the NC membrane was incubated at room temperature for 1.5 h with HRP-conjugated goat anti-mouse antibodies. The membrane was rinsed three times with TBS-T for 25 min, and specific protein bands were visualized using ECL (Santa Cruz Biotechnology, Inc.) and a Bio-Rad (Thermo, USA) system.
The A2780 cell line was originally derived from a female ovarian adenocarcinoma, and the HO8910 cell line was originally derived from a female ovarian serous carcinoma. These two cell lines were preserved in our laboratory. Cells were seeded on glass cover slips in six-well plates and cultured in high-glucose Dulbecco’s modified Eagle's medium (HyClone, Thermo, UT) supplemented with 10% (V/V) fetal calf serum (FCS, Sigma), 100 IU/ml penicillin and 100 mg/ml streptomycin at 37 °C in a humidified chamber with 5% CO2. Afterward, the cells were fixed by incubation in 4% paraformaldehyde for 5 min and permeabilized in PBS containing 0.1% Triton X-100 for 10 min. Non-specific binding was blocked with 10% BSA for 30 min. CIAPIN1 was stained using a 1:800 dilution of the antibody in 1% BSA overnight at 4 °C. A mouse FITC-conjugated phalloidin secondary antibody (Invitrogen) was then used at a 1:1,000 dilution and incubated for 2 h in a humidified chamber with minimal exposure to light. All washes were performed in 1× PBS. An anti-fade solution containing DAPI (Vector Laboratories, CA) was used in mounting the slides. Images were taken with a fluorescence microscope (Olympus BX51, Tokyo, Japan), and Adobe Photoshop was used to merge the images.
Nominal variables were compared using the χ2 test, and ordinal categorical variables were evaluated by a non-parametric Spearman’s rank test. The survival probabilities of patients were described by Kaplan-Meier curves and compared using the log-rank test. The Cox proportional hazards model with likelihood ratio statistics was employed to further evaluate the risk factors for survival. Two-tailed P < 0.05 was considered to be statistically significant. The SPSS18.0 software package (SPSS, Inc., Chicago, IL) was used for the statistical analyses.
Elevated expression of CIAPIN1 in EOC
Quantitative analysis of CIAPIN1 expression in clinical specimens
Correlation between the subcellular localization of CIAPIN1 and clinicopathological features
The correlation between the subcellular localization of CIAPIN1 and clinicopathological features in EOC was further evaluated. The nuclear expression level of CIAPIN1 increased from well-differentiated to poorly differentiated EOC tissues (Figure1b-d). In contrast, the level of CIAPIN1 cytoplasmic expression did not obviously differ between non-cancerous epithelial tissues and well or moderately differentiated tumor tissues (Figure1a-c). As shown in Table1, positive nuclear expression of CIAPIN1 positively correlated with the degree of differentiation, indicating that the CIAPIN1 nuclear expression in poorly differentiated cancer was significantly higher than that in well-differentiated cancer (P < 0.0001). Moreover, the nuclear expression was also significantly higher in patients with an advanced FIGO stage (III + IV) than in those with an early FIGO stage (I + II) ( P = 0.034). No significant association was observed between CIAPIN1 nuclear expression and patients’ age, lymph node metastasis or pathology subtype ( P > 0.05). In addition, no statistically significant correlation between CIAPIN1 cytoplasmic expression and clinicopathological features was observed (see Additional file1: Table S1, P > 0.05).
Relationship between CIAPIN1 subcellular expression and differentiation in EOC cell lines
Univariate analysis of the association between clinical characteristics and survival in patients with EOC
Median survival time (months)
Kaplan-Meier P- value
I + II
III + IV
Lymph node status
Cox multivariate analysis
95% confidence interval
CIAPIN1 has been reported to be involved in proliferation, multidrug resistance, angiopoiesis and anti-apoptosis[4, 15] in many solid tumors and hematological malignancies. The intracellular distribution of CIAPIN1 has been demonstrated to play a cell death-defying role in a variety of mouse and human embryonic cells[4, 5, 7, 9]. However, the subcellular distribution of CIAPIN1 in tumors and the relationship between CIAPIN1 expression and EOC had not been examined. The present study indicated that CIAPIN1 nuclear localization is associated with the histological differentiation, FIGO stage and prognosis for EOC.
This study demonstrated that CIAPIN1 is highly expressed in EOC tissues compared with paired non-cancerous epithelial tissues by immunohistochemistry and Western blotting. Consistently, CIAPIN1 has also been found to be elevated in hepatocellular carcinoma and diffuse large B cell lymphoma. These data indicate that CIAPIN1 may play an oncogenic role in diverse cancers. More importantly, this study revealed that high nuclear expression of CIAPIN1 is significantly associated with poor histological differentiation and an advanced FIGO stage in EOC. However, no correlation between CIAPIN1 cytoplasmic localization and clinical pathological features was observed in the EOC tissues. Interestingly, these results were in accordance with the observation that the levels of CIAPIN1 nuclear expression in A2780 cells were higher than those in HO8910 cells. The differentiation status of the A2780 cell line has previously been shown to be poorer than that of HO8910. Moreover, one expression pattern might be strictly regulated by the subcellular localization of various proteins and varied with alterations in function proteins, such as the subcellular localization of LIMK1, cathepsin L and ALCAM altered the prognosis of correlated cancers[16–18]. Thus, the study findings suggested that the nuclear expression of CAIPIN1 might be associated with the development of poorly differentiated EOC. Proper transport of a protein to its final destination is known to be crucial for the function of the protein. The data from this study suggest that CIAPIN1 nuclear localization is also associated with carcinogenesis and differentiation in EOC, and at least partially with poor clinical outcome of EOC patients. These associations may be a result of the distinct differentiation status of the EOC cells or interactions with specific molecules. Further studies would be necessary to address this notion. From these data, we conclude that the nuclear distribution of CIAPIN1, but not the cytoplasmic distribution, plays an important role in EOC progression. We hypothesize that nuclear CIAPIN1 expression may be involved in neoplastic alterations, while the function of the cytoplasmic protein does not contribute to cancer progression.
This study demonstrated that CIAPIN1 expression has prognostic value in several human tumors[8, 9, 15] and revealed that patients with high levels of CAIPIN1 nuclear expression displayed shorter postoperative survival times than those with weak nuclear expression. This finding is in accord with previous studies that have indicated that subcellular localization is associated with poor prognosis in other tumors[17, 18]. The studies suggest that nuclear expression of CIAPIN1 is closely related to the poor prognosis of patients with EOC. Moreover, multivariate Cox proportional hazards regression analysis revealed that CIAPIN1 nuclear localization is an independent poor prognostic factor in EOC. These data demonstrate that CIAPIN1 nuclear localization is a promising prognostic marker associated with shorter overall survival in EOC. This information might be useful for clinicians in providing individualized therapy for EOC patients with optimal benefit. However, the FIGO stage, pathological subtype and lymph node status were poor prognostic factors according to Cox multivariate analysis. These variables may be potential predictive factors for poor overall survival in EOC patients because of the potential correlations between clinicopathological variables and CIAPIN1 nuclear localization. Moreover, the differences may be caused by the cellular components among the ovarian specimens. Further studies of additional patient samples are necessary to address the significance of such correlations.
Bioinformatics prediction (PROSITE) analysis has indicated that CIAPIN1 is primarily localized in the nucleus and, to a lesser extent, in the cytoplasm. The nuclear localization of CIAPIN1 is established either through specific nuclear localization signal sequences or via interaction with specific molecules. In fact, during mitosis, CIAPIN1 cooperates with posttranslational modifications of cell-cycle-dependent proteins, including cyclinD1[21, 22]. CyclinD1 can accelerate ovarian cancer carcinogenesis[23–26]. Thus, we hypothesize that CIAPIN1 in the nucleus might induce the development of EOC. In addition, the interaction of CIAPIN1 with PICOT (PKCθ interacting cousin of thioredoxin) at the N-terminal regions might lead to the growth of Ba/F3 cells. Moreover, phosphorylated PKC can activate proliferation and differentiation through various signaling pathways. Recent studies have demonstrated that the stability and anti-apoptotic function of CIAPIN1 are the result of interactions with TXNL2 and PICOT. TXNL2 is involved in the activation of the c-Jun N-terminal kinase/AP-1 and NF-kB pathways. These data imply that molecules in the cytoplasm that interact with CIAPIN1 might play crucial roles in causing the translocation of CIAPIN1 into the nucleus.
To our knowledge, this study is the first to associate the subcellular expression of CIAPIN1 in EOC tissues with clinical parameters and patient outcomes using immunohistochemical methods. The results suggest that CIAPIN1 nuclear accumulation might be responsible for EOC progression and is likely associated with the neoplastic outcomes of EOC. The nuclear localization of CIAPIN1 may represent a useful diagnostic and prognostic marker for EOC.
We would like to thank Prof. Xin Wang for the mouse monoclonal anti-CIAPIN1 antibody. We also thank Jingfeng Zhou, Qiao Yang and Yong Guo for their technical support with the immunohistochemistry. Thanks to the statistical assistant Dr. Ming Bai.
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