Expressions of Osteopontin (OPN), αVβ3 and Pim-1 Associated with Poor Prognosis in Non-small Cell Lung Cancer (NSCLC)

Yi Jin, Da-yue Tong, Lu-ying Tang, Jian-ning Chen, Jing Zhou, Zhi-ying Feng, Chun-kui Shao*Department of Pathology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 50630, China

2Department of Forensic medicine, ZhongShan Medical School, Sun Yat-sen University, Guangzhou 510080, China

Expressions of Osteopontin (OPN), αVβ3 and Pim-1 Associated with Poor Prognosis in Non-small Cell Lung Cancer (NSCLC)

Yi Jin1, Da-yue Tong2, Lu-ying Tang1, Jian-ning Chen1, Jing Zhou1, Zhi-ying Feng1, Chun-kui Shao1*1Department of Pathology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China

2Department of Forensic medicine, ZhongShan Medical School, Sun Yat-sen University, Guangzhou 510080, China

Objective:To examine the expressions of osteopontin (OPN), α V β3 and Pim-1 in non-small cell lung cancer (NSCLC), and investigate their potential pathogenic roles in the development of NSCLC.

Methods:Immunohistochemistry was used to examine the expressions of OPN, α V β3 and Pim-1 in cohort (136 cases) of NSCLC samples and their adjacent normal lung tissue specimens. Statistical analysis was performed to evaluate the relationships among expressions of OPN, α V β3 and Pim-1 and their associations with patients clinicopathological parameters.

Results:The expressions of OPN and Pim-1 were predominantly observed in cytoplasm. The expression of α V β3 was mostly detected in cytoplasm and/or membrane. In NSCLC samples, the positive rates of OPN, α V β3 and Pim-1 expressions were 68.4% (93/136), 77.2% (105/136) and 57.4% (78/136), respectively. In normal lung tissues, in contrast, the positive rates of OPN, α V β3 and Pim-1 were 24.0% (12/50), 26.0% (13/50) and 16.0% (8/50), respectively. There were significant differences of the positive expression rates of OPN, α V β3 and Pim-1 between NSCLCs samples and normal lung tissues (P＜0.01). In addition, the positive expression of OPN, α V β3 and Pim-1 in NSCLCs samples was significantly associated with increased pathological grade, lymph node metastasis and advanced clinical stage (P＜0.01), and they were independent of other clinicopathological parameters (P＞0.05). Furthermore, a significantly positive correlation between the expression of OPN and α V β3 (r=0.38,P＜0.01), OPN and Pim-1 (r=0.37,P＜0.01), or α V β3 and Pim-1 (r=0.20,P＜0.05) was evaluated in our NSCLC cohort.

Conclusion:OPN, α V β3 and Pim-1 proteins are frequently overexpressed in NSCLC, and they may play important roles in the development and/or progression of NSCLC.

NSCLC; OPN; α V β3; Pim-1; Immunohistochemistry

INTRODUCTION

Primary bronchogenic carcinomas have the highest mortality rate of malignant tumors in the world. Among them, non-small cell lung cancer (NSCLC) accounts for 85%, most patients who have been already clinically diagnosed are in middle-advanced stage, and the 5-year survival rate is very low[1]. Thus, early diagnosis and early treatment are particularly important to improve the survival rate. It is now considered that various pathogenic factors were involved in the evolution of NSCLC.

Osteopontin (OPN) is a multifunctional secretephosphorylated glycoprotein, and it can promote cell chemotaxis, adhesion and migration, which mediate invasion and metastasis of tumor cells, and it is closely related to the occurrence, development, metastasis and prognosis of a variety of cancers[2,3]. Recent studies have indicated that OPN is involved in NSCLC progression and metastasis through interaction with its receptor, alphaV beta3 (α V β3) integrin, and overexpression of OPN is associated with progression and poor prognosis of NSCLC[2,3]. α Vβ3 is a peptide of heparin binding factor and is an important molecule of integrin family. α Vβ3 can mediate adhesion of cell to cell and cell to matrix, regulate intracellular signaling pathways, and induce the activation of protein dissolving enzymes, thereby contributing to extracellular matrix and basement membrane degradation, and promoting invasion and migration migration of tumor cells[4]. Previous studyfound that α Vβ3 is detectable in a variety of tumors, and is closely associated with the tumorigenesis and the degree of malignancy of tumor[5]. Other factors which are closely related with genes of cell cycle regulation and proliferation, including Pim-1 (coded bypim-1oncogene)，are involved in tumorigenesis[6]. It has been reported that OPN acts through α Vβ3 integrin, which in turn activates the FAK, PI3K, Akt, ERK, NF-κB and Pim-1 pathways, contributing to the migration of lung cancer cells[6]. Taken together, these results suggest OPN mediates migration in human lung cancer cells via the α Vβ3 integrin, FAK, PI3K, Akt, ERK, NF-κB and Pim-1 signaling pathways. Therefore, we chose three factors of signaling pathways, OPN, α Vβ3 integrin and Pim-1 in this study. To date, however, the expression dynamics of OPN, α Vβ3 and Pim-1 in NSCLCs, and their potential biological roles in tumorigenesis of NSCLC have not been elucidated.

In the present study, immunohistochemistry was used to examine the expression dynamics of OPN, α Vβ3 and Pim-1 in cohort (136 cases) of NSCLC samples and their adjacent normal lung tissue specimens. Next, the potential correlations among the 3 protein expressions and their associations with NSCLC patients’ clinicopathological features were evaluated.

MATERIALS AND METHODS

Clinical Data

In this study, specimens were obtained from archived paraffin-embedded tissue sections of 136 patients with NSCLC at the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou from January 1st, 2009 to December 31st, 2010. A group of 50 normal lung tissue cases was conducted as control. In this cohort of NSCLC patients, 97 were men and 39 were women, with a median age of 60 years (range 30-82 years). According to the World Health Organization criteria of lung cancer published in 2004[7], NSCLC patients were classified as follows: adenocarcinoma 72 cases, squamous cell carcinoma 40 cases, and other types 24 cases; well and moderately differentiated carcinoma 88 cases, and poorly differentiated carcinoma 48 cases. According to the staging standard of the TNM system of International Association for the Study of Lung Cancer[8], the NSCLC patients were classified as stage I/II 96 cases, and stage III/IV 40 cases. In 136 NSCLC cases of the present study, 35 had lymph node metastasis.

Protein Expression of OPN, α Vβ3 and Pim-1 in NSCLC

Immunohistochemical technique using streptavidinperoxidase (SP) was employed for OPN, α Vβ3 andPim-1detection. Mouse-anti-human monoclonal antibodies of OPN, αVβ3, Pim-1 and SP kit were purchased from Maxim biological and technical company, Fuzhou, China; ready-to-use. All the sections were routinely deparaffinized and rehydrated, then the sections were rinsed in phosphate-buffered saline (PBS, pH=7.4), subsequently were treated for antigen retrieval. Sections were treated in EDTA buffer (pH=8.0) in an autoclave sterilizer. After cooling at room temperature for 20 min, the sections were rinsed in PBS, then immersed in 3% H2O2for 15 min to block the endogenous enzymes. After being rinsed in PBS, the sections were incubated with normal goat serum at 37°C for 15 min to block nonspecific antibodies. After interaction with OPN antibody, αVβ3 and Pim-1 antibodies (monoclonal antibodies), the sections were rinsed in PBS, then incubated with biotinylated secondary antibodies and rinsed in PBS again. After interaction with streptavidinhorseradish peroxidase (HRP) and being rinsed in PBS, the sections were visualized by reaction with 3,3’-diaminobenzidine and counterstained with hematoxylin. They were then dehydrated, transparentized and covered with coverslips and sealed with neutral gum. PBS substituting the primary antibody was used as negative control.

Judgment of Positive Result of OPN,αVβ3 and Pim-1

The judgment that whether the tumor and the normal tissues were positive or not was performed by two pathology doctors. The positive expression of OPN was mostly in cytoplasm with brown-yellow staining, α Vβ3 was mostly in cytoplasm and membrane with brownyellow staining, and Pim-1 was mostly in cytoplasm with brown-yellow staining. A tumor or normal tissue in which more than 10% of cells were stained with those antibodies was recognized as being positive; while less than 10% was recognized as being negative.

Statistical Analysis

Data were analyzed with computer aided SPSS 13.0 statistical software (SPSS Inc., Chicago, IL, USA). Chisquare test was used in comparing the expressions of OPN, α Vβ3 and Pim-1 in NSCLC samples and in normal lung tissue specimens. The associations between the expressions of OPN, α Vβ3 and Pim-1 and NSCLC patients’ clinicopathological parameters were also evaluated by the Chi-square test. The correlation between two variables was evaluated by the Spearman rank correlation test. A value ofP＜0.05 was considered statistically significant.

RESULTS

Relationship between Protein Expression of OPN and Clinicopathological Parameters in NSCLC

The expression of OPN in NSCLC tissues was predominantly a cytoplasmic pattern (Figure 1 A, B). In our study, 93 (68.4%) of 136 NSCLC cases showed positive expression of OPN, while the positive rate of OPN in normal lung tissues was 24.0% (12/50). Therewas a significant difference of the expression of OPN between NSCLC and normal lung tissues (P＜0.05) (Table 1). Further correlation analysis demonstrated that the expression of OPN was significantly associated with tumor differentiation degree, lymph node metastasis and clinical staging in NSCLC patients (P＜0.01), but was not correlated with other clinicopathological parameters studied (P＞0.05) (Table 2).

Figure 1.Protein expressions of OPN, α V β3 and Pim-1 in NSCLC. Protein expression of OPN is mostly in cytoplasm with yellow or brownyellow staining. Positive expression of OPN was examined in a squamous carcinoma (A) and an adenocarcinoma (B) of the lung. In normal lung tissue, the expression of OPN was negative (C). α Vβ3 is mostly expressed in membrane or cytoplasm with yellow or brownyellow staining. αVβ3 is positive in another squamous carcinoma (D) and adenocarcinoma (E) of the lung. In normal lung tissue, the expression of α V β3 was negative (F). The expression of Pim-1 is predominantly a cytoplasmic pattern. Pim-1 is positive in a squamous carcinoma (G) and an adenocarcinoma (H) of the lung. In normal lung tissue, the expression of Pim-1 was negative (I) (SP ×200).

Relationship between Protein Expression of α Vβ3 and Clinicopathological Parameters in NSCLC

In NSCLC, we observed that α Vβ3 protein was mostly expressed in membrane or cytoplasm (Figure 1 D, E). The positive rate of α Vβ3 expression in NSCLCs was 77.2% (105/136), which was significantly higher than that (26.0%, 13/50) in normal lung tissues (P＜0.05) (Table 1). In addition, the expression of α Vβ3 was also positively associated to NSCLC histopathological differentiation, lymph node metastatic status and clinical stage (P＜0.01) (Table 2).

Relationship between Protein Expression of Pim-1 andClinicopathological Parameters in NSCLC

The expression of Pim-1 was mostly observed in cytoplasm (Figure 1 G, H). In our NSCLC cohort, 78 (57.4%) of the 136 cases had positive expression of Pim-1. The positive rate of Pim-1 in normal lung tissues was 16.0% (8/50). There was a significant difference of Pim-1 expression between NSCLC and normal lung groups (P＜0.05) (Table 1). The expression of Pim-1 was significantly correlated to differentiation degree, lymph node metastasis and clinical staging in NSCLC (P＜0.01), while no correlations were observed between the expression of Pim-1 and other clinicopathological parameters studied (P＞0.05) (Table 2).

Table 1．The expression of OPN, α Vβ3 and Pim-1 between NSCLC and normal lung tissue

Correlations among Protein Expression of OPN,α V β3 and Pim-1 in NSCLCs

In our study, the potential correlations among protein expression of OPN, α Vβ3 and Pim-1 in NSCLC were further evaluated. Spearman rank correlation analysis showed that the expression of OPN was positively correlated αVβ3 expression in our NSCLC cohort (r=0.38,P＜0.01) (Table 3). The expression of OPN in NSCLC was also positively correlated with Pim-1 expression (r=0.37,P＜0.01) (Table 4). Furthermore, a significant positive correlation between expressions of αVβ3 and Pim-1 was observed (r=0.20,P＜0.05) (Table 5).

Table 2．Relationship between expressions of OPN, α V β3 and Pim-1 and clinicopathological parameters in NSCLC

Table 3.Relativity of protein expressions of OPN and α V β3 in NSCLC

Table 4.Relativity of protein expressions of OPN and Pim-1 in NSCLC

Table 5.Relativity of α V β3 and Pim-1 expressions in NSCLC

DISCUSSION

It is known that malignant transformation of cells needs changes of gene phenotype and angiogenesis. OPN is considered to be the most important factor. OPN is an extracellular matrix-secreted phosphorylated glycoprotein which is also called the transformationrelated protein phosphatase, and it was found by Senger, et al.[9]for the first time in the epithelial cell strain of malignant transformation. In recent years, studies have confirmed that overexpression of OPN can promote tumor growth, invasion and/or metastasis[3].

Previously, it was reported that the expression of OPN was 68.8% in NSCLC[10]. Other groups reported that OPN expression was associated with tumor growth, tumor staging, and lymph node invasion of patients with NSCLC[11]. In the present study, the expression of OPN protein was detected in 68.4% of NSCLC, while only 24.0% of normal lung tissues expressed OPN protein, suggesting that the positive expression of OPN may provide a selective advantage for the development of NSCLC. In our study, further statistical analysis showed that the expression of OPN was correlated closely to NSCLC’s differentiation degree, lymph node metastasis and clinical staging, and it was independentof other clinicopathological parameters. The positive expression of OPN was more frequently observed in poorly differentiated cancer, tumors with lymph node metastasis and/or tumors in more advanced clinical stage III/IV. A current study suggested that OPN can produce a marked effect by binding to receptors on endothelial cell membrane. After OPN binds to the receptors such as αVβ3 integrins, it can directly stimulate the differentiation and proliferation of lung cancer cells, and might be capable of regulating genesis and migration of lung cancer cells, increase vascular permeability, change extracellular matrix, induce angiogenesis, activate intracellular signaling pathways and promote the growth of NSCLC[12]. These data suggested that the increased expression of OPN may facilitate the development and/or progression of NSCLC and OPN might be used as a therapeutic target and useful biomarker for NSCLC.

The reason why OPN is highly expressed in NSCLC is that it is regulated by some transcription factors. Among them, αVβ3 and Pim-1 are more important. Previous studies have demonstrated that αVβ3 regulates the expressions of Pim-1 and VEGF, and mediates tumor angiogenesis through the signaling pathways of PI13/AKT. In turn, they also promote the expression of OPN[13,14]. Recently, it has been reported that the overexpression of αVβ3 integrin on tumor is associated with an aggressive phenotype of several solid tumor types[15,16]. In this study, we further found that the expression rate of αVβ3 was 77.2% in NSCLC, and significantly higher than that (26.0%) in normal lung tissue, suggesting that αVβ3 might be involved in the development of NSCLC. In addition, the statistical analysis showed that the protein expression of αVβ3 was positively associated with NSCLC’s differentiation degree, lymph node metastasis and clinical staging. These results further suggested that the expression of αVβ3 might be involved in the development of NSCLC, and closely related to the degree of malignancy, invasion and metastasis of NSCLC. Possible molecular mechanism why αVβ3 promotes the development of NSCLC is that αVβ3 integrin plays an important role in promoting angiogenesis, and adhesion of cell to matrix so that it enhances the development of NSCLC[17]. Thus, αVβ3 can be used as an important indicator to evaluate the malignant degree and invasion of NSCLC. These results also suggest that αVβ3 could be a surrogate marker in the diagnosis of NSCLC and the prediction of therapeutic response for treatment with anti-αVβ3 antibody in NSCLC.

The gene,pim-1, is a potential oncogene, which is located on chromosome 6p21.2. The encoded protein of Pim-1 is a serine/threonine kinase[18]. Recent studies have confirmed that it is highly expressed in some malignant tumors[19,20]. It is involved in the regulation of proliferation, differentiation and apoptosis of lung cancer cells[21]. In our present study, the positive expression of Pim-1 was detected in the majority of NSCLC, while in few normal lung tissues. This result was in consistent with the literature reported by Zhang, et al. and He, et al.[22,23]. It has been documented that Pim-1 can promote G2/M process of cell cycle, activate growth, differentiation and proliferation of cells[6]. In addition, we also found that the expression of Pim-1 in NSCLC with poor differentiation, clinical stage of III and IV and lymph node metastasis was significantly higher than that in clinical stage of I and II and without lymph node metastasis. Based on the results mentioned above, collectively, we proposed that Pim-1 might also be involved in the tumorigenesis/progression of NSCLC.

In this study, Spearman rank correlation analysis showed that there was an obvious positive correlation of protein expression between OPN and αVβ3, in which the higher the expression level of OPN, the higher the expression of αVβ3. It was suggested that OPN acts through αVβ3 integrin, which in turn activates the FAK pathways, contributing to the overexpression of αVβ3[24]. Other groups also revealed that OPN is involved in tumor growth and angiogenesis of lung cancer by upregulating vascular endothelial cell migration and proliferation via interacting with αVβ3 integrin[25]. Upregulation of OPN specifically activates the activity of integrin receptor αVβ3, and may accelerate tumor angiogenesis, and induce activation of a variety of kinases such as Pim-1, PI3K, and AKT[13,14]. Therefore, when the expression level of OPN is higher, it can elevate the expressions of αVβ3 and Pim-1 through regulating signaling pathways. In NSCLC, the expression of OPN, Pim-1 and the expression of αVβ3, Pim-1 are also positively correlated. Therefore, our results, together with others’ findings, suggested that OPN plays a crucial role for tumor growth and/or progression of human lung cancer cells by interacting with αVβ3 integrin, and thus, regulating signaling pathways and activating Pim-1[13,14,18,24], resulting in the overexpression of OPN, αVβ3 and Pim-1.

With regards to the molecular targets studied in this report, it was concluded that OPN can promote extracellular matrix degradation, inhibit apoptosis, and accelerate tumor angiogenesis in the process of invasive growth and metastasis. The other one, Pim-1 may promote cell cycle G2/M process[6], and promote cell proliferation through enhancing the cell cycle promoter activity, such as Cdc25A and Cdc25C, so that the decline of homotypic adhesion, degradation of extracellular matrix and cell proliferation can be a vicious cycle and promote each other. This may indicate that a synergistic effect among the three working together might be capable of regulating migration of lung cancer cells and promote the occurrence, invasion and metastasis of NSCLC. The expressions of OPN, αVβ3 and Pim-1 may be early diadynamic criteria of NSCLC. Taken together,our results suggested that targeting the interaction among OPN, αVβ3 and/or Pim-1 could be effective for future development of anti-angiogenic therapeutic agents for patients with NSCLC.

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

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10.1007/s11670-012-0103-1

2011-09-16;Accepted2012-03-13

*Corresponding author.

E-mail: chunkuishao2011@163.com

?Chinese Anti-Cancer Association and Springer-Verlag Berlin Heidelberg 2012