Prognostic value of osteopontin expression in breast cancer: A meta-analysis

  • Authors:
    • Ying-Yi Xu
    • Ya-Ya Zhang
    • Wei-Feng Lu
    • Yan-Jun Mi
    • Yu-Qiang Chen
  • View Affiliations

  • Published online on: December 22, 2014     https://doi.org/10.3892/mco.2014.480
  • Pages: 357-362
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Abstract

Osteopontin (OPN) has been implicated in tumor development and progression over the last few years. However, the prognostic value of OPN overexpression in patients with breast cancer remains controversial. We performed a meta‑analysis to investigate the association of OPN expression in the tumor with the clinicopathological characteristics and survival of breast cancer patients. A total of 8 studies met the inclusion criteria and were entered in the meta‑analysis. The data analysis demonstrated that OPN expression was positively associated with lymph node metastasis [pooled odds ratio = 2.026, 95% confidence interval (CI): 1.199‑3.425, P=0.008, random‑effects model]. we also found that OPN expression was positively associated with overall survival [hazard ratio (HR) = 3.69, 95% CI: 1.45‑9.42, P=0.000, random‑effects model) and disease‑free survival (pooled HR=2.40, 95% CI: 1.27‑4.55, P=0.007, fixed‑effects model). Based on the results of this study, we concluded that OPN overexpression in the tumor is a candidate positive prognostic biomarker for breast cancer patients.

Introduction

Breast cancer is the most commonly diagnosed cancer in women. Up to 2013, breast cancer reportedly accounted for 29% of all new cancer cases and 14% of all cancer -related deaths among women worldwide (1). Breast cancer-related mortality is closely associated with the development of metastatic potential of the primary tumor. Despite the significant efforts to reduce breast cancer metastasis and mortality, its prognosis remains poor. Therefore, we must identify novel biomarkers to improve the prognosis of breast cancer. It was previously demonstrated that the expression of osteopontin (OPN) may reflect breast cancer progression and metastasis (2).

OPN is a secreted glycophosphoprotein that has been implicated in physiologic al as well as pathological processes (3). Over the last few years, a number of studies have reported that aberrant OPN expression is closely associated with tumorigenesis and metastasis in several tumors, including breast cancer (46). In addition, several studies demonstrated that OPN overexpression was associated with poor prognosis of patients with breast cancer (711). OPN may also be used in conjunction with other markers of known prognostic and predictive value that are commonly evaluated in the primary tumor, such as estrogen receptors (ER), progesterone receptors (PR) and HER2 (12, 13). However, the emerging data regarding the ability of OPN to predict disease progression, overall survival (OS) and disease-free survival (DFS) in patients with breast cancer have been inconsistent. To address this issue, we conducted a meta-analysis aimed at estimating the value of OPN as a prognostic marker for breast cancer and to confirm the association between OPN and several clinicopathological characteristics of breast cancer.

Materials and methods

Study selection

A search was conducted through the PubMed electronic database to identify studies investigating the association of clinicopathological parameters and prognosis with OPN expression in breast cancer up to February 14, 2014, for inclusion in the present meta-analysis. The search terms were ‘breast cancer’ and ‘OPN’. The published studies that were included in this meta-analysis were required to meet the following criteria: i) the type of tumor investigated was breast cancer; ii) the studies assessed the association between OPN expression and clinicopathological characteristics and/or survival and only full peer-reviewed papers had been published as full texts; and iii) the protein expression was evaluated in tumor tissues by immunohistochemistry (IHC). There were no limitations regarding the language or the patient numbers.

Data extraction

Two investigators independently reviewed all potentially relevant studies to minimize bias and improve reliability. The following data were extracted from the eligible studies: name of first author, name of journal, year of publication, sample size, test method, cut-off value, age, HER2, PR, ER, p53, menopausal status, differentiation, lymph node metastasis, stage and OPN expression-related survival. When the prognosis was plotted as a Kaplan-Meier curve, the GetData Graph Digitizer 2.24 software (http://getdata-graph-digitizer.com) and HR digitizer Engauge 4.0 software (http://engauge-digitizer.software.informer.com/) were used to digitize and extract the data. In brief, the Kaplan-Meier curve was saved as a graph and open ed in the GetData Graph Digitizer 2.24 and Engauge Digitizer 4.0 software, the scale was set (coordinate system) and, finally, the points of the Kaplan-Meier curve were manually digitized.

Quality assessment

The methodological quality of each included study was assessed on basis of the Newcastle-Ottawa scale (NOS) (14) by two independent reviewers. A star or point system of NOS has been developed for the evaluation. The scores are shown in Table 1. The publications included in our meta-analysis, with scores of ≥ 5, were rated as high-quality.

Table I.

Main characteristics and results of the eligible studies.

Table I.

Main characteristics and results of the eligible studies.

First authors (Refs.)JournalYearCountryMethodsDuration of follow-up (months)Cut-off point (high/low)No. of patientsNo. of deceased/alive/lostHR estimationQuality assessment (0–8)
de Silva Rudland (15)Clin Cancer Res2006UKIHC216≥1% (143/148)291RR+95 %CI5
Kim (16)J Korean Med Sci1998KoreaIHC160儥5% (221/32)25352/153/38RR+95 %CI5
Ribeiro-Silva A and Oliveira da Costa (25)Int J Biol Markers2008BrazilIHC≥1% (65/35)100 5
Wang (31)Radiology2010ChinaIHCScore ≥2 (92/49)1417
Rudland (17)Cancer Res2002UKIHC228>5% (221/112)333168/165/-RR+95 %CI6
Pang (18)Cancer Epidemiol2013ChinaIHC92Score ≥2 (119/51)170HR+95 %CI4
Wang (19)Eur J Clin Invest2008ChinaIHC62.4Score >4 (33/84)117Survival curves5
Tuck (9)Int J Cancer1998CanadaIHC195.6Score >4 (11/143)15445/109/-Survival curves4

[i] IHC, immunohistochemistry; RR, risk ratio; HR, hazard ratio; CI, confidence interval.

Statistical analysis

All the statistical analyses were performed using Stata 12.0 software for Windows (Stata Corporation, College Station, TX, USA). The pooled estimates of odds ratios (ORs) with their 95% confidence intervals (CIs) were applied to assess the association between OPN expression and the clinical parameters of breast cancer, including age, HER2, PR, ER, p53, menopausal status, differentiation, lymph node metastasis and stage. The pooled estimates of hazard ratios (HRs) with their 95% CIs were applied to estimate the association between OPN expression and the survival outcome of breast cancer. The statistical heterogeneity within studies was detected with the Chi-squared based Q-test (P>0.10) and I2. When I2<50%, there was no heterogeneity and the fixed-effects model was used. In the opposite case, the random-effects model was used. The assessment of publication bias was performed by Egger's and Begg's tests and the potential publication bias was deemed significant at P<0.05.

Results

Description of studies

Following a combined search in PubMed using the terms ‘breast cancer’ and ‘OPN’ 209 potentially relevant citations were retrieved. After excluding animal experiments, non-breast cancer-related studies, non-original articles, or studies lacking data on the association of OPN with clinicopathological characteristics and/or OS, only 8 studies met the inclusion criteria for the present analysis (Fig. 1). Two of these publications lacked information on survival and follow-up and could not be included in the survival analysis. The sample size ranged between 100 and 333 patients. The expression of OPN was detected by IHC in all the studies. Detailed information on the parameters of the included publications is provided in Table I.

Correlation of OPN expression with clinicopathological characteristics

The main results of the meta-analysis are summarized in Table II. In certain studies, presented data on clinicopathological characteristics could not be extracted and when parameters were provided by >3 publications, a meta-analysis was performed. There was no correlation between OPN expression and age (pooled OR= 1.132, 95% CI: 0.737-1.737, P=0.572), HER2 (pooled OR= 1.780, 95% CI: 0.533-5.950, P=0.349), PR (pooled OR= 0.716, 95% CI: 0.333-1.538, P=0.392), ER (pooled OR= 0.915, 95% CI: 0.477-1.753, P=0.798), p53 (pooled OR= 1.190, 95% CI: 0.557-2.545, P=0.654), menopausal status (pooled OR= 0.844, 95% CI: 0.368-1.935, P=0.688), tumor differentiation (pooled OR= 0.699, 95% CI: 0.386-1.265, P=0.237) and stage (pooled OR= 0.479, 95% CI: 0.202-1.136, P=0.095). However, OPN expression was positively correlated with lymph node metastasis compared to the absence of lymph node metastasis. (pooled OR=2.026, 95% CI: 1.199-3.425, P=0.008).

Table II.

Main results of the meta-analysis between confidence interval.

Table II.

Main results of the meta-analysis between confidence interval.

Clinical parametersStudies (refs.)Overall OR (95% CI)Heterogeneity test Q, I2, P (model)
Age (≤ 60 vs. >60 years)16, 25, 181.132 (0.737-1.737)0.23, 0.0%, 0.572 (fixed-effects)
HER2 (positive vs. negative)25, 31, 181.780 (0.533-5.950)5.87, 65.9%, 0.349 (random-effects)
ER (positive vs. negative)15, 16, 25, 31, 180.915 (0.477-1.753)16.27, 75.4%, 0.798 (random-effects)
PR (positive vs. negative)25, 31, 17, 180.716 (0.333-1.538)14.95, 79.9%, 0.392 (random-effects)
p53 (positive vs. negative)16, 25, 171.190 (0.557-2.545)7.07, 71.7%, 0.654 (random-effects)
Differentiation (poor vs. high)15, 16, 25, 31, 17, 180.699 (0.386-1.265)13.29, 62.4%, 0.237 (random-effects)
LN metastasis (+ vs. -)15, 16, 25, 31 17, 182.026 (1.199-3.425)16.77, 70.2%, 0.008 (random-effects)
Stage (III/IV vs. I/II)25, 31, 180.479 (0.202-1.136)6.32, 68.3%, 0.095 (random-effects)
Menopausal status (premenopausal vs. postmenopausal)25, 31, 180.844 (0.368-1.935)7.49, 73.3%, 0.688 (random-effects)

[i] OPN, o steop o ntin; HER2, human epidermal growth factor receptor-2; ER, estrogen receptor; PR, progesterone receptor; LN, lymph node; OR, odd s ratio; CI, confidence interval.

Effect of OPN expression on OS of breast cancer

The different results were extracted from previous studies on the effect of OPN expression on OS. A total of 6 studies (9, 1519) provided data on OS. All 6 studies investigating OS were pooled into the meta-analysis. The results demonstrated that OPN overexpression was correlated with poor OS (HR=3. 69, 95% CI: 1. 45-9.42, P=0.000) (Fig. 2), with heterogeneity in the data (χ2 =33.04, I2 =84.9%, P=0.000). In order to test the heterogeneity in OS, we performed sensitivity analyses to assess the stability of the results. Our results suggested that the heterogeneity for OS was significantly decreased by exclusion of the study of Rudland et al (17) (χ2 =7.77, I2 =48.5%, P=0.100), with a combined OR of 2.16 (95% CI: 1.5 1 −3.1 1, P=0.000) (Fig. 3), demonstrating that the sensitivity is low and the result is more robust and credible.

Effect of OPN expression on DFS of breast cancer

The different results were extracted from previous studies on the effect of OPN expression on DFS. A total of 3 studies (9, 18, 19) provided information on DFS. The combined data of the 3 studies indicated that patients with OPN overexpression exhibited a shorter DFS (pooled HR=2.40, 95% CI: 1.2 7 −4.56, P=0.007) (Fig. 4), without any heterogeneity in the data (χ2 =0.08, I2 =0.0%, P=0.959), suggesting that the sensitivity is low and the result is more robust and credible. These studies indicated that OPN overexpression is associated with the prognosis of breast cancer.

Publication bias

Begg's funnel plot with pseudo 95% confidence limits and Egger's test were applied to estimate the publication bias of the included literature (Figs. 5 and 6). Begg's and Egger's tests did not reveal any evidence of obvious asymmetry in the overall meta-analysis of all the studies.

Discussion

Meta-analyses based on individual data are currently considered the gold en standard for systematic reviews (20). Meta-analysis has been successfully applied in the evaluation of prognostic indicators in patients with malignant diseases (2124). To the best of our knowledge, this meta-analysis is the first to systematically review the association of OPN with clinicopathological parameters and prognostic factors in breast cancer.

In our study, a combined analysis of all the included articles that compared breast cancer patients according to the tumor expression of OPN, revealed a poor prognostic outcome in patients expressing high levels of OPN. OPN is a prognostic factor in breast cancer; alt hough OPN overexpression was reportedly associated with lower tumor grade (17, 18) and lower tumor stage (18), PR status (18, 25), ER status (25) and p53 status (17), our results indicated that the positive expression of OPN was not correlated with these clinicopathological parameters. The results indicated that OPN expression is significantly associated with lymph node metastasis, OS and DFS. Tumor invasion and metastasis have been frequently correlated with poor prognosis of breast cancer (26, 27), as described above. Previous studies have reported high OPN levels in the blood and primary tumors of breast cancer patients and, in certain cases, this was correlated with a poor prognosis (6, 9, 10, 17). A highly metastatic human breast cancer cell line was shown to express significantly higher levels of OPN compared to a cell line of low metastatic potential (28). Dai et al (29) used a humaniz ed OPN-specific antibody to effectively prevent breast cancer cell invasion in vitro and inhibit pulmonary metastasis of breast cancer in nude mice. OPN may act as a diagnostic marker as well as a potential therapeutic target for breast cancer metastasis. Tuck et al (30) demonstrated that OPN was crucial for the metastasis of breast cancer, which may be regulated through activation of the protein kinase C, phospholipase C and phosphoinositide 3-kinase pathways. Consequently, OPN may be a marker for poor prognosis and lymph node metastasis in breast cancer.

There were several important limitations to this meta-analysis. First, we searched studies only from one database and the number of included studies was relatively small. Second, 4 of the 8 studies were from Asia (3 from China and 1 from Korea), 3 were from Europe and 1 was from Brazil. Distinct differences among different locations may result in publication bias. Third, the cut-off values for determining the positive or negative expression of OPN were different among the included studies, which may contribute to heterogeneity. New studies with the same cut-off values must be included in a combined analysis for further evaluation. Finally, there are only a few studies specifically investigating OPN and the prognosis of breast cancer.

In summary, in this meta-analysis, we demonstrated that OPN expression was not correlated with clinicopathological parameters, apart from lymph node metastasis. Therefore, we conclude that OPN overexpression is associated with poor OS and DFS and may serve as a potential molecular target for the clinical management of breast cancer.

Acknowledgements

This study was supported by the National Natural Scientific Foundation of China (grant no. 81100225).

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Xu Y, Zhang Y, Lu W, Mi Y and Chen Y: Prognostic value of osteopontin expression in breast cancer: A meta-analysis. Mol Clin Oncol 3: 357-362, 2015
APA
Xu, Y., Zhang, Y., Lu, W., Mi, Y., & Chen, Y. (2015). Prognostic value of osteopontin expression in breast cancer: A meta-analysis. Molecular and Clinical Oncology, 3, 357-362. https://doi.org/10.3892/mco.2014.480
MLA
Xu, Y., Zhang, Y., Lu, W., Mi, Y., Chen, Y."Prognostic value of osteopontin expression in breast cancer: A meta-analysis". Molecular and Clinical Oncology 3.2 (2015): 357-362.
Chicago
Xu, Y., Zhang, Y., Lu, W., Mi, Y., Chen, Y."Prognostic value of osteopontin expression in breast cancer: A meta-analysis". Molecular and Clinical Oncology 3, no. 2 (2015): 357-362. https://doi.org/10.3892/mco.2014.480