- Open Access
Astrocyte elevated gene-1 (AEG-1) is a marker for aggressive salivary gland carcinoma
- Wen-Ting Liao†1, 2,
- Ling Guo†1, 3,
- Yi Zhong†1, 4,
- Yan-Heng Wu6,
- Jun Li5 and
- Li-Bing Song1, 4Email author
© Liao et al; licensee BioMed Central Ltd. 2011
- Received: 31 August 2011
- Accepted: 1 December 2011
- Published: 1 December 2011
Astrocyte elevated gene-1 (AEG-1) is associated with tumorigenesis and progression in diverse human cancers. The present study was aimed to investigate the clinical and prognostic significance of AEG-1 in salivary gland carcinomas (SGC).
Real-time PCR and western blot analyses were employed to examine AEG-1 expression in two normal salivary gland tissues, eight SGC tissues of various clinical stages, and five pairs of primary SGC and adjacent salivary gland tissues from the same patient. Immunohistochemistry (IHC) was performed to examine AEG-1 protein expression in paraffin-embedded tissues from 141 SGC patients. Statistical analyses was applies to evaluate the diagnostic value and associations of AEG-1 expression with clinical parameters.
AEG-1 expression was evidently up-regulated in SGC tissues compared with that in the normal salivary gland tissues and in matched adjacent salivary gland tissues. AEG-1 protein level was positively correlated with clinical stage (P < 0.001), T classification (P = 0.008), N classification (P = 0.008) and M classifications (P = 0.006). Patients with higher AEG-1 expression had shorter overall survival time, whereas those with lower tumor AEG-1 expression had longer survival time.
Our results suggest that AEG-1 expression is associated with SGC progression and may represent a novel and valuable predictor for prognostic evaluation of SGC patients.
- Salivary gland carcinomas
Salivary gland carcinoma (SGC) is a relatively rare cancer that accounts for less than 5% of all head and neck cancers [1, 2]. It is among the most complex malignancies owing to diverse histological characteristics and biological behaviors. According to the World Health Organization (WHO) classification, SGC is one of the most complex malignancies for it has up to 24 different histological subtypes . Although there have been some remarkable advances, treating SGC is still challenging, and the clinical outcomes of advanced SGC have not significantly improved . More than 5% of patients suffer a recurrence at the primary site and/or distant metastasis, and the incidence of occult lymph node metastasis is also high in major SGC types [5, 6]. Due to the limited number of cases available in most series of salivary gland tumors, the molecular mechanism of the development and progression of SGC is still poorly understood. Therefore, it is of great value to better understand the etiology and to identify valuable diagnostic and prognostic markers as well as novel therapeutic strategies of the disease.
AEG-1 was originally discovered as a novel protein induced by HIV-1 or tumor necrosis factor-α in primary human fetal astrocytes [7–9]. In recent years, numerous researches have revealed the essential role of AEG-1 in the development and progression of cancer. Aberrant elevation of AEG-1 expression frequently occurs in human cancers, including breast cancer, glioma, melanoma, esophageal squamous cell carcinoma, prostate cancer, hepatocellular carcinoma and gastric cancer [10–16]. As a downstream target of Ha-Ras, AEG-1 has an essential role in regulating tumorigenesis, invasion, metastasis and angiogenesis . AEG-1 can promote proliferation via suppression of FOXO1, induce serum-independent cell growth and suppress apoptosis through activation of PI3K-Akt signaling [18–21], and increase anchorage-independent growth of non-tumorigenic astrocytes through activation of PI3K-Akt and NF-κB pathway [18, 22]. In addition, knockdown of AEG-1 inhibits the progression of prostate cancer through up-regulation of FOXO3a activity . Moreover, overexpression of AEG-1 promotes tumorigenesis and progression via activation of the Wnt/β-Catenin and NF-κB pathways in hepatocellular carcinoma . Further more, AEG-1 can regulate human malignant glioma invasion through up-regulation of matrix metalloproteinase-9 and activating the NF-κB signaling pathway [10, 19, 22, 23]. These findings suggest that AEG-1 plays a dominant positive role in development and progression of diverse cancers.
However, whether AEG-1 deregulation also occurs in SGC remains unclear. To address this question, we investigated the expression of AEG-1 in SGC and evaluate its prognostic significance by correlating AEG-1 expression levels with clinicopathologic features and survival in 141 archived SGC samples.
Patients and tissue specimens
Clinicopathological characteristics of patient samples and expression of AEG-1 in salivary gland cancer
All cases (%)
All cases (%)
Adenoid cystic carcinoma
Acinar cell carcinoma
Squamous cell carcinoma
Salivary duct carcinoma
Basal cell carcinoma
Vital status (at follow-up)
Death (all SGC-related)
Expression of AEG-1
RNA extraction and real-time PCR
Total RNA from tissue samples were extracted using the Trizol reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's instruction. Real-time PCR was performed according to standard methods as described previously . Sequences of the real-time PCR primers and probes have been reported previously . Expression data were normalized to the geometric mean of the housekeeping gene GAPDH and calculated as 2-[(Ct of AEG-1)-(Ct of GAPDH)], where Ct represents the threshold cycle for each transcript.
Western blots were performed according to standard methods as described previously , using a rabbit anti-AEG-1 polyclonal antibody (1:500; Zymed). A mouse anti-α-Tubulin antibody (1:1,000; Sigma, Saint Louis, MI) was used as an inner control.
Immunohistochemical (IHC) analysis
IHC analysis were carried out similarly to previously described methods . Briefly, tissue sections were incubated with a rabbit anti-AEG-1 antibody (1:200; Zymed) overnight at 4°C. For negative controls, the rabbit anti-AEG-1 antibody was replaced with normal non-immune serum.
The degree of I of paraffin-embedded sections was reviewed and scored independently by two observers, based on both the proportion of positively stained tumor cells and the intensity of staining . The proportion of tumor cells was scored as follows: 0 (no positive tumor cells), 1 (< 10% positive tumor cells), 2 (10-50% positive tumor cells) and 3 (> 50% positive tumor cells). The intensity of staining was graded according to the following criteria: 0 (no staining); 1 (weak staining = light yellow), 2 (moderate staining = yellow brown) and 3 (strong staining = brown). The staining index (SI) was calculated as staining intensity score × proportion of positive tumor cells. Using this method of assessment, we evaluated the expression of AEG-1 in benign salivary gland tissues and SGC lesions by determining the SI, which scores as 0, 1, 2, 3, 4, 6 and 9. Cutoff values for AEG-1 were chosen on the basis of a measure of heterogeneity with the log-rank test statistical analysis with respect to overall survival. An optimal cutoff value was identified: the SI score of ≥ 4 was used to define tumors as having high AEG-1 expression and ≤ 3 as having low expression of AEG-1.
To account for inconsistencies in IHC stain intensities, the mean optical density (MOD) method, which was used for the scoring of the staining intensity, was applied in the current study. In brief, the stained slides were evaluated at 200× magnification using the SAMBA 4000 computerized image analysis system with Immuno 4.0 quantitative program (Image Products International, Chantilly, VA). Ten representative staining fields of each tumor sample were analyzed to determine the MOD, which represented the concentration of the stain or proportion of positive pixels within the whole tissue. A negative control for each staining batch was used for background subtraction in the quantitative analysis. The data were statistically analyzed using t-test to determine the differences in average MOD values between different groups of tissues. P < 0.05 was considered significant.
All statistical analyses were carried out using the SPSS 13.0 statistical software package. Comparisons between groups for statistical significance were performed with a two-tailed paired Student's t test. The chi-square test was used to analyze the relationship between AEG-1 expression and clinicopathologic features. Bivariate correlations between variables were calculated by Spearman's correlation coefficients. Survival curves were plotted by the Kaplan-Meier method and compared using the log-rank test. Survival data were evaluated using univariate and multivariate Cox regression analyses. P < 0.05 in all cases was considered statistically significant.
AEG-1 is up-regulated in SGC
Further comparative analysis was done in the five pairs of primary SGC tissues and their matched adjacent non-cancerous tissues by Western blot and real-time PCR analysis. The results revealed that the expression level of AEG-1 protein was significantly up-regulated in all five of the SGC tumors (Figure 1C). By real-time PCR analysis, the tumor/adjacent non-cancerous (T/N) ratio of AEG-1 mRNA expression was > 2-fold in all these samples, and the highest ratio was up to about 8-fold (Figure 1D). In the mean time, the expression of the AEG-1 protein was also found to be up-regulated in all 5 human primary SGC tissue samples as compared to the expression in their matched adjacent noncancerous tissues by IHC analyses (Figure 1E).
Overexpression of AEG-1 protein in archived SGC samples
Figure 2B shows representative IHC stained tumor sections of each of the four WHO grades of SGC. Moderate to strong cytoplasmic staining of AEG-1 protein was observed in tumor cells in these primary SGC tissues. By contrast, weak or negative signals were observed in control normal tissues (Figure 2B). Quantitative IHC analysis revealed that the MOD values of AEG-1 staining in all primary SGC were higher than that in control normal tissues and increased along with the progression of tumor grades I to IV (P < 0.001, Figure 2C).
Increased AEG-1 expression correlates with clinicopathologic features of SGC
Correlation between AEG-1 expression and clinicopathologic characteristics of SGC
Chi-square test P-value
Low or none No. cases (%)
No. cases (%)
Adenoid cystic carcinoma
Acinar cell carcinoma
Squamous cell carcinoma
Salivary duct carcinoma
Basal cell carcinoma
Spearman correlation analysis between AEG-1 and clinical pathologic factors
AEG-1 expression level
High AEG-1 expression is associated with poor prognosis of patients with SGC
Univariate and multivariate analyses of various prognostic parameters in patients with SGC Cox-regression analysis
Regression coefficient (SE)
95% confidence interval
Expression of AEG-1
In this study, we presented the first evidence of AEG-1 up-regulation in SGC biopsies at both the mRNA and protein levels compared with adjacent non-cancerous tissues. We also examined 141 SGC that covered a wide spectrum of histological types. AEG-1 protein was observed in 96.5% of archived SGC specimens, and the expression level of AEG-1 protein was found to be significantly correlated with advanced tumor stage and TNM classification, as well as unfavorable prognosis of SGC patients. Our results suggested the important role for AEG-1 protein in the development and progression of SGC.
Due to the rarity and complexity of this type of cancer, it has been difficult to make clinical judgments regarding diagnosis and treatment, as well as the prognosis [1, 4, 5]. Meanwhile, little is known about its pathogenesis, and few reliable prognostic markers have been identified to predict aggressive biological behavior of SGC. In early studies, HER-2 was found to be an independent marker of poor prognosis of SGC [26, 27]. HER-2/neu was found to be amplified and overexpressed in mucoepidermoid carcinomas, as markers of poor prognosis independent of histopathologic grade, tumor size and involvement of regional lymph nodes . The mutated p53 was also shown to be expressed in 7 of 63 (11%) primary SGC in one report . In another study, patients with parotid gland cancer, moderate and high expression of mutated p53 protein were associated more frequently with metastases and poor survival . Other studies also showed that ras-p21  and cyclin D1  are overexpressed in a small subset of SGC, while C-kit is up-regulated in a large percentage of SGC [32, 33]. Moreover, vascular endothelial growth factor (VEGF) was found to be up-regulated in 62% of SGC tissues, and its expression is significantly correlated with lymph node metastasis, clinical stage and disease-specific survival . In a previous study, we had found that sphingosine kinase 1 (SPHK1) was associated with SGC progression . In this study, we found that up-regulation of AEG-1 correlated with poor prognosis and reduced survival of patients with SGC. Multivariate analysis showed that AEG-1 protein levels could be used as an independent prognostic predictor for SGC patients, especially in subgroups with advanced clinical stages (III-IV), higher T classification (T3-4), and involvement of distant metastasis (M1). Thus, testing the AEG-1 protein level may be useful for formulating prognosis and guiding the follow-up schedule in SGC patients with advanced and aggressive SGC.
In this study, we found that up-regulation of AEG-1 correlated with poor prognosis and reduced survival of patients with SGC. Multivariate analysis showed that AEG-1 protein levels could be used as an independent prognostic predictor for SGC patients, especially in subgroups with advanced clinical stages (III-IV), higher T classification (T3-4), and involvement of distant metastasis (M1). Thus, testing the AEG-1 protein level may be useful for formulating prognosis and guiding the follow-up schedule in SGC patients with advanced and aggressive SGC.
This study was supported by: The Natural Science Foundation of China (No. 30901791, 81071780, 81030048, 30870963, 30831160517); The Science and Technology Department of Guangdong Province, China (No. 8251008901000006, 2008A030201006).
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