Decreased expression of granulocyte-macrophage colony-stimulating factor is associated with adverse clinical outcome in patients with gastric cancer undergoing gastrectomy
- Authors:
- Published online on: August 9, 2017 https://doi.org/10.3892/ol.2017.6738
- Pages: 4701-4707
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Copyright: © Liu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Despite decreased incidence and mortality rates in previous decades, gastric cancer remains the fourth most common malignancy and the third leading cause of cancer-associated mortality worldwide (1,2). Due to the mild and atypical symptoms at the early stage, >80% of the patients are clinically diagnosed at an advanced stage, which generally indicates a poor outcome (1,3). For the stratification of patient risk, the underlying molecular and cellular processes during gastric carcinogenesis are ignored in the widely-used Union for International Cancer Control/American Joint Committee on Cancer (UICC/AJCC) Tumor Node Metastasis (TNM) staging systems (4), while previous evidence has demonstrated its heterogeneity, with an unpredictable clinical outcome (4). There is an urgent requirement to illuminate the molecular events involved in the development and progression of gastric cancer, making it possible to improve disease prognosis and provide novel therapeutic targets for treatment.
Since the 19th century, cancer has been associated with inflammation. Emerging evidence has revealed that inflammation serves an important role in the initiation, development and progression of human malignancy (5,6). As the most abundant immune cell in the tumor microenvironment, macrophages have received attention for their pro-tumoral role by facilitating neoangiogenesis in the primary tumor site, and promoting metastasis in distant sites (7–9). Macrophages that infiltrated into the tumor microenvironment were primed to adopt a pro-tumoral M2-phenotype rather than a tumoricidal M1-phenotype (10). In the process of the polarization and activation of macrophages, a variety of chemokines were identified, of which granulocyte-macrophage colony-stimulating factor (GM-CSF) may be the essential orchestrator (10,11). The role of GM-CSF, also termed CSF-2, in the tumor microenvironment is controversial. Certain studies revealed that GM-CSF promoted tumorigenesis via stimulating the epithelial release of VEGF (12), while others stated that GM-CSF released by tumor cells was associated with improved survival (13) in colorectal cancer. In breast cancer, GM-CSF was identified to inhibit cancer growth and metastasis (14), and GM-CSF triggered and maintained the alternative activation of tumor-associated macrophages (TAM), and promoted tumor growth and angiogenesis in glioma (15). However, the clinical significance of intratumoral GM-CSF and its prognostic value in gastric cancer remains obscure.
The prognostic role of diametrically polarized TAMs in gastric cancer has been identified in our previous study (16). The present study aimed to investigate the expression of GM-CSF in gastric cancer and its correlation with the clinicopathological characteristics and clinical outcomes, including overall survival (OS) and disease-free survival (DFS) times. In addition, nomograms were generated to evaluate the 3- and 5-year DFS and OS rates for the patients with gastric cancer following surgery.
Patients and methods
Clinical specimens
A total of 408 patients diagnosed with gastric cancer at Zhongshan Hospital, Fudan University (Shanghai, China) from January 1, 2008 to December 31, 2008 were enrolled in the present study. The male:female ratio was 2.37 and the median age of the patients was 60 (range, 27–88) years old. Written informed consent from each patient was obtained, and the use of human specimens was approved by the Clinical Research Ethics Committee of Zhongshan Hospital. All the patients received a radical resection (R0) with a D2 lymphadenectomy from the same surgical team and the resultant formalin-fixed paraffin-embedded surgically resected specimens were used in the present study. The specimens were fixed in 10% formalin for 12 h at room temperature and were embedded in paraffin for 4 h at 60°C. The section width was 5 µm. No patients had received any anti-cancer therapy prior to surgery. The clinicopathological and baseline demographic characteristics of the patients were retrospectively collected, including age, sex, tumor size, tumor histological classification (17), Lauren's classification (18) and TNM stage (4). A total of 2 independent gastroenterology pathologists from the Department of Pathology of Zhongshan Hospital provided reassessments for the tumor stage according to the 7th Edition of the UICC/AJCC TNM staging system (4). DFS was defined as the time from the date of surgery to the date of recurrence or the last visit. OS was defined as the time from the date of surgery to the date of death from all causes or the last visit.
Tissue microarray and immunohistochemistry
The construction of the tissue microarray and the immunohistochemical protocols were as previously described (19). An anti-GM-CSF antibody (dilution, 1:100 at 5 µg/ml; cat. no. ab9741, Abcam, Cambridge, MA, USA) was used as the primary antibody in the immunohistochemical analysis. The semi-quantitative H-score, which ranged from 0 to 300, was calculated by multiplying the staining intensities (0, negative; 1, weak; 2, moderate; 3, strong) by the distribution areas (percentage of positive staining cancer cells, 0–100%) at each intensity level for each sample. A total of 2 independent observers who were blinded to the patient outcomes and clinicopathological characteristics provided the evaluation of the immunostaining.
Statistical analysis
The cut-off point for the definition of high/low expression subgroups was determined by X-tile plot analysis (20). SPSS 19.0 (IBM Corp., Armonk, NY, USA) was used to perform the analyses. The Pearson χ2 test or Kruskal-Wallis test was used to compare categorical variables. Continuous variables were analyzed with an unpaired Student's t-test. Survival estimates were conducted with Kaplan-Meier curves, and statistical significance was determined using the log-rank test. Multivariable Cox proportional hazards models were used to identify the independent prognosticator. A nomogram was generated by R software v3.2.2 with ‘rms’ package (R Foundation for Statistical Computing, Vienna, Austria). Calibration plots for 3- and 5-year survival rates were constructed to examine the performance characteristics of the generated nomograms. The prognostic accuracy was measured by calculating the Harrell's concordance indices (c-indices). All statistical analyses were two-sided, and P<0.05 was considered to indicate a statistically significant difference.
Results
Associations between GM-CSF immunohistochemical expression and the clinicopathological features
Immunohistochemical staining analysis was performed in 408 clinical specimens resected from primary tumor sites. GM-CSF staining greatly varied in intensity in the tumor tissues (Fig. 1A and B). The positive staining of GM-CSF was observed primarily in the cytoplasm and/or on the membrane of neoplastic epithelia, and partially in the stroma. According to the semi-quantitative H-score, 239 (58.6%) cases were included in the GM-CSF low expression group. The clinicopathological features of the patients dichotomized by intratumoral GM-CSF expression are summarized in Table I. No significant association was identified between GM-CSF expression patterns and the clinicopathological features.
Table I.Correlations between GM-CSF expression and clinicopathological features in patients with gastric cancer (n=408). |
Prognostic evaluation of GM-CSF expression in patients with gastric cancer
The Kaplan-Meier method and log-rank tests were performed to assess the association between GM-CSF expression and clinical outcome in patients with gastric cancer. At the last follow-up, the mean duration of OS was 40.2 months (median, 44.5 months) and DFS was 37.9 months (median, 41.0 months). Patients with low GM-CSF expression were more likely to exhibit poorer survival [Hazard ratio (HR), 2.26; 95% confidence interval (CI), 1.65–3.11; P<0.001; Fig. 1C] and suffer from earlier recurrence (HR, 1.68; 95% CI, 1.26–2.26; P=0.001; Fig. 1D) compared with those with high expression. The median DFS and OS times for the GM-CSF low expression subgroup were 52 and 55 months, respectively, while those for the high expression subgroup were 30.1 and 34 months, respectively.
In order to eliminate the effects of tumor stage on prognosis, Kaplan-Meier analysis was also applied to compare OS according to GM-CSF expression in different TNM stages. A statistically significant difference was identified in advanced stages of tumors when stratified by GM-CSF expression levels (Fig. 2A and B), while the DFS and OS of the patients with TNM I stage tumors were not significantly different (Fig. 2C and D).
In the univariate Cox regression analysis of OS, intratumoral GM-CSF expression was defined as a prognostic factor (P<0.001). Multivariable Cox proportional hazards models that included depth of tumor invasion, lymph node metastasis, GM-CSF expression and Lauren's classification as co-variables were constructed. For OS, depth of tumor invasion (P<0.001), lymph node metastasis (P<0.001), adjuvant chemotherapy (P<0.001) and GM-CSF expression (P<0.001) were identified to be independent prognostic factors for patients with gastric cancer, while for DFS, depth of tumor invasion (P<0.001), lymph node metastasis (P<0.001), Lauren's classification (P=0.029), adjuvant chemotherapy (P=0.001) and GM-CSF expression (P=0.009) were identified to be independent prognostic factors (Table II).
Predictive nomogram for OS in gastric cancer patients
In order to provide a quantitative assessment for outcomes of patients with gastric cancer, 2 nomograms were constructed to provide a more sensitive prognostic model (Figs. 3A and 4A). The factors incorporated in the nomogram were independent factors for OS selected subsequent to multivariate analysis, with the exception of adjuvant chemotherapy, to generate a model that only included the characteristics of the tumor without artificial interventions. A higher number of total points predicted a poorer prognosis. The total point was raised by the addition of the score of each factor for each patient correspondingly. Calibration curves for the internal validation of the nomogram predictions of 3- and 5-year survival rate were constructed, and the nomograms performed well with the ideal model (Fig. 3B and C; Fig. 4B and C). Harrell's c-index for the generated nomogram was 0.714 (95% CI, 0.679–0.749) for OS and 0.743 for DFS (95% CI, 0.708–0.778). The area under the receiver operating curve of the generated nomogram for OS was 0.804, which was significantly larger compared with that of TNM stage (0.742; P<0.001; Fig. 3D). The area under the receiver operating curve of the generated nomogram for DFS was 0.807, which was also larger compared with that of TNM stage (0.779; P=0.015; Fig. 4D). These data indicated that the nomograms performed well in predicting the OS of the patients.
Discussion
Previous studies have revealed the important role of tumor-associated macrophages in the process of tumor development and progression (10,21). Our previous study also demonstrated the prognostic value of infiltrated polarized macrophages in gastric cancer (16). However, the role of cytokines that are involved in the orchestration of the polarization of TAM remains controversial. To the best of our knowledge, the present study is the first study that identified intratumoral GM-CSF expression as an independent prognostic factor for patients following gastrectomy. In addition, the generated nomograms performed better compared with the TNM staging system in predicting the DFS and OS for the patients.
Much attention has been paid to TAMs for their crucial role in the carcinogenesis of various tumors (10). For gastric cancer, Ohno et al (22) stated that the aggregation of TAMs within the tumor nest demonstrated a tumoricidal effect, while Ishigami et al (23) identified that the presence of TAMs in tumor tissue was correlated with an adverse prognosis. However, our previous study revealed that the infiltration of M2-polarized TAM in tumor tissue was associated with a favorable outcome, while M1-TAM infiltration exhibited the opposite effect (16). These raised lead to the investigation of the cytokines that are involved in the polarization of TAMs. In a previous study, a high expression of C-C motif chemokine 2 (CCL-2) in the tumor tissue of gastric cancer was revealed to be associated with the poor OS of the patients (24). The present study identified that high intratumoral expression of GM-CSF was correlated with an improved clinical outcome. Therefore, it is conceivable that increased GM-CSF may promote M2 to M1 polarization of macrophages, which would impede infiltration and invasion of the primary tumor, while CCL-2 possibly directed the opposite polarization.
Since Lauren's classification was introduced in 1965 (18), debates have continued on whether this may provide risk stratification in patients with gastric cancer. Lauren diffuse-type gastric cancer is frequently associated with a mutation of the Cadherin 1 (CDH1) gene (25–27). Mutation or loss and methylation of CDH1 leads to the aberrant expression of E-cadherin, disturbing the normal cell-cell adhesion (27). Therefore, gastric cancer cells of diffuse-type may be more likely to disperse and disseminate. This may provide a potential explanation for the results of the present study, which suggest that Lauren's classification was an independent prognostic factor for DFS, but not for OS.
The prognostic value of GM-CSF expression in gastric cancer, particularly in advanced tumors, was investigated in the present study. According to intratumoral GM-CSF expression, patients were separated into two subgroups. GM-CSF expression was demonstrated to be an independent adverse prognosticator for OS and DFS in patients with gastric cancer. Furthermore, nomograms were constructed by integrating GM-CSF expression, depth of tumor invasion and lymph node metastasis status to provide a prediction for the 3- and 5-year OS and DFS rates of the patients. Calibration plots and c-indices indicated that the generated nomograms performed better than the TNM staging system in terms of discriminating between patients with different clinical outcomes. However, a limitation exists that the study design is retrospective in nature and the number of patients enrolled was relatively small. A large, multi-center, prospective study is required to validate these results.
It is known that anticancer therapies, including cytotoxic drugs, radiotherapy and targeted agents, depend on the activation of anticancer immune responses (28). Studies on the reversion of M1/M2 polarization, the prognostic value of TAMs (29,30) and GM-CSF expression, as in the present study, have raised the possibility that by altering the level of cytokines, for example, increasing the concentration of GM-CSF in the tumor microenvironment, the reversal of the polarization of TAMs may provide a novel target for the treatment of gastric cancer.
In conclusion, intratumoral expression of GM-CSF in gastric cancer has been identified as an independent prognostic factor for OS and DFS. Furthermore, intratumoral GM-CSF expression may be integrated with the depth of tumor invasion and lymph node metastasis status to provide improved risk stratification for patients with gastric cancer with different prognosis, particularly in advanced stages.
Acknowledgements
The present study was funded by grants from the National Key Projects for Infectious Diseases of China (grant nos. 2012ZX10002012-007 and 2016ZX10002018-008), the National Natural Science Foundation of China (grant nos. 31100629, 31270863, 81372755, 31470794, 81401988, 81402082, 81402085, 81471621, 81472227, 81472376, 31570803, 81501999 and 81572352) and the Program for New Century Excellent Talents in University (grant no. NCET-13-0146).
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