Level of circulating PD-L1 expression in patients with advanced gastric cancer and its clinical implications

Introduction

Gastric cancer is one of the most common cancers worldwide and has the second leading cancer-related mortality rate with much poorer survival (1,2). Even with advances in diagnosis and therapy, the total prognosis of gastric cancer patients is still poor (3). Cell-mediated immune responses against tumor are either present spontaneously in human cancer patients as a critical component of tumor immune surveillance or can be elicited by cancer vaccination and adoptive T-cell transfer (4-7). Recent evidence showed that experimental depletion of regulatory T cells (Tregs) improves immune-mediated tumor clearance and enhances the response to immune-based therapy (8,9). Tregs have been shown to suppress tumor-specific T cell immunity and therefore may contribute to the progression of human tumors (10,11).

At present, tumor-associated macrophages (TAMs) and T cells are the most commonly used immune cells within the tumor microenvironment for research. The family of T-cell inhibitory receptors (12-16) limits T-cell functions by negatively regulating signals in immune cells (e.g., T cells and natural killer cells), including activating signals mediated by the T cell receptor (TCR) (17). Recently, various molecules have been identified, that can modulate TCR signals, such as the well known CD28 and CTLA-4. Programmed cell death-1 (PD-1), an immunoinhibitory receptor of the CD28 family, which plays a major role in tumor immune escape (18,19), is an inhibitory receptor expressed on the surface of T cells that functions to physiologically limit T-cell activation and proliferation (20). Its ligand, PD-L1 (B7-H1/CD274), is expressed on antigen-presenting cells. The PD-1/PD-L1 pathway is another major receptor-ligand network that functions primarily to provide a coinhibitory signal. Binding of PD-L1 to its receptor inhibits T lymphocyte proliferation and effector functions (cytotoxicity, cytokine release), induces apoptosis of tumor-specific T cells, promotes the differentiation of CD4+ T cells into Foxp3+ Tregs, as well as the resistance of tumor cells to cytotoxic lymphocyte (CTL) attack (21-25). The expression of PD-L1 in tumors has been described in many histological types of carcinoma, such as renal cell carcinoma, breast cancer, pancreatic cancer, ovarian cancer, urothelial cancer, melanoma, esophageal cancer, hepatocellular carcinoma, as well as gastric carcinoma (26-34). Less invasive and more efficient biomarkers are needed for detection and evaluation of gastric cancer by mass screening. The current biomarkers, pepsinogen, carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9), are not sufficient for accurately predicting gastric cancer (35-37). The aim of this study is to identify circulating PD-L1 level in patients with advanced gastric cancer by using enzyme-linked immunosorbent assay (ELISA) procedures, and evaluate the relation of the PD-L1 expression and clinicopathological features and their prognostic significance.

Materials and methods

Patients

A total of 80 patients with advanced gastric cancer, who were treated at the Department of Gastrointestinal Surgery of Beijing Cancer Hospital from 2006 to 2009, were included in this retrospective analysis, and 40 healthy subjects served as controls. Patients were excluded from this analysis due to incomplete clinical data or inadequate follow-up or inadequate blood sampling. All patients had histologically confirmed carcinoma of the stomach. Staging was based on clinical assessment and histopathological analysis by the International Union Against Cancer (UICC) TNM staging system recommended by the American Joint Committee on Cancer (AJCC) stage (7th edition) and Japanese Gastric Cancer Association (JGCA) guidelines. Clinicopathological characteristics of the patients were collected from our hospital electronic patient records. None of the gastric cancer patients had synchronous cancers, previous gastrointestinal diseases, abdominal surgery, chemotherapy or radiotherapy. All samples were taken from endoscopic biopsy or surgically resected material. Follow-up data of patients were retrieved from hospital records and by contacting the general practitioners. Three of them were lost to follow-up because of unable to contact. The study was approved by the Ethics Committee of Peking University Cancer Hospital. Informed consent was obtained from each patient.

Blood sampling

Blood samples were drawn prior to any treatment. Sera derived from advanced gastric cancer patients and from sex, age-matched controls were collected prior to definitive treatment using a standardized protocol. The serum was obtained by centrifugation (at 3,000 g for 10 min), aliquoted and stored at –80 °C until analysis. Blood collection and analyses were approved by the Ethics Committee of Peking University Cancer Hospital. All samples were analyzed retrospectively, and cases and controls were processed simultaneously. Patient recruitment and sample collection were performed within the guidelines of protocols approved by the institutional review boards. All cases have been analyzed by clinicians.

ELISA assay

Serum samples obtained from 80 advanced gastric cancer patients and 40 health controls were assayed by a commercially available ELISA Kit for PD-L1 (Uscn Life Science Inc.), following the manufacturer’s protocol. Briefly, 96-well plates were incubated with standards at different concentrations, and serum samples were incubated for 2 h at 37 °C. After covering biotinylated antibodies and several aspiration/wash processes, horseradish peroxidase (HRP)-conjugated streptavidin was prepared at 37 °C for 15-25 min, and protected from light. The liquid will turn blue by the addition of substrate solution. Enzymatic reactions were developed and the absorbance was measured at 450 nm (A450) in Bio-Rad Model 680 Microplate Reader immediately (Bio-Rad Laboratories, Inc., California, USA). Protein levels were calculated according to standard curves. For a correct evaluation of the results, parallel investigations were made in healthy non-treated controls.

Statistical analysis

Continuous variables were summarized using and median (range). The ^χ2-test was used to determine the associations between PD-L1 expression and clinicopathological characteristics. The overall survival time was calculated from the date of gastric cancer treatment to the gastric cancer-specific death or censored at the time of death by other causes or the end of follow-up. The Kaplan-Meier method was used to determine the cumulative probability of survival. The log rank test was used for comparison of cumulative survival rate in the patient group. All the statistical analyses and graphics were performed with the SPSS 20.0 statistical package (SPSS Inc., Chicago, IL, USA). P

Results

Circulating level of PD-L1 in advanced gastric cancer patients and health controls

The overall data from the 80 patients and 40 health controls in Beijing Cancer Hospital were analyzed. The serum level of PD-L1 was tested by ELISA. The mean value of serum PD-L1 level in advanced gastric cancer was 0.8928±0.0900 ng/mL, and in health person was 0.5899±0.0617 ng/mL. The expression level of PD-L1 showed significant difference between normal controls and advanced gastric cancer patients (P=0.006). A cut-off value of 0.5993 ng/mL was best distinguished in patients without lymph node metastasis and with lymph node metastasis, which was used as a cut-off value for correlations and survival analysis, and the area under curve (AUC) value was 0.613 [95% confidence interval (95% CI): 0.509-0.717, P=0.044] (Figure 1).

Figure 1 Receiver operating characteristics (ROC) curve for predicting lymph node metastasis for patients with gastric cancer.

Correlations between serum PD-L1 level and characteristics of advanced gastric cancer patients

The advanced gastric cancer cohort includes 62 men and 18 women and the median age was 59 years (range, 30-72 years). Twenty (25.0%) patients were at clinical stage I or II, and 60 (75.0%) were at stage III. Sixty-four (80.0%) patients had lymph node metastasis, and 16 (20.0%) didn’t. A total of 20 patients (25.0%) were well-moderately differentiated, and 60 (75.0%) were poorly differentiated/undifferentiated. The expression of PD-L1 in serum was found to be low up-regulated in 33 (41.2%) of 80 cases, whereas the remaining 47 cases (58.8%) were classified as having highly up-regulated expression. As shown in Table 1, the PD-L1 expression appeared to be significantly associated with differentiation and lymph node metastasis (P=0.026 and P=0.041, respectively) in univariate analysis. There were more patients with differentiated cancer and/or without lymph node metastasis had higher expression of PD-L1 in serum. No significant association was observed between serum PD-L1 level and other clinicopathological variables. Multivariate logistic regression analysis found that the differentiation of advanced gastric cancer was statistically significant with soluble PD-L1 (sPD-L1) expression (RR=0.267, 95% CI: 0.080-0.894, P=0.032).

Table 1 Correlations between serum programmed cell death-1 ligands (PD-L1) level and clinical characteristics of advanced gastric cancer patients
Full table

Correlation of PD-L1 expression with prognosis of advanced gastric cancer patients

The overall survival rates of advanced gastric cancer patients were statistically estimated with the expression of serum PD-L1. The median follow-up duration since the time of diagnosis was 39.6 months (range, 1.5-76.6 months). The advanced gastric cancer patients with different PD-L1 expression had similar overall survival with no significant differences (P=0.636, Figure 2A). But the overall 5-year survival rate in advanced gastric adenocarcinoma patients with high and low up-regulated PD-L1 expression levels was nearly 65.6% and 44.7%, respectively. The survival difference between these two groups was statistically significant (P=0.028, Figure 2B). We found that there were no significant differences in the serum expression of PD-L1 between the differentiated cancer patients and undifferentiated patients (P>0.05).

Figure 2 Kaplan-Meier overall survival curves. (A) Advanced gastric cancer patients; (B) Advanced gastric adenocarcinoma patients. Survival analysis was performed according to the expression of serum PD-L1.

Discussion

A lot of studies have shown that immune escape is an active process in which tumor cells and immune cells within the tumor microenvironment actively suppress the antitumor immune response. The most notably Tregs have been shown to suppress tumor-specific T cell immunity and account for tumor progression (38,39). PD-L1 (B7-H1), with its receptor PD-1, plays a critical role in suppressing T cell-based immunity and could mediate tumor immunosuppression (40). PD-1/PD-L1 interactions contribute to the maintenance of peripheral tolerance of self-antigens in normal hosts (41). One in vitro study showed that PD-L1 (B7-H1) specifically interacts with B7-1 to inhibit T and B cell activation and proliferation. Additionally, both B and T cell function can be modulated by engagement of cell-surface PD-L1 (42,43). Different from membrane-bound forms, soluble forms have been found for several members of B7 family (44,45), but no study has been reported soluble PD-L1 expression in gastric cancer patient until now. sPD-L1 may play an important role in the immunoregulation of PD-1/PD-L1 pathway, and could afford distant effect to the activated T cells by the intervention between PD-1/membrane PD-L1 (mPD-L1). The soluble ligands can bind receptors in a similar manner as their membrane-bound counterparts and as a result may play an important role in the regulation of receptor activity. Circulating sPD-L1 remains the biological activity and has the ability of binding to PD-1 receptor. The existence of sPD-L1 in human peripheral blood increases the complexity of PD-1/PD-L1 co-inhibitory signal in immune regulation.

To further explore the existence of sPD-L1 and evaluate the pathological significance of this circulating factor in human cancer serum, we developed this study for the detection and quantification of sPD-L1 in advanced gastric cancer patients. Although the sPD-L1 level in advanced gastric cancer is lower than some earlier reported in other cancers in the present study, but it also indicates that the sPD-L1 expression in advanced gastric cancer was much higher than health controls, which is in agreement with previous findings (46). The patients with differentiated tumor and/or without lymph node metastasis had higher sPD-L1 level. However, despite the lack of statistical significance, there was a lower level of sPD-L1 expression with increasing stage and/or deeper depth of gastric cancer. Therefore, it was considered to be an early event during tumor progression. In line with these findings, Wang et al. observed the similar results in hepatocellular carcinoma tissues (47), although there still have more different cancer observations (48,49). Several studies have shown that the PD-1/PD-L1 pathway plays critical roles in compromised chronic infections and tumor immunity. It is interesting that chronic infections and tumors may have exploited the PD-1 pathway to evade eradication by the immune system. PD-1 is up-regulated upon T cell activation in infection but declines with resolution of the infection and establishment of memory (50). Interactions between PD-L1 and PD-1 are thought to maintain peripheral tolerance. PD-L1/PD-1 has been shown to mediate T-cell exhaustion, an important mechanism underlying T-cell dysfunction during chronic inflammation and chronic infection (51,52). Therefore, the increased level of sPD-L1 occurred in the early staged tumor which was considered to be caused by longlasting chronic infections and may represent an important contribution to immune evasion during tumor progression. Recent reports demonstrated that PD-L1 expressed in tumor cells or peritumoral activated monocytes contributed to tumor aggressiveness and postoperative recurrence in hepatocellular carcinoma patients (53-55).

When we explored in depth the survival rates of patients according to different level of sPD-L1 expression, the most striking finding was that patients with advanced adenocarcinoma with higher sPD-L1 expression had better overall survival although all the patients in this study have similar prognosis. This observation indicates that sPD-L1 may be a novel and unexpected feature of advanced gastric adenocarcinoma, more importantly, and predict certain patients with completely different clinical outcomes. In spite of our findings, the relationship of PD-L1 expression with survival of gastric cancer patients has remained largely debated. Previous studies had indicated that the increase of PD-L1 expression in carcinomas can cause poor clinical prognosis of many tumors, as well as gastric cancer (32,34,35). These controversial results may have been affected by different strategies in selecting the study population and mostly by different kinds of test methods that we detect the PD-L1 in peripheral circulating serum using ELISA unlike other studies of carcinoma tissues. In light of our own findings, sPD-L1 may be a useful marker to define the survival of patients with advanced gastric adenocarcinoma.

This study observed the circulating level of PD-L1 expression in advanced gastric cancer. The potential limitations should be considered that the cohort is small, and we should enlarge the samples in order to confirm the results. Further prospective studies need to monitor the alteration of PD-L1 expression during perioperative period/chemotherapy and follow-up. Despite these limitations, the findings offer an effective and easy method to predict the special clinical feature and outcome of advanced gastric cancer patients.

In conclusion, high up-regulated expression of circulating serum PD-L1 in advanced gastric cancer was correlated with differentiated tumor and without lymph node metastasis. Furthermore, the expression level of sPD-L1 might be also a potential prognostic factor for advanced gastric adenocarcinoma patients.

Acknowledgements

Disclosure: The authors declare no conflict of interest.

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