Diagnostic and prognostic value of the peripheral natural killer cell levels in gastric cancer
- Authors:
- Published online on: August 5, 2020 https://doi.org/10.3892/etm.2020.9101
- Pages: 3816-3822
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Copyright: © Chen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Gastric cancer (GC) is the fourth leading cause of cancer-associated mortality among the most common malignancies, with nearly 760,000 deaths resulting from GC each year (1,2). GC has no specific manifestation at the early stage and >80% of patients with GC present with advanced or late-stage GC upon diagnosis (3). Thus, early diagnosis of GC is particularly important and more effective non-invasive diagnostic markers for early GC are urgently required.
Peripheral lymphocyte subsets are important cells in the immune system (4,5). Peripheral blood lymphocyte subsets mainly include T lymphocytes, B lymphocytes (CD19+) and natural killer (NK) cells (CD3-CDl6+CD56+). According to the presence of different cell surface markers, T lymphocytes may be divided into various phenotypic and functional groups, including CD3+, CD4+ and CD8+ T cells, and regulatory T cells (Tregs; CD4+CD25+CD127-). T cells and NK cells are mainly involved in cellular immunity, while B cells are involved in humoral immunity (5-8).
Changes in the peripheral lymphocyte subsets of tumor patients not only reflect the state of immune functions but are also closely linked to the clinical phenotype of tumors (9). Low levels of CD3+ T cells in peripheral blood are associated with the poor prognosis of patients with colon, endometrial or lung cancer (10-12), while low levels of CD4+ and CD8+ T cells are associated with the poor prognosis of patients with breast (13), colorectal (14) and cervical cancer (15). Certain studies have indicated that the proportion of CD4+ and CD8+ T cells tends to be stable, fluctuating between 1.3 and 2.0% in healthy individuals and may also be a good prognostic marker for lung and cervical cancer (16,17). CD19 is able to specifically reflect changes in B lymphocytes and CD19+ B cells were proven to be a prognostic marker for nasopharyngeal carcinoma (18). Tregs are a group of lymphocytes that negatively regulate the immune response and have an important role in maintaining self-tolerance and avoiding excessive immune damage to the body. Studies have suggested that high levels of Tregs lead to poor prognosis in patients with colorectal or esophageal cancer (19,20). NK cells are a group of lymphocytes with innate immune function. Low levels of NK cells have been indicated to be associated with a favorable prognosis in patients with esophageal or pancreatic cancer (21,22). In spite of the increase of clinical research on lymphocyte subsets in peripheral blood, only a few systematic studies have reported on the distribution of lymphocyte subsets in the peripheral blood of patients with GC (23).
In the present study, the distribution of peripheral lymphocyte subsets in healthy donors (HDs), patients with gastric ulcer (GU) and patients with GC was explored and the value of NK cells as a diagnostic and prognostic marker for GC was revealed.
Materials and methods
Patients
To determine the minimum sample size in the HD, GU and GC groups for inclusion in the present study, the following formula was used to calculate the sample capacity: n1=Zα2Sen(1-Sen)/Δ2, n2=Zβ2Spe(1-Spe)/Δ2, where n1 is the case sample capacity, n2 the control sample capacity, Sen is the sensitivity, Spe is the specificity, Zα=Zβ=95% CI=1.96 and Δ=0.1. The minimum sample capacity was determined to be 72 for GC and 68 for GU and HD. Peripheral blood samples were collected from 122 patients with GC prior to radical D2 surgery for GC at the Affiliated Hospital of Nantong University (Nantong, China) from January 2013 to December 2013. Informed consent was obtained from all included participants. A total of 122 patients with primary GC scheduled for radical D2 surgery for GC were selected according to the following criteria: i) Patients were not older than 80 years; ii) patients did not receive any chemotherapy drugs prior to or after surgery; iii) patients had no known infectious diseases within 1 month prior to surgery; iv) patients had no obvious symptoms of fever; v) no blood transfusion was performed during surgery and within 1 month after surgery or 3 months prior to surgery; vi no infection or other complications occurred after surgery; and vii) tumors were TNM stage I, II or III. A uniform follow-up procedure was performed based on the clinical guidelines of the Japanese GC Association Classification of Gastric Carcinoma, 13th edition (24). The present study was approved by the Ethics Committee of the Affiliated Hospital of Nantong University (Nantong, China) in accordance with the tenets of the Declaration of Helsinki.
Blood sample collection and flow cytometry
Fasting venous blood samples were collected in heparin anticoagulant tubes and the samples were incubated with four-color monoclonal antibodies at room temperature for 15 min as follows: A CD3-FITC/CD8-PE/CD45-peridinin chlorophyll (PerCP)/CD4-allophycocyanin (APC) four-color kit (Mindray Medical International Co., Ltd.; cat. no. 340443; 1:1) and a CD3-FITC/CD16+56-phycoerythrin (PE)/CD45-PerCP/CD19-APC four-color kit (Mindray Medical International Co., Ltd.; cat. no. 652834, 1:1) were used to identify CD3+, CD4+, CD8+ and CD19+ T cells and NK cells, respectively, while a CD45-PerCP/CD4-APC/CD25-PE/CD127-FITC four-color kit (BD Biosciences; cat. no. 6029623, 1:1) was used to identify Tregs. After 15 min, flow cytolytic lysing agent (Mindray Medical International Co., Ltd.; cat. no. 2018110601) was added. The aforementioned kits were used according the manufacturers' protocols and all of the prepared samples were assayed using a BriCyte E6 flow cytometer (Mindray) and a minimum of 3x103 cells were recorded. A particular uniform protocol was followed that was published previously (9).
Immunohistochemical (IHC) analysis
In brief, GC or GU tissues were paraffin-embedded and cut into sections (4 µm thick). The sections were dewaxed in xylene and then rehydrated using a graded ethanol series. After three washes with PBS, the sections were incubated overnight at 4˚C with the anti-CD56 antibody (Fuzhou Maixin Biotech Co., Ltd.; cat. no. Kit-0028, 1:100), an NK cell marker. After three washes with PBS, the sections were incubated with a horseradish peroxidase-conjugated secondary antibody (Dako, Agilent Technologies, Inc.; cat. no. S0809; 1:150) for 2 h at room temperature. Finally, hematoxylin and xylene were used to counterstain the sections. The staining intensity was scored manually in the microscope by two independent experienced pathologists. Brown-stained lymphocytes were defined as positively stained cells. The final IHC score was calculated using the average proportion of positively stained cells among lymphocyte cells in five random fields.
Statistical analysis
Statistical analysis was performed using SPSS version 17.0 statistical software (SPSS Inc.). The results are expressed as mean ± standard deviation (SD). One-way analysis of variance followed by the Student-Neumann-Keuls post hoc test was used for comparison among the GC, GU and HD groups. The Student's t-test was used for comparing the NK cell ratio between cancer associated death and those who were still alive after 5 years. The correlation of NK cell levels between serum and paired tumor tissue samples was analyzed by Spearman correlation analysis. The sensitivity and specificity to identify GC and HD based on the peripheral NK cell level were analyzed and the best cutoff was determined by receiver-operating characteristic (ROC) curve analysis. The χ2 test was used to determine the association between the level of peripheral NK cells and clinicopathological features. Clinical and pathological data at the time of resection were analyzed to identify factors that influenced the prognosis via the Cox proportional hazards model. Multivariate analysis was performed by the Cox proportional hazards regression model. Kaplan-Meier analysis with a log-rank test was performed to determine the overall survival (OS) of patients with GC based on the level of peripheral NK cells. P<0.05 was considered to indicate statistical significance.
Results
Distribution of lymphocyte subsets in patients with gastric diseases
Flow cytometry was used to detect the distribution of peripheral blood lymphocyte subsets in 80 HDs (age, 59.77±12.06 years; 50 male, 30 female), 80 cases of GU (age, 60.26±11.23 years; 42 male, 38 female) and 122 cases of GC (age, 56.41±11.92 years;37 male, 85 female) (Fig. 1). CD3+, CD4+ and CD8+ T cells, as well as CD19+ B cells, were lower in patients with GC than in HDs and GU cases but with no statistical significance (P>0.05; Fig. 1A-D). Tregs levels were higher in patients with GC than in HDs or cases of GU, but there was no significant difference (P>0.05; Fig. 1E). Of note, the level of NK cells in patients with GC was significantly higher than that in HDs (P<0.001; 95% CI=7.51-12.51) and patients with GU (P<0.001; 95% CI=8.31-13.67; Fig. 1E).
NK cell levels are correlated between paired serum and tumor samples from patients with GC
Next, IHC analysis of NK cells (CD56) was performed in samples from patients with GC (n=20) and ulcer tissue samples from patients with GU (n=3), revealing that the NK cell level in GC tissues was notably higher compared with in GU tissues (Fig. 2A). Further comparison revealed a strong positive correlation between the NK cell levels of paired tumor serum and tissue samples from patients with GC (Spearman R=0.898; P<0.001, Fig. 2B).
Peripheral NK cell levels are able to effectively distinguish patients with GC from HDs
The median proportion of NK cells among lymphocytes in patients with GC (n=122) was 18.77% and the interquartile range (IQR) was 13.54-31.18%. However, in HDs (n=80) and patients with GU (n=80), the median proportion of NK cells was 12.19% (IQR, 10.32-14.77%) and 12.74% (IQR, 11.42-16.01%), respectively. In addition, the one-way analysis of variance revealed that the level of peripheral NK cells was increased in the GU group as compared with that in the HD group, and in the GC group as compared with that in the GU group (P=0.026 and P<0.001, respectively), indicating that the level of NK cells increased with the progression of the disease. An ROC curve was generated and demonstrated that the peripheral NK cell levels were able to effectively identify patients with GC and HD (Fig. 3). The area under the curve was 0.846 (95% CI: 0.789-0.893; P<0.001), while the best cut-off diagnostic threshold of NK cells for GC was 15.16%. For this critical value, a diagnostic sensitivity of 75.41% and a specificity of 77.45% were determined. The false-positive rate was 24.59% and the false-negative rate was 22.55%. At the critical value of 15.16%, the proportion of patients with high levels of NK cells in the GC, HD and GU groups were 75.41% (92/122), 22.55% (18/80) and 26.25% (21/80), respectively.
Peripheral NK cell levels in patients with GC are associated with clinicopathological features
To determine the clinical importance of peripheral NK cell levels in patients with GC, the association of the peripheral levels of NK cells with various clinicopathological features in 122 patients with GC was determined. High NK cell levels were defined as >15.16% and low NK cell levels as ≤15.16% based on the previously determined NK cell level cutoff in patients with GC. χ2 test indicated that high levels of peripheral NK cells were associated with the N stage, T stage and TNM stage (Table I). However, multivariate analysis suggested that high levels of peripheral NK cells were only independently associated with the T stage [P=0.031; hazard ratio (HR)=3.278; 95% CI: 1.113-9.656].
 | Table IAssociation between the characteristics of patients with gastric cancer and NK cell ratios in peripheral blood. |
High levels of NK cells in patients with GC are linked to poor survival
Kaplan-Meier survival curves were drawn to determine the association of the levels of peripheral NK cells with OS. The results indicated that patients with high peripheral NK cell levels had a shorter OS than those with low levels of NK cells (P=0.004; Fig. 4A). In addition, at the 5-year follow-up, 69 patients had died, while 53 patients remained alive, with a 5-year mortality rate of 56.6%. The median proportion of NK cells was significantly higher in patients who had deceased (20.77%; IQR, 16.38-34.38%) than in those who were still alive after 5 years (17.50%; IQR, 12.80-20.82%; P=0.002; Fig. 4B). Next, multivariate analysis suggested that the level of peripheral NK cells were independent predictors of OS in patients with GC (P=0.018; HR=2.637; 95% CI: 1.305-5.328; Table II).
| Table IIUnivariate and multivariate analyses of prognostic factors for overall survival in patients with gastric cancer. |
Discussion
The present study aimed to investigate the diagnostic and prognostic value of peripheral lymphocyte subsets in GC. The levels of peripheral CD3+, CD4+ and CD8+ T cells, CD19+ B cells and Tregs in patients with GC were not significantly different from those in HDs, but the proportion of peripheral NK cells in patients with GC (18.77%) was significantly higher than that in HDs (10.85%, P<0.001) and cases of GU (11.89%, P<0.001). ROC curve analysis suggested that the peripheral NK cell levels may be used as a diagnostic marker for patients with GC. In addition to CEA, CA19-9 and CA72-4 serum markers are widely used for the early diagnosis of GC (25-27). Recent studies have indicated that non-coding RNAs, including Homo sapiens circular RNA 0000467, as well as epigenetic changes such as RAS association domain family member 10 (RASSF10) hypermethylation, Helicobacter pylori infection, T stage and other molecular markers (28), may also act as diagnostic markers for GC (29-32). In a previous study, the sensitivity and specificity of CA19-9 were determined to be 0.605 and 0.559, respectively, while those for CEA were 0.686 and 0.593, respectively, and those for CA72-4 were 0.667 and 0.592, respectively (29). In the present study, an ROC curve was generated and the sensitivity and specificity of NK cells were determined to be 75.41 and 77.45%, respectively, which were significantly higher than those for CEA, CA19-9 and CA72-4. These results suggested that the peripheral NK cell levels may be used as a marker for the early diagnosis of GC.
The peripheral NK cell level is associated with various clinicopathological factors. It has been indicated that the level of peripheral NK cells is associated with lymph node metastasis in esophageal cancer (21). The present study determined that the level of peripheral NK cells in patients with GC was associated with the T stage, suggesting that it may be used to assess tumor progression in patients with GC. However, this requires further validation in future studies with larger sample sizes.
Numerous factors affect the prognosis of GC, with the most widely used factor being the TNM stage (33,34). However, according to our clinical experience, it appears that patients with GC and the same TNM stage have different prognoses, and patients with the same TNM stage may have different molecular phenotypes. Molecular typing of GC also has an important role in the prognosis of patients (35). In recent years, an increasing number of studies have reported that certain factors, including high co-overexpression of epidermal growth factor receptor and receptor tyrosine kinase 3, low levels of microRNA-214 and high methylation of RASSF10, are associated with poor prognosis in patients with GC (30,36,37). In the present study, the peripheral NK cell levels were determined to be an independent prognostic factor in patients with GC and patients who died within 5 years had a higher level of peripheral NK cells. Furthermore, the detection of NK cells only requires peripheral blood extraction, which is convenient to test and associated with low cost for patients. In the present study, the specificity and sensitivity of the NK cell ratio were slightly better than those for established prognostic markers for GC, including CEA and CA19-9. The present study determined that the NK cell ratio in the serum exhibited a positive correlation with that in matched GC tumor tissue samples. In the future, the NK cell ratio may be implemented in routine diagnostic/prognostic procedures for GC. However, the present study was limited by the sample size of patients with GC and HDs. In addition, only common peripheral blood lymphocytes were examined and the role of the proportion of NK cells in the prognosis and diagnosis of GC patients was demonstrated. However, there may be other lymphocyte clusters that warrant exploration.
In conclusion, the present study indicated that the peripheral NK cell levels may be used to identify patients with GC and are associated with certain clinicopathological factors of malignancy. Of note, high levels of peripheral NK cells were associated with poor prognosis. The present study demonstrated that the peripheral NK cell levels may be a good diagnostic and prognostic marker for patients with GC.
Acknowledgements
The authors thank Dr Nicole Okoh (Liwen Bianji, Edanz Editing China; www.liwenbianji.cn/ac) for editing the English text of a draft of this manuscript.
Funding
This study was supported by the National Natural Science Foundation of China (grant no. 81672409), Jiangsu Provincial Medical Youth Talent (grant no. QNRC2016700), ‘333 Talent’ Cultivating Project of Jiangsu Province (grant no. BRA2018394), Postgraduate Research & Practice Innovation Program of Jiangsu Province (grant no. SJCX20_1153; SJCX20_1159; KYCX20_2674) and the Scientific and Technological Innovation and Demonstration Project of Nantong City (grant no. MS12018061).
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
Authors' contributions
WJX and YLH conceived and designed the experiments. YYC and YF performed the experiments. QSM, JZL, XC and PM analyzed the data. YYC and YFL wrote the manuscript. WL and YFL searched the literature and performed statistical analysis. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The present study was approved by the Ethics Committee of Nantong University (Nantong, China). Written informed consent was obtained from each participant.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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