- Research article
- Open Access
- Open Peer Review
Clinical significances of preoperative serum interleukin-6 and C-reactive protein level in operable gastric cancer
- Do-Kyong Kim†1,
- Sung Yong Oh†1,
- Hyuk-Chan Kwon1,
- Suee Lee1,
- Kyung A Kwon1,
- Byung Geun Kim1,
- Seong-Geun Kim1,
- Sung-Hyun Kim1,
- Jin Seok Jang1,
- Min Chan Kim2,
- Kyeong Hee Kim3,
- Jin-Yeong Han3 and
- Hyo-Jin Kim1Email author
© Kim et al; licensee BioMed Central Ltd. 2009
- Received: 01 January 2009
- Accepted: 20 May 2009
- Published: 20 May 2009
The interleukin-6 (IL-6) pathway is one of the mechanisms that link inflammation and angiogenesis to malignancy. Because the C-reactive protein (CRP) is a representative marker for inflammation, CRP has recently been associated with the progression of disease in many cancer types. The principal objective of this study was to determine the preoperative serum levels of IL-6 and CRP in gastric carcinoma, and to correlate them with disease status and prognosis.
A total of 115 patients who underwent gastrectomy were enrolled in this study. Serum levels of IL-6 were assessed via Enzyme-Linked Immuno-Sorbent Assay (ELISA), and CRP was measured via immunoturbidimetry. Histological findings included tumor size, depth of tumor invasion, lymph node (LN) metastasis, and TNM stage (6th AJCC Stage Groupings: The staging systems; Primary tumor, regional LN, metastasis).
Increases in cancer invasion and staging are generally associated with increases in preoperative serum IL-6 levels. IL-6 and CRP levels were correlated with invasion depth (P < 0.001, P = 0.001), LN metastasis (P < 0.001, P = 0.024) and TNM stage (P < 0.001, P < 0.001). The presence of peritoneal seeding metastasis is associated with IL-6 levels (P = 0.012). When we established the cutoff value for IL-6 level (6.77 pg/dL) by ROC curve, we noted significant differences in time to progression (TTP; P < 0.001) and overall survival (OS; P = 0.010). However, CRP evidenced no significance with regard to patients' TTP and OS levels. Serum IL-6 levels were correlated positively with CRP levels (r 2 = 0.049, P = 0.018).
Preoperative serum IL-6 and CRP levels might be markers of tumor invasion, LN metastasis, and TNM stage. Preoperative high IL-6 levels were proposed as a poor prognostic factor for disease recurrence and overall survival in patients with gastric cancers.
- Gastric Cancer
- Lymph Node Metastasis
- Peritoneal Metastasis
- Peritoneal Seeding
- Myeloma Bone Disease
Interleukin-6 (IL-6) is a multi-poietic cytokine that induces the growth and differentiation of immune cells, the production and expression of other cytokines, and acute-phase protein synthesis. IL-6 also exerts several effects on cancer cells [1, 2].
In cancer, IL-6 is generally known to be involved in host defense mechanisms. IL-6 binds to the IL-6 receptor, activates the Janus kinase (JAK), and subsequently phosphorylates the signal transducers and activators of transcription (STAT). The phosphorylated STAT gene translocates into the nucleus and activates the target gene (JAK/STAT) pathway. Suppressor of cytokine signaling-1 (SOCS-1) is one of the STAT-activated genes, which is upregulated by IL-6 and is involved in the downregulation of the JAK/STAT pathway [3–5]. In many cancer types, recent studies have demonstrated that the hypermethylation of SOCS-1 is not controlled by the JAK/STAT pathway, and IL-6 cannot perform a role in cancer defense; on the contrary, it is involved in cancer development [3, 6].
In the development and progression of cancer, angiogenesis is a crucial and essential process. IL-6 is associated with angiogenesis by virtue of its ability to induce the mRNA of vascular endothelial growth factor (VEGF), which is typically a direct angiogen . Additionally, IL-6 activates the Rho protein, which is associated with cell-cell adhesion and invasion in malignancy .
C-reactive protein (CRP) is a representative marker for inflammatory conditions, and performs a crucial anti-infection function in the immune system. In many cancers, it has been reported that chronic inflammation is involved with malignant change, and the risks of cancer are increased when pre-diagnostic CRP levels are high . Cancer invasion begins with inflammation around cancer cells. Thus, it has been reported that serum CRP levels are higher in cases of invasive cancer than in cases of non-invasive cancer [9, 10].
Gastric cancer is the fourth most-frequent source of morbidity worldwide, and the second most-frequent source of mortality [11, 12]. In Korea, gastric cancer is the most frequent source of morbidity among malignant tumors . These high levels of gastric cancer mortality can be attributed to the high incidence of serosal invasion, direct invasion into the adjacent organs, peritoneal seeding, lymph node metastasis, and distant metastasis of gastric cancer. In cases of gastric cancer, the failure of downregulation of the JAK/STAT pathway due to the hyper-methylation of SOCS-1 has been surveyed, and angiogenesis has been identified as an indispensable process for high tendencies toward malignancy [3, 14, 15]. The principal objective of this study was to determine the relationship between serum IL-6 and CRP levels and malignant tendencies and prognosis in gastric cancer patients.
From March 2005 to August 2008, a total of 115 patients with histologically-confirmed gastric carcinomas from surgically resected specimens of gastric tumors at the Dong-A University Hospital were enrolled in this study. After operation, the disease status of patients was evaluated via gastroendoscopy and abdominal computed tomography (CT). During the first 2 years, we checked CT and endoscopy at six-month intervals, and afterwards CT and endoscopy were conducted every 12 months. We also conducted abdomen CT when we observed abdominal distension, acute abdominal pain, severe diarrhea, and chest X-ray abnormalities suggestive of lung metastasis. Endoscopy was conducted in cases in which patients complained of unexplained abdominal discomfort and dyspepsia. On average, in the stage III and IV patients, the first evaluation was conducted within 3 months after operation. All patients provided informed consent, and the hospital review board approved the study.
Assay of serum IL-6 and CRP
Venous blood sampling was conducted within 7 days before the patients underwent operations. The blood collected for IL-6 serum level assessments was collected in plain tubes, and the levels of serum IL-6 were measured using commercially available enzyme-linked immunosorbent assays (ELISAs) (Quantikine h IL-6 Immunoassay, R&D Systems, USA). The blood samples were centrifuged for 10 min at 3,000 r/min at -4°C. The serum was subsequently removed and stored at -80°C until biochemical analysis. The blood samples for CRP analysis were collected in serum separation tubes, and the serum CRP levels were measured via immunoturbidimetry (Denka Seiken Co. Ltd., Japan).
Serum levels of IL-6 and CRP were expressed as the means ± SD. A p value of < 0.05 was considered to be statistically significant. The Spearman rho correlation coefficient (r) was employed to evaluate the correlation between the IL-6 and CRP levels and the clinical findings. The IL-6 and CRP cut-off values for survival analysis were determined by the ROC curve. The duration of recurrence of gastric cancer and death measured from the date of surgery was referenced against time to progression and overall survival time. Survival durations were calculated via the Kaplan-Meier method. The log-rank test was employed to compare the cumulative survival rate and time to progression in the patient groups. Linear regression analysis was conducted to estimate the relationship between the IL-6 values and CRP values. The Statistical Package for Social Sciences (SPSS) Version 15.0 for Windows was utilized to perform all statistical analyses.
No. of patients
Total number of patients
Depth of tumor invasion
Clinicopathological significance of IL-6
Correlation between the IL-6, CRP and clinicopathological parameters
Median ± SD
Median ± SD
6.83 ± 7.34
0.11 ± 0.25
7.07 ± 12.30
0.06 ± 0.43
6.48 ± 12.26
0.07 ± 0.30
7.31 ± 5.56
0.11 ± 0.38
6.48 ± 5.04
0.09 ± 0.28
7.56 ± 12.93
0.09 ± 0.39
6.25 ± 1.41
0.05 ± 0.10
6.60 ± 5.42
0.07 ± 0.31
7.62 ± 16.02
0.17 ± 0.36
9.76 ± 6.06
0.64 ± 0.64
6.36 ± 5.61
0.06 ± 0.30
7.70 ± 13.99
0.11 ± 0.36
6.83 ± 2.10
0.09 ± 0.08
7.80 ± 6.96
0.19 ± 0.51
7.56 ± 11.24
0.11 ± 0.35
7.36 ± 5.52
0.06 ± 0.29
7.66 ± 2.24
0.07 ± 0.15
11.87 ± 14.90
0.12 ± 0.30
13.92 ± 10.76
0.39 ± 0.50
6,83 ± 8.83
0.08 ± 0.29
23.70 ± 14.55
0.41 ± 0.69
Clinicopathological significance of CRP
0.145 mg/dl was taken as the cutoff value of CRP by ROC curve, after which the patients were divided into two groups. The sensitivity and specificity of 0.145 mg/dl as the cutoff value were 57.1% and 65.3% on OS. We noted no significant difference in the TTP values (70.7% vs 75.0%, P = 0.5245) and OS values (81.4% vs 91.7%, P = 0.0791) among the groups.
Association between IL-6 and CRP
In this study, the serum levels of both IL-6 and CRP evidenced statistically significant differences in tumor size, tumor invasion depth, and LN metastasis. In the TNM stage, as the stage of the disease increased, serum IL-6 and CRP levels were significantly higher. Additionally, the median levels of IL-6 were significantly higher in the patients with peritoneal seeding than in those without peritoneal seeding, but in CRP, this was not proven. In terms of survival rate and time to cancer progression, the results of this study showed that IL-6 levels were associated with poor prognoses. As IL-6 and CRP levels were associated strongly with disease status, in our multivariate analysis, IL-6 and CRP were not identified as independent factors. In some papers, it has been reported that IL-6 was an effective prognostic indicator in stages II and III . In this study, we conducted multivariate analysis in stage II and III, but we were unable to detect any tendency that would point to IL-6 as an independent prognostic factor.
There have been a great many studies conducted concerning the values and functions of IL-6 in malignancy. The majority of these studies have shown that IL-6 levels were higher in malignancies than in non-malignancies, and increased with increasing tumor size and depth [17–19]. We detected a statistically significant relationship between IL-6 levels and existing LN metastasis. However, some studies have reported no relationship between IL-6 levels and LN metastasis . LN metastasis was shown to be affected by independent predictors in cases of advanced cancers. Many previous studies have also noted that IL-6 levels increased in cases of distant metastasis, especially hepatic metastasis [17, 18]. This result has been attributed to a host of mechanisms, including the autocrine and paracrine pathways. With regard to the autocrine pathway, IL-6 activated the production of IL-6 by tumor cells with the IL-6 receptor. With regard to the paracrine pathway, IL-6-stimulated stromal cells promoted the secretion of tumor growth and adhesion molecules containing VEGF and hepatocyte growth factor (HGF) [2, 17, 19, 21].
CRP has been identified in many previous studies as a poor prognostic factor in several diseases, including coronary artery disease, chronic obstructive pulmonary disease, diabetes mellitus, myeloma bone disease, and a variety of cancers [22–30]. In many studies of cancer patients, it has been noted that elevated CRP levels are associated with tumor size, cancer stage, cancer cachexia, and poor prognosis as independent prognostic indicators [19, 26, 28, 31]. In this paper, we described the relationship between CRP levels and tumor invasion depth, LN metastasis, and TNM stage. The operant mechanism in this regard remains unknown. However, elevations of CRP levels have been reported previously in patients with impaired T lymphocyte response, and thus this mechanism is considered to be related to the immunity system and poor survival rate .
CRP is generated by the liver and other organs in response to the release of IL-6 by monocytes and other immune cells . Thus, when IL-6 levels increased, CRP levels also increased. Although CRP was not found, in this study, to be related to TTP and OS in cancer patients, CRP has generally been connected with IL-6, and IL-6 is associated with cancer prognosis. This study was somewhat limited in that the patients' group was restricted in patients who underwent operations. Thus, this study included more patients who could undergo surgery at a lower stage than those who evidenced contraindications for curative operations, including those patients in stage IV. In particular, as compared with another study concerning the relationship between CRP levels and cancer prognosis, a small number of advanced-stage patients were enrolled in this study .
Elevated serum IL-6 levels have been implicated in many different conditions characterized by chronic inflammation, including viral and bacterial infections, autoimmune disease, ischemia, diabetes mellitus, severe exercise, and malignancy [6, 32]. Actually, when the IL-6 cutoff value was established at 6.77 pg/ml, the TTP and OS differed significantly between patients with IL-6 levels in excess of 6.77 pg/ml, and those with lower IL-6 levels. When the IL-6 cutoff value was established at 6.77 pg/ml, the sensitivity was 80.0% in TTP and 85.7% in OS; the specificity was 55.3% and 50.1%. Although there were many disturbance factors that complicated the elevation of IL-6 levels, the sensitivity of IL-6 in association with TTP and OS was found, in this study, to be sufficiently high. Thus, we surmise that the prognoses in gastric cancer patients with high IL-6 levels would be generally poor.
However, high IL-6 and CRP levels were related to advanced stage, including distant metastasis, in this study, and elevated IL-6 levels were associated with poor outcomes in cases of gastric cancer.
Preoperative serum IL-6 and CRP levels were related to cancer stage and might be markers of tumor invasion, LN metastasis and TNM stage. Especially high IL-6 levels were prospected as a poor prognostic factor of disease recurrence and overall survival in patients with gastric cancer.
This Paper was supported by the Dong-A University Research Fund.
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