L1 and epithelial cell adhesion molecules associated with gastric cancer progression and prognosis in examination of specimens from 601 patients
© Wang et al.; licensee BioMed Central Ltd. 2013
Received: 27 July 2013
Accepted: 2 September 2013
Published: 16 September 2013
L1 cell adhesion molecule (L1CAM) and epithelial cell adhesion molecule (EPCAM) have been implicated in the development and progression of gastric cancer. The present study investigated the clinical significance of L1CAM and EPCAM in the development, progression and prognosis of gastric cancer.
Expression of L1CAM and EPCAM were examined immunochemically in 601 clinicopathologically characterized gastric cancer cases.
L1CAM protein was detected in 23.9% of human non-tumor mucosa samples. All samples expressed L1CAM protein at low levels. High expression of L1CAM protein was detected in 163 (27.1%) tumors. Expression of L1CAM correlated with age, tumor location, size of tumors, Lauren’s classification, depth of invasion, lymph node and distant metastases, regional lymph node stage, Tumor-Node-Metastasis (TNM) stage and prognosis. EPCAM protein was detected in 45.7% of human non-tumor mucosa samples. All samples expressed EPCAM protein at low levels. High expression of EPCAM protein was detected in 247 (41.1%) tumors. Expression of EPCAM correlated with age, tumor location, size of tumors, Lauren’s classification, depth of invasion, lymph node and distant metastases, regional lymph node stage, TNM stage and prognosis. Cumulative 5-year survival rates of patients with high expression of both L1CAM and EPCAM were significantly lower than in patients with low expression of both.
Expression of L1CAM and EPCAM in gastric cancer was significantly associated with lymph node and distant metastasis, and poor prognosis. L1CAM and EPCAM proteins could be useful markers to predict tumor progression and prognosis.
KeywordsGastric carcinoma L1CAM EPCAM Immunohistochemistry Progression Prognosis
Although global incidence of gastric cancer has decreased in recent years, its mortality rate in China is the highest among all tumors. The main cause of death is invasion and metastasis of tumor. Tumor invasion and metastasis is a very complicated and continuous process involving multiple steps, regulated at the molecular level by adhesion molecules, protein catabolic enzymes, cellular growth factors and various angiogenic factors. L1 cell adhesion molecule (L1CAM) is a cell adhesion molecule of the immunoglobulin superfamily of cell adhesion molecules (IgCAM), initially identified in the nervous system. Recent studies demonstrated L1CAM expression in various types of cancer, predominantly at the invasive front of tumors and metastases. Overexpression of L1CAM in normal and cancer cells increased motility, enhanced growth rate and promoted cell transformation and tumorigenicity. The epithelial cell adhesion molecule (EPCAM) is a glycoprotein of approximately 40 kD that was originally identified as a marker for carcinoma. EPCAM’s effects are not limited to cell adhesion; they include diverse processes such as signaling, cell migration, proliferation, and differentiation. Cell surface expression of EPCAM may actually prevent cell–cell adhesion.
The current study examined expression of L1CAM and EPCAM in surgical specimens of gastric carcinoma, to explore possible correlations between L1CAM and EPCAM expression and clinicopathological variables and prognosis.
Materials and methods
Cell culture and frozen tissues
Human gastric cancer cell lines AGS, MKN-28, BGC-823, HCG-27, SGC-7901, 9811P, MKN-45 and non-malignant gastric epithelial cell line GES-1 were obtained from Key Laboratory of Gastroenterology of Zhejiang Province (Hangzhou, China), and cultured in RPMI1640 containing 10% foetal bovine serum (FBS), 50U/ml penicillin and 50 μg/ml streptomycin. All cells were maintained at 37°C under an atmosphere of 5% CO2.
Patients and frozen tissue samples
Our study included 42 patients (29 male, 13 female; mean age: 59 years; range: 30–86) collected from gastrectomy specimens from the Department of Surgery, Zhejiang Provincial People’s Hospital from January 2010 and January 2011. None of the patients were treated with radiotherapy or perioperative chemotherapy, and all had undergone total gastrectomies. Resected specimens were studied pathologically according to the criteria described in the AJCC classification (2009). There were 24 tubular adenocarcinomas, 3 papillary adenocarcinomas, 10 mucinous adenocarcinomas, 5 signet-ring cell carcinomas. Two cases were categorized as stage I, 8 as stage II, 29 as stage III, and 3 as stage IV. The study items included age, sex, tumor location, tumor size, gross (Borrmann) type, gastric wall invasion, resection margin, histological type, lymph node metastasis, vascular invasion, lymphatic invasion, and perineural invasion. Fresh samples of tumor tissue, and matched normal gastric mucosa were obtained immediately after gastric resection. The samples were dissected carefully from resected specimens by a pathologist, and immediately snap-frozen in separate vials using liquid nitrogen. These frozen specimens were stored at −80°C in a tumor bank before use.
Patients and paraffin-embedded tissue samples
Gastric cancer tissues were collected from gastrectomy specimens of 601 patients from the Department of Surgery, Zhejiang Provincial People’s Hospital from January 1998 to January 2004. Tissues had been formalin-fixed and paraffin-embedded, and clinically and histopathologically diagnosed at the Departments of Gastrointestinal Surgery and Pathology. All patients had follow-up records over at least 5 years. The follow-up deadline was December 2008. Survival times were counted from the dates of surgery to the follow-up deadline or dates of death, which were mostly caused by carcinoma recurrence or metastasis. Ninety-two noncancerous human gastric tissues were obtained from gastrectomies of adjacent gastric cancers beyond margins >5 cm. Routine chemotherapy was given to patients with advanced-stage disease after operation, but no radiation treatment was administered to any patients included in our study.
Real-time quantitative RT-PCR
Expressions of L1CAM and EPCAM in 42 tumor tissue samples and matched normal gastric mucosa were confirmed by RT-PCR. Total RNA was extracted by TRIzol and cDNAs were reverse-transcribed by RevertAid TM reverse transcriptase. Real-time PCR was carried out using the ABI PRISM 7700 Sequence Detection System (Applied Biosystems) at 50°C for 2 min, 95°C for 10 min, followed by 50 cycles at 95°C for 15 s, and at 60°C for 1 min. The primers for GAPDH (224 bp) were 5′-TGAAGGTCGGAGTCAACGG-3′ (sense) and 5′- CTGGAAGATGGTGATGGGATT-3′ (antisense). The primers for L1CAM (187 bp) were 5′-TGTCCTTCCCTTTACGCCAC-3′ (sense) and 5′- GACCAAGCACAGGCATACAGG-3′ (antisense). The primers for EPCAM (101 bp) were 5′-ATAATAATCGTCAATGCCAGTG-3′ (sense) and 5′- ATTCATTTCTGCCTTCATCAC-3′ (antisense). The expression of GAPDH was used to normalize that of the target genes. Each assay was done in triplicate and the average calculated. The expression level of L1CAM/EPCAM was expressed as 2–ΔΔCt, ΔCt = Ct(Target) – Ct(GAPDH).
Immunohistochemical analysis was used to study altered protein expression in 92 noncancerous human gastric tissue controls and 601 human gastric cancer tissues [3, 4]. In brief, slides were baked at 60°C for 2 h, followed by deparaffinization with xylene and rehydration. The sections were submerged into EDTA antigenic retrieval buffer and microwaved for antigenic retrieval, after which they were treated with 3% hydrogen peroxide in methanol to quench endogenous peroxidase activity, followed by incubation with 1% bovine serum albumin to block nonspecific binding. Sections were incubated with rabbit anti-EPCAM(Epitomics), and with mouse anti-L1CAM (Abcam), overnight at 4°C. Normal goat serum was used as a negative control. After washing, tissue sections were treated with secondary antibody. Tissue sections were then counterstained with hematoxylin, dehydrated, and mounted. Cytoplasm with L1CAM and EPCAM was stained as buffy. The degree of immunostaining was reviewed and scored independently by two observers based on the proportion of positively stained tumor cells and intensity of staining [5–7].
All statistical analyses were performed using SPSS16.0 software. Measurement data were analyzed using Student’s t test, while categorical data were studied using χ 2 or Fisher exact tests. Survival curves were estimated using the Kaplan–Meier method; the log-rank test was used to compute differences between curves. Multivariate analysis using the Cox proportional hazards regression model was performed to assess prognostic values of protein expression. Correlation coefficients between protein expression and clinicopathological findings were estimated using the Pearson correlation method. Statistical significance was set at P < 0.05.
Expression of L1CAM and EPCAM mRNA in gastric tumor tissue and cell lines
Expression of L1CAM and EPCAM in archived gastric cancer tissue and non-cancer mucosa
L1CAM and EPCAM overexpression and clinicopathological features
Relationship of L1CAM expression with pathological parameters of tumor
57.86 ± 11.88
61.20 ± 11.85
Signet-ring cell carcinoma
Regional lymph nodes
Relationship of EPCAM expression with pathological parameters of tumor
56.85 ± 11.4
61.51 ± 12.22
Signet-ring cell carcinoma
Regional lymph nodes
Correlation between L1CAM and EPCAM expression and patient prognosis
As TNM stage, lymph node and distant metastasis are used as prognostic factors for gastric cancer , we further analyzed the correlation between L1CAM/EPCAM expression and patient prognosis according to Lauren classification, TNM stage and regional lymph nodes.
Correlation between the expression of L1CAM and prognosis
Low expression of L1CAM
High expression of L1CAM
Correlation between the expression of EPCAM and prognosis
Low expression of EPCAM
High expression of EPCAM
Factors with possible prognostic effects in gastric carcinoma were analyzed by Cox regression analysis. The study revealed that depth of invasion (P=0.007), lymph node (P = 0.009) and distant metastasis (P = 0.01), TNM stage (P = 0.008), expression of L1CAM (P = 0.007), and of EPCAM (P = 0.009) were independent prognostic factors in patients with gastric carcinoma. However, the location of the tumor, tumor size, histological type, differentiation, and vessel invasion had no prognostic value.
Association among expression of L1CAM and EPCAM
Three hundred and sixteen gastric cancer cases had low expression of both L1CAM and EPCAM; 125 gastric cancer cases had high expression of both L1CAM and EPCAM. L1CAM and EPCAM expressions were significantly correlated (χ2 = 117.0, P = 0.0001). Cumulative 5-year survival rates of patients with high expression of both L1CAM and EPCAM were significantly lower than in patients with low expression of both (60.1% vs 11.2%, χ2 = 261.52, P = 0.0001).
Tumor invasion and metastasis is a very complicated and continuous process involving multiple steps, regulated at the molecular level by adhesion molecules, protein catabolic enzymes, cellular growth factors and various angiogenic factors.
The L1 cell adhesion molecule (L1CAM) belongs to the immunoglobulin superfamily and was originally identified in the nervous system. Recent studies demonstrated L1CAM expression in various types of cancer, predominantly at the invasive front of tumors and in metastases, which indicates its involvement in advanced stages of tumor progression. Overexpression of L1CAM in normal and cancer cells increases motility, enhances growth rate and promotes cell transformation and tumorigenicity. Moreover, L1CAM expression in tumor cells conferred the capacity to form metastases [9, 10]. L1CAM was overexpressed in esophageal adenocarcinoma , pancreatic cancer [12, 13], colorectal cancer , gallbladder carcinoma , extrahepatic cholangiocarcinoma , gastric cancer , and cholangiocarcinoma , notably at the invasive front of the tumors. Our study indicated L1CAM protein was highly expressed in 163 (27.1%) tumors. L1CAM was localized mainly in the cytoplasm of primary cancer cells. The present study shows L1CAM expression in tumors correlated with histologic grade, Lauren’s classification, depth of invasion, lymph node and distant metastases, and prognosis. Kodera detected L1CAM expression in 15 of 72 pT3-stage gastric cancer specimens with L1CAM expression more common in intestinal cancer types. Prognosis of patients with L1CAM+ cancer was significantly inferior, particularly among those with diffuse-type cancers . Positive L1CAM expression was significantly correlated with histological grade, lymph node involvement, distant metastasis and survival . Positive L1CAM expression in pancreatic ductal adenocarcinoma was associated with node involvement, vascular invasion, perineural invasion, higher degree of pain, and poor survival . L1CAM expression in gallbladder carcinomas was significantly associated with high histologic grade, advanced pathologic T stage and clinical stage, and positive venous/lymphatic invasion. Multivariate analyses showed that L1CAM expression and clinical stage were independent risk factor for disease-free survival . High expression of L1CAM in extrahepatic cholangiocarcinoma was detected at the invasive front of tumors and was significantly associated with perineural invasion. Univariate analysis indicated that various prognostic factors such as histologic grade 3, advanced pathologic T stage and clinical stage, perineural invasion, nodal metastasis, and high L1CAM expression were risk factors predicting poorer patient survival. Multivariate analyses using Cox’s proportional hazards model showed that high L1CAM expression and nodal metastasis were independent risk factors for patient death . Aberrant L1CAM expression in colorectal cancer correlated with advanced stage and presence of lymph node and distant metastases .
Epithelial cell adhesion molecule (EPCAM) is overexpressed in most solid cancers and it has recently been identified as a cancer stem cell marker . EPCAM overexpression was observed in esophageal cancer , pancreatic cancer and ampullary cancer samples , colon cancers, gastric cancers, prostate cancers, and lung cancers . Our study showed high expression of EPCAM protein was detected in 247(41.1%) gastric cancers. Further study revealed EPCAM expression correlated with age, tumor location, tumor size, Lauren’s classification, depth of invasion, lymph node and distant metastases, regional lymph node stage, TNM stage and prognosis. EPCAM was found to be overexpressed in gastric cancer tissues . Patients with EPCAM expression had a significantly better 10-year survival than patients with no EPCAM expression: 42% vs 22%. Loss of EPCAM expression identifies aggressive tumors, especially in patients with stage I and II disease . The high EPCAM expression group showed significantly good prognosis in both overall survival and disease-free survival compared with the low-expression group. In multivariate analysis, EPCAM expression was an independent prognostic factor, along with histology and lymph node metastasis . EPCAM overexpression correlated with shorter overall survival among patients with ampullary cancer and advanced stage pancreatic cancer, and was found to correlate with tumor stage of ampullary cancer . EPCAM expression in human esophageal cancer correlated with tumor depth, stage, blood-vessel invasion and infiltrative growth pattern. Survival rates for patients with tumors with high EPCAM expression was significantly higher than for patients with tumors with low EPCAM expression .
The most important prognostic factor for gastric cancer is lymph node metastasis [28, 29]. We did not find literature about the relationship between expression of EPCAM/L1CAM and prognosis of patients according to regional lymph nodes. We therefore analyzed the relationship between expression of EPCAM/L1CAM and prognosis of patients with gastric cancer according to regional lymph nodes. Cumulative 5-year survival rates for patients with low L1CAM was significantly higher than for patients with high L1CAM expression in PN1. Cumulative 5-year survival rates for patients with low EPCAM was significantly higher than for patients with high EPCAM expression in PN0, in PN1, and in PN2. Lauren classification is helpful from an epidemiological standpoint , Lauren classification has been useful in evaluating the natural history of gastric carcinoma, especially with regard to incidence trends, clinicopathological correlations, and etiological precursors . We investigated the intestinal and diffuse types in our study. Patients with the mixed and unclassified types were not investigated because we did not have these patients. We analyze the relationship between the expression of EPCAM/L1CAM and the prognosis of patients with gastric cancer according to Lauren classification. The cumulative 5-year survival rates for both the low-L1CAM expression group and the low-EPCAM expression group were higher than for their respective high-expression groups in intestinal-type gastric cancer and diffuse-type gastric cancer. There was no literature about the relationship between expression of EPCAM/L1CAM and prognosis of patients according to Lauren classification. To avoid biasing the prognostic value of EPCAM/L1CAM by tumor stage, we analyzed the relationship between expression of EPCAM/L1CAM and prognosis of patients with gastric cancer according to TNM stage. The cumulative 5-year survival rates for both the low-L1CAM expression group and the low-EPCAM expression group were higher than for their respective high-expression groups in stages I–III.
Our study suggests that overexpression of EPCAM and L1CAM is common in gastric cancer, and plays an important role in the progression and metastasis of gastric cancer. These results imply that EPCAM and L1CAM could be useful prognostic and survival indicators. Our study provides a basis for the development of a novel biomarker for the diagnosis and prognosis of gastric cancer.
Work was supported by Zhejiang Provincial Department of Science and Technology Research Foundation (2008C33040), and Zhejiang Provincial Medical Science Research Foundation (201337120).
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