Background
Esophageal cancer is one of the most malignant solid tumors with a five-year survival rate estimated at <19% [
1]. Data reported by the International Union Against Cancer/ American Joint Committee on Cancer (UICC/AJCC) showed that approximately 44% of initially resected cancers of the esophagus and esophagogastric junction had lymph node metastasis and this high incidence contributed to the causes of poor survival [
2]. Nevertheless some surgeons, especially those in Japan, have been conducting extended lymphadenectomy to provide better prognosis, most prospective trials have failed to demonstrate its survival benefit and its clinical significance is now considered to be limited [
3‐
6].
One potential approach that might provide a breakthrough in this situation is the clarification of the mechanism of lymph node metastasis. A report by Müller et al. yielded important and noteworthy findings [
7]. They found that the interaction between a chemokine and its corresponding chemokine receptor had a critical role in organ-specific cancer metastasis and they suggested that the CC-chemokine receptor 7 (CCR7) and CC-chemokine ligand 21/secondary lymphoid-tissue chemokine (CCL21/SLC) axis might be responsible for lymph node metastasis. Chemokine receptor CCR7 was first identified as a gene receptor of the Epstein–Barr virus (EBV), while CCL21/SLC and CC-chemokine ligand 19/ EBV-induced molecule ligand chemokine (CCL19/ELC) have since then been reported to be specific ligands for CCR7 [
8]. CCR7 has been shown to be a homing receptor that controls the migration of immune cells to secondary lymphoid tissue organs in response to CCL21/SLC. Müller et al. demonstrated that this cell homing mechanism applied equally to CCR7-expressing cancer cells, allowing lymph node metastasis to be established as a consequence.
Although CCR7 and clinical associations have been revealed in a large variety of malignant tumors [
9], only a few are currently known for esophageal cancer. In addition, little is known about the
in vitro and
in vivo behavior of CCR7-expressing cells in the sequence of lymph node metastasis. In this study, we hypothesized that patients with esophageal squamous cell carcinoma (ESCC) have a close relationship between CCR7 expression and lymph node metastasis because a functional CCR7 on ESCC cells plays a crucial role in lymph node metastasis in response to CCL21/SLC.
Methods
Study patients
We retrospectively surveyed ESCC patients who underwent radical esophagectomy in Keio University hospital between 1997 and 2007. Of these patients, we selected 105 consecutive patients from 1997 to 2002 who were diagnosed with Stage IA-IIIC and 61 patients from 1997 to 2007 who were diagnosed with pathological T1 cancer (tumor invasion into the lamina propia or submucosa), according to the UICC staging system (7th edition).
Immunohistochemistry
CCR7 expression in tissue samples was assessed by immunohistochemistry (IHC) using the ENVISION + system (Dako, Glostrup, Denmark). A rabbit anti-human polyclonal IgG CCR7 antibody (1:100; Medical and Biological Laboratories, Aichi, Japan) was used as a primary antibody. Paraffin-embedded human normal spleen and tonsil tissues were used as positive controls for CCR7. Negative control sections were treated with a non-immunized rabbit immunoglobulin fraction (Dako) under equivalent conditions.
To assess the immunoreactivity, the sections were scored in terms of their proportion (score 0: -10%, 1; 10%–40%, 2: 40%–70%, 3: >70%) and intensity (score 0: none, 1: weak, 2: strong) by two investigators (T.I. and H.T.) who had no knowledge of clinicopathological factors. The total score was calculated by multiplying the two scores and they were defined as positive at ≥1.
Esophageal cell line
We used 10 established ESCC cell lines from the TE series (TE-1, 4, 5, 6, 8, 9, 10, 11, 14, and 15) kindly provided by Dr. Nishihira (Tohoku University, Miyagi, Japan). Identity of each cell line was confirmed by short tandem repeat (STR) analysis (data not shown).
RNA extraction and quantitative real-time RT-PCR
Total RNA from each of the 10 TE cell lines was extracted and analyzed by quantitative real-time RT-PCR using the 7300 Real Time PCR system (Applied BioSystems, Carlsbad, CA), TaqMan Gene Expression Master Mix (Applied BioSystems), and ready-to-use CCR7 primers (Assay ID: Hs99999080_m1; Applied BioSystems). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as an internal control. We used human lymphocyte from a healthy donor as a positive control and distilled water without the template as a negative control. The relative quantity of CCR7 mRNA in 10 TE cell lines was calculated using ΔΔCt method in which TE1 expression level is defined as 1.
Establishment of a stable CCR7-overexpressing cell line
CCR7 mRNA was extracted from TE8 and its full-length open reading frame (ORF) was amplified and inserted into the plasmid vector pFLAG-CMV-4 (Sigma Aldrich, St. Louis, MO). The plasmids were electroporated into E.coli 5DHα (Takara Bio Inc., Shiga, Japan) and transfected to TE4 cells using Lipofectamine 2000 Reagent (Invitrogen, Carlsbad, CA). We defined this stable transfectant as TE4CCR7+ in which CCR7 overexpression was confirmed by western blotting, cell enzyme-linked immunosorbent assay (ELISA), and real-time RT-PCR.
Adhesion assay
TE4 and TE4CCR7+ cells were labeled with green 5-chloromethylfluorescein diacetate (CMFDA; Invitrogen). To investigate the effect of epithelial cells on cell adhesion, normal human lung lymphatic microvascular endothelial cells (HMVEC-LLy; Lonza Walkersville Inc., Walkersville, MD) were used in this assay, and HMVEC-LLy was labeled with a red fluorescent dye (CMPTX; Invitrogen). Chambers were confluent with a monolayer of HMVEC-LLy. We seeded 5 × 104 cells/well TE4 or TE4CCR7+ and incubated for 10 min at 37°C with or without human recombinant CCL21/SLC (R&D Systems). A blocking assay was performed using mouse monoclonal anti-CCR7 antibody (10 μg/ml; R&D Systems), mouse monoclonal anti-intercellular adhesion molecule (ICAM)-1 (10 μg/ml; Abcam, Cambridge, England), or anti-ICAM-2 antibody (10 μg/ml; Abcam). The number of attached cells in five randomly-selected fields was semiautomatically counted using BIOREVO BZ-9000 microscope (Keyence, Osaka, Japan). These procedures were repeated at least three times.
Our heterotopic transplantation mouse model of lymph node metastasis was developed as follows: 1) a subcutaneously growing tumor was established by injecting 1 × 107 TE4 or TE4CCR7+ cells into five-week-old nude mice; 2) after the tumors had developed (4–6 weeks after injection), they were excised and a small piece (approximately 1 mm3) was transplanted into the right and left elbows of additional five-week-old nude mice (defined as the TE4 and TE4CCR7+ groups, respectively); 3) the accessory axillary lymph nodes were excised and examined at 3, 4, and 5 weeks after transplantation. Ten lymph nodes from five nude mice were examined each week, and DNA of each node was extracted.
We used a human Alu sequence to quantitatively assess lymph node metastasis. We quantified 90 ng of DNA from each lymph node using primers for the Alu sequence [
10]. The primers were 5’-CGCCTGTAATCCCAGCACTTT-3’ (forward), 3’-CCCAGGCTGGAGTGCAGT-5’ (reverse), and 5’-FAMCGAGGCGGGCGGATCACCTBHQ1-3’ (TaqMan Probe). We used DNA extracted from TE4 cells as a positive control while that from the lymph nodes of a non-treated nude mouse was used as a negative control. The estimated number of cells was calculated based on a standard curve prepared prior to this experiment (data not shown,
r
2
= 0.998).
Statistical analyses
For statistical analyses, Student’s t-test, Pearson’s χ2 test or Fisher’s exact probability test was used for assessing the correlation between CCR7 expression and clinicopathological characteristics. The Kaplan–Meier and log-rank test were used for survival analysis. Student’s t-test or Welch’s t-test with Bonferroni correction was used for analysis in adhesion assay. In the mouse model, the Mann–Whitney U test was used to calculate statistical significances of the estimated number of cells. All statistical procedures were performed using IBM SPSS Statistics (Version 19; IBM, Armonk, NY). A p value of less than 0.05 was considered statistically significant. This study was approved by the Institutional Review Board at Keio University School of Medicine (ref. 20–125).
Discussion
Our study had three significant findings about CCR7 and lymph node metastasis in ESCC. First, we demonstrated that positive CCR7 expression was significantly correlated with lymph node metastasis and the five-year survival rate using the largest population of patients with ESCC. In addition, we also showed that exclusive pT1 patients denoted the same tendency. Second, the adhesive abilities of CCR7-expressing cells were significantly enhanced in response to CCL21/SLC, which has never been reported in prior studies. Third, CCR7-expressing cells had higher metastatic potential in the lymph node of our heterotopic transplantation mouse model, which was a newly-developed model in the study of lymph node metastasis.
Previous studies have described clinical correlations between CCR7 and lymph node metastasis in malignant solid tumors [
7,
13‐
15]. However, only three studies have investigated esophageal cancer [
12,
16,
17]. Our results confirmed the results obtained in these previous studies, but with a larger population of patients and we provided further evidence of the correlation with ESCC. Another key finding was that patients with pathological T1 ESCC denoted the same tendency. This fact has rarely been described because of low incidence of lymph node metastasis in patients at an early stage of other carcinomas, whereas it can occur in 25%–35% of T1 ESCC patients [
18]. These relationships between positive CCR7 expression and frequent lymph node metastasis imply the possible functional correlation of CCR7 with lymph node metastasis in ESCC.
Lymphatic invasion seems to have a significant relationship with positive CCR7 since CCR7 expression significantly correlated with lymph node metastasis, but there was no significant difference in lymphatic invasion when all patients with ESCC were analyzed. One possible reason for this is that lymphatic invasion was seen in most of patients with ESCC (83%), which, if any, required us more patients to be analyzed to demonstrate a significant difference. However, patients with both positive CCR7 and lymphatic invasion accounted for 93% of all patients with positive CCR7. Moreover, we showed significant differences in lymphatic and vessel invasion in pT1 patient population. These facts suggest a potential relationship between CCR7 expression and lymphatic invasion.
The adhesion assay demonstrated an enhanced adhesive ability of CCR7-expressing cells in response to CCL21/SLC, especially in the presence of lymphatic endothelial cells. Yin et al. investigated the functional and genetic importance of heparan sulfate lining on the lymphatic endothelial cells, demonstrating that heparan sulfate plays a critical role in mediating chemokine-dependent tumor cell trafficking in the lymphatic microenvironment [
19]. Another study by Peramo et al. showed that heparan sulfate is a preferred substrate for adhesion while it is attenuated by heparin use [
20]. Taken together, CCR7-mediated cell adhesion may be facilitated in the presence of lymphatic endothelial cells, presumably through heparan sulfate glycosaminoglycans. For naïve T cells, subsequent firm binding was established by ICAM-1 and ICAM-2; however, for cancer cells, this binding could not be blocked by anti-ICAM-1 and ICAM-2 antibodies. Further study will be required to clarify which molecule is involved in this firm binding to lymphatic cells since it can be a potential target for preventing cancer cell adhesion as well.
Transferring these findings to clinical practice demands a clinically accurate and reliable animal model. We demonstrated the high metastatic potential of CCR7-expressing cells using a heterotopic transplantation mouse model. With regard to animal models, Cunningham et al. and Wiley et al. have also reported the high metastatic potential of CCR7-expressing cells for breast cancer and malignant melanoma metastasis, respectively [
21,
22]. Our results objectively demonstrated not only the high metastatic potential of CCR7-expressing cells but also an earlier metastasis compared with wild-type cells. This result was comparable with that of our clinical study of T1 ESCC. Therefore, this may provide a molecular explanation for early lymph node metastasis in ESCC patients.
Our findings suggest potential therapeutic strategies for lymph node metastasis, i.e., CCR7 may be a promising biomarker and molecular target for lymph node metastasis. First, CCR7 could be a candidate that can predict lymph node metastasis. T1 patients with CCR7-negative ESCC may be at a low risk of lymph node metastasis; therefore, they could receive less invasive therapy, thereby avoiding radical esophagectomy. Second, in terms of molecular therapy, Lanati et al. showed Chemotrap-1, an engineered CCL21-soluble inhibitor that could block the chemokine-induced migration of cancer cells, reduced lymphatic invasion, tracking, and metastasis
in vivo[
23]. Taken together, our results and this evidence of an inhibitory molecule could bring CCR7-targeted therapy closer to clinical reality. Our findings provide further evidence for the mechanism of CCR7-mediated lymph node metastasis, leading to novel therapeutic strategies for regulating lymph node metastasis.
Conclusions
In this study, we demonstrated the significant clinicopathological relationship and functional causality between CCR7 expression and lymph node metastasis in ESCC patients. CCR7 expression significantly correlated with poor outcomes in ESCC patients.
The adhesive abilities of CCR7-expressing cells were significantly enhanced in response to CCL21/SLC. CCR7-expressing cells had higher metastatic potential in the lymph node of our heterotopic transplantation mouse model, which was a newly-developed model in the study of lymph node metastasis.
Acknowledgments
The authors would like to thank Dr. Masakazu Ueda of the Keio University School of Medicine for valuable experimental advice. This study was supported by grants from the Ministry of Education, Culture, Sports, Science and Technology in Japan (Grant number: 20790970, 21591712, and 19591561).
Competing interests
All of the authors declare no competing interests.
Author’s contributions
IT collected data of ESCC patients, carried out all experiments, wrote this paper and discussed results; TH conceived the study and supervised all experiments performed; MS supported and carried out all experiments performed; TH and KY supervised the study as principal investigator. All participants contributed commentary on and corrected the manuscript. All authors read and approved the final manuscript.