Abstract
The aim of the present study was to investigate whether the expression levels of CC-chemokine receptor 7 (CCR7) combined with computed tomography (CT) was associated with lymph node metastasis in bladder transitional cell carcinoma (BTCC). For this purpose, 115 cases of BTCC were analyzed at the Department of Urology of Xiangya Hospital, Central South University (Changsha, China). Preoperative CT scans of abdomen and pelvis, immunohistochemistry of CCR7 expression in the tumor specimens and pathological findings for lymph node metastasis were assessed. In addition, the sensitivity, specificity and accuracy of CCR7 and CT for the diagnosis of lymph node metastasis in BTCC were evaluated separately and jointly. The expression levels of CCR7 were observed to be significantly higher in BTCC than in normal controls (P<0.01). Multivariate analysis indicated that the overexpression of CCR7 was an independent predictor for lymph node metastasis in BTCC (P<0.05). The sensitivity, specificity and accuracy of CCR7 combined with CT scan for the diagnosis of lymph node metastasis in BTCC were 92.3, 83.6 and 70.0%, respectively. By contrast, the sensitivity, specificity and accuracy of CCR7 alone were 88.1, 69.9 and 76.5%, respectively, while the sensitivity, specificity and accuracy of CT alone were 52.4, 79.5 and 69.6%, respectively. The results of the present study indicated that CCR7 is an independent predictor of lymph node metastasis in BTCC. Therefore, the use of CCR7 combined with CT may improve the accuracy of the diagnosis of lymph node metastasis in BTCC.
Keywords: CCR7, computed tomography, bladder carcinoma, lymph node metastasis
Introduction
Bladder transitional cell carcinoma (BTCC) is one of the most common types of malignant tumor of the urinary system. The treatment of BTCC is challenging, due to its high occurrence of metastasis (1). Survival in muscle-invasive BTCC depends mainly on the pathological stage of the disease (2), and lymph node metastasis is currently considered to be the most highly-dependent variable associated with survival (3).
Evidence from previous studies suggests that chemokines and their receptors participate in tumor metastasis (4). CC-chemokine receptor 7 (CCR7) is naturally a homeostatic chemokine receptor expressed by various subtypes of immune cells that migrate to and within lymphoid organs (5). Previous studies have demonstrated that the overexpression of CCR7 in tumor cells is significantly associated with lymph node metastasis in gastric, non-small cell lung, breast and bladder cancer (6,7). Spiral computed tomography (CT) is commonly used to evaluate lymph metastasis in bladder cancer. However, the sensitivity and accuracy of CT is limited (8). A previous study by Li et al (9) reported that the use of CT combined with vascular endothelial growth factor C may improve the accuracy of the diagnosis of lymph node metastasis in bladder carcinoma.
Therefore, in the present study, the potential role of CCR7 as an independent predictor for lymph node metastasis in BTCC was investigated. Furthermore, the sensitivity, specificity and accuracy of CCR7 and CT for the diagnosis of lymph node metastasis were evaluated separately and jointly. The results indicated that CCR7 is a predictive biomarker associated with CT for the diagnosis of lymph node metastasis in BTCC.
Materials and methods
Patients and treatment
The present study included 115 patients with BTCC who underwent laparoscopic radical cystectomy and pelvic lymphadenectomy in the Department of Urology of Xiangya Hospital, Central South University (Changsha, China) between January 2010 and December 2013. The study was approved by the ethics committee at Xiangya Hospital, Central South University. Written informed consent was obtained from all the participants in the study. The patients included in the study had undergone radical surgery of the bladder, surrounding fat tissue, remote end of the ureter and pelvic lymphadenectomy. The cranial, lateral and caudal borders of the pelvic lymphadenectomy were the level of the inferior mesenteric artery, genitofemoral nerve and pelvic floor, respectively.
The BTCC tissue specimens obtained following the above surgical procedure were fixed in 10% formaldehyde solution for postoperative histopathological examination. Normal urothelium tissue specimens were obtained from ten patients with benign prostatic hypertrophy via transurethral resection of the bladder. The histological cell type of the BTCC specimens was determined according to the 2004 World Health Organization (10) classification by an experienced pathologist who did not possess any prior knowledge of the patient's disease data. A total of 14, 42 and 59 specimens were classified as papillary urothelial neoplasm of low malignant potential, low-grade urothelial carcinoma and high-grade urothelial carcinoma, respectively. Tumor staging was reviewed based on the 2009 Union for International Cancer Control-tumor node metastasis staging system (11). Accordingly, 7, 26, 58 and 24 tumors were staged T1, T2, T3 and T4, respectively.
Immunohistochemical staining
Immunohistochemical staining of CCR7 was performed using a ready-to-use SP kit (Zhongshan Jinqiao Biotechnology Co., Ltd., Beijing, China), according to the manufacturer's protocol. Briefly, the 4-µm paraffin-embedded tissue sections were subjected to deparaffinization and rehydration prior to be immersed in 0.01 M citric buffer (pH 6.0). The slides were then incubated with 3% hydrogen peroxide for 10 min, followed by incubation in normal goat serum for 10 min at room temperature. Anti-CCR7 rabbit monoclonal immunoglobulin (Ig)G antibody (catalogue no. ab32527; Abcam, Cambridge, MA, USA) was used at a dilution of 1:200 as primary antibody. Next, the sections were incubated with goat anti-rabbit polyclonal antibody for 10 min, and subsequently exposed to streptavidin peroxidase (Zhongshan Jianqaio Biotechnology) for 10 min. The slides were visualized with 3,3′-diaminobenzidine (Zhongshan Jianqaio Biotechnology), counterstained with hematoxylin (Auragene, Changsha, China), prior to be examined by microscopy (Olympus BH2; Olympus Corporation, Tokyo, Japan). For the negative controls, the primary antibody was substituted for phosphate-buffered saline.
Under a low-power microscopy field, each slide was evaluated in ten randomly selected areas that contained tumor cells, ensuring that ≥100 tumor cells/field were examined. The evaluation was conducted by two independent investigators, who were unaware of the clinicopathological data. Two scoring systems were used, including staining intensity and percentage of positive cells. The staining intensity was scored on a semiquantitative 4-points scale as follows: i) A score of 0 was assigned to the negative control; ii) a score of 1 indicated weak cytoplasmic and nuclear staining, which was slightly darker than the negative control; iii) a score of 2 was indicative of moderate staining, defined as an intensity exhibiting a score of 1–3; and iv) 3 corresponded to strong staining, which was equivalent to or darker than the positive control. The percentage of stained cells was also scored on a semiquantitative 4-points scale as follows: i) 0 indicated <10% positive cells; ii) 1 was assigned if the percentage of positive cells in the sample was 10–25%; iii) 2 corresponded to 25–50% positive cells present in the sample; and iv) 3 was assigned to those samples displaying >50% positive cells. The staining intensity and percentage of stained cells scores were then combined as follows: i) Those specimens presenting a total score of 0–1 were assigned a value of I; ii) II was assigned to those specimens with a total score of 2; iii) III indicated a total score of 3–4; and iv) IV was assigned to samples exhibiting a total score of 5–6.
CT evaluation
All patients included in the study had undergone CT scanning of the abdomen and pelvis ≥5 days prior to cystectomy and pelvic lymphadenectomy, which had been conducted on SOMATOM Sensation 64 eco (Siemens AG, Munich, Germany), with a slice thickness and layer of 5 mm. As contrast agent, 80 ml Ultravist® (Bayer AG, Leverkusen, Germany) was used. The CT images were reevaluated by urologists and uroradiologists who were unaware of the final pathological results. A pelvic lymph node >10 mm in size was considered as positive lymph node metastasis.
Statistical analysis
Statistical analyses were performed using SPSS software, version 13.0 (SPSS, Inc., Chicago, IL, USA). The association between the variables was assessed by χ2 test, Fisher's exact probability test, Mann-Whitney U test or stepwise logistic regression analysis. Logistic regression analysis was employed for univariate analysis, while multiple logistic regressions were used for multivariate analysis. P<0.05 was considered to indicate a statistically significant difference.
Results
CCR7 levels in patients with BTCC and normal controls
Expression of CCR7 was detected in the cytoplasm and membrane of tumor cells, but low or no staining for CCR7 was observed in the normal transitional epithelium (Fig. 1). The frequency of detectable CCR7 in the BTCC samples was markedly higher than in the normal bladder tissues (P<0.01; Table I).
Figure 1.
Immunohistochemical staining of CCR7 in bladder transitional cell carcinoma tissues. (A) Negative staining, indicating no expression of CCR7 (score I). (B) Weak positive staining, indicating low expression levels of CCR7 (score II). (C) Moderate positive staining, indicating moderate expression levels of CCR7 (score III). (D) Strong positive staining, indicating high expression levels of CCR7 (magnification, ×400). CCR7, CC-chemokine receptor 7
Table I.
Expression levels (score I–IV) of CC-chemokine receptor 7 in patients with bladder transitional cell carcinoma and normal controls.
| CC-chemokine receptor 7 (no.) | |||||
|---|---|---|---|---|---|
| Tissues (no. of patients) | I | II | III | IV | P-value |
| Bladder transitional cell carcinoma (115) | 16 | 29 | 48 | 22 | <0.01 |
| Normal (10) | 8 | 2 | 0 | 0 | – |
Association of CCR7 with lymph node metastasis in BTCC
In the positive lymph node metastasis group, 0, 5, 14 and 23 samples displayed expression of CCR7 of score I, II, III and IV, respectively. By contrast, in the negative lymph node metastasis group, the number of cases displaying expression levels of CCR7 of score I, II, III and IV were 15, 36, 22 and 0, respectively. These results indicated that the overexpression of CCR7 was significantly associated with pelvic lymph node metastasis (P<0.05; Table II).
Table II.
Association between the expression levels (score I–IV) of CC-chemokine receptor 7 and lymph node metastasis in bladder transitional cell carcinoma.
| CC-chemokine receptor 7 (no.) | |||||
|---|---|---|---|---|---|
| Lymph node metastasis (no. of patients) | I | II | III | IV | P-value |
| Positive (42) | 0 | 5 | 14 | 23 | <0.05 |
| Negative (73) | 15 | 36 | 22 | 0 | – |
Association of BTCC lymph node metastasis with clinicopathological features
BTCC pelvic lymph node metastasis was closely associated with certain clinicopathological features of the patients, including tumor size, pathological grade, clinical stage, recurrence and expression levels of CCR7. Among these, overexpression of CCR7 was identified as an independent indicator for lymph node metastasis in multivariate analysis, based on the results of stepwise logistic regression analysis (Table III).
Table III.
Univariate and multivariate analyses for bladder transitional cell carcinoma lymph node metastasis.
| Univariate | Multivariate | ||||
|---|---|---|---|---|---|
| Variable | Comparison | OR (95% CI) | P-value | OR (95% CI) | P-value |
| Age (years) | <60 or ≥60 | – | >0.05 | – | – |
| Tumor size (cm) | <3 or ≥3 | – | >0.05 | – | – |
| Pathological grade (WHO 2004) | PUNLMP-LGPUC or HGPUC | 0.409 (0.061–0.813) | <0.05 | – | >0.05 |
| Clinical stage (UICC-TNM) | T1-T2 or T3-T4 | 0.233 (0.042–0.671) | <0.01 | – | >0.05 |
| Detection (time) | First or recurrence | – | >0.05 | – | – |
| CCR7 expression levels (score) | I–II or III–IV | 3.860 (1.710–7.590) | <0.01 | 2.930 (1.650–6.710) | <0.05 |
OR, odds ratio; CI, confidence interval; WHO, World Health Organization; PUNLMP, papillary urothelial neoplasm of low malignant potential; LGPUC, low-grade urothelial carcinoma; HGPUC, high-grade urothelial carcinoma; UICC, Union for International Cancer Control; TNM, tumor node metastasis; CCR7, CC-chemokine receptor 7.
Separate and joint evaluation of CCR7 and CT scan for the detection of BTCC lymph node metastasis
Based on the expression levels of CCR7, the samples were classified into two groups, according to their score levels. Thus, CCR7 scores of I and II were included in the low expression or negative group, whereas CCR7 scores of III and IV corresponded to the high expression or positive group. Among the 115 cases with BTCC analyzed, 37 displayed CCR7 scores of III–IV and lymph node metastasis; 22 displayed CCR7 scores of III–IV but no lymph node metastasis; 51 exhibited CCR7 scores of I–II but no lymph node metastasis; and 5 presented CCR7 scores of I–II in addition to lymph node metastasis. The sensitivity, specificity and accuracy of CCR7 in the evaluation of lymph node metastasis were 88.1, 69.9 and 76.5%, respectively.
CT examination revealed 37 patients with lymph node metastasis, including 29 in stage T3 and 8 in stage T4. The positive rate was 32.2% (37/115). Positive CT and presence of lymph node metastasis were observed in 22 patients, while 15 patients presented positive CT but negative lymph node metastasis, 20 displayed negative CT but positive lymph node metastasis, and 58 exhibited negative CT and absence of lymph node metastasis. The sensitivity, specificity and accuracy of CT in the evaluation of lymph node metastasis were 52.4, 79.5 and 69.6%, respectively.
When CCR7 was combined with CT scan in the detection of lymph node metastasis, the sensitivity, specificity and accuracy were 92.3% (39/42 cases), 83.6% (61/73 cases) and 87.0% (100/115 cases), respectively (Table IV).
Table IV.
Sensitivity, specificity and accuracy of CCR7 alone, CT alone and CCR7 combined with CT for the diagnosis of bladder transitional cell carcinoma lymph node metastasis.
| Lymph node metastasis (no. of patients) | |||||
|---|---|---|---|---|---|
| Predictor | Positive | Negative | Sensitivity (%) | Specificity (%) | Accuracy (%) |
| CCR7 | 88.1 | 69.9 | 76.5 | ||
| Positive | 37 | 22 | |||
| Negative | 5 | 51 | |||
| CT | 52.4 | 79.5 | 69.6 | ||
| Positive | 22 | 15 | |||
| Negative | 20 | 58 | |||
| CCR7 plus CT | 92.3 | 83.6 | 87.0 | ||
| Positive | 39 | 12 | |||
| Negative | 3 | 61 | |||
CCR7, CC-chemokine receptor 7; CT, computed tomography.
Discussion
Despite remarkable advances in the treatment of bladder cancer, the morbidity and mortality rates for this disease remain high. In USA, the estimated incidence and number of mortalities associated with bladder cancer in 2012 were 73,510 and 14,880 cases, respectively (12). Thus, the identification of the risks behind disease recurrence and mortality in bladder cancer is critical for adequate surveillance and selection of adjuvant therapies (13,14). Numerous studies have previously investigated potential prognostic factors for patients with bladder cancer, in order to guide therapeutic approaches and improve survival outcomes (15). Lymph node metastasis was previously identified as an important prognostic factor in patients with BTCC, since the survival rate of patients with lymph node metastasis of bladder cancer is usually low (16).
Chemokines are small secreted proteins that may contribute to the regulation of leukocyte adherence to endothelial cells, leukocyte migration through transendothelial membranes and tissue invasion (17). Previous studies revealed that the binding of chemokines to their specific receptors led to the activation of numerous signaling pathways involved in the growth and metastasis of tumor cells (18). CCR7, which was formerly considered to be an orphan receptor, has recently been identified as a chemokine receptor for chemokine (C-C motif) ligand 12, which is expressed in several human cell lines and vascular endothelial cells (19). The expression of CCR7 on tumor cells has mainly been reported for breast, non-small cell lung, prostate, head and neck, stomach and colorectal cancer, in addition to melanoma, chronic lymphocytic and T cell leukemia and non-Hodgkin's lymphoma (20). Yates et al (21) demonstrated that the expression of CCR7 in bladder carcinoma cells regulated processes such as proliferation, chemotactic motility and formation of signaling complexes in these cells and the expression levels of CCR7 were observed to be upregulated in bladder tumor tissues and exfoliated urothelial cells present in the urine of patients with bladder carcinoma, which was associated with prognosis
According to previous studies, the overexpression of CCR7 appears to be implicated in lymph node metastasis in patients with esophageal, pancreatic, gastric and breast cancer, and demonstrated that the overexpression of CCR7 was an independent factor of lymph node metastasis in these patients (22–24). In the present study, CCR7 was observed to be highly expressed in BTCC tissues, compared with normal bladder tissues. In addition, the frequency of detectable CCR7 expression was observed to be significantly higher in patients with pelvic lymph node metastasis, which is consistent with previous data reported in the literature (21). Furthermore, the logistic regression analysis conducted in the present study identified the overexpression of CCR7 as an independent factor influencing pelvic lymph node metastasis in BTCC.
CT is commonly used to evaluate bladder cancer and provide information on lymph node metastasis. However the sensitivity and accuracy of diagnosing lymph node metastasis remains poor (8). In previous studies, Ficarra et al (25) diagnosed pathological lymph node involvement in 45 patients, but CT only identified 19 of these patients. CT appears to be limited to the detection of metastatic lymph nodes of ≥0.5 cm in size. In the present study, postoperative pathological examination results were used as standards, and the sensitivity, specificity and accuracy of CT for the evaluation of lymph node metastasis were calculated to be 52.4, 79.5 and 69.6%, respectively, which is somewhat in agreement with previous studies. These results confirm the limitations of CT for detecting lymph node metastasis in bladder carcinoma. Thus, a more sensitive method to detect lymph node metastasis at early stage is required.
In the present study, the diagnosis of lymph node metastasis using CCR7 identified 42 cases that were positive for lymph node metastasis, 37 of which were confirmed to be correct. In 56 cases that appeared to be absent of lymph node metastasis based on their expression levels of CCR7, 5 presented lymph nodes metastasis, according to pathological diagnosis. The sensitivity, specificity and accuracy of CCR7 in the evaluation of lymph node metastasis were observed to be 88.1, 69.9 and 76.5%, respectively. Thus, the sensitivity of CCR7 appeared to be higher than that of CT (88.1 vs. 52.4%, respectively), but its specificity was lower (69.9 vs. 79.5%). Therefore, the expression levels of CCR7 were combined with the results of CT scan, and the combined sensitivity increased to 92.3% (39/42 cases), whereas the combined specificity and accuracy were determined to be 83.6% (61/73 cases) and 87.0% (100/115 cases, respectively). Thus, a combination of CT and CCR7 detection may improve the sensitivity of the diagnosis of lymph node metastasis in BTCC.
In conclusion, the results of the present study suggest the potential clinical application of CCR7 as a predictive biomarker for diagnosing lymph node metastasis in BTCC. Furthermore, the combined evaluation of CCR7 and CT appears to be a more reliable marker for lymph node metastasis in BTCC, compared to the diagnosis by CT or CCR7 alone. These results require further confirmation by large sample and multi-center prospective studies.
Acknowledgements
The present study was supported by the National Natural Science Foundation of China (Beijing, China) (grant no. 30700832) and the Fundamental Research Funds for the Central Universities of Central South University (Changsha, China) (grant no. 72150050586).
Glossary
Abbreviations
- CCR7
CC-chemokine receptor 7
- CT
computed tomography
- BTCC
bladder transitional cell carcinoma
- PUNLMP
papillary urothelial neoplasm of low malignant potential
- LGPUC
low-grade urothelial carcinoma
- HGPUC
high-grade urothelial carcinoma
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