Clinical significance of CD24 as a predictor of bladder cancer recurrence
- Authors:
- Published online on: May 21, 2013 https://doi.org/10.3892/ol.2013.1357
- Pages: 96-100
Abstract
Introduction
Bladder cancer is the second most common urological malignancy and represents a significant cause of morbidity and mortality worldwide (1). The disease consists of two principal forms of cancer, superficial and invasive, with the majority of bladder carcinomas as the former type at the time of diagnosis. Superficial cancers exhibit papillary and multifocal tumor growth, which often recurs following transurethral surgery and occasionally progresses to become an invasive disease. By contrast, invasive cancer is usually nodular, metastasizes to distant organs during the early phase of the disease and has a poor prognosis. The treatment for these cancers usually involves transurethral resection of the bladder tumors or a combination of chemotherapy, immunotherapy and radical cystectomy. However, a significant number of patients suffer from disease recurrence and progression. Therefore, a greater understanding of the molecular characteristics involved in bladder cancer recurrence is required to develop improved, more effective treatments.
Cluster of differentiation (CD)24 is a small, heavily glycosylated, mucin-like cell surface protein (27 amino acids long) that binds to the membrane via a glycosyl-phosphatidylinositol anchor (2). CD24 molecules are expressed in hematopoietic cells, such as B lymphocytes and neutrophils, and in certain epithelial cells, including keratinocytes and renal tubular epithelial cells (2,3). It has been reported that CD24 is important in cell selection and maturation for specific cellular functions (4). CD24 has also been reported to be a ligand for P-selectin, an adhesion receptor on activated endothelial cells and platelets (5,6), suggesting that the molecule functionally enhances the metastatic potential of cancer cells. CD24 has recently received attention in tumor biology research, as several studies have reported that the protein is broadly overexpressed in numerous types of cancer cell from the lung, breast, prostate, liver, kidney, pancreas and ovary, as well as in lymphomas (3,4). These studies demonstrated that CD24 overexpression was markedly associated with a more aggressive course of the disease. However, the correlation of CD24 expression with bladder cancer and its prognostic significance remain largely unknown.
The present study evaluated the CD24 expression in resected tumor specimens of bladder cancer and analyzed the correlation between this expression and the clinicopathological parameters. Since the association between CD24 overexpression and bladder cancer recurrence has not been reported previously, the study was focused on the CD24 expression in cancer tissues and the intra-bladder tumor recurrence following transurethral surgical resection.
Materials and methods
Patients and tissue samples
The present study included 125 patients with primary superficial bladder cancer (Ta and T1) who were treated in the Department of Urology, Zhujiang Hospital of Southern Medical University (Guangzhou, China) between 2005 and 2008. Cases of muscle invasive cancer (T2, T3 and T4), carcinoma in situ (CIS) or diseases other than urothelial carcinoma were excluded from the study and none of the patients included in the analysis had received pre-operative treatment. All patients were classified according to the 1997 UICC TNM classification for pathological staging and the 1973 World Health Organization classification for pathological grading. The bladder tumor lesions of the 125 patients were treated with transurethral resection of bladder tumor (TUR-Bt) surgery, and the paraffin-embedded samples were prepared for hematoxylin and eosin (HE) staining and immunohistochemical examination. Follow-up examinations were conducted cystoscopically to detect any tumor recurrence for three to six months following the transurethral surgery.
This study was approved by the ethics committee of Zhujiang Hospital of Southern Medical University, Haizhu, Guangzhou, Guangdong, China. Written informed consent was obtained from the patients.
Immunohistochemical staining of CD24
The bladder cancer tissue specimens were fixed in 10% neutral buffered formalin and subsequently embedded in paraffin. The specimens were sectioned to a thickness of 4.5 μm, then de-paraffinized with xylene and rehydrated for further staining with HE or immunohistochemistry. The immunohistochemical staining for the CD24 expression was performed as described previously (7,8). Briefly, the endogenous peroxidase activity in the rehydrated sections was blocked with 3% H2O2 and the antigen was retrieved by heat treatment for 30 min in 10 mmol/l citrate buffer. The sections were incubated for 10 min in 10% normal goat serum, then incubated overnight at 4°C with a primary rabbit polyclonal antibody against the CD24 antigen (1:100 dilution, ab110448; Abcam, Cambridge, MA, USA). The tissue sections were then incubated at room temperature for 1 h with anti-rabbit peroxidase-conjugated secondary antibody. The bound antibodies were detected using diaminobenzidine-tetrahydrochloride as the substrate and the sections were counterstained with hematoxylin. The sections were then dehydrated, mounted and observed using light microscopy.
Immunohistochemical analysis of CD24 expression
The sections immunostained for CD24 were evaluated by two independent pathologists or urologists who were blinded to the clinicopathological data and clinical outcomes of the patients. CD24 expression was assessed by calculating the percentage of tumor cells that showed immunoreactivity in the microscopic field and then classified as negative (∼1%) or positive (>1%) for each tumor specimen (9). The number of positively-stained tumor cells showing immunoreactivity in the cytoplasm and the number of negatively-stained cells were counted in 10 representative microscopic fields. The percentage of positive cells was then calculated. In addition, the staining intensity was determined as reported previously (10), where the degree of intensity was classified into three categories; weak, moderate and strong. The most frequently recorded staining intensity of the 10 representative microscopic fields was determined as the intensity of the tumor sections. The results of these assessments were obtained from the two researchers and compared. Any discrepancies were resolved by reassessment of the sections by the two researchers until a consensus was reached.
Statistical analysis
The SPSS version 17.0 software program (SPSS Inc., Chicago, IL, USA) was used for the statistical analysis. The data are presented as the mean ± standard error. Fisher’s exact test was used to evaluate the association between the CD24 expression and the clinicopathological parameters. The recurrence-free rate of bladder cancer following transurethral surgery was estimated based on the Kaplan-Meier method. P<0.05 was considered to indicate a statistically significant difference.
Results
Clinicopathological characteristics
The clinicopathological characteristics of the bladder cancer patients are shown in Table I. A total of 125 patients with an average age 61.4 years (range, 18–88 years) were enrolled in the present study. The pathological stages were Ta (intramucosal, n=71) or T1 (submucosal invasive, n=54) and the cancer grade was either G1 (n=29), G2 (n=62) or G3 (n=34). Bladder cancer recurrence developed in 67 (53.6%) of the 125 patients, as detected by cystoscopic examination following transurethral surgery. Disease recurrence was defined as any evidence of a tumor in the bladder at least three months subsequent to treatment.
CD24 expression and cellular distribution
The expression and cellular distribution of the CD24 protein were determined by immunohistochemical staining in 125 paraffin-embedded bladder cancer tissues. Several specimens of adjacent normal bladder tissues were included in these paraffin blocks for comparison. The CD24 expression was typically negative in the normal urothelial cells of the bladder epithelium (data not shown). The specific signals of the CD24 protein were localized mainly in the cytoplasm of the cancer cells and were indicated by brown staining (Fig. 1). The CD24 protein expression was positive in 79 (63.2%) of the bladder cancer cases and the representative staining pattern [negative or positive (weak, moderate or strong)] is shown in Fig. 1.
Association of CD24 expression with clinicopathological parameters of bladder cancer
CD24 immunoreactivity was positively correlated with certain clinicopathological parameters (Table II). There was a significant association between CD24 expression and the cancer grade and the recurrence of the bladder tumors [low-grade (G1, 8 out of 29, 27.6%) and high-grade (G2–G3, 71 out of 96, 74.0%); recurrence-negative (22 out of 58, 37.9%) and recurrence-positive (57 out of 67, 85.1%)].
Correlation between CD24 expression and bladder cancer recurrence-free rate
The recurrence-free rate of the bladder tumors following surgical treatment was analyzed using the Kaplan-Meier method. The recurrence-free rate was determined from the date of the TUR-Bt surgery to the time of the detection of intra-bladder cancer recurrence or the last follow-up. The 5-year overall recurrence-free rates of bladder cancer in the CD24-negative and -positive populations were 63.7 and 13.4%, respectively (Fig. 2A). The association between the intensity of CD24 expression and the recurrence-free rate was further analyzed during the follow-up period. There tended to be an association between the CD24 staining intensity and a poor recurrence-free rate (Fig. 2B). Log-rank tests revealed that there was a statistically significant difference between the negative/weak, weak/moderate and weak/strong staining categories.
The impact of the tumor stage and cancer grade on the recurrence-free rate was also investigated. The Ta and T1 tumor stages exhibited no significant association with the recurrence-free rate (Fig. 3A). By contrast, the higher cancer grades (G2–G3) had a significant correlation with a poor recurrence-free rate (Fig. 4A). A significant association between positive CD24 staining and the incidence of tumor recurrence was observed in each tumor category [stages Ta and T1, low (G1) and high grades (G2–G3); Figs. 3B and C, 4B and C].
Discussion
Intra-bladder tumor recurrence is a common feature of human bladder cancer and a major clinical concern for patients following transurethral treatment. Several studies have suggested a clonal nature for the recurrent urothelial carcinomas and also that these tumors are often derived from disseminated cancer cells that remain following surgery (11–13). CD24 is considered to function as an adhesion molecule and is known to bind to P-selectin, a protein expressed on the surface of thrombin-activated platelets and endothelial cells (5,6), and to L1, a member of the immunoglobulin superfamily that is expressed on neural and lymphoid cells (3,6). It is hypothesized that CD24 is able to support the adhesion of neutrophils or monocytes to thrombin-activated platelets or activated endothelial cells (4–6). In addition, the interaction of cancer cells with P-selectin via CD24 may be an important adhesion pathway involved in cancer metastasis and progression (3–5). It is possible that CD24-expressing tumor cells may disseminate more easily as a result of their enhanced ability to attach to normal endothelial cells.
Accumulating evidence suggests that CD24 is a significant marker for cancer metastasis and prognosis (3–5,14). Studies have suggested that CD24 overexpression may contribute to the metastasis and subsequent poor prognosis of various metastatic tumors (3,4). Based on this background, the present study focused on the expression of CD24, a possible cancer cell dissemination-related factor, in human superficial bladder cancer and investigated its correlation with intra-bladder tumor recurrence following transurethral surgical treatment. Immunohistochemical analysis clearly indicated that there was a positive correlation between CD24 expression and the pathological cancer grade (low and high) that indicates the degree of malignancy. Positive CD24 expression was significantly associated with intra-bladder tumor recurrence following surgery. The association between CD24 expression and tumor recurrence was observed in each tumor category [stages Ta and T1, low- (G1) and high-grades (G2–G3)]. Notably, the intensity of CD24 expression was also correlated with the intra-bladder tumor recurrence following treatment for bladder cancer. This demonstrated that CD24 expression was significantly associated with the recurrence of bladder cancer. The significant association of CD24 expression with the cancer grade and tumor recurrence rate suggests that CD24 induced a more malignant phenotype in the bladder cancer cells and that it may be involved in tumor recurrence by enhancing the attachment of tumors cells to the normal endothelium.
The present study is the first to show the potential involvement of CD24 in the development of more malignant bladder cancer and in the recurrence of tumors. The results clearly indicated that higher CD24 protein expression may predict a higher risk of bladder cancer recurrence. CD24 expression may therefore be used not only as a prognostic marker in bladder cancer, but also as a target for the development of new therapeutic approaches, including antibody-based immunotherapeutic agents.
Acknowledgements
The present study was supported by the National Natural Scientific Foundation of China (Grant No. 81101559) and scientific research grants (KAKENHI 22591767 and 24390368) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
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