Abstract
Cyclooxygenase is the rate-limiting enzyme that catalyzes the conversion of arachidonic acid to prostaglandins. The inducible form, cyclooxygenase-2, is known to be overexpressed in various human cancers including the colon, stomach, and urinary bladder. In this study, we evaluated the overexpression of cyclooxygenase-2 in 64 cases of breast cancer and correlated the results with clinicopathologic parameters. Immunohistochemical staining for cyclooxygenase-2 demonstrated positivity of the tumor cells in 46 of 64 cases (72%). Cyclooxygenase-2 overexpression was significantly correlated with larger tumor size and advanced clinical stage. Cyclooxygenase-2 overexpression tended to be more frequently observed in cases with presence of lymph node metastasis and in cases without expression of estrogen and progesterone; however, there was no significant correlation statistically. Nuclear and histologic grade were not well correlated with cyclooxygenase-2 overexpression. When ductal carcinoma in situ was considered separately, 32 of 42 cases (76%) were positive for cyclooxygenase-2. We conclude that cyclooxygenase-2 is up-regulated in a high proportion of breast cancers. The overexpression of cyclooxygenase-2 was associated with larger tumor size and advanced clinical stage, although lymph node status, estrogen and progesterone expression, and nuclear and histologic grade were not significantly correlated. Therefore, cyclooxygenase-2 overexpression may be a feature of the aggressive phenotype and may be useful as a prognostic indicator in breast cancer.
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Main
Cyclooxygenase (COX) is a rate-limiting enzyme that catalyzes the conversion of arachidonic acid to prostaglandins, and two isoforms, COX-1 and COX-2, have been characterized. Although COX-1 is constitutively expressed in many tissues and is present under homeostatic conditions, COX-2 is not detectable in most normal tissue but is induced by growth factors, cytokines, hormones, and mitogens and is involved in inflammatory reactions (1, 2, 3, 4).
Recent studies have indicated that the up-regulation of COX-2 is associated with many human cancers of the colon, stomach, prostate, and bladder (5, 6, 7, 8). Moreover, a number of studies have suggested that the use of nonsteroidal anti-inflammatory drugs (NSAIDs) and COX-2 inhibitors reduced the incidence of colon cancer (9) and that NSAIDs are also useful in providing protection against breast cancer (10). Through these observations, it was suggested that COX-2 may be involved in tumorigenesis in various organs. The exact mechanism by which COX-2 contributes to tumorigenesis is still unclear, although recent studies have suggested that promotion of angiogenesis, suppression of apoptosis, stimulation of cell growth, and immune suppression may play a role (11).
In breast cancer, a high level of prostaglandin and COX-2 expression was reported in breast cancer tissue as well as in breast cancer cell lines (12, 13). Numerous in vivo studies in rodents have shown that NSAIDs inhibit mammary tumor growth (14), and Celecoxib, a selective COX-2 inhibitor, was also reported to reduce the incidence, multiplicity, and volume of carcinogen-induced breast cancers in rats (15). However, studies on the role of COX-2 in the development and the progression of human breast cancer are relatively few when compared with the case of colon cancer.
The aim of this study was to further determine the role of COX-2 in the development and progression of breast cancer by evaluation of COX-2 expression and correlation with clinicopathologic prognostic parameters, including tumor size, lymph node status, stage, estrogen (ER) and progesterone (PR) status, and nuclear and histologic grade.
MATERIALS AND METHODS
Case Selection
Sixty-four patients who underwent surgery for breast cancer at Bundang CHA Hospital from 1995 to 2001 were examined. The TNM staging system was used for clinical staging. Pathological evaluation was performed using previously stained hematoxylin-eosin–stained sections. The histologic type of the tumor was determined according to the WHO classification of breast cancer. There were 47 invasive ductal carcinomas, 4 DCIS, 4 mucinous carcinomas, 3 apocrine carcinomas, 2 mixed ductal and lobular carcinomas, 1 medullary carcinoma, 1 atypical medullary carcinoma, 1 metaplastic carcinoma, and 1 papillary carcinoma. In invasive ductal carcinomas, the nuclear and histologic grades of the tumor were also determined. The nuclear grade was categorized as follows: Grade 1 = poorly differentiated, Grade 2 = intermediate, Grade 3 = well differentiated, using the grading system of Black and Speer (16). The histologic grade was categorized as grade I = well differentiated, grade II = intermediate, and grade III = poorly differentiated, using the Elston-modified Bloom and Richardson grading system (17).
Clinicopathologic characteristics including tumor size, lymph node status, stage, ER and PR status, and nuclear and histologic grades were evaluated.
Immunohistochemical Staining
Immunohistochemistry using representative formalin-fixed, paraffin-embedded tissue blocks was performed after microwave pretreatment. A monoclonal antibody to COX-2 (dilution 1:200; Cayman chemical, Ann Arbor, MI) was reacted overnight at 4° C, and polyclonal antibodies to ER and PR (dilution 1:50; Zymed Laboratories, San Francisco, CA) were reacted for 1 hour 30 minutes at room temperature. A streptavidin peroxidase detection system with diaminobenzidine tetrachloride (Vector Laboratories, Burlington, CA) was used.
For COX-2, the results of immunohistochemistry were interpreted as positive when >10% of the tumor cells demonstrated clear cytoplasmic staining. The immunoreactive score was calculated for ER and PR by multiplication of the percentage of positive cells and the staining intensity (18). The percentage of positive cells was categorized as 0 = negative, 1 = <10% positive cells, 2 = 10–50% positive cells, 3 = 51–80% positive cells, and 4 = >80% positive cells. The staining intensity was categorized as 0 = negative, 1 = weak, 2 = moderate, 3 = strong. An immunoreactive score of >2 was considered positive.
Statistical analysis of the correlation between COX-2 expression and clinicopathologic characteristics was calculated with the χ2 test.
RESULTS
COX-2 was positive in 46 of 64 carcinomas (72%) including invasive and DCIS. It showed granular positivity in the cytoplasm of the tumor cells. Nonneoplastic tissue in the immediate vicinity of the tumor occasionally expressed COX-2 in lobules, ducts, blood vessels, and stromal cells, but the staining intensity was much weaker than in the tumor cells. The normal tissue away from the tumor did not stain with COX-2.
COX-2 was positive in 34 of 47 cases (72%) of invasive ductal carcinomas (Fig. 1) and in 11 of 13 cases (85%) of invasive carcinomas of other histologic types. There was no significant correlation between COX-2 expression and histologic type (P = .821).
The results of the correlation between COX-2 expression and clinicopathologic characteristics including stage, tumor size, lymph node status, ER and PR status, and histologic and nuclear grade are summarized in Tables 1 and 2 and in Figure 2. COX-2 was positive in 1 of 4 cases (25%) in Stage 0, 9 of 16 cases (56%) in Stage I, 29 of 37 cases (78%) in Stage II, and 6 of 7 cases (86%) in Stage III, which was statistically significant (P = .034). Of the 60 cases of invasive carcinoma, COX-2 was positive in 19 of 30 cases (63%) measuring ≤2 cm, 22 of 27 cases (81%) measuring >2 cm and <5 cm, and all 3 cases (100%) measuring ≥5 cm, which was statistically significant (P = 0.046). Although cases showing positive lymph node status and positive ER/PR tended to more frequently overexpress COX-2, there was no significant correlation. Nuclear and histologic grade were not well correlated to cyclooxygenase-2 overexpression.
Four cases were composed solely of DCIS, whereas 38 cases of invasive ductal carcinoma contained areas of DCIS (Table 3). Thirty-two of the 42 cases, including pure DCIS cases and the DCIS component of invasive ductal carcinoma (76%), demonstrated COX-2 positivity (Fig. 3). Of the cases in which DCIS and invasive carcinoma coexisted, 31 cases showed COX-2 overexpression in both DCIS and invasive components (Fig. 3). Of these, 5 cases demonstrated stronger staining intensity in the DCIS component than in the invasive component, whereas the staining intensity was decreased in the DCIS component in 1 case. The remaining cases showed similar staining intensity in both the invasive and DCIS components.
DISCUSSION
Cyclooxygenase (COX) is a key enzyme that catalyzes the biosynthesis of prostaglandins and thromboxanes from arachidonic acid. Two isoforms of this enzyme, COX-1 and COX-2, have been identified: COX-1 is expressed ubiquitously, whereas COX-2 is an immediate-early response gene that is inducible by various extracellular stimuli, including growth factors, cytokines, carcinogens, tumor promoters (1, 2, 3, 4), and several oncogenes, including v-src, v-Ha-ras, Her-2/neu, and Wnt genes (19, 20, 21). Recent studies have demonstrated that high levels of prostaglandins and COX-2 were expressed in a variety of tumors, including colon, stomach, and bladder tumors (5, 6, 7, 8). Further evidence for a role of COX-2 and its products in tumorigenesis of various organs comes from studies demonstrating that the use of NSAIDs, such as celecoxib and sulindac, decreased the incidence of colorectal cancers (22, 23).
Although the exact mechanism through which COX-2 contributes to carcinogenesis remains to be elucidated, several explanations seem to be more relevant: during tumorigenesis, transcriptional activation is likely to occur in response to growth factors, oncogenes, or loss of function of the p53 tumor suppressor gene, resulting in the up-regulation of COX-2. It was recently reported that the up-regulated COX-2 promotes angiogenesis, suppresses apoptosis, stimulates cell growth, and mediates immune suppression (11). It has also been shown that COX-2 overexpression is sufficient to induce tumorigenesis in transgenic mice (24).
Several studies have provided support for the role of prostaglandins and COX-2 in the growth and invasiveness of human breast tumors (13, 25). Nonetheless, the role of COX-2 in breast cancer is less clear than its role in colon cancer, and few studies to date have focused on the expression of COX-2 in human breast cancers. Furthermore, conflicting data have been found regarding the frequency of COX-2 expression in breast cancers. In contrast to nearly 85% in human colorectal cancers, COX-2 overexpression has been reported in 37–56% of breast cancers (26, 27, 28). In the present study, we found COX-2 overexpression in 72% of breast cancers, which is the highest frequency that has ever been reported. The discordance in the proportion of COX-2 positivity in breast cancers may be due to different methods in the evaluation of immunohistochemistry results. We used a cutoff value of >10% positive cells regardless of the intensity in the interpretation of COX-2. We have studied the correlation of COX-2 expression with various clinicopathologic parameters, including tumor size, lymph node status, stage, ER and PR expression, and nuclear and histologic grade. Larger size and advanced stage in tumors were significantly correlated with COX-2 overexpression. COX-2 overexpression was more frequently observed in the cases with lymph node metastasis, although there was no statistical significance. These results suggest that COX-2 overexpression is associated with aggressive features and poor prognostic parameters in breast cancer. A previous study with breast cancer cell lines has also demonstrated that COX-2 was overexpressed in the estrogen-independent, highly invasive metastatic cell line (29). More recently, it was reported that a high level of COX-2 protein was more frequently noted in breast cancers with overexpression of HER-2/neu, compared with HER-2/neu-negative breast cancers (30). Taken together, COX-2 overexpression may be associated with the aggressive phenotype with metastatic potential and may be influenced by hormone status.
When DCIS was considered separately, COX-2 was positive in 76% of cases, including pure DCIS cases and the DCIS component of invasive ductal carcinoma. This result is in accordance with that of previous studies reporting COX-2 positivity in 80% of DCIS (26). Thus, it can be suggested that COX-2 overexpression is involved in the progression to invasive carcinoma. Further studies including more cases of pure DCIS are needed to determine the role of COX-2 in the development of DCIS.
The first report of COX-2 localization has demonstrated COX-2 expression specifically in tumor cells, not in normal stromal cells (13). However, the expression of COX-2 in normal breast tissue has been observed subsequently by several investigators (26, 28). It has been reported that the COX-2 protein was localized predominantly to carcinoma cells but could also be detected in some stromal cells, vascular endothelial cells, and inflammatory mononuclear cells. In the present study, COX-2 was also found to be occasionally positive in normal lobules and ducts in the immediate vicinity of the tumor, as well as in stromal cells and blood vessels. However, the staining intensity was much weaker than that of the tumor cells. The COX-2 expression in adjacent normal tissue may possibly be explained by a paracrine effect of the tumor cells. Some investigators have suggested the possibility of a “field” or “landscaping” effect for this phenomenon; that is, COX-2–derived prostaglandins synthesized by neoplastic cells may act as positive modulators of the cross-talk between the transformed cell and the stromal cells; therefore, the area adjacent to the tumor shows increased COX-2 expression, and this area may provide an increased risk of developing additional cancers (26).
In conclusion, the present study demonstrated COX-2 positivity in 72% of breast cancer, and COX-2 overexpression was significantly correlated to large tumor size and advanced stage. These results indicate that COX-2 may contribute to the development of breast cancer and can be used as a prognostic indicator in breast cancer. Our results further suggest that selective COX-2 inhibitors may be useful in the chemoprevention and adjuvant therapy of breast cancer.
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Shim, J., An, H., Lee, Y. et al. Overexpression of Cyclooxygenase-2 Is Associated with Breast Carcinoma and Its Poor Prognostic Factors. Mod Pathol 16, 1199–1204 (2003). https://doi.org/10.1097/01.MP.0000097372.73582.CB
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DOI: https://doi.org/10.1097/01.MP.0000097372.73582.CB
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