Denkert Carsten, Winzer Klaus-Jürgen, Müller Berit-Maria, Weichert Wilko, Pest Sören, Köbel Martin, Kristiansen Glen, Reles Angela, Siegert Antje, Guski Hans, Hauptmann Steffen
Institute of Pathology, Charité Hospital, Berlin, Germany.
Cancer. 2003 Jun 15;97(12):2978-87. doi: 10.1002/cncr.11437.
Cyclooxygenases regulate the production of prostaglandins and play a role in tumor development and progression. The authors investigated the prognostic impact of expression of the cyclooxygenase (COX) isoforms, COX-1 and COX-2, on disease-free survival and progression-free survival in patients with primary breast carcinoma as well as the association between COX expression and other clinicopathologic parameters.
In this study COX isoform expression was determined by immunohistochemistry in a cohort of 221 patients with primary breast carcinoma.
Expression of COX-2 was detected in 36% of breast carcinoma samples and was associated significantly with several clinicopathologic parameters, including positive lymph node status (P < 0.0005), larger tumor size (P < 0.0005), poor differentiation (P < 0.0005), vascular invasion (P = 0.03), and negative estrogen receptor status (P = 0.04). In contrast, COX-1 was expressed in 45% of tumors and was associated with smaller tumor size (P = 0.02) and with negative lymph node status (P = 0.01). In a univariate survival analysis, a significant association was observed between elevated COX-2 expression and decreases in disease-free survival (P = 0.0007) and overall survival (P = 0.02). In a multivariate analysis, expression of COX-2 was of borderline significance for disease-free survival (relative risk, 1.90; 95% confidence interval, 1.00-3.59), adjusting for tumor size, histologic grade, number of positive lymph nodes, and patient age. Elevated expression of COX-1 in tumor tissue had no statistically significant influence on patient prognosis.
The current data suggest that increased expression of COX-2 may play a role in the progression of primary breast carcinoma. It remains to be investigated whether treatment with selective inhibitors of COX-2 may be an additional therapeutic option for patients with breast carcinoma.
环氧化酶调节前列腺素的产生,并在肿瘤发生和发展中起作用。作者研究了环氧化酶(COX)同工型COX-1和COX-2的表达对原发性乳腺癌患者无病生存期和无进展生存期的预后影响,以及COX表达与其他临床病理参数之间的关联。
在本研究中,通过免疫组织化学法测定了221例原发性乳腺癌患者队列中的COX同工型表达。
在36%的乳腺癌样本中检测到COX-2表达,且与多个临床病理参数显著相关,包括淋巴结阳性状态(P<0.0005)、肿瘤较大(P<0.0005)、低分化(P<0.0005)、血管侵犯(P=0.03)和雌激素受体阴性状态(P=0.04)。相比之下,45%的肿瘤表达COX-1,且与肿瘤较小(P=0.02)和淋巴结阴性状态(P=0.01)相关。在单变量生存分析中,观察到COX-2表达升高与无病生存期降低(P=0.0007)和总生存期降低(P=0.02)之间存在显著关联。在多变量分析中,调整肿瘤大小、组织学分级、阳性淋巴结数量和患者年龄后,COX-2表达对无病生存期具有临界显著性(相对风险,1.90;95%置信区间,1.00-3.59)。肿瘤组织中COX-1表达升高对患者预后无统计学显著影响。
目前的数据表明,COX-2表达增加可能在原发性乳腺癌进展中起作用。COX-2选择性抑制剂治疗是否可能成为乳腺癌患者的另一种治疗选择,仍有待研究。