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环氧化酶2(COX-2)作为预后标志物在乳腺癌中的免疫组化表达及其与临床病理参数的相关性

Immunohistochemical Expression of Cyclooxygenase 2 (COX-2) as a Prognostic Marker and Its Correlation With Clinicopathological Parameters in Breast Cancer.

作者信息

Perazhi Pulikkal Archana, K Mamatha

机构信息

Pathology, Shri B. M. Patil Medical College Hospital and Research Centre, Bijapur Lingayat District Education (BLDE) (Deemed to be University), Vijayapura, IND.

出版信息

Cureus. 2024 Jul 27;16(7):e65550. doi: 10.7759/cureus.65550. eCollection 2024 Jul.

DOI:10.7759/cureus.65550
PMID:39192935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11349250/
Abstract

Introduction Breast cancer is considered the most common cancer among women. According to the literature, cyclooxygenase-2 (COX-2) expression in breast carcinoma is associated with aggressive tumor biology and acts as an independent prognostic marker. As COX-2 is a newly identified marker, studies are required to understand its immunoexpression and correlation with hormone receptor status and other prognostic factors, which helps in the therapeutic management of patients. Hence, this study evaluates the expression of COX-2 in breast carcinoma. Methods A hospital-based cross-sectional study was done on 55 mastectomy specimens collected at the Histopathology and Surgical Pathology Section of the Department of Pathology. The patient's age, histological type, tumor size, lymph node status, histological grade, and vascular invasion were noted. Immunohistochemical staining for estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2/neu protooncogene (HER2/neu), and COX-2 markers was performed, and its results were compared with these clinicopathological and prognostic parameters. Results were subjected to statistical analysis. Results COX-2 expression was seen in 37 out of 55 cases (67.2%). Expression of COX-2 showed a statistically significant correlation with vascular invasion, ER-negative status, and PR-negative status. No statistical association was found between other parameters like age, tumor size, histological type, histological grade, lymph node status, and HER2/neu status. Conclusion The expression of COX-2 correlated strongly with well-established poor prognostic markers, such as vascular invasion, ER-negative status, and PR-negative status. Thus, expression of COX-2 suggests aggressive tumor biology, and it can be used as an independent prognostic marker.

摘要

引言

乳腺癌被认为是女性中最常见的癌症。根据文献,环氧化酶-2(COX-2)在乳腺癌中的表达与侵袭性肿瘤生物学相关,并作为独立的预后标志物。由于COX-2是一种新发现的标志物,需要开展研究以了解其免疫表达以及与激素受体状态和其他预后因素的相关性,这有助于患者的治疗管理。因此,本研究评估了COX-2在乳腺癌中的表达。

方法

在病理学系组织病理学和外科病理学科室收集的55份乳房切除术标本上进行了一项基于医院的横断面研究。记录患者的年龄、组织学类型、肿瘤大小、淋巴结状态、组织学分级和血管侵犯情况。对雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2/neu原癌基因(HER2/neu)和COX-2标志物进行免疫组织化学染色,并将其结果与这些临床病理和预后参数进行比较。对结果进行统计学分析。

结果

55例中有37例(67.2%)出现COX-2表达。COX-2的表达与血管侵犯、ER阴性状态和PR阴性状态在统计学上具有显著相关性。在年龄、肿瘤大小、组织学类型、组织学分级、淋巴结状态和HER2/neu状态等其他参数之间未发现统计学关联。

结论

COX-2的表达与血管侵犯、ER阴性状态和PR阴性状态等已明确的不良预后标志物密切相关。因此,COX-2的表达提示侵袭性肿瘤生物学特性,它可作为独立的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/773b6a0949ff/cureus-0016-00000065550-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/3ad5a8559c95/cureus-0016-00000065550-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/2ed4bee460c2/cureus-0016-00000065550-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/7b6e9746ca01/cureus-0016-00000065550-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/ef511e7f7d0f/cureus-0016-00000065550-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/c27fa53d3aec/cureus-0016-00000065550-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/e39f860aeafb/cureus-0016-00000065550-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/773b6a0949ff/cureus-0016-00000065550-i07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/3ad5a8559c95/cureus-0016-00000065550-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/2ed4bee460c2/cureus-0016-00000065550-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/7b6e9746ca01/cureus-0016-00000065550-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/ef511e7f7d0f/cureus-0016-00000065550-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/c27fa53d3aec/cureus-0016-00000065550-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/e39f860aeafb/cureus-0016-00000065550-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d99b/11349250/773b6a0949ff/cureus-0016-00000065550-i07.jpg

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