To study the utility of COX-2 as immunohistochemical prognostic marker in comparison to various histopathological parameters and TNM staging in breast carcinoma: an observational, cross-sectional study protocol
Jayashree Bhawani, Samarth Shukla, Sourya Acharya, Sunita Vagha, Miheer Jagtap, Shaan Khetrapal, Amit Kumar Chowhan, Jayashree Bhawani

TL;DR
This study aims to evaluate COX-2 as a potential prognostic marker in breast cancer by comparing it with standard histopathological and staging parameters.
Contribution
The novelty lies in assessing COX-2's prognostic value in breast cancer alongside established clinical and pathological markers.
Findings
COX-2 overexpression is expected to correlate with poor prognostic factors like larger tumor size and lymph node involvement.
The study will determine if COX-2 expression can provide additional prognostic information beyond TNM staging and histological grading.
Results may support COX-2 as a useful immunohistochemical marker in breast cancer prognosis.
Abstract
Background: Breast cancer is the most prevalent cancer among women worldwide and is a well-known cause for cancer mortality in females. COX-2 (cyclooxygenase) plays a vital role in development of some human cancers such as lung, colon and breast. It is a potent enzyme that is important for the conversion of arachidonic acid into prostaglandins. These prostaglandins mediate cellular proliferation, apoptosis and angiogenesis which contributes to carcinogenesis. Overexpression of COX-2 has been detected in several malignancies including breast cancer. COX-2 overexpression is regarded as a poor prognostic marker of breast cancer. The present study will aim to study the immunohistochemical expression of COX-2 in breast cancer and compare it with known histopathological parameters thus assessing its prognostic value. Methods: This will be an observational study conducted in the Department…
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Taxonomy
TopicsInflammatory mediators and NSAID effects · Estrogen and related hormone effects · Cancer, Stress, Anesthesia, and Immune Response
