医学
结直肠癌
结直肠腺瘤
血管生成
腺瘤
癌症研究
病态的
肿瘤进展
塞来昔布
恶性转化
炎症
肿瘤科
细胞凋亡
免疫系统
内科学
肿瘤微环境
生物标志物
免疫监视
大肠癌小鼠模型的建立
免疫疗法
细胞生长
生物信息学
不利影响
肿瘤发生
个性化医疗
癌症
细胞
作者
Zhongsen Dou,Kang Zhou,Fanglai Zhu
标识
DOI:10.1177/10849785261415777
摘要
Background: Cyclooxygenase-2 (COX-2) serves as a pivotal molecule bridging inflammation and tumor development, playing a central role in the initiation, progression, and malignant transformation of colorectal adenomas. Methods: This review systematically examines COX-2 expression patterns, molecular regulatory networks, and its potential applications in clinical diagnosis, prognosis assessment, and chemoprevention. Results: Evidence indicates that COX-2 exhibits significantly elevated expression in adenoma tissues (e.g., 54.8% positive rate in polyps vs. 18.5% in adjacent tissue), driving pathological progression through multiple mechanisms including cell proliferation induction, apoptosis inhibition, angiogenesis promotion, and tumor immune microenvironment remodeling. Nonsteroidal anti-inflammatory drugs and selective COX-2 inhibitors have demonstrated clear promise in adenoma chemoprevention (with agents such as celecoxib reducing advanced adenoma recurrence risk by 33%−45%). Conclusions: COX-2 is a critical early-event biomarker and therapeutic target in colorectal adenomas. Targeting the COX-2 pathway represents a viable strategy for prevention, although challenges regarding safety and personalized application remain.
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