Department of Oral Surgery, University of Porto, Porto, Portugal.
Oral Oncol. 2009 Oct;45(10):e124-8. doi: 10.1016/j.oraloncology.2009.03.016. Epub 2009 May 19.
Cyclooxygenase-2 (COX-2) levels are increased in various tumors, particularly those involving the esophagus, stomach, breast, pancreas, lung, colon, skin, urinary bladder, prostate and head and neck. Nevertheless, the tumorigenic mechanisms of COX-2 overexpression still remain poorly understood and may include mechanisms that may act at different stages of the disease. Thus, the literature shows increasing evidence that overexpression of the COX-2 plays an important role in tumor growth and spread of tumors by interfering with different biological processes such as cell proliferation, cellular adhesion, immune surveillance, apoptosis, and angiogenesis. Furthermore, the expression of COX-2 might shed some light over the physiopathology and clinical behavior of tumors of the head and neck, including benign odontogenic neoplasms of the jaws with an aggressive behavior, such as keratocystic odontogenic tumors (KCOT). Ultimately, the research of molecular markers associated with the biological behavior of tumors will help to understand the underlying molecular mechanisms and to predict the clinical outcome, leading to the development of new therapeutic applications, such as molecular-targeted treatment and patient tailored therapy.
环氧化酶-2(COX-2)水平在各种肿瘤中升高,特别是涉及食管、胃、乳腺、胰腺、肺、结肠、皮肤、膀胱、前列腺和头颈部的肿瘤。然而,COX-2 过表达的肿瘤发生机制仍知之甚少,可能包括在疾病不同阶段起作用的机制。因此,文献显示越来越多的证据表明,COX-2 的过表达通过干扰细胞增殖、细胞黏附、免疫监视、细胞凋亡和血管生成等不同的生物学过程,在肿瘤生长和肿瘤扩散中发挥重要作用。此外,COX-2 的表达可能揭示了头颈部肿瘤的病理生理学和临床行为,包括具有侵袭性行为的颌骨良性牙源性肿瘤,如角化囊肿性牙源性肿瘤(KCOT)。最终,与肿瘤生物学行为相关的分子标志物的研究将有助于理解潜在的分子机制,并预测临床结果,从而开发新的治疗应用,如分子靶向治疗和个体化治疗。