Ballaz Santiago, Mulshine James L
Department of Histology and Pathology, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Clin Lung Cancer. 2003 Jul;5(1):46-62. doi: 10.3816/CLC.2003.n.021.
A number of lines of evidence suggests that chronic inflammation contributes to the process of carcinogenesis. In this article, this theme is explored with particular emphasis on the involvement of inflammation in the development of lung cancer. A number of molecular pathways activated in chronic inflammation may contribute to lung carcinogenesis. The challenge is to conceptualize a cohesive picture of this complex biology that allows for effective pharmaceutical intervention. Initial therapeutic efforts involve strategies to block single pathways, such as with cyclooxygenase (COX) activity. However, the more that is learned about the consequences of COX activity, the more evident are the relationships of this enzyme to other classes of regulatory molecules such as the potent nuclear factor-kB. In light of this emerging picture, more global intervention strategies, such as with drug combinations, may be essential for success. Further basic study is essential to sort out possible molecular relationships and to permit elucidation of the most critical regulatory circuits. Given the complexity of these molecular interactions, well-designed clinical trials that specifically evaluate the precise effects of particular antiinflammatory drugs on lung carcinogenesis will also be critical to sort out the complexity and to validate successful approaches to arresting lung carcinogenesis.
多项证据表明,慢性炎症会促进癌症发生过程。在本文中,将探讨这一主题,尤其着重于炎症在肺癌发展中的作用。慢性炎症中激活的一些分子途径可能导致肺癌发生。挑战在于构建一个关于这种复杂生物学的连贯图景,以便进行有效的药物干预。最初的治疗努力涉及阻断单一途径的策略,例如抑制环氧化酶(COX)的活性。然而,对COX活性后果了解得越多,就越能清楚地看到这种酶与其他类别的调节分子(如强效核因子-κB)之间的关系。鉴于这一逐渐清晰的情况,更全面的干预策略,如联合用药,可能对成功至关重要。进一步的基础研究对于理清可能的分子关系以及阐明最关键的调节回路必不可少。鉴于这些分子相互作用的复杂性,精心设计的临床试验专门评估特定抗炎药物对肺癌发生的确切影响,对于理清这种复杂性并验证阻止肺癌发生的成功方法也至关重要。