国际肿瘤学杂志››2013,Vol. 40››Issue (11): 820-823.doi:10.3760/cma.j.issn.1673-422X.2013.11.006
龙成, 姜永梅, 李国权
出版日期:
2013-11-08发布日期:
2013-10-15通讯作者:
李国权, E-mail:lgqjym@163.com E-mail:lgqjym@163.com基金资助:
大连市科技计划
LONG Cheng, JIANG Yong-Mei, LI Guo-Quan
Online:
2013-11-08Published:
2013-10-15Contact:
LI Guo-Quan, E-mail:lgqjym@163.com E-mail:lgqjym@163.comSupported by:
2008E13SF216
摘要:环氧合酶-2(COX-2)是花生四烯酸生物合成前列腺素的限速酶,在多种恶性肿瘤中高表达,在其发生、发展过程中发挥重要作用,而且与恶性肿瘤预后密切相关,目前已成为潜在的治疗靶点之一。实验研究发现选择性COX-2抑制剂可通过多种分子途径提高恶性肿瘤的放疗增敏性,对正常组织体现出放疗保护作用,是极具前景的放疗调节剂,其分子机制仍需继续深入研究。
龙成, 姜永梅, 李国权. 选择性环氧合酶-2抑制剂在肿瘤放疗中的应用[J]. 国际肿瘤学杂志, 2013, 40(11): 820-823.
LONG Cheng, JIANG Yong-Mei, LI Guo-Quan. Application of selective cyclooxygenase-2 inhibitors in tumor radiotherapy[J]. Journal of International Oncology, 2013, 40(11): 820-823.
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