Cyclooxygenase-2 inhibitors in lung cancer treatment: Bench to bed

被引:42
|
作者
Liu, Rui [1 ,2 ]
Xu, Kang-Ping [2 ]
Tan, Gui-Shan [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Sch Pharmaceut Sci, Changsha 410013, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung cancer; Cyclooxygenase-2; Celecoxib; Clinical trials; Combination therapy; ENDOTHELIAL GROWTH-FACTOR; CELECOXIB INDUCES APOPTOSIS; PROGNOSTIC-SIGNIFICANCE; COX-2; INHIBITION; PHASE-I; PANCREATIC-CANCER; PROSTATE-CANCER; MULTIPLE ROLES; CLINICAL-TRIAL; KAPPA-B;
D O I
10.1016/j.ejphar.2015.11.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The most common and leading cause of cancer-related death in men is lung cancer. Despite the recent advances in chemotherapy, advanced lung cancer still remains incurable. For this, the understanding of molecular mechanisms involved in lung carcinogenesis is necessary to provide potentially effective therapeutic targets for the treatment of lung cancer, and thus the therapeutic limitations can be overcome. Cyclooxygenase-2 (COX-2) is an important inflammation factor that is reported to be up-regulated in different cancers. A number of COX-2 inhibitors have been developed, but most of them are restricted due to the different risk factors. Currently, the FDA has allowed celecoxib to remain on the market but advised physicians to apply this drug with alternative therapies or to use at a low dosage. Some other COX-2 inhibitors, such as, apricoxib and etoricoxib are under critical investigation currently. Celecoxib is being tested in clinical trials against lung cancer, as a single agent or in combination with other agents. Recent studies have suggested celecoxib as a feasible and clinically active regimen in the treatment of patients with lung cancer. However, more clinical trials are necessary for the better understanding of the role of selective COX-2 inhibitors in the prevention and treatment of lung cancer along with their assessment of toxicity. In this review, we have discussed the mechanism of actions of COX-2 in cancer progression and the therapeutic use of COX-2 inhibitors in the treatment of lung cancer with subsequent clinical studies and future management. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 133
页数:7
相关论文
共 50 条
  • [11] Selective cyclooxygenase-2 inhibitors and non-small cell lung cancer
    Gridelli, C
    Maione, P
    Airoma, G
    Rossi, A
    CURRENT MEDICINAL CHEMISTRY, 2002, 9 (21) : 1851 - 1858
  • [12] Cyclooxygenase-2 inhibitors
    Nies, AS
    Gresser, MJ
    ADVANCES IN PROTEIN CHEMISTRY, VOL 56: DRUG DISCOVERY AND DESIGN, 2001, 56 : 115 - +
  • [13] Cyclooxygenase-2 inhibitors
    Gajraj, NM
    ANESTHESIA AND ANALGESIA, 2003, 96 (06): : 1720 - 1738
  • [14] Cyclooxygenase-2 inhibitors
    Terrett, N
    DRUG DISCOVERY TODAY, 1997, 2 (11) : 501 - 501
  • [15] Cyclooxygenase-2 inhibitors
    Hawkey, CJ
    Fortun, PJ
    CURRENT OPINION IN GASTROENTEROLOGY, 2005, 21 (06) : 660 - 664
  • [16] Cyclooxygenase-2 inhibitors
    Turnheim, K
    WIENER KLINISCHE WOCHENSCHRIFT, 2001, 113 (15-16) : 558 - 565
  • [17] Multifaceted roles of cyclooxygenase-2 in lung cancer
    Riedl, K
    Krysan, K
    Pold, M
    Dalwadi, H
    Heuze-Vourc'h, N
    Dohadwala, M
    Liu, M
    Cui, XY
    Figlin, R
    Mao, JT
    Strieter, R
    Sharma, S
    Dubinett, SM
    DRUG RESISTANCE UPDATES, 2004, 7 (03) : 169 - 184
  • [18] Treatment of pain with cyclooxygenase-inhibitors: Cyclooxygenase-2 as a new target?
    Geisslinger, G
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1997, 355 (04) : S19 - S19
  • [19] The effects of cyclooxygenase-2 inhibitors on urological cancer cells
    Yoshimura, R
    Matsuyama, M
    Kawahito, Y
    Takemoto, Y
    Tsuchida, K
    Kuratsukuri, K
    Segawa, Y
    Shinnka, T
    Sano, H
    Nakatani, T
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2004, 13 (06) : 789 - 793
  • [20] Cyclooxygenase-2 inhibitors in colorectal cancer prevention: Point
    Arber, Nadir
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2008, 17 (08) : 1852 - 1857