5-Lipoxygenase: A Promising Drug Target Against Inflammatory Diseases-Biochemical and Pharmacological Regulation

被引:15
作者
Anwar, Yasir [1 ]
Sabir, Jamal S. M. [1 ]
Qureshi, Muhammad I. [1 ]
Saini, Kulvinder S. [1 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Biol Sci, Jeddah 21589, Saudi Arabia
关键词
Cytokines; 5-Lipoxygenase; leukotrienes; new drug discovery; small molecules; GROWTH-FACTOR-BETA; HUMAN POLYMORPHONUCLEAR LEUKOCYTES; COLONY-STIMULATING FACTOR; LEUKOTRIENE C-4 SYNTHASE; ARACHIDONIC-ACID; HUMAN-NEUTROPHILS; ACTIVATING PROTEIN; PRODUCT FORMATION; DUAL INHIBITOR; RECEPTOR BLT1;
D O I
10.2174/1389450114666131209110745
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5-Lipoxygenase (5-LO) is the key enzyme involved in the synthesis of pro-inflammatory leukotrienes (LTs) and has become a prime target for new drug discovery research and development efforts by the pharmaceutical and biotech industry. The pathophysiological effects of LTs can be modulated by the selective inhibition of 5-LO. In this review, we summarize the established dogma and recent progress on the biochemical and pharmacological regulation of 5-LO and its diverse cellular partners. In the last decade, significant research efforts have led to the exploitation of 5-LO pathway for developing new drugs against inflammatory diseases. Despite few setbacks, a number of promising molecules have moved into clinical development. These fundamental discoveries and proof-of-concept studies will ultimately be helpful in delineating how 5-LO pathway participates in the development of disease phenotype and what are possible key biomarkers of disease progression and regression. Elucidation of molecular mechanism-of-action of 5-LO in individual cell types will pave the way for improving efficacy parameters. Taken together, this combined knowledge about the 5-LO pathway would be helpful in planning collaborative and targeted R&D efforts, by the academic laboratories and pharmaceutical/biotech industry, for the discovery and development of novel, efficacious and safer drugs against multiple diseases.
引用
收藏
页码:410 / 422
页数:13
相关论文
共 154 条
[1]   Hyperforin is a dual inhibitor of cyclooxygenase-1 and 5-lipoxygenase [J].
Albert, D ;
Zündorf, I ;
Dingermann, T ;
Müller, WE ;
Steinhilber, D ;
Werz, O .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (12) :1767-1775
[2]   Licofelone - clinical update on a novel LOX/COX inhibitor for the treatment of osteoarthritis [J].
Alvaro-Gracia, JM .
RHEUMATOLOGY, 2004, 43 :I21-I25
[3]   Montelukast for the treatment of asthma in the adult population [J].
Amlani, Salima ;
Nadarajah, Thanu ;
McIvor, Richard Andrew .
EXPERT OPINION ON PHARMACOTHERAPY, 2011, 12 (13) :2119-2128
[4]   Resolvin E1 selectively interacts with leukotriene B4 receptor BLT1 and ChemR23 to regulate inflammation [J].
Arita, Makoto ;
Ohira, Taisuke ;
Sun, Yee-Ping ;
Elangovan, Siva ;
Chiang, Nan ;
Serhan, Charles N. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (06) :3912-3917
[5]   The leukotriene E4 puzzle: Finding the missing pieces and revealing the pathobiologic implications [J].
Austen, K. Frank ;
Maekawa, Akiko ;
Kanaoka, Yoshihide ;
Boyce, Joshua A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2009, 124 (03) :406-416
[6]   Functional characteristics of cysteinyl-leukotriene receptor subtypes [J].
Bäck, M .
LIFE SCIENCES, 2002, 71 (06) :611-622
[7]   Association of 5-lipoxygenase gene polymorphisms with bronchial asthma [J].
Bai, Chunying ;
Yu, Xiaoming ;
Yun, Rui ;
Shi, Tiewei ;
Zhang, Chaojun ;
Zhou, Jing ;
Sachurangui ;
Tong, Lijuan ;
Li, Xiujun ;
Gao, Lifeng .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2012, 4 (06) :967-971
[8]   Pharmacodynamics and Pharmacokinetics of AM103, a Novel Inhibitor of 5-Lipoxygenase-Activating Protein (FLAP) [J].
Bain, G. ;
King, C. D. ;
Rewolinski, M. ;
Schaab, K. ;
Santini, A. M. ;
Shapiro, D. ;
Moran, M. ;
de Rooij, S. van de Wetering ;
Roffel, A. F. ;
Schuilenga-Hut, P. ;
Milne, G. L. ;
Lorrain, D. S. ;
Li, Y. ;
Arruda, J. M. ;
Hutchinson, J. H. ;
Prasit, P. ;
Evans, J. F. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2010, 87 (04) :437-444
[9]   Zileuton: clinical implications of 5-Lipoxygenase inhibition in severe airway disease [J].
Berger, W. ;
De Chandt, M. T. M. ;
Cairns, C. B. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2007, 61 (04) :663-676
[10]   MK-0633, a potent 5-lipoxygenase inhibitor, in chronic obstructive pulmonary disease [J].
Bernstein, Jonathan A. ;
Liu, Nancy ;
Knorr, Barbara A. ;
Smugar, Steven S. ;
Hanley, William D. ;
Reiss, Theodore F. ;
Greenberg, Steven .
RESPIRATORY MEDICINE, 2011, 105 (03) :392-401