Small Molecule Inhibitors of CXCR4

被引:222
作者
Debnath, Bikash [1 ]
Xu, Shili [1 ]
Grande, Fedora [2 ]
Garofalo, Antonio [2 ]
Neamati, Nouri [1 ]
机构
[1] Univ So Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90089 USA
[2] Univ Calabria, Dipartimento Sci Farmaceut, I-87036 Arcavacata Di Rende, CS, Italy
关键词
CXCR4; antagonists; HIV; cancer; rheumatoid arthritis; WHIM syndrome; lupus; CHEMOKINE RECEPTOR CXCR4; CHRONIC LYMPHOCYTIC-LEUKEMIA; SYNTHETIC MULTIVALENT LIGANDS; FACTOR-I; DIPEPTIDE ISOSTERES; STEREOSELECTIVE-SYNTHESIS; PLASMODIUM-FALCIPARUM; PANCREATIC-CANCER; POTENT ACTIVITY; HIV-1; ENTRY;
D O I
10.7150/thno.5376
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
CXCR4 is a G-protein-coupled receptor involved in a number of physiological processes in the hematopoietic and immune systems. The SDF-1/CXCR4 axis is significantly associated with several diseases, such as HIV, cancer, WHIM syndrome, rheumatoid arthritis, pulmonary fibrosis and lupus. For example, CXCR4 is one of the major co-receptors for HIV entry into target cells, while in cancer it plays an important role in tumor cell metastasis. Several promising CXCR4 antagonists have been developed to block SDF-1/CXCR4 interactions that are currently under different stages of development. The first in class CXCR4 antagonist, plerixafor, was approved by the FDA in 2008 for the mobilization of hematopoietic stem cells and several other drugs are currently in clinical trials for cancer, HIV, and WHIM syndrome. While the long-term safety data for the first generation CXCR4 antagonists are not yet available, several new compounds are under preclinical development in an attempt to provide safer and more efficient treatment options for HIV and cancer patients.
引用
收藏
页码:47 / 75
页数:29
相关论文
共 121 条
[21]  
Carrour L.C., 2010, The Open Bioinformatics Journal, V4, P5, DOI DOI 10.2174/1875036201004010005
[22]   Synthesis of a novel tricyclic 1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline ring system and CXCR4 antagonists with potent activity against HIV-1 [J].
Catalano, John G. ;
Gudmundsson, Kristjan S. ;
Svolto, Angilique ;
Boggs, Sharon D. ;
Miller, John F. ;
Spaltenstein, Andrew ;
Thomson, Michael ;
Wheelan, Pat ;
Minick, Doug J. ;
Phelps, Dean P. ;
Jenkinson, Stephen .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (07) :2186-2190
[23]   Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1 [J].
Ceradini, DJ ;
Kulkarni, AR ;
Callaghan, MJ ;
Tepper, OM ;
Bastidas, N ;
Kleinman, ME ;
Capla, JM ;
Galiano, RD ;
Levine, JP ;
Gurtner, GC .
NATURE MEDICINE, 2004, 10 (08) :858-864
[24]  
Cervia JS, 2003, CLIN INFECT DIS, V37, P1102, DOI 10.1086/378302
[25]   Targeting the CXCR4/CXCL12 axis in systemic lupus erythematosus [J].
Chong, Benjamin F. ;
Mohan, Chandra .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2009, 13 (10) :1147-1153
[26]   CXC chemokine receptor 4 expressed in T cells plays an important role in the development of collagen-induced arthritis [J].
Chung, Soo-Hyun ;
Seki, Keisuke ;
Choi, Byung-Il ;
Kimura, Keiko B. ;
Ito, Akihiko ;
Fujikado, Noriyuki ;
Saijo, Shinobu ;
Iwakura, Yoichiro .
ARTHRITIS RESEARCH & THERAPY, 2010, 12 (05)
[27]   Change in coreceptor use correlates with disease progression in HIV-1-infected individuals [J].
Connor, RI ;
Sheridan, KE ;
Ceradini, D ;
Choe, S ;
Landau, NR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :621-628
[28]   Solution structure and basis for functional activity of stromal cell-derived factor-1; dissociation of CXCR4 activation from binding and inhibition of HIV-1 [J].
Crump, MP ;
Gong, JH ;
Loetscher, P ;
Rajarathnam, K ;
Amara, A ;
Arenzana-Seisdedos, F ;
Virelizier, JL ;
Baggiolini, M ;
Sykes, BD ;
Clark-Lewis, I .
EMBO JOURNAL, 1997, 16 (23) :6996-7007
[29]   The effect of a trans-locked Gly-Pro alkene isostere on collagen triple helix stability [J].
Dai, Nan ;
Wang, Xiaodong J. ;
Etzkorn, Felicia A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (16) :5396-+
[30]   Recent advances on the use of the CXCR4 antagonist plerixafor (AMD3100, Mozobil™) and potential of other CXCR4 antagonists as stem cell mobilizers [J].
De Clercq, Erik .
PHARMACOLOGY & THERAPEUTICS, 2010, 128 (03) :509-518