Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review

被引:183
作者
McLoughlin, Eavan C. [1 ]
O'Boyle, Niamh M. [1 ]
机构
[1] Trinity Coll Dublin, Sch Pharm & Pharmaceut Sci, Trinity Biomed Sci Inst, Dublin D02, Ireland
关键词
anti-cancer; anti-tubulin; tubulin binding; microtubule-targeting agents; colchicine; colchicine binding site; combretastatin; CA-4; tubulin destabilizing; COMBRETASTATIN A4 PHOSPHATE; TUBULIN POLYMERIZATION INHIBITOR; VASCULAR TARGETING AGENT; COLON-CANCER CELLS; BIOLOGICAL EVALUATION; ANTITUMOR-ACTIVITY; ANTINEOPLASTIC AGENTS; ANTICANCER AGENTS; COVALENT INHIBITORS; TUMOR VASCULATURE;
D O I
10.3390/ph13010008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
It is over 50 years since the discovery of microtubules, and they have become one of the most important drug targets for anti-cancer therapies. Microtubules are predominantly composed of the protein tubulin, which contains a number of different binding sites for small-molecule drugs. There is continued interest in drug development for compounds targeting the colchicine-binding site of tubulin, termed colchicine-binding site inhibitors (CBSIs). This review highlights CBSIs discovered through diverse sources: from natural compounds, rational design, serendipitously and via high-throughput screening. We provide an update on CBSIs reported in the past three years and discuss the clinical status of CBSIs. It is likely that efforts will continue to develop CBSIs for a diverse set of cancers, and this review provides a timely update on recent developments.
引用
收藏
页数:43
相关论文
共 171 条
[61]   Etoposide: Four decades of development of a topoisomerase II inhibitor [J].
Hande, KR .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (10) :1514-1521
[62]   Genomic dissection of an extended phenotype: Oak galling by a cynipid gall wasp [J].
Hearn, Jack ;
Blaxter, Mark ;
Schonrogge, Karsten ;
Nieves-Aldrey, Jose-Luis ;
Pujade-Villar, Juli ;
Huguet, Elisabeth ;
Drezen, Jean-Michel ;
Shorthouse, Joseph D. ;
Stone, Graham N. .
PLOS GENETICS, 2019, 15 (11)
[63]  
Herdman CA, 2016, MEDCHEMCOMM, V7, P2418, DOI [10.1039/c6md00459h, 10.1039/C6MD00459H]
[64]   VINCA ALKALOIDS - ANTIVASCULAR EFFECTS IN A MURINE TUMOR [J].
HILL, SA ;
LONERGAN, SJ ;
DENEKAMP, J ;
CHAPLIN, DJ .
EUROPEAN JOURNAL OF CANCER, 1993, 29A (09) :1320-1324
[65]  
Hua JY, 2003, ANTICANCER RES, V23, P1433
[66]   Structural Optimization of Indole Derivatives Acting at Colchicine Binding Site as Potential Anticancer Agents [J].
Hwang, Dong-Jin ;
Wang, Jin ;
Li, Wei ;
Miller, Duane D. .
ACS MEDICINAL CHEMISTRY LETTERS, 2015, 6 (09) :993-997
[67]   Synthesis of phenstatin/isocombretastatin-chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers [J].
Kamal, Ahmed ;
Kumar, G. Bharath ;
Vishnuvardhan, M. V. P. S. ;
Shaik, Anver Basha ;
Reddy, Vangala Santhosh ;
Mahesh, Rasala ;
Bin Sayeeda, Ibrahim ;
Kapure, Jeevak Sopanrao .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2015, 13 (13) :3963-3981
[68]   The tumor vascular targeting agent combretastatin A-4-phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells [J].
Kanthou, C ;
Tozer, GM .
BLOOD, 2002, 99 (06) :2060-2069
[69]   Therapeutic efficacy of a novel βIII/βIV-tubulin inhibitor (VERU-111) in pancreatic cancer [J].
Kashyap, Vivek K. ;
Wang, Qinghui ;
Setua, Saini ;
Nagesh, Prashanth K. B. ;
Chauhan, Neeraj ;
Kumari, Sonam ;
Chowdhury, Pallabita ;
Miller, Duane D. ;
Yallapu, Murali M. ;
Li, Wei ;
Jaggi, Meena ;
Bin Hafeez, Bilal ;
Chauhan, Subhash C. .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2019, 38 (1)
[70]   Rituximab A Review of its Use in Chronic Lymphocytic Leukaemia, Low-Grade or Follicular Lymphoma and Diffuse Large B-Cell Lymphoma [J].
Keating, Gillian M. .
DRUGS, 2010, 70 (11) :1445-1476