Literature DB >> 20166845

Inhibitors of Cdc25 phosphatases as anticancer agents: a patent review.

Antonio Lavecchia1, Carmen Di Giovanni, Ettore Novellino.   

Abstract

IMPORTANCE OF THE FIELD: The cell division cycle 25 (Cdc25) family of proteins are highly conserved dual specificity phosphatases that regulate cyclin-dependent kinases, the main gatekeepers of the eukaryotic cell division cycle. The three isoforms of Cdc25, including Cdc25A, Cdc25B and Cdc25C, appear to act on different cyclin-dependent kinase/cyclin complexes at different stages of the cell cycle. Overexpression of Cdc25A and/or Cdc25B, but not Cdc25C, has been detected in numerous cancers and is often correlated with a poor clinical prognosis. Thus, inhibition of these phosphatases may represent a promising therapeutic approach in oncology. AREAS COVERED IN THIS REVIEW: The main focus of the present review is to describe the development of Cdc25 inhibitors over the years. We describe different compounds according to the decade of discovery and focus attention on molecules that were published in patents. WHAT THE READER WILL GAIN: Insight into the most clinically relevant therapeutic Cdc25 analogues that have been published in over 40 patents over the past 19 years. TAKE HOME MESSAGE: Some Cdc25 inhibitors have suppressed in vivo the growth of human tumor xenografts in animals; this confirmed the validity of using Cdc25 phosphatase inhibition as an anticancer strategy, but side effects and toxicity remain to be investigated.

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Year:  2010        PMID: 20166845     DOI: 10.1517/13543771003623232

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  24 in total

1.  Targeting cannabinoid receptor-2 pathway by phenylacetylamide suppresses the proliferation of human myeloma cells through mitotic dysregulation and cytoskeleton disruption.

Authors:  Rentian Feng; Qin Tong; Zhaojun Xie; Haizi Cheng; Lirong Wang; Suzanne Lentzsch; G David Roodman; Xiang-Qun Xie
Journal:  Mol Carcinog       Date:  2015-01-16       Impact factor: 4.784

Review 2.  DNA repair dysregulation from cancer driver to therapeutic target.

Authors:  Nicola J Curtin
Journal:  Nat Rev Cancer       Date:  2012-12       Impact factor: 60.716

3.  Synthesis, anticancer activity, and molecular modeling of 1,4-naphthoquinones that inhibit MKK7 and Cdc25.

Authors:  Igor A Schepetkin; Alexander S Karpenko; Andrei I Khlebnikov; Marina O Shibinska; Igor A Levandovskiy; Liliya N Kirpotina; Nadezhda V Danilenko; Mark T Quinn
Journal:  Eur J Med Chem       Date:  2019-09-18       Impact factor: 6.514

4.  Inhibition of Cdc25A suppresses hepato-renal cystogenesis in rodent models of polycystic kidney and liver disease.

Authors:  Tatyana V Masyuk; Brynn N Radtke; Angela J Stroope; Jesús M Banales; Anatoliy I Masyuk; Sergio A Gradilone; Gabriella Bedekovicsne Gajdos; Natasha Chandok; Jason L Bakeberg; Christopher J Ward; Erik L Ritman; Hiroaki Kiyokawa; Nicholas F LaRusso
Journal:  Gastroenterology       Date:  2011-12-07       Impact factor: 22.682

5.  Discovering the distinct inhibitory effects between C4-epimeric glycosyl amino acids: new insight into the development of protein tyrosine phosphatase inhibitors.

Authors:  Xiao-Peng He; Cui Li; Zhi-Zhou Wang; Li-Xin Gao; Xiao-Xin Shi; Yun Tang; Juan Xie; Jia Li; Guo-Rong Chen; Kaixian Chen
Journal:  Glycoconj J       Date:  2011-09-06       Impact factor: 2.916

6.  Solution NMR studies reveal no global flexibility in the catalytic domain of CDC25B.

Authors:  George Lund; Tomasz Cierpicki
Journal:  Proteins       Date:  2014-04-29

7.  Identification of the quinolinedione inhibitor binding site in Cdc25 phosphatase B through docking and molecular dynamics simulations.

Authors:  Yushu Ge; Marc van der Kamp; Maturos Malaisree; Dan Liu; Yi Liu; Adrian J Mulholland
Journal:  J Comput Aided Mol Des       Date:  2017-10-09       Impact factor: 3.686

Review 8.  CuAAC click chemistry accelerates the discovery of novel chemical scaffolds as promising protein tyrosine phosphatases inhibitors.

Authors:  X-P He; J Xie; Y Tang; J Li; G-R Chen
Journal:  Curr Med Chem       Date:  2012       Impact factor: 4.530

9.  Reactivation of the p90RSK-CDC25C Pathway Leads to Bypass of the Ganetespib-Induced G2-M Arrest and Mediates Acquired Resistance to Ganetespib in KRAS-Mutant NSCLC.

Authors:  Suman Chatterjee; Eric H-B Huang; Ian Christie; Timothy F Burns
Journal:  Mol Cancer Ther       Date:  2017-05-31       Impact factor: 6.261

10.  GeneFriends: an online co-expression analysis tool to identify novel gene targets for aging and complex diseases.

Authors:  Sipko van Dam; Rui Cordeiro; Thomas Craig; Jesse van Dam; Shona H Wood; João Pedro de Magalhães
Journal:  BMC Genomics       Date:  2012-10-06       Impact factor: 3.969

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