Targeting the Ataxia Telangiectasia Mutated Protein in Cancer Therapy

Author(s): Donatella Vecchio, Guido Frosina

Journal Name: Current Drug Targets

Volume 17 , Issue 2 , 2016

  Journal Home
Translate in Chinese
Become EABM
Become Reviewer

Graphical Abstract:


Genotoxic anticancer drugs explicate their effects damaging DNA, thus triggering a coordinated signal-transduction network called DNA Damage Response (DDR). Ataxia Telangiectasia Mutated (ATM) protein plays a central role in this response: activated by DNA damage, ATM phosphorylates itself and downstream effectors that arrest cell cycle allowing for DNA repair or, should DNA damage be too severe and not retrievable, inducing apoptosis. ATM is a worth-investigating target for tumor radio- and chemosensitization. During last years, pharmaceutical industries and research laboratories have developed a series of small molecules, capable to inhibit ATM with increasing specificity. Several preclinical studies have demonstrated that these inhibitors alone or in association with other treatments may improve therapeutic outcomes. In this review we discuss ATM inhibitors so far developed, focussing on recent acquisitions on their potential antineoplastic usefulness.

Keywords: ATM, chemotherapy, glioma, inhibitor, radiotherapy, resistance, sensitization.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2016
Page: [139 - 153]
Pages: 15
DOI: 10.2174/1389450115666141110154621
Price: $65

Article Metrics

PDF: 48
PRC: 1