4.5 Review

Molecular inhibitors of DNA repair: searching for the ultimate tumor killing weapon

期刊

FUTURE MEDICINAL CHEMISTRY
卷 7, 期 12, 页码 1543-1558

出版社

FUTURE SCI LTD
DOI: 10.4155/fmc.15.95

关键词

cancer therapy; clustered DNA lesions; DNA damage; DNA repair; DNA repair inhibitors; multipathway lethality; synthetic lethality

资金

  1. EU Marie Curie Reintegration Grant [MC-CIG-303514]
  2. Greek National funds through the Operational Program 'Educational and Lifelong Learning of the National Strategic Reference Framework (NSRF)-Research Funding Program: THALES [MIS 379346]
  3. COST Action 'Biomimetic Radical Chemistry' [CM1201]
  4. BRFFA

向作者/读者索取更多资源

DNA repair (DR) inhibitors are small molecules that interact with DR proteins in order to disrupt their function and induce a strike' to the high fidelity of the mammalian DNA repair systems. Many anticancer therapies aim to harm the DNA of the usually highly proliferative cancer cell, causing it to undergo apoptosis. In response to this, cancer cells attempt to fix the induced lesion and reconstitute its genomic integrity, in turn reducing the efficacy of treatment. To overcome this, DR inhibitors suppress DNA repair proteins' function, increasing the potency and tumor killing effect of chemotherapy or radiotherapy. In this review, we discuss clinically applied novel inhibitors under translational investigation and we apply bioinformatic tools in order to identify repair proteins implicated in more than two phenomenically distinct DNA repair pathways (e.g., base excision repair and nonhomologous end joining), that is, the concept of synthetic lethality'. Our study can aid towards the optimization of this therapeutic strategy and, therefore, maximizing treatment effectiveness like in the case of radiation therapy.

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