Literature DB >> 29757235

Clinically Applicable Inhibitors Impacting Genome Stability.

Anu Prakash1, Juan F Garcia-Moreno2, James A L Brown3, Emer Bourke4.   

Abstract

Advances in technology have facilitated the molecular profiling (genomic and transcriptomic) of tumours, and has led to improved stratification of patients and the individualisation of treatment regimes. To fully realize the potential of truly personalised treatment options, we need targeted therapies that precisely disrupt the compensatory pathways identified by profiling which allow tumours to survive or gain resistance to treatments. Here, we discuss recent advances in novel therapies that impact the genome (chromosomes and chromatin), pathways targeted and the stage of the pathways targeted. The current state of research will be discussed, with a focus on compounds that have advanced into trials (clinical and pre-clinical). We will discuss inhibitors of specific DNA damage responses and other genome stability pathways, including those in development, which are likely to synergistically combine with current therapeutic options. Tumour profiling data, combined with the knowledge of new treatments that affect the regulation of essential tumour signalling pathways, is revealing fundamental insights into cancer progression and resistance mechanisms. This is the forefront of the next evolution of advanced oncology medicine that will ultimately lead to improved survival and may, one day, result in many cancers becoming chronic conditions, rather than fatal diseases.

Entities:  

Keywords:  DSB; HR; NHEJ; amplification; centrosome; chromatin; clinical; clustering; inhibitor; trial

Mesh:

Substances:

Year:  2018        PMID: 29757235      PMCID: PMC6100577          DOI: 10.3390/molecules23051166

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  390 in total

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Journal:  Dev Cell       Date:  2009-09       Impact factor: 12.270

2.  Distribution of topoisomerase II cleavage sites in simian virus 40 DNA and the effects of drugs.

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3.  Valproic acid defines a novel class of HDAC inhibitors inducing differentiation of transformed cells.

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4.  ENMD-2076 is an orally active kinase inhibitor with antiangiogenic and antiproliferative mechanisms of action.

Authors:  Graham C Fletcher; Richard D Brokx; Trisha A Denny; Todd A Hembrough; Stacy M Plum; William E Fogler; Carolyn F Sidor; Mark R Bray
Journal:  Mol Cancer Ther       Date:  2010-12-21       Impact factor: 6.261

Review 5.  Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template.

Authors:  R Scott Williams; Jessica S Williams; John A Tainer
Journal:  Biochem Cell Biol       Date:  2007-08       Impact factor: 3.626

Review 6.  Mesenchymal stem cells derived from dental tissues vs. those from other sources: their biology and role in regenerative medicine.

Authors:  G T-J Huang; S Gronthos; S Shi
Journal:  J Dent Res       Date:  2009-09       Impact factor: 6.116

7.  Stat3 activity is required for centrosome duplication in chinese hamster ovary cells.

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Journal:  J Biol Chem       Date:  2004-08-04       Impact factor: 5.157

Review 8.  The DNA damage response and cancer therapy.

Authors:  Christopher J Lord; Alan Ashworth
Journal:  Nature       Date:  2012-01-18       Impact factor: 49.962

9.  Stat3 regulates centrosome clustering in cancer cells via Stathmin/PLK1.

Authors:  Edward J Morris; Eiko Kawamura; Jordan A Gillespie; Aruna Balgi; Nagarajan Kannan; William J Muller; Michel Roberge; Shoukat Dedhar
Journal:  Nat Commun       Date:  2017-05-05       Impact factor: 14.919

Review 10.  Targeting cancer using KAT inhibitors to mimic lethal knockouts.

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Journal:  Biochem Soc Trans       Date:  2016-08-15       Impact factor: 5.407

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Review 3.  Small Molecules Targeting HATs, HDACs, and BRDs in Cancer Therapy.

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4.  Editorial: Mechanisms guarding the genome.

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5.  Cisplatin Resistance in Osteosarcoma: In vitro Validation of Candidate DNA Repair-Related Therapeutic Targets and Drugs for Tailored Treatments.

Authors:  Marilù Fanelli; Elisa Tavanti; Maria Pia Patrizio; Serena Vella; Amira Fernandez-Ramos; Federica Magagnoli; Silvia Luppi; Claudia Maria Hattinger; Massimo Serra
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