Evidence map›Paper›PMID 29757235›Full record

ReviewMolecules (Basel, Switzerland)2018

Clinically Applicable Inhibitors Impacting Genome Stability.

Anu Prakash, Juan F Garcia-Moreno, James A L Brown, Emer Bourke

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Editorial: Mechanisms guarding the genome.Frontiers in cell and developmental biology · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Cisplatin Resistance in Osteosarcoma:Frontiers in oncology · 2020
    Article
  13. Review
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Anu PrakashDiscipline of Pathology, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, H91 YR71 Galway, Ireland. A.PRAKASH2@nuigalway.ie.
Juan F Garcia-MorenoDiscipline of Surgery, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, H91 YR71 Galway, Ireland. juan_fernandez93@hotmail.com.
James A L BrownDiscipline of Surgery, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, H91 YR71 Galway, Ireland. james.brown@nuigalway.ie.ORCID 0000-0002-3155-0334
Emer BourkeDiscipline of Pathology, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, H91 YR71 Galway, Ireland. emer.bourke@nuigalway.ie.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnimalsAntineoplastic AgentsBiomarkersCentrosomeChromosomal InstabilityDNA DamageDNA RepairGenomic InstabilityHistone Deacetylase InhibitorsHumansMolecular Targeted TherapyPhthalazinesProtein Kinase InhibitorsSignal TransductionAntineoplastic AgentsAZ0108BiomarkersHistone Deacetylase InhibitorsPhthalazinesProtein Kinase InhibitorsamplificationcentrosomechromatinclinicalclusteringDSBHRinhibitorNHEJtrial

Identifiers

PMID29757235
PMCPMC6100577

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.