
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.
topoisomerase-i inhibitors, lysine methyltransferase setd8, DNA Repair, Antineoplastic Agents, Review, amplification, histone deacetylase inhibitors, t-cell lymphoma, induced centrosome amplification, Genomic Instability, clinical, DNA-damage-response, strand break repair, Chromosomal Instability, hr, Animals, Humans, dependent kinase inhibitor, Molecular Targeted Therapy, Protein Kinase Inhibitors, Centrosome, trial, nhej, dsb, Histone Deacetylase Inhibitors, inhibitor, small-molecule inhibitors, centrosome, poly(adp-ribose) polymerase inhibitor, Phthalazines, chromatin, Biomarkers, DNA Damage, Signal Transduction, clustering
topoisomerase-i inhibitors, lysine methyltransferase setd8, DNA Repair, Antineoplastic Agents, Review, amplification, histone deacetylase inhibitors, t-cell lymphoma, induced centrosome amplification, Genomic Instability, clinical, DNA-damage-response, strand break repair, Chromosomal Instability, hr, Animals, Humans, dependent kinase inhibitor, Molecular Targeted Therapy, Protein Kinase Inhibitors, Centrosome, trial, nhej, dsb, Histone Deacetylase Inhibitors, inhibitor, small-molecule inhibitors, centrosome, poly(adp-ribose) polymerase inhibitor, Phthalazines, chromatin, Biomarkers, DNA Damage, Signal Transduction, clustering
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 21 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
