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Clinically Applicable Inhibitors Impacting Genome Stability
Anu Prakash1, Juan F Garcia-Moreno2, James A L Brown3
1Discipline of Pathology, Lambe Institute for Translational Research, School of Medicine, National University of Ireland Galway, H91 YR71 Galway, Ireland. A.PRAKASH2@nuigalway.ie.
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.
Insights
Advances in tumor molecular profiling enable personalized cancer treatments. Novel therapies targeting genomic pathways and DNA damage responses are crucial for overcoming treatment resistance and improving patient survival.
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Technological advances enable comprehensive tumor molecular profiling (genomic and transcriptomic).
- Personalized medicine requires targeted therapies to disrupt tumor compensatory and resistance pathways.
Purpose of the Study:
- To review novel therapies targeting cancer's genome and signaling pathways.
- To discuss compounds in clinical and pre-clinical trials for cancer treatment.
Main Methods:
- Review of recent advances in genome-targeting therapies.
- Focus on inhibitors of DNA damage response and genome stability pathways.
- Analysis of compounds in clinical and pre-clinical development.
Main Results:
- Emerging therapies target specific molecular pathways in cancer.
- Compounds inhibiting DNA damage responses show promise for synergistic combinations.
- Tumor profiling data combined with new treatment insights reveal cancer progression and resistance mechanisms.
Conclusions:
- Targeted therapies disrupting compensatory pathways are key to personalized oncology.
- Novel genome-focused treatments are advancing cancer care, potentially leading to improved survival and chronic disease management.
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