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Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Druggable genome and precision medicine in cancer: current challenges
Camille Amandine Dupont1, Kristina Riegel1, Malvika Pompaiah1
1Cell Biology Unit, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Abstract:
The past decades have seen tremendous developments with respect to "specific" therapeutics that target key signaling molecules to conquer cancer. The key advancements with multiomics technologies, especially genomics, have allowed physicians and molecular oncologists to design "tailor-made" solutions to the specific oncogenes that are deregulated in individual patients, a strategy which has turned out to be successful though the patients quickly develop resistance. The swift integration of multidisciplinary approaches has led to the development of "next generation" therapeutics and, with synergistic therapeutic regimes combined with immune checkpoint inhibitors to reactivate the dampened immune response, has provided the much-needed promise for cancer patients. Despite these advances, a large portion of the druggable genome remains understudied, and the role of druggable genome in the immune system needs further attention. Establishment of patient-derived organoid models has fastened the preclinical validation of novel therapeutics for swift clinical translation. We summarized the current advances and challenges and also stress the importance of biobanking and collection of longitudinal data sets with structured clinical information, as well as the critical role these "high content data sets" will play in designing new therapeutic regimes in a tailor-made fashion.
Insights
Targeted cancer therapies show promise but face resistance. Future strategies involve exploring the druggable genome, combining treatments, and utilizing patient-derived models with comprehensive data for personalized medicine.
Area of Science:
- Oncology
- Genomics
- Immunotherapy
Background:
- Significant progress in developing targeted cancer therapeutics based on multiomics, particularly genomics.
- Tailor-made solutions targeting specific oncogenes have shown success but are limited by acquired resistance.
- Next-generation therapeutics integrate multidisciplinary approaches and immune checkpoint inhibitors to overcome treatment resistance.
Purpose of the Study:
- To summarize current advances and challenges in cancer therapeutics.
- To highlight the understudied druggable genome and its role in the immune system.
- To emphasize the importance of biobanking and longitudinal data for personalized cancer treatment.
Main Methods:
- Review of advancements in targeted therapies and multiomics.
- Discussion of synergistic therapeutic regimes and immune checkpoint inhibitors.
- Exploration of patient-derived organoid models for preclinical validation.
Main Results:
- Targeted therapies offer personalized treatment but face rapid resistance.
- A significant portion of the druggable genome remains unexplored, particularly concerning its immunological functions.
- Patient-derived organoid models accelerate the preclinical testing of novel drugs.
Conclusions:
- Further research into the druggable genome and its immune interactions is crucial.
- Biobanking and longitudinal data collection are essential for developing future tailor-made cancer therapies.
- Integrating multiomics, advanced models, and comprehensive data will drive personalized oncology.
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