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Published on: December 9, 2015
The role of emerging genomics and proteomics technologies in cancer drug target discovery
1Department of Medicine, Johns Hopkins University School of Medicine, 1064 Ross, 720, Rutland Avenue, Baltimore, MD 21205, USA. Onyango@jhmi.edu
Abstract:
Cancer drugs have traditionally been identified in screens designed to produce broad biological end points such as cell death. A serious undesired outcome of drugs discovered in these screens is that the mechanism of drug action is unknown and such drugs often have adverse side effects. Designing cancer drugs that act on specific targets offer the advantage that the mechanism of drug action can be understood and accurately monitored in clinical trials leading to development of better drugs. The pharmacological industry has recently shifted to a target directed drug discovery model. However, until recently potential cancer drug targets comprised of only a small fraction of the human genome. The human genome project and high-throughput structural and functional genomics have dramatically increased the number of cancer drug targets. Deciphering cancer drug targets requires the understanding of biochemical pathways that are affected in the cancer genome. It has been suggested that utilization of Single-nucleotide polymorphisms (SNPs) will aid in identifying individuals at high risk of developing certain cancers, and will also help in development of tailored medication or identify genetic profiles of specific drug action and toxicity. Achieving successful new cancer drug development schemes will require a merger of research disciplines that include pharmacology, genomics, comparative genomics, functional genomics, proteomics and bioinformatics. In this review the significance and challenges of these rapidly evolving technologies in cancer drug target discovery are discussed.
Insights
Discovering targeted cancer drugs improves treatment efficacy and safety. Advances in genomics and bioinformatics are crucial for identifying novel drug targets and developing personalized cancer therapies.
Area of Science:
- Oncology
- Pharmacology
- Genomics
- Bioinformatics
Background:
- Traditional cancer drug discovery relied on broad biological endpoints, often resulting in unknown mechanisms of action and adverse side effects.
- The shift towards target-directed drug discovery is gaining momentum, driven by advancements in understanding cancer genomics.
Purpose of the Study:
- To review the significance and challenges of emerging technologies in cancer drug target discovery.
- To highlight the importance of understanding biochemical pathways affected in cancer for effective drug development.
Main Methods:
- Review of current research in pharmacology, genomics, comparative genomics, functional genomics, proteomics, and bioinformatics.
- Discussion on the role of high-throughput screening and the human genome project in identifying potential cancer drug targets.
- Exploration of Single-nucleotide polymorphisms (SNPs) for personalized medicine and predicting drug response.
Main Results:
- The human genome project and functional genomics have significantly expanded the landscape of potential cancer drug targets.
- Understanding cancer-specific biochemical pathways is essential for deciphering drug mechanisms.
- SNPs offer potential for identifying at-risk individuals and tailoring cancer treatments.
Conclusions:
- Target-directed cancer drug discovery offers improved understanding of mechanisms and enhanced clinical trial monitoring.
- Successful cancer drug development necessitates an interdisciplinary approach integrating various 'omics' fields and bioinformatics.
- Emerging technologies present both opportunities and challenges in the ongoing quest for effective cancer therapies.
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