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Pharmacogenomics for the efficacy of platinum-based chemotherapy: Old drugs, new integrated perspective
Chen-Xue Mao1, Min Li2, Wei Zhang3
1Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, PR China; Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha 410078, PR China; Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, Changsha 410078, PR China.
Abstract:
Platinum-based chemotherapy remains the cornerstone of treatment for many malignancies. However, although therapeutic efficiency varies greatly among individuals, there is a lack of pharmacogenomic biomarkers that can be used in clinical settings to identify chemosensitive patients and allow stratification. With the development of high-throughput screening techniques and systems biology approaches, a growing body of evidence has shown that platinum resistance is a multifactorial, multi-dimensional, dynamic process incorporating genetic background, tumor evolution and gut microbes. This review critically summarizes potential pharmacogenomic biomarkers for predicting the efficacy of platinum drugs and provides a comprehensive, time-varying perspective that integrates multiple markers.
Insights
Identifying effective platinum-based chemotherapy requires new biomarkers. This review explores multifactorial markers, including genetics and gut microbes, to predict patient response and overcome platinum resistance.
Area of Science:
- Oncology and Pharmacology
- Genomics and Microbiomics
Background:
- Platinum-based chemotherapy is a primary cancer treatment.
- Individual patient response varies significantly.
- Current clinical practice lacks biomarkers for predicting platinum drug efficacy and stratifying patients.
Purpose of the Study:
- To critically review potential pharmacogenomic biomarkers for platinum drug efficacy.
- To provide a comprehensive, time-varying perspective integrating multiple markers.
- To address the need for biomarkers in personalized cancer therapy.
Main Methods:
- Literature review of high-throughput screening techniques.
- Systems biology approaches to understand platinum resistance.
- Analysis of multifactorial determinants of drug response.
Main Results:
- Platinum resistance is a complex, dynamic process influenced by genetic background, tumor evolution, and gut microbiota.
- Multiple pharmacogenomic biomarkers show potential for predicting treatment outcomes.
- Integration of diverse markers offers a more holistic view of drug response.
Conclusions:
- Pharmacogenomic biomarkers are crucial for optimizing platinum-based chemotherapy.
- A multifactorial and dynamic approach is needed to predict treatment efficacy.
- Future research should focus on integrating diverse markers for clinical application.
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