Related Experiment Video
Updated: Aug 8, 2025

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Microsatellite instability assessment is instrumental for Predictive, Preventive and Personalised Medicine: status
Jakub Styk1,2,3, Zuzana Pös2,3,4, Ondrej Pös2,3
1Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University, 811 08 Bratislava, Slovakia.
Abstract:
A form of genomic alteration called microsatellite instability (MSI) occurs in a class of tandem repeats (TRs) called microsatellites (MSs) or short tandem repeats (STRs) due to the failure of a post-replicative DNA mismatch repair (MMR) system. Traditionally, the strategies for determining MSI events have been low-throughput procedures that typically require assessment of tumours as well as healthy samples. On the other hand, recent large-scale pan-tumour studies have consistently highlighted the potential of massively parallel sequencing (MPS) on the MSI scale. As a result of recent innovations, minimally invasive methods show a high potential to be integrated into the clinical routine and delivery of adapted medical care to all patients. Along with advances in sequencing technologies and their ever-increasing cost-effectiveness, they may bring about a new era of Predictive, Preventive and Personalised Medicine (3PM). In this paper, we offered a comprehensive analysis of high-throughput strategies and computational tools for the calling and assessment of MSI events, including whole-genome, whole-exome and targeted sequencing approaches. We also discussed in detail the detection of MSI status by current MPS blood-based methods and we hypothesised how they may contribute to the shift from conventional medicine to predictive diagnosis, targeted prevention and personalised medical services. Increasing the efficacy of patient stratification based on MSI status is crucial for tailored decision-making. Contextually, this paper highlights drawbacks both at the technical level and those embedded deeper in cellular/molecular processes and future applications in routine clinical testing.
Insights
Microsatellite instability (MSI) detection is shifting from low-throughput methods to high-throughput massively parallel sequencing (MPS). This advancement enables predictive, preventive, and personalized medicine (3PM) through efficient patient stratification.
Area of Science:
- Genomics
- Cancer Biology
- Bioinformatics
Background:
- Microsatellite instability (MSI) is a genomic alteration resulting from DNA mismatch repair (MMR) failure.
- Traditional MSI detection methods are low-throughput and require both tumor and healthy samples.
- Recent advancements highlight the potential of massively parallel sequencing (MPS) for MSI assessment.
Purpose of the Study:
- To comprehensively analyze high-throughput strategies and computational tools for MSI calling and assessment.
- To discuss the detection of MSI status using current MPS blood-based methods.
- To explore the potential of MSI detection in advancing Predictive, Preventive, and Personalised Medicine (3PM).
Main Methods:
- Analysis of whole-genome, whole-exome, and targeted sequencing approaches for MSI detection.
- Review of computational tools for MSI event assessment.
- Discussion of current blood-based MPS methods for MSI status determination.
Main Results:
- High-throughput strategies, particularly MPS, offer significant advantages over traditional methods for MSI detection.
- Minimally invasive MPS methods show promise for clinical integration.
- MPS facilitates patient stratification for tailored medical decisions.
Conclusions:
- MPS technologies are poised to revolutionize MSI detection, enabling a shift towards 3PM.
- Further development is needed to address technical and cellular/molecular challenges for routine clinical application.
- Efficient MSI status determination is crucial for personalized cancer care and decision-making.
More Related Videos
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
05:58Digital Polymerase Chain Reaction Assay for the Genetic Variation in a Sporadic Familial Adenomatous Polyposis Patient Using the Chip-in-a-tube Format
Published on: August 20, 2018