Cancer Researchers Can Assess Microsatellite Instability (MSI) Through New Lens with Expanded Promega System

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MADISON, Wis.– A new microsatellite instability (MSI) system launched today by Promega Corporation enables cancer researchers to evaluate a new set of unique MSI markers that may offer additional precision in the characterization of their tumor samples. MSI testing measures changes in DNA sequence length that occur when cells are unable to repair mistakes in DNA replication as a result of a functional deficiency in one or more major DNA mismatch repair proteins (dMMR).

Promega LMR MSI Analysis System

The Promega LMR MSI Analysis System is a PCR-based research tool with novel markers for detecting MSI. The panel consists of eight markers, including four gold-standard markers and four novel long mononucleotide repeat (LMR) markers. Early research indicates the addition of the LMR markers may offer more clarity in assessing MSI status in challenging samples with subtle MSI phenotypes, ambiguous results or small shifts.

“Our eight-marker panel with novel LMR markers may offer a more complete view of MSI,” says Jeff Bacher, Senior Research Scientist at Promega. “This technology offers cancer researchers a broad new lens to assess the MSI status of their samples.”

Analyzing MSI

MSI analysis typically involves comparing allelic profiles of microsatellite markers generated by amplification from matched pairs of tumor and normal samples. The presence of alleles in the tumor sample that are not found in the matched normal sample indicates MSI.

The panel of markers in the new Promega LMR MSI Analysis System is comprised of four gold standard MSI markers (BAT-25, BAT-26, MONO-27, and NR-21) as well as four markers with increased repeat length (BAT-52, BAT-56, BAT-59, and BAT-60). This set of markers enables researchers to combine long markers that bring additional MSI detection alongside known and trusted markers, expanding MSI detection ability in difficult samples while maintaining overlap with data gathered using traditional markers. The assay has been optimized to enable strong and balanced amplification, even from degraded samples such as formalin-fixed, paraffin-embedded (FFPE) tissue.