4.6 Review

Microsatellite Instability in Colorectal Cancer Liquid Biopsy-Current Updates on Its Potential in Non-Invasive Detection, Prognosis and as a Predictive Marker

Journal

DIAGNOSTICS
Volume 11, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/diagnostics11030544

Keywords

circulating tumor cells; circulating tumor DNA; cell-free DNA; microsatellite instability; colorectal cancer; non-invasive; liquid biopsy

Funding

  1. Dana Impak Perdana Grant by Universiti Kebangsaan Malaysia (UKM) (Kuala Lumpur, Malaysia) [DIP-2018-010]
  2. Monash University Malaysia (Selangor, Malaysia)

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CRC is the third most commonly-diagnosed cancer worldwide and MSI is an indicator for LS and a prognostic marker for immunotherapy response. Traditional tissue-based MSI testing may be hindered when surgery is not an option or tissues are insufficient, but next-generation sequencing in combination with liquid biopsy presents a promising alternative.
Colorectal cancer (CRC) is the third most commonly-diagnosed cancer in the world and ranked second for cancer-related mortality in humans. Microsatellite instability (MSI) is an indicator for Lynch syndrome (LS), an inherited cancer predisposition, and a prognostic marker which predicts the response to immunotherapy. A recent trend in immunotherapy has transformed cancer treatment to provide medical alternatives that have not existed before. It is believed that MSI-high (MSI-H) CRC patients would benefit from immunotherapy due to their increased immune infiltration and higher neo-antigenic loads. MSI testing such as immunohistochemistry (IHC) and PCR MSI assay has historically been a tissue-based procedure that involves the testing of adequate tissue with a high concentration of cancer cells, in addition to the requirement for paired normal tissues. The invasive nature and specific prerequisite of such tests might hinder its application when surgery is not an option or when the tissues are insufficient. The application of next-generation sequencing, which is highly sensitive, in combination with liquid biopsy, therefore, presents an interesting possibility worth exploring. This review aimed to discuss the current body of evidence supporting the potential of liquid biopsy as a tool for MSI testing in CRC.

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