AI Article Synopsis

  • - Multiple myeloma (MM) is an incurable blood cancer traditionally monitored through invasive bone marrow biopsies, but recent advancements suggest liquid biopsies using cell-free DNA (cfDNA) could serve as a less invasive alternative for tracking the disease.
  • - This pilot study focused on assessing the feasibility of detecting oncogenic mutations in key genes (NRAS, KRAS, BRAF) that are involved in the MAPK pathway using cfDNA from the blood of 13 MM patients, alongside matched bone marrow samples.
  • - Preliminary findings indicate that mutations were present in both cfDNA and bone marrow DNA, suggesting that cfDNA could be a useful tool for screening mutations and predicting treatment outcomes in MM, although results are based on

Article Abstract

Multiple myeloma (MM) is an incurable haematological malignancy which relies heavily on bone marrow biopsies for disease monitoring and prediction of treatment response. In recent years, liquid biopsy derived cell-free DNA (cfDNA) has emerged as alternative for invasive biopsies. This pilot study aimed to evaluate the feasibility of using cfDNA for the detection of oncogenic mutations in the mitogen-activated protein kinase (MAPK) pathway genes NRAS, KRAS, and BRAF in MM patients. Matched peripheral blood and bone marrow aspirates were collected from thirteen MM patients at various disease stages. cfDNA was isolated using the Qiagen Circulating Nucleic Acid Kit while bone marrow DNA was extracted using the Maxwell Promega platform. The presence of NRAS, KRAS, and BRAF mutations was analysed by ddPCR and compared between the cfDNA and gDNA samples. Although our data come from a small patient cohort, mutations were detected, which supports cfDNA utility for mutational screening and prognostication in MM.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613886PMC
http://dx.doi.org/10.1016/j.lrr.2023.100393DOI Listing

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