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December 8, 2025BloodOpen Access

Single-cell DNA sequencing uncovers synergistic co-mutations in multiple myeloma

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Authors

ELElizabeth LyubchenkoSFStephanie FernandesMKMarcella Kaddoura

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Overview

Single-cell DNA sequencing uncovers somatic mutations in multiple myeloma, suggesting genomic factors may influence treatment resistance.

Key Points

  • To investigate the co-occurrence of somatic mutations within individual multiple myeloma cells using single-cell DNA sequencing.
  • Collected bone marrow aspirates from 46 patients with multiple myeloma (newly diagnosed and relapsed).
  • Enriched CD138⁺ plasma cells through magnetic-activated cell sorting for detailed analysis.
  • Utilized single-cell DNA sequencing to profile genomic and proteomic characteristics.
  • Conducted variant allele frequency comparisons between tumor and reference cells.
  • Identified multiple somatic mutations, including common alterations in TP53.
  • Revealed co-occurring mutations that suggest treatment-driven selection pressures in tumor cells.
  • Documented divergent mutations in subclonal populations, indicating complex evolutionary dynamics.

Cite This Study

Lyubchenko et al. (2025) studied this question.

synapsesocial.com/papers/69362f5a4fa91c937236db66https://doi.org/10.1182/blood-2025-2157
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