4.8 Article

Determining therapeutic susceptibility in multiple myeloma by single-cell mass accumulation

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-01593-2

Keywords

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Funding

  1. US National Institutes of Health [R33 CA191143, PO1-155258, P50-100707]
  2. Cancer Center Support (core) Grant [P30 CA14051]
  3. Cancer Systems Biology Consortium from the National Cancer Institute [U54 CA217377]
  4. Department of Veterans Affairs Merit Review Award [1 I01BX001584-01]
  5. Koch Institute for Integrative Cancer Research at MIT
  6. Dana-Farber/Harvard Cancer Center (D.F./H.C.C.)
  7. Koch Institute Quinquennial Cancer Research fellowship

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Multiple myeloma (MM) has benefited from significant advancements in treatment that have improved outcomes and reduced morbidity. However, the disease remains incurable and is characterized by high rates of drug resistance and relapse. Consequently, methods to select the most efficacious therapy are of great interest. Here we utilize a functional assay to assess the ex vivo drug sensitivity of single multiple myeloma cells based on measuring their mass accumulation rate (MAR). We show that MAR accurately and rapidly defines therapeutic susceptibility across human multiple myeloma cell lines to a gamut of standard-of-care therapies. Finally, we demonstrate that our MAR assay, without the need for extended culture ex vivo, correctly defines the response of nine patients to standard-of-care drugs according to their clinical diagnoses. This data highlights the MAR assay in both research and clinical applications as a promising tool for predicting therapeutic response using clinical samples.

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