Murie, Carl https://orcid.org/0009-0007-2565-0615
Turkarslan, Serdar
Patel, Anoop P. https://orcid.org/0000-0001-7078-9535
Coffey, David G.
Becker, Pamela S.
Baliga, Nitin S. https://orcid.org/0000-0001-9157-5974
Funding for this research was provided by:
U.S. Department of Health & Human Services | National Institutes of Health (NCI-5R01AI141953-04, NSF1565166, NCI-5R01CA259469-02, NSF2042948, NCI-5R01AI141953-04, NSF1565166, NCI-5R01CA259469-02, NSF2042948, NCI-5R01AI141953-04, NSF1565166, NCI-5R01CA259469-02, NSF2042948, NCI-5R01CA259469-02, P30 CA015704, P30 CA015704)
Washington Research Foundation
Brotman Baty Institute for for Precision Medicine Catalytic Collaboration Grant
Article History
Received: 17 July 2024
Revised: 7 February 2025
Accepted: 12 March 2025
First Online: 1 April 2025
Competing interests
: NB is a co-founder and member of the Board of Directors of Sygnomics, Inc., which will commercialize the SYGNAL technology. AP and ST have equity stakes in Sygnomics, Inc. The terms of these arrangements have been reviewed and approved by ISB and Duke University in accordance with their conflict-of-interest policies. PB received institutional research support from Glycomimetics, Pfizer, Notable labs, and is an advisor to Accordant Health Services (CVS Caremark).
: This study utilizes publicly available human RNA sequencing datasets (GSE19784, GSE24080, GSE136337) from the Gene Expression Omnibus (GEO) repository, a previously published study on ex vivo drug sensitivity profiles of CD138+ cells from bone marrow aspirates from 8 patients [] and the CoMMpass study. The data used in this study is considered not human subjects research, as it is publicly available open-access data [, , ]. All data were originally collected with appropriate ethical approval from their respective original studies and made publicly available in accordance with relevant guidelines and regulations. Informed consent was obtained from all participants by the original authors as documented in the previously published studies. The CoMMpass study (NCT01454297, dbGaP: phs000748.v7.p4) was conducted in accordance with recognized ethical guidelines in the United States and European Union and the Institutional Review Board at each participating center approved the study protocol. The CoMMpass trial is in accordance with the Declaration of Helsinki. Ex vivo drug sensitivity profiles for CD138+ cells from bone marrow aspirates of 8 (Patient IDs 9944-01, 9944-02, 9944-04, 9944-10, 9944-14, 9944-20, 9944-21, 9944-25) of the 23 patients, obtained at the Seattle Cancer Care Alliance (SCCA) on a Fred Hutchinson Cancer Center-approved IRB protocol (9944), were previously published []. The remaining 15 patients (IDs: MM26, MM48, MM59, MM68, MM80, MM83, MM84, MM137, MM144, MM154, MM160, MM173, MM184, MM194, MM209) were enrolled under a Fred Hutchinson Cancer Center-approved IRB protocol (1757). Informed consent was obtained from all participants, and all data were collected in accordance with recognized ethical guidelines. All methods in this study were conducted in accordance with the relevant guidelines and regulations (e.g., 45 CFR 46). Ethical approval for the use of data in this research was granted by the Institute of Systems Biology Compliance Manager, with the data designated as not human subjects research, as all data is de-identified and publicly accessible for the relevant datasets. Appropriate data use agreements were established for any data classified as controlled access.