BMC CancerBioinformaticsPeer-reviewed journal article
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Noah BerlowiD, Rishi Raj RikhiiD, Mathew N. GeltzeileriD, Jinu AbrahamiD, Matthew N. SvalinaiD, Lara Emily DavisiD, Erin Wise, Maria ManciniiD, Jonathan Christopher NoujaimiD, Atiya MansooriD, Michael J. Quist, Kevin L. Matlock, Martin W. GorosiD, Brian S. HernandeziD, Yee C. Doung, Khin ThwayiD, Tomohide TsukaharaiD, Jun NishioiD, Elaine HuangiD, Susan D. AirhartiD, Carol J. BultiD, Regina F. Gandour‐EdwardsiD, Robert G. MakiiD, Robin L. JonesiD, Joel Edmund MichalekiD, , Charles KelleriD
Abstract
Cancer patients with advanced disease exhaust available clinical regimens and lack actionable genomic medicine results, leaving a large patient population without effective treatments options when their disease inevitably progresses. To address the unmet clinical need for evidence-based therapy assignment when standard clinical approaches have failed, we have developed a probabilistic computational modeling approach which integrates sequencing data with functional assay data to develop patient-specific combination cancer treatments. This computational modeling approach addresses three major challenges in personalized cancer therapy, which we validate across multiple species via computationally-designed personalized synergistic drug combination predictions, identification of unifying therapeutic targets to overcome intra-tumor heterogeneity, and mitigation of cancer cell resistance and rewiring mechanisms. These proof-of-concept studies support the use of an integrative functional approach to personalized combination therapy prediction for the population of high-risk cancer patients lacking viable clinical options and without actionable DNA sequencing-based therapy.
- organism: mouse
- assay: bulk RNA-seq
- research focus: drug response / drug discovery
- approach: statistical model
- Citations
- 21
- FWCI
- 2.39
- Field percentile
- top 11%
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