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Project Details
Description
PROJECT SUMMARY
Patients with aggressive cancers often present with no pharmacologically actionable mutations and poor or no
sensitivity to immune checkpoint blockade, thus deriving only modest improvement in disease-free survival from
targeted therapy and immunotherapy. Tumor heterogeneity adds further complexity by fostering reprogramming,
adaptation, selection, and ultimately expansion of drug-resistant cells, as well as emergence of an
immunosuppressive tumor microenvironment (TME), both of which are ultimately responsible for patient relapse
and poor outcome. Addressing these challenges—i.e., identifying more universal, mechanism-based targets for
pharmacological intervention and assessing their potential value in highly heterogeneous tumors—is critically
dependent on the availability of accurate, comprehensive, and cell type-specific molecular interaction networks
(cellular networks, hereafter), which underlie both the cell-autonomous behavior of cancer cells and their
interaction with other TME subpopulations. The proposed Cancer Systems Therapeutics (CaST) Center, will
continue its highly productive collaboration within the U54 Cancer Systems Biology Center (CSBC) network by
extending its successful network-based methodologies—which integrate cutting edge computational advances
and novel experimental technologies, including use of 3D structure and multi-omics-based evidence. This will
support studying cancer as a fully integrated system of co-evolving, interacting subpopulations, comprising both
molecularly distinct, coexisting malignant cell states as well as non-malignant cell states recruited to the tumor
microenvironment and potentially reprogrammed to implement a pro-malignant, immunosuppressive milieu. The
ultimate goal of this proposal is to leverage recent advances by CaST center investigators to elucidate the
Mechanism of Action of clinically relevant drugs and late-stage experimental compounds to target individual
subpopulation to either drive combination therapy or to rescue immunotherapy in drug resistant tumors.
Status | Finished |
---|---|
Effective start/end date | 9/19/23 → 8/31/24 |
ASJC Scopus Subject Areas
- Cancer Research
- Oncology
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Projects
- 6 Finished
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Single-Cell, Spatial and Functional Dissection of Cancer Cell States, Co-Evolving Ecosystems, and Vulnerabilities During Tumor Progression and Metastasis
Izar, B. (PI)
9/1/23 → 8/31/24
Project: Research project
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Drug Mechanism of Action-based targeting of tumor subpopulations
Califano, A. A. (PI)
9/1/23 → 8/31/24
Project: Research project