Genetic Dissection of Therapeutic Intervention Targets in Triple Negative Breast CancerPublic Deposited
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MLAMaxfield, Kimberly. Genetic Dissection of Therapeutic Intervention Targets In Triple Negative Breast Cancer. Chapel Hill, NC: University of North Carolina at Chapel Hill Graduate School, 2015. https://doi.org/10.17615/6h87-cq39
APAMaxfield, K. (2015). Genetic Dissection of Therapeutic Intervention Targets in Triple Negative Breast Cancer. Chapel Hill, NC: University of North Carolina at Chapel Hill Graduate School. https://doi.org/10.17615/6h87-cq39
ChicagoMaxfield, Kimberly. 2015. Genetic Dissection of Therapeutic Intervention Targets In Triple Negative Breast Cancer. Chapel Hill, NC: University of North Carolina at Chapel Hill Graduate School. https://doi.org/10.17615/6h87-cq39
- Last Modified
- March 19, 2019
- Affiliation: School of Medicine, Department of Pharmacology
- Triple negative breast cancer (TNBC) is the most aggressive and metastatic type of breast cancer, accounting for 20% of all breast cancer diagnoses. Currently, there are no TNBC-specific targeted therapies in the clinic and therefore, broad-spectrum cytotoxic chemotherapeutic regimens remain the standard of care. Due to high rates of innate drug resistance, many TNBC patients do not respond to these regimens and, therefore, have no other therapeutic options. Our group employed a pan-genomic loss of function screen to systematically dissect the molecular architecture that functionally supports TNBC to uncover new therapeutic entry points. We further applied a paclitaxel-based synthetic lethal approach to increase our discovery space to also identify those molecular components that modulate chemoresponsiveness. To encompass the heterogeneity found within the TNBC patient population, we screened four triple negative tumor-derived breast cancer cell lines that represent the spectrum of TNBC oncogenic aberrations and chemoresponse profiles. We also accounted for the two molecular subtypes, claudin-low and basal-like that comprise the majority of TNBC cases. These screens revealed a number of core modulators of tumor cell viability and paclitaxel-induced cellular stress that have not been previously appreciated for supporting TNBC biology at the cell autonomous level. In particular, this strategy implicated the signaling supported by the cytokine receptor, CXCR3, and its ligand, CXCL9, to promote mitotic fidelity and tumor cell survival in the basal-like TNBC molecular subtype. In addition, we uncovered a requirement for the AMPK family member, SIK2, as a key nutrient sensor that may inhibit excessive autophagy. Inhibition of SIK2 enhanced autophagic flux and a loss of cell viability in a variety of TNBC genetic backgrounds. Finally, we discovered that cancer testes antigen transcription factor, ZNF165, directly repressed expression of negative TGFβ regulators thereby specifying a pro-tumorigenic TGFβ gene expression profile. Given that the expression of ZNF165 is otherwise restricted to the male testes, ZNF165 may represent a mechanism by which tumors engage anomaly-expressed proteins to promote survival. Taken together, our screening approach uncovered novel TNBC tumor cell vulnerabilities that identified cellular processes that could lead to new therapeutic approaches.
- Date of publication
- December 2015
- Resource type
- Rights statement
- In Copyright
- Whitehurst, Angelique
- Baldwin, Albert
- Perou, Charles
- McLeod, Howard L.
- Sondek, John
- Johnson, Gary
- Doctor of Philosophy
- Degree granting institution
- University of North Carolina at Chapel Hill Graduate School
- Graduation year
- Place of publication
- Chapel Hill, NC
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