Abstract
dc:description.abstract<p>The integrated stress response (ISR) is a highly conserved pathway that senses diverse stresses and responds by limiting total protein synthesis and redirecting translation to stress response transcripts. The ISR has the potential to modify a broad range of processes in cancer, but the major cancer-relevant functions of the pathway have remained elusive due to the complex and redundant nature of the upstream kinases that sense stress and activate the pathway. To overcome this challenge, we genetically targeted the central, regulatory node of the pathway, eIF2α-serine 51, directly, in primary squamous cell carcinoma cells to generate "ISR-null" SCCs. We surprisingly found that the ISR acted as a tumor suppressor early in tumorigenesis, but also promoted proteostasis in response to the chemotherapy and proteasome inhibitor, bortezomib. We found this second finding to be mechanistically linked to a previously-undescribed role for the ISR in regulating the microtubule cytoskeleton to promote the removal of aggregated proteins. As a second goal of this project we sought to develop small molecule inhibitors of the ISR for anticancer therapy, focusing on the alternative translation initiation factor, EIF2A, which we previously found to be critical for oncogenesis. Utilizing dual luciferase reporters for alternative translation (Atf4-firefly) and housekeeping translation (HBB-renilla) we performed a high throughput screen and have identified promising hits with potential as novel EIF2A inhibitors. </p>
Degree
thesis:*- Name thesis:degree_name
- Doctor of Philosophy (PhD)
- Level thesis:degree_level
- Thesis
- Year
- 2022
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Hurwitz, Brian
- Contributors dc:contributor
-
- Elaine Fuchs
Subjects
dc:subject × 7Identifiers
dc:identifier.*- Repository record dc:identifier
- https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/665
- OAI identifier oai:identifier
- oai:digitalcommons.rockefeller.edu:student_theses_and_dissertations-1656