The Role of RUVBL1/RUVBL2 and Their Potential as Therapeutic Targets in Non-Small Cell Lung Cancer
| dc.contributor.advisor | DeBerardinis, Ralph J. | en |
| dc.contributor.committeeMember | Minna, John D. | en |
| dc.contributor.committeeMember | Kittler, Ralf | en |
| dc.contributor.committeeMember | Mangelsdorf, David J. | en |
| dc.contributor.committeeMember | Kraus, W. Lee | en |
| dc.creator | Yenerall, Paul Matthew, II | en |
| dc.creator.orcid | 0000-0003-3912-0571 | |
| dc.date.accessioned | 2021-09-17T18:00:02Z | |
| dc.date.available | 2021-09-17T18:00:02Z | |
| dc.date.created | 2019-08 | |
| dc.date.issued | 2019-07-31 | |
| dc.date.submitted | August 2019 | |
| dc.date.updated | 2021-09-17T18:00:02Z | |
| dc.description.abstract | Behind heart disease, cancer is the leading cause of death today in Americans. Among cancers, lung cancer is the deadliest, killing as many individuals as next 3 most lethal cancer types combined. Approximately 80% of lung cancers are a type known as non-small cell lung cancer (NSCLC), and despite numerous advances in the treatment of NSCLC, only 18% of all NSCLC patients live 5 years after their initial diagnosis. To identify new therapeutic targets in NSCLC, we performed a viability-based RNA interference (RNAi) screen targeting nuclear receptors, their coregulators and chromatin remodelers. This screen identified RUVBL1 and RUVBL2 (collectively referred to as RUVBL1/2) as differentially required for the viability of NSCLC. We show that RUVBL1/2 require their ATPase activity to support NSCLC viability and have developed an orally bioavailable, potent and specific inhibitor of RUVBL1/2 ATPase activity, known as Compound B. Multiple unbiased analyses suggested that RUVBL1/2 may have roles in DNA replication in NSCLC, and inhibition or depletion of RUVBL1/2 in sensitive NSCLC lines delays S-phase progression and ultimately results in cancer cell death via replication catastrophe. While Compound B treatment in vivo produces modest anti-tumor activity, only a subset of NSCLC cell lines show a therapeutically meaningful response. To enhance the efficacy of Compound B, we searched for therapies that may synergize with Compound B. Various analyses indicated that RUVBL1/2 may have roles in the response to ionizing radiation (IR), and indeed, genetic depletion or pharmacological inhibition of RUVBL1/2 radiosensitized NSCLC cell lines and patient tumors both in vitro and in vivo. Interestingly, Compound B, did not radiosensitize models of non-transformed cells, potentially because key DNA damage proteins such as ATM and DNA-PKcs were more stable after Compound B treatment in normal cells than in tumor cells. The combined necessity of RUVBL1/2 for NSCLC viability and the recovery from radiation, specifically in tumor cells, make RUVBL1/2 an attractive target for future preclinical development as a radiosensitizer in NSCLC. | en |
| dc.format.mimetype | application/pdf | en |
| dc.identifier.oclc | 1268338270 | |
| dc.identifier.uri | https://hdl.handle.net/2152.5/9628 | |
| dc.language.iso | en | en |
| dc.subject | Carcinoma, Non-Small-Cell Lung | en |
| dc.subject | Carrier Proteins | en |
| dc.subject | DNA Helicases | en |
| dc.subject | DNA Repair | en |
| dc.subject | Lung Neoplasms | en |
| dc.title | The Role of RUVBL1/RUVBL2 and Their Potential as Therapeutic Targets in Non-Small Cell Lung Cancer | en |
| dc.type | Thesis | en |
| dc.type.material | text | en |
| thesis.degree.department | Graduate School of Biomedical Sciences | en |
| thesis.degree.discipline | Cancer Biology | en |
| thesis.degree.grantor | UT Southwestern Medical Center | en |
| thesis.degree.level | Doctoral | en |
| thesis.degree.name | Doctor of Philosophy | en |