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RUVBL1/RUVBL2 ATPase Activity Drives PAQosome Maturation, DNA Replication and Radioresistance in Lung Cancer
- Source :
- Cell Chem Biol
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- Summary RUVBL1 and RUVBL2 (collectively RUVBL1/2) are essential AAA+ ATPases that function as co-chaperones and have been implicated in cancer. Here we investigated the molecular and phenotypic role of RUVBL1/2 ATPase activity in non-small cell lung cancer (NSCLC). We find that RUVBL1/2 are overexpressed in NSCLC patient tumors, with high expression associated with poor survival. Utilizing a specific inhibitor of RUVBL1/2 ATPase activity, we show that RUVBL1/2 ATPase activity is necessary for the maturation or dissociation of the PAQosome, a large RUVBL1/2-dependent multiprotein complex. We also show that RUVBL1/2 have roles in DNA replication, as inhibition of its ATPase activity can cause S-phase arrest, which culminates in cancer cell death via replication catastrophe. While in vivo pharmacological inhibition of RUVBL1/2 results in modest antitumor activity, it synergizes with radiation in NSCLC, but not normal cells, an attractive property for future preclinical development.
- Subjects :
- DNA Replication
Lung Neoplasms
Multiprotein complex
ATPase
Clinical Biochemistry
Antineoplastic Agents
Biology
Radiation Tolerance
01 natural sciences
Biochemistry
Article
Carcinoma, Non-Small-Cell Lung
Radioresistance
Drug Discovery
RUVBL2
medicine
Humans
Enzyme Inhibitors
Lung cancer
Molecular Biology
Pharmacology
Molecular Structure
010405 organic chemistry
DNA Helicases
DNA replication
medicine.disease
Phenotype
0104 chemical sciences
Multiprotein Complexes
Cancer cell
biology.protein
Cancer research
ATPases Associated with Diverse Cellular Activities
Molecular Medicine
Carrier Proteins
Subjects
Details
- ISSN :
- 24519456
- Volume :
- 27
- Database :
- OpenAIRE
- Journal :
- Cell Chemical Biology
- Accession number :
- edsair.doi.dedup.....9c145330326ced598cd01d78c09569ea
- Full Text :
- https://doi.org/10.1016/j.chembiol.2019.12.005