9-Deazaadenosine directly binds PYCR1 and inhibits cancer cell proliferation through disruption of NAD+ metabolism
Cancer cells exhibit abnormal proliferation and dysregulated cell cycle checkpoints. Therefore, discovering cell cycle inhibitors is a promising strategy for cancer treatment. The pyrroline-5-carboxylate reductase 1 (PYCR1) is a key enzyme that controls proline metabolism by regulating the conversion of pyrroline-5-carboxylate to proline. PYCR1 is highly expressed in various cancers, including colon cancer. In this study, we discovered a novel role of 9-deazaadenosine (9-DAA) as a cell cycle inhibitor and demonstrated that this compound directly binds to PYCR1. Our results suggest that the inhibitory effects of 9-DAA are due to nicotinamide adenine dinucleotide. We further demonstrated that PYCR1 was elevated under hypoxia and in 3D spheroids in colon cancer and that 9-DAA effectively inhibited cancer progression under cancer-mimicking conditions and in vivo.
Authors
- Sung‐Kyun Ko (ORCID: https://orcid.org/0000-0002-8202-1205)
- Jongtae Roh (ORCID: https://orcid.org/0000-0003-1114-8580)
- In Sook Ahn
- Jong‐Ryoo Choi
Institutions
- Jusung Engineering (South Korea) (KR)
- Korea Research Institute of Bioscience and Biotechnology (KR)
Publication Details
- Journal
- Translational Oncology
- Published
- 2025-07-24
- DOI
- https://doi.org/10.1016/j.tranon.2025.102478
- Primary Topic
- Histone Deacetylase Inhibitors Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministry of Science, ICT and Future Planning
- Korea Research Institute of Bioscience and Biotechnology
- National Research Foundation of Korea
- National Research Council of Science and Technology