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.

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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

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article

9-Deazaadenosine directly binds PYCR1 and inhibits cancer cell proliferation through disruption of NAD+ metabolism

Sung‐Kyun Ko, Jongtae Roh, In Sook Ahn, Jong‐Ryoo Choi
1 links
Translational Oncology
Histone Deacetylase Inhibitors Research
article

9-Deazaadenosine directly binds PYCR1 and inhibits cancer cell proliferation through disruption of NAD+ metabolism

Sung‐Kyun Ko, Jongtae Roh, In Sook Ahn, Jong‐Ryoo Choi
article en

Abstract

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.

Translational OncologyVol. 60
Jusung Engineering (South Korea) (KR), Korea Research Institute of Bioscience and Biotechnology (KR)
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
Zero hunger
Openalex Percentile: Top 84%
Histone Deacetylase Inhibitors Research
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9-Deazaadenosine directly binds PYCR1 and inhibits cancer cell proliferation through disruption of NAD+ metabolism — Sung‐Kyun Ko, Jongtae Roh, et al. · Translational Oncology (2025) | TGRS Research Map | TGRS