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Jung Yun Kim

As seen in: Nature, PLOS ONE, MDPI, Cell Press
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Articles

Disruption of WNT/Notch signaling in pancreatic cancer reveals tumors depend on the intricate equilibrium of malignant cell states

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By Stefan R. Torborg, Jung Yun Kim, Anupriya Singhal, Olivera Grbovic-Huezo, Matilda Friberg Holm, Katherine J. Wu Verified, Xuexiang Han, Yu-Jui Ho, Caj Haglund, Michael Mitchell, Scott Lowe, Lukas Dow, Kenneth L Pitter, Francisco J. Sanchez-Rivera, Andre Levchenko, Tuomas Tammela
| Cell Press Verified
Keywords intratumoral heterogeneity pancreas cancer tissue organization lineage tracing lineage ablation WNT Notch gene perturbation Get full text access Log in, subscribe or purchase for full access. References 1. Barker, N. ∙ Clevers, H. Leucine-rich repeat-containing G-protein-coupled receptors as markers of adult stem cells Gastroenterology. 2010; 138:1681-1696 2. Murtaugh, L.C. ∙ Keefe, M.D. Regeneration and repair of the exocrine pancreas Annu. Rev. Physiol. 2015; 77:229-249 3. Ge, Y. ∙ Fuchs, E.
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Cancer-wide in silico analyses using differentially expressed genes demonstrate the functions and clinical relevance of JAG, DLL, and NOTCH

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By Jung Yun Kim, Nayoung Hong, Sehyeon Park, Sunyoung Seo
| PLOS ONE
Loading metrics Open Access Peer-reviewed Research Article Citation: Kim JY, Hong N, Ham SW, Park S, Seo S, Kim H (2024) Cancer-wide in silico analyses using differentially expressed genes demonstrate the functions and clinical relevance of JAG, DLL, and NOTCH. PLoS ONE 19(7): e0307943. https://doi.org/10.1371/journal.pone.0307943 Editor: Kenji Tanigaki, Shiga Medical Center, JAPAN Received: November 13, 2023; Accepted: July 16, 2024; Published: July 29, 2024 Copyright: © 2024 Kim et al.
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Jagged1 intracellular domain/SMAD3 complex transcriptionally regulates TWIST1 to drive glioma invasion - Cell Death & Disease

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By Jung Yun Kim, Jong-Whi Park
| Nature Verified
Abstract Jagged1 (JAG1) is a Notch ligand that correlates with tumor progression. Not limited to its function as a ligand, JAG1 can be cleaved, and its intracellular domain translocates to the nucleus, where it functions as a transcriptional cofactor. Previously, we showed that JAG1 intracellular domain (JICD1) forms a protein complex with DDX17/SMAD3/TGIF2. However, the molecular mechanisms underlying JICD1-mediated tumor aggressiveness remains unclear.
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