Jin-Haeng Chung
Seoul National University · Medicine
About the Lab
Professor Jin-Haeng Chung's research lab specializes in translational lung cancer research, focusing on the molecular and immunological characterization of non-small cell lung cancer (NSCLC). The lab investigates biomarkers such as PD-L1 protein and mRNA expression, explores the correlation between histomorphological features and genetic alterations (e.g., ALK rearrangements), and evaluates the reliability and interchangeability of PD-L1 immunohistochemistry assays across different clones and platforms. Their work aims to improve patient stratification for immune checkpoint inhibitor therapy and enhance the accuracy of mediastinal staging using PET imaging and pathological correlation.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Blockade of the programmed cell death-1 (PD-1) axis has already been established as an effective treatment of non-small cell lung cancer. Immunohistochemistry (IHC) for programmed death-ligand 1 (PD-L1) protein is the only available biomarker that can guide treatment with immune checkpoint inhibitors in non-small cell lung cancer. Because each PD-1/PD-L1 blockade was approved together with a specific PD-L1 IHC assay used in the clinical trials, pathologists have been challenged with performing v
UNLABELLED: The evaluation of mediastinal lymph node involvement in non-small cell lung carcinoma (NSCLC) is very important for the selection of surgical candidates. PET using (18)F-FDG has remarkably improved mediastinal staging in NSCLC. However, false (18)F-FDG PET results remain a problem. This study was undertaken to identify histologic and immunohistochemical differences between cases showing false and true results of mediastinal lymph node involvement assessed by (18)F-FDG PET. METHODS: P
Molecular classification of lung cancer correlates well with histomorphological features. However, specific histomorphological features that differentiate anaplastic lymphoma kinase (ALK)-rearranged tumors from ALK-negative tumors have not been fully evaluated. Eighty ALK-rearranged and 213 ALK-negative (91 epidermal growth factor receptor-mutated; 29 K-ras-mutated; 93 triple-negative) resected lung adenocarcinomas were analyzed for several histomorphological parameters and histological subtype.
Research Areas
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