Jin Sung Kim

Dr. Jin Sung Kim


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 March 2012 in Nucleic Acids Research
Verified
Journal Article
Open access
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JSJungmin Seo
Jungmin Seo
SKSang Cheol Kim
Sang Cheol Kim
HLHeun-Sik Lee
Heun-Sik Lee
JKJung Kyu Kim
Jung Kyu Kim
HSHye Jin Shon
Hye Jin Shon
JCJung Kyoon Choi
Jung Kyoon Choi
Phosphorylation of the histone variant H2AX forms γ-H2AX that marks DNA double-strand break (DSB). Here, we generated the sequencing-based maps of H2AX and γ-H2AX positioning in resting and proliferating cells before and after ionizing irradiation. Genome-wide locations of possible endogenous and exogenous DSBs were identified based on γ-H2AX distribution in dividing cancer cells without irradiation and that in resting cells upon irradiation, respectively. γ-H2AX-enriched regions of endogenous origin in replicating cells included sub-telomeres and active transcription start sites, apparently reflecting replication- and transcription-mediated stress during rapid cell division. Surprisingly, H2AX itself, prior to phosphorylation, was specifically located at these endogenous hotspots. This phenomenon was only observed in dividing cancer cells but not in resting cells. Endogenous H2AX was concentrated on the transcription start site of actively transcribed genes but was irrelevant to pausing of RNA polymerase II (pol II), which precisely coincided with γ-H2AX of endogenous origin. γ-H2AX enrichment upon irradiation also coincided with actively transcribed regions, but unlike endogenous γ-H2AX, it extended into the gene body and was not specifically concentrated on the pausing site of pol II. Sub-telomeres were less responsive to external DNA damage than to endogenous stress. Our findings provide insight into DNA repair programs of cancer and may have implications for cancer therapy.

24 October 2024 in Nature Communications
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Journal Article
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YOYujin Oh
Yujin Oh
SPSangjoon Park
Sangjoon Park
HBHwa Kyung Byun
Hwa Kyung Byun
YCYeona Cho
Yeona Cho
ILIk Jae Lee
Ik Jae Lee
JYJong Chul Ye
Jong Chul Ye
Target volume contouring for radiation therapy is considered significantly more challenging than the normal organ segmentation tasks as it necessitates the utilization of both image and text-based clinical information. Inspired by the recent advancement of large language models (LLMs) that can facilitate the integration of the textural information and images, here we present an LLM-driven multimodal artificial intelligence (AI), namely LLMSeg, that utilizes the clinical information and is applicable to the challenging task of 3-dimensional context-aware target volume delineation for radiation oncology. We validate our proposed LLMSeg within the context of breast cancer radiotherapy using external validation and data-insufficient environments, which attributes highly conducive to real-world applications. We demonstrate that the proposed multimodal LLMSeg exhibits markedly improved performance compared to conventional unimodal AI models, particularly exhibiting robust generalization performance and data-efficiency.

1 December 2020 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
MCMin Seo Choi
Min Seo Choi
BCByeong Su Choi
Byeong Su Choi
SCSeung Yeun Chung
Seung Yeun Chung
NKNalee Kim
Nalee Kim
JCJaehee Chun
Jaehee Chun
JKJin Sung Kim
Jin Sung Kim

13 January 2022 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
YCYeona Cho
Yeona Cho
YKYejin Kim
Yejin Kim
ICIbrahim Chamseddine
Ibrahim Chamseddine
WLWon Hee Lee
Won Hee Lee
HKHye Ryun Kim
Hye Ryun Kim
CGClemens Grassberger
Clemens Grassberger

25 February 2021 in Radiation Oncology
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Journal Article
Open access
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SCSeung Yeun Chung
Seung Yeun Chung
JCJeesuk Chang
Jeesuk Chang
MCMin Seo Choi
Min Seo Choi
YCYongjin Chang
Yongjin Chang
BCByong Su Choi
Byong Su Choi
YKYong Bae Kim
Yong Bae Kim
Background: In breast cancer patients receiving radiotherapy (RT), accurate target delineation and reduction of radiation doses to the nearby normal organs is important. However, manual clinical target volume (CTV) and organs-at-risk (OARs) segmentation for treatment planning increases physicians’ workload and inter-physician variability considerably. In this study, we evaluated the potential benefits of deep learning-based auto-segmented contours by comparing them to manually delineated contours for breast cancer patients. Methods: CTVs for bilateral breasts, regional lymph nodes, and OARs (including the heart, lungs, esophagus, spinal cord, and thyroid) were manually delineated on planning computed tomography scans of 111 breast cancer patients who received breast-conserving surgery. Subsequently, a two-stage convolutional neural network algorithm was used. Quantitative metrics, including the Dice similarity coefficient (DSC) and 95% Hausdorff distance, and qualitative scoring by two panels from 10 institutions were used for analysis. Inter-observer variability and delineation time were assessed; furthermore, dose-volume histograms and dosimetric parameters were also analyzed using another set of patient data. Results: The correlation between the auto-segmented and manual contours was acceptable for OARs, with a mean DSC higher than 0.80 for all OARs. In addition, the CTVs showed favorable results, with mean DSCs higher than 0.70 for all breast and regional lymph node CTVs. Furthermore, qualitative subjective scoring showed that the results were acceptable for all CTVs and OARs, with a median score of at least 8 (possible range: 0–10) for (1) the differences between manual and auto-segmented contours and (2) the extent to which auto-segmentation would assist physicians in clinical practice. The differences in dosimetric parameters between the auto-segmented and manual contours were minimal. Conclusions: The feasibility of deep learning-based auto-segmentation in breast RT planning was demonstrated. Although deep learning-based auto-segmentation cannot be a substitute for radiation oncologists, it is a useful tool with excellent potential in assisting radiation oncologists in the future. Trial registration Retrospectively registered.

1 January 2015 in Radiation Oncology Journal
Verified
Journal Article
Open access
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KCKwangzoo Chung
Kwangzoo Chung
YHYoungyih Han
Youngyih Han
JKJin Sung Kim
Jin Sung Kim
SASung Hwan Ahn
Sung Hwan Ahn
SJSang Gyu Ju
Sang Gyu Ju
DCDoo Ho Choi
Doo Ho Choi
Chung K, et al. Radiat Oncol J. 2015 Dec;33(4):337-343. http://dx.doi.org/10.3857/roj.2015.33.4.337