Yoon Jae Kim

Dr. Yoon Jae Kim

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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24 May 2012 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
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YKYoon Jae Kim
Yoon Jae Kim
EKEun‐Hee Kim
Eun‐Hee Kim
KHKi Baik Hahm
Ki Baik Hahm

22 January 2009 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
Closed access
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JPJeong Youp Park
Jeong Youp Park
SHSung Pil Hong
Sung Pil Hong
YKYoon Jae Kim
Yoon Jae Kim
HKHong Jeoung Kim
Hong Jeoung Kim
HKHee Man Kim
Hee Man Kim
SBSeungmin Bang
Seungmin Bang

1 October 2010 in Cancer Prevention Research
Verified
Journal Article
Open access
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YKYoon Jae Kim
Yoon Jae Kim
KHKyung Sook Hong
Kyung Sook Hong
JCJun Won Chung
Jun Won Chung
JKJu Hyun Kim
Ju Hyun Kim
KHKi Baik Hahm
Ki Baik Hahm
The emergence of infliximab was an epochal event in the treatment of inflammatory bowel disease (IBD). Because colitis-associated cancers arose in the setting of chronic inflammation, during which “inflammation-dysplasia-carcinoma sequence” prevails and anti-inflammatory agents can prevent carcinogenesis, we hypothesized whether infliximab can prevent colitic cancer in animal models for which C57BL/6 mice were exposed to 15 cycles of dextran sulfate sodium (DSS), with each cycle consisting of 0.7% DSS for 1 week followed by sterilized water for 10 days. Infliximab (4 mg/kg i.v.) was given on the 1st, 3rd, and 7th weeks or 25th, 27th, and 31st weeks of cycle according to “step-up” versus “top-down” strategy. Molecular change about inflammation and carcinogenesis was compared between groups. Multiple colorectal tumors developed in 75% to 80% of control mice, whereas only 16.7% of mice treated with infliximab on the 1st, 3rd, and 7th weeks developed colon tumors. Significant decreases in tumor necrosis factor-α level, mast cell number, and the expression of inflammatory cytokines were observed in top-down strategy using infliximab. The expression and activity of matrix metalloproteinase-9 (MMP-9) and MMP-11 were significantly decreased in mice treated with infliximab accompanied with attenuated numbers of “β-catenin–accumulated crypts.” In animal group where infliximab was administered at later stage of 25th, 27th, and 31st weeks, no reduction in tumorigenesis was noted. These biological effects of infliximab were further explored in in vitro experiment using Raw264.7 and Jurkat T cells. Conclusively, earlier and intensive therapy with infliximab should be considered for either mitigating clinical course or preventing ultimate development of colitic cancer in high-risk IBD patients. Cancer Prev Res; 3(10); 1314–33. ©2010 AACR.

1 January 2016 in World Journal of Gastroenterology
Verified
Journal Article
Open access
EKEui Joo Kim
Eui Joo Kim
YKYoon Jae Kim
Yoon Jae Kim
Since the development of uncovered self-expanding metal stents (SEMS) in the 1990s, endoscopic stents have evolved dramatically. Application of new materials and new designs has expanded the indications for enteral SEMS. At present, enteral stents are considered the first-line modality for palliative care, and numerous types of enteral stents are under development for extended clinical usage, beyond a merely palliative purpose. Herein, we will discuss the current status and the future development of lower enteral stents.

1 June 2009 in Gastrointestinal Endoscopy
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Journal Article
Closed access
JCJae Hee Cho
Jae Hee Cho
JPJeong Youp Park
Jeong Youp Park
YKYoon Jae Kim
Yoon Jae Kim
HKHee Man Kim
Hee Man Kim
HKHong Jeong Kim
Hong Jeong Kim
SBSeungmin Bang
Seungmin Bang

29 October 2012 in Journal of Gastroenterology and Hepatology
Verified
Journal Article
Closed access
PDF file
JCJun-Won Chung
Jun-Won Chung
YJYoung Kul Jung
Young Kul Jung
YKYoon Jae Kim
Yoon Jae Kim
KKKwang Ahn Kwon
Kwang Ahn Kwon
JKJung Ho Kim
Jung Ho Kim
SYSung‐Cheol Yun
Sung‐Cheol Yun