Seong-taek Oh

Dr. Seong-taek Oh

Division of Coloproctology, Department of Surgery, Uijeongbu St. Mary’s Hospital, College of Medicine The Catholic University of Korea, Seoul, Korea

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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1 January 2014 in Annals of Surgical Treatment and Research
Verified
Journal Article
Open access
SKSeung-Jin Kwag
Seung-Jin Kwag
JKJun-Gi Kim
Jun-Gi Kim
WKWon-Kyung Kang
Won-Kyung Kang
JLJin-Kwon Lee
Jin-Kwon Lee
SOSeong-taek Oh
Seong-taek Oh
The authors evaluate the prevalence of malnutrition and its effect on the postoperative morbidity of patients after surgery for colorectal cancer. Three hundred fifty-two patients were enrolled prospectively. Nutritional risk screening 2002 (NRS 2002) score was calculated through interview with patient on admission. Clinical characteristics, tumor status and surgical procedure were recorded. The prevalence of patients at nutritional risk was 28.1 per cent according to the NRS 2002. The rate of postoperative complication was 27%. There was a significant difference in postoperative complication rates between patients at nutritional risk and those not at risk (37.4% vs. 22.9%, P = 0.006). Nutritional risk was identified as an independent predictor of postoperative complications (odds ratio, 3.05; P = 0.045). Nutritional risk increased the rate of anastomotic leakage (P = 0.027) and wound infection (P = 0.01). NRS may be a prognostic factor for postoperative complication after surgery for colorectal cancer. A large scaled prospective study is needed to confirm whether supplementing nutritional deficits reduces postoperative complication rates.

22 January 2015 in BMC Gastroenterology
Verified
Journal Article
Open access
PDF file
WKWon Kyung Kang
Won Kyung Kang
JLJin Kwon Lee
Jin Kwon Lee
SOSeong-taek Oh
Seong-taek Oh
SLSung Hak Lee
Sung Hak Lee
Chan Kwon JungChan Kwon Jung
Chan Kwon Jung
MicroRNA-21 (miR-21) is an oncogenic microRNA that regulates the expression of multiple cancer-related target genes. miR-21 has been associated with progression of some types of cancer. Metastasis-associated protein1 expression and loss of E-cadherin expression are correlated with cancer progression and metastasis in many cancer types. In advanced colorectal cancer, the clinical significance of miR-21 expression remains unclear. We aimed to investigate the impact of miR-21 expression in advanced colorectal cancer and its correlation with target proteins associated with colorectal cancer progression. From 2004 to 2007, 277 consecutive patients with T3-4a colorectal cancer treated with R0 surgical resection were included. Patients with neoadjuvant therapy and distant metastasis at presentation were excluded. The expression of miR-21 was investigated by in situ hybridization. Immunohistochemistry was used to detect E-cadherin and metastasis-associated protein1 expression. High stromal expression of miR-21 was found in 76 of 277 (27.4%) colorectal cancer samples and was correlated with low E-cadherin expression (P = 0.019) and high metastasis-associated protein1 expression (P = 0.004). T3-4a colorectal cancer patients with high miR-21 expression had significantly shorter recurrence-free survival than those with low miR-21 expression. When analyzing colon and rectal cancer separately, high expression of miR-21 was an independent prognostic factor of unfavorable recurrence-free survival in T3-4a colon cancer patients (P = 0.038, HR = 2.45; 95% CI = 1.05-5.72) but not in T3-4a rectal cancer patients. In a sub-classification analysis, high miR-21 expression was associated with shorter recurrence-free survival in the stage II cancer (P = 0.001) but not in the stage III subgroup (P = 0.267). Stromal miR-21 expression is related to the expression of E-cadherin and metastasis-associated protein1 in colorectal cancer. Stage II colorectal cancer patients with high levels of miR-21 are at higher risk for tumor recurrence and should be considered for more intensive treatment.

24 February 2014 in BMC Cancer
Verified
Journal Article
Open access
PDF file
MLMyung Ah Lee
Myung Ah Lee
JPJin-Hee Park
Jin-Hee Park
SRSi Young Rhyu
Si Young Rhyu
SOSeong-taek Oh
Seong-taek Oh
WKWon-Kyoung Kang
Won-Kyoung Kang
HKHee-Na Kim
Hee-Na Kim
The wnt/β-catenin signaling pathway is known to affect in cancer oncogenesis and progression by interacting with the tumor microenvironment. However, the roles of wnt3a and wnt5a in colorectal cancer (CRC) have not been thoroughly studied. In the present study, we investigated the expression of wnt protein and the concordance rate in primary tumor and metastatic sites in CRC. To determine the relationship of wnt proteins with invasion related protein, we also analyzed the association between wnt protein expression and the expression of matrix metalloproteinase-9 (MMP-9) and vascular endothelial growth factor receptor-2 (VEGFR-2).

16 April 2010 in Surgical Endoscopy
Verified
Journal Article
Closed access
PDF file
HKHyung Jin Kim
Hyung Jin Kim
JLJae Im Lee
Jae Im Lee
YLYoon Suk Lee
Yoon Suk Lee
ILIn Kyu Lee
In Kyu Lee
JPJung Hyun Park
Jung Hyun Park
SOSeong-taek Oh
Seong-taek Oh

1 September 2006 in International Journal of Colorectal Disease
Verified
Journal Article
Closed access
PDF file
ILIn Kyu Lee
In Kyu Lee
NSNa Young Sung
Na Young Sung
YLYoon Suk Lee
Yoon Suk Lee
SLSang Chul Lee
Sang Chul Lee
WKWon Kyung Kang
Won Kyung Kang
SCSuk Kyun Chang
Suk Kyun Chang

31 January 2012 in Colorectal Disease
Verified
Journal Article
Closed access
PDF file
BKB.‐H. Kye
B.‐H. Kye
HKH. J. Kim
H. J. Kim
WKW. K. Kang
W. K. Kang
HCH.‐M. Cho
H.‐M. Cho
YHY.‐K. Hong
Y.‐K. Hong
SOSeong-taek Oh
Seong-taek Oh