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박중진 교수

Jung-jin Park

고려대학교 의학과 · 생화학·유전·분자생물학

연구실 소개

박중진 교수의 연구실은 당뇨병, 암 전이 및 근육 형성과 관련된 세포 신호 전달 경로를 중심으로, 당단백질의 글리코실화 조절, 미토콘드리아 생합성, 그리고 단백질 유비퀴틴화 메커니즘을 규명하고 있습니다. 특히 결장암에서의 ST6Gal I 효소 활성과 그가 유도하는 세포 표면 당단백질의 사일릴화가 전이 및 방사선 저항성에 미치는 영향을 집중적으로 연구하고 있으며, 이와 관련된 신호 분자들인 인테그린 β1, AKT, SIRT1 등에 대한 기전적 분석을 수행하고 있습니다. 또한, 근육에서 인슐린 수용체 신호 전달을 조절하는 MG53-IRS-1 상호작용을 억제하는 약물 후보를 발굴하는 데에도 기여하고 있습니다.

글리코실화암 전이ST6Gal I미토콘드리아 생합성인슐린 신호 전달

연구 현황

논문 수
11
총 인용 수
485
최근 5년 논문
8
주요 분야
생화학·유전·분자생물학

연구 성과 추이

표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.

5개년 연도별 논문 게재 수
8총합
2010
2012
2013
2014
2016
5개년 연도별 피인용 수
467총합
20102012201320142016

주요 논문

11
1
논문|인용수 128·2012
Sialylation of epidermal growth factor receptor regulates receptor activity and chemosensitivity to gefitinib in colon cancer cells
Jung-Jin Park, Jae Youn Yi, Yeung Bae Jin, Yoon-Jin Lee, Jae‐Seon Lee, Yun‐Sil Lee, Young‐Gyu Ko, Min Young Lee
SJR Q1Biochemical Pharmacology
Molecular BiologyBiochemistry, Genetics and Molecular Biology
2
리뷰|인용수 119·2013
Increasing the α 2, 6 Sialylation of Glycoproteins May Contribute to Metastatic Spread and Therapeutic Resistance in Colorectal Cancer
Jung-Jin Park, Min‐Young Lee
SJR Q1Gut and LiverOA

Abnormal glycosylation due to dysregulated glycosyltransferases and glycosidases is a key phenomenon of many malignancies, including colorectal cancer (CRC). In particular, increased ST6 Gal I (β-galactoside α 2, 6 sialyltransferase) and subsequently elevated levels of cell-surface α 2, 6-linked sialic acids have been associated with metastasis and therapeutic failure in CRC. As many CRC patients experience metastasis to the liver or lung and fail to respond to curative therapies, intensive rese

Molecular BiologyBiochemistry, Genetics and Molecular Biology
3
논문|인용수 88·2012
Berberine inhibits human colon cancer cell migration via AMP-activated protein kinase-mediated downregulation of integrin β1 signaling
Jung-Jin Park, Seon-Mi Seo, Eun Ju Kim, Yoon-Jin Lee, Young‐Gyu Ko, Joohun Ha, Minyoung Lee
SJR Q2Biochemical and Biophysical Research Communications
PharmacologyMedicine
4
논문|인용수 42·2010
Adhesion of ST6Gal I-mediated human colon cancer cells to fibronectin contributes to cell survival by integrin beta1-mediated paxillin and AKT activation.
Minyoung Lee, Jung-Jin Park, Yun‐Sil Lee
PubMed

We have recently demonstrated that ionizing radiation (IR) of cells increased the expression of beta-galactoside alpha-(2,6)-sialyltransferase (ST6Gal I) and the level of glycoprotein sialylation, especially for the key adhesion molecule integrin beta1. In addition, ST6Gal I-mediated sialylation of integrin beta1 contributed to cell adhesion-mediated radioresistance in colon cancer cells. In this study, we examined IR-induced cell adhesion to the extracellular matrix and evaluated the role of in

Immunology and AllergyMedicine
5
논문|인용수 31·2014
Mitochondrial Complex I Deficiency Enhances Skeletal Myogenesis but Impairs Insulin Signaling through SIRT1 Inactivation
Jin Hee Hong, Bong-Woo Kim, Hyo‐Jung Choo, Jung-Jin Park, Jae-Sung Yi, Dong‐Min Yu, Hyun Lee, Gye-Soon Yoon, Jae‐Seon Lee, Young‐Gyu Ko
SJR Q1Journal of Biological ChemistryOA

To address whether mitochondrial biogenesis is essential for skeletal myogenesis, C2C12 myogenesis was investigated after knockdown of NADH dehydrogenase (ubiquintone) flavoprotein 1 (NDUFV1), which is an oxidative phosphorylation complex I subunit that is the first subunit to accept electrons from NADH. The NDUFVI knockdown enhanced C2C12 myogenesis by decreasing the NAD(+)/NADH ratio and subsequently inactivating SIRT1 and SIRT1 activators (pyruvate, SRT1720, and resveratrol) abolished the NDU

Geriatrics and GerontologyMedicine
6
논문|인용수 30·2012
Cleavage of ST6Gal I by Radiation-Induced BACE1 Inhibits Golgi-Anchored ST6Gal I-Mediated Sialylation of Integrin β1 and Migration in Colon Cancer Cells
Min Young Lee, Jung-Jin Park, Young‐Gyu Ko, Yun‐Sil Lee
SJR Q1Radiation OncologyOA

Our results suggest that soluble ST6Gal I, possibly in cooperation with the Golgi-bound form, may participate in cancer progression and metastasis prior to being secreted from cancer cells.

Molecular BiologyBiochemistry, Genetics and Molecular Biology
7
논문|인용수 16·2016
MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) Interaction Disruptor Sensitizes Insulin Signaling in Skeletal Muscle
Hyun Lee, Jung-Jin Park, Nga Nguyen, Jun Sub Park, Jin Hee Hong, Seung-Hyeob Kim, Woon Song, Hak Joong Kim, Kwangman Choi, Sungchan Cho, Jae‐Seon Lee, Bong-Woo Kim
SJR Q1Journal of Biological ChemistryOA

Mitsugumin 53 (MG53) is an E3 ligase that interacts with and ubiquitinates insulin receptor substrate-1 (IRS-1) in skeletal muscle; thus, an MG53-IRS-1 interaction disruptor (MID), which potentially sensitizes insulin signaling with an elevated level of IRS-1 in skeletal muscle, is an excellent candidate for treating insulin resistance. To screen for an MID, we developed a bimolecular luminescence complementation system using an N-terminal luciferase fragment fused with IRS-1 and a C-terminal lu

Molecular BiologyBiochemistry, Genetics and Molecular Biology
8
논문|인용수 13·2010
Expression pattern of the class I homeobox genes in ovarian carcinoma
홍진화, 이재관, 박중진, 이낙우, 이규완, 나정열

Objective: Although some sporadic reports reveal the link between the homeobox (HOX) genes and ovarian carcinoma, there is no comprehensive analysis of the expression pattern of the class I homeobox genes in ovarian carcinoma that determines the candidate genes involved in ovarian carcinogenesis. Methods: The different patterns of expression of 36 HOX genes were analyzed, including 4 ovarian cancer cell lines and 4 normal ovarian tissues. Using a reverse transcription-polymerase chain reaction (

9
논문|인용수 10·2007
Short-Term Cold Exposure May Cause a Local Decrease of Neuropeptide Y in the Rat Hypothalamus
박중진, Woo Sung Yu, Heung Kyung Lee, Min Woo Shin, Sung Jin Kim, Seung Yeon Noh, Jin Shin
10
논문|인용수 8·2007
Patterns of Plasma Fatty Acids in Rat Models with Adenovirus Infection
백만정, 신규태, 안영환, 박중진, 이광, Ki Ho Park, 김경례
11
논문|인용수 0·2008
Recent Progress in Biotechnology-based Gene Manipulating Systems to Produce Knock-In/Out Mouse Models
Woon Kyu Lee, 박중진, 차석호, 윤철희

Gene-manipulated mice were discovered for the first time about a quarter century ago. Since then, numerous sophisticated technologies have been developed and applied to answer key questions about the fundamental roles of the genes of interest. Functional genomics can be characterized into gain-of-function and loss-of-function, which are called transgenic and knock-out studies, respectively. To make transgenic mice, the most widely used technique is the microinjection of transgene-containing vect

대표 연구 분야

Molecular BiologyPharmacologyImmunology and AllergyGeriatrics and Gerontology

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