Ji-Hyeok Lee

Dr. Ji-Hyeok Lee

Korea Mouse Metabolic Phenotyping Center, Lee Gil Ya Cancer and Diabetes Institute, Gachon University Gil Medical center, Incheon 21999, Republic of Korea

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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30 March 2015 in Marine Drugs
Verified
Journal Article
Open access
PDF file
EKEun-Kyung Kim
Eun-Kyung Kim
YTYujiao Tang
Yujiao Tang
YKYon-Suk Kim
Yon-Suk Kim
JHJin-Woo Hwang
Jin-Woo Hwang
ECEun-Ju Choi
Eun-Ju Choi
PPPyo-Jam Park
Pyo-Jam Park
We investigated the effect of Ecklonia cava (E. cava)-derived dieckol on movement behavior and the expression of migration-related genes in MCF-7 human breast cancer cell. Phlorotannins (e.g., dieckol, 6,6′-biecko, and 2,7″-phloroglucinol-6,6′-bieckol) were purified from E. cava by using centrifugal partition chromatography. Among the phlorotannins, we found that dieckol inhibited breast cancer cell the most and was selected for further study. Radius™-well was used to assess cell migration, and dieckol (1–100 µM) was found to suppress breast cancer cell movement. Metastasis-related gene expressions were evaluated by RT-PCR and Western blot analysis. In addition, dieckol inhibited the expression of migration-related genes such as matrix metalloproteinase (MMP)-9 and vascular endothelial growth factor (VEGF). On the other hand, it stimulated the expression of tissue inhibitor of metalloproteinase (TIMP)-1 and TIMP-2. These results suggest that dieckol exerts anti-breast cancer activity via the regulation of the expressions of metastasis-related genes, and this is the first report on the anti-breast cancer effect of dieckol.

30 May 2017 in Marine Drugs
Verified
Journal Article
Open access
PDF file
JKJung-Il Kang
Jung-Il Kang
MKMin-Kyoung Kim
Min-Kyoung Kim
Ji-Hyeok LeeJi-Hyeok Lee
Ji-Hyeok Lee
You-Jin JeonYou-Jin Jeon
You-Jin Jeon
EHEun-Kyoung Hwang
Eun-Kyoung Hwang
HKHee-Kyoung Kang
Hee-Kyoung Kang
In this study, we investigated the effect and mechanism of Undariopsis peterseniana, an edible brown alga, on hair growth. The treatment of vibrissa follicles with U. peterseniana extract ex vivo for 21 days significantly increased the hair-fiber lengths. The U. peterseniana extract also significantly accelerated anagen initiation in vivo. Moreover, we found that U. peterseniana extract was able to open the KATP channel, which may contribute to increased hair growth. The U. peterseniana extract decreased 5α-reductase activity and markedly increased the proliferation of dermal papilla cells, a central regulator of the hair cycle. The U. peterseniana extract increased the levels of cell cycle proteins, such as Cyclin D1, phospho(ser780)-pRB, Cyclin E, phospho-CDK2, and CDK2. The U. peterseniana extract also increased the phosphorylation of ERK and the levels of Wnt/β-catenin signaling proteins such as glycogen synthase kinase-3β (GSK-3β) and β-catenin. These results suggested that the U. peterseniana extract had the potential to influence hair growth by dermal papilla cells proliferation through the activation of the Wnt/β-catenin and ERK pathways. We isolated a principal of the U. peterseniana extract, which was subsequently identified as apo-9′-fucoxanthinone, a trichogenic compound. The results suggested that U. peterseniana extract may have a pivotal role in the treatment of alopecia.

28 June 2016 in Fisheries and Aquatic Sciences
Verified
Journal Article
Open access
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HKHyung-Ho Kim
Hyung-Ho Kim
HKHyun-Soo Kim
Hyun-Soo Kim
JKJu-Young Ko
Ju-Young Ko
CKChul-Young Kim
Chul-Young Kim
Ji-Hyeok LeeJi-Hyeok Lee
Ji-Hyeok Lee
You-Jin JeonYou-Jin Jeon
You-Jin Jeon
One of the main compounds in Ishige okamurae, diphlorethohydroxycarmalol (DPHC), is known to exhibit antiviral and anti-inflammatory effects. However, it has not been investigated extensively. In this study, preparative centrifugal partition chromatography (CPC) coupled with 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS+) online HPLC was employed for effectively separating considerable amounts of antioxidant compounds from marine algae. Two main antioxidant compounds, DPHC and octaphlorethol A (OPA), respectively, were confirmed and isolated from the ethyl acetate (EtOAc) fraction of I. okamurae by ABTS+ online HPLC and preparative CPC systems. The presence of DPHC and OPA was confirmed in the EtOAc fraction of I. okamurae by both liquid chromatography with diode array detection and electrospray ionization mass spectrometry (LC-DAD-ESI/MS) and ABTS+ online HPLC systems: DPHC (39 mg) and OPA (23 mg) were successfully isolated from I. okamurae (500 mg) with optimum solvent composition (0.5:10:4:6; n-hexane/EtOAc/MeOH/water, v/v) with corresponding partition coefficients (K) of 1.62 and 2.71, respectively, by preparative CPC. Hence, CPC coupled with ABTS+ online HPLC is convenient for the efficient and simple isolation of these antioxidant compounds from I. okamurae.

10 May 2021 in Marine Drugs
Verified
Journal Article
Open access
PDF file
SKSeo-Young Kim
Seo-Young Kim
Ji-Hyeok LeeJi-Hyeok Lee
Ji-Hyeok Lee
NKNalae Kang
Nalae Kang
Kil-Nam KimKil-Nam Kim
Kil-Nam Kim
You-Jin JeonYou-Jin Jeon
You-Jin Jeon
Skeletal muscle is an important tissue in energy metabolism and athletic performance. The use of effective synthetic supplements and drugs to promote muscle growth is limited by various side effects. Moreover, their use is prohibited by anti-doping agencies; hence, natural alternatives are needed. Therefore, we evaluated the muscle growth effect of substances that can act like synthetic supplements from edible marine algae. First, we isolated six marine algal polyphenols belonging to the phlorotannin class, namely dieckol (DK), 2,7″-phloroglucinol-6,6′-bieckol (PHB), phlorofucofuroeckol A (PFFA), 6,6′-bieckol (6,6-BK), pyrogallol-phloroglucinol-6,6′-bieckol (PPB), and phloroglucinol (PG) from an edible brown alga, Ecklonia cava and evaluated their effects on C2C12 myoblasts proliferation and differentiation. Of the six phlorotannin isolates evaluated, DK and PHB induced the highest degree of C2C12 myoblast proliferation. In addition, DK and PHB regulates myogenesis by down-regulating the Smad signaling, a negative regulator, and up-regulating the insulin-like growth factor-1 (IGF-1) signaling, a positive regulator. Interestingly, DK and PHB bind strongly to myostatin, which is an inhibitor of myoblast proliferation, while also binding to IGF-1 receptors. Moreover, they bind to IGF-1 receptor. These results suggest that DK and PHB are potential natural muscle building supplements and could be a safer alternative to synthetic drugs.

24 November 2016 in Journal of Applied Phycology
Verified
Journal Article
Closed access
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Ji-Hyeok LeeJi-Hyeok Lee
Ji-Hyeok Lee
JKJu-Young Ko
Ju-Young Ko
EKEun-A Kim
Eun-A Kim
EHEun-Kyoung Hwang
Eun-Kyoung Hwang
CPChan Sun Park
Chan Sun Park
You-Jin JeonYou-Jin Jeon
You-Jin Jeon

7 March 2015 in Journal of Applied Phycology
Verified
Journal Article
Closed access
PDF file
Ji-Hyeok LeeJi-Hyeok Lee
Ji-Hyeok Lee
JHJong Won Han
Jong Won Han
JKJu-Young Ko
Ju-Young Ko
WLWonwoo Lee
Wonwoo Lee
GAGinnae Ahn
Ginnae Ahn
You-Jin JeonYou-Jin Jeon
You-Jin Jeon