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Induction of Apoptosis and Inhibition of Cell Migration by Ethyl Alcohol Extract of Hizikia fusiforme in Human Breast cancer Cells

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98 The 49th International Symposium of Korean Society of Life Science

P141

Induction of Apoptosis and Inhibition of Cell Migration by Ethyl Alcohol

Extract of Hizikia fusiforme in Human Breast cancer Cells

Sun Hwa Jung

1

, Cheol Park

1

, Cheng-Yun Jin

2

, Min Ho Han

2

, Il-Whan Choi

3

,

Taek-Jeong Nam

4

, Se-Kwon Kim

5

and Yung Hyun Choi

1,2

*

1

Department of Biomaterial Control, Dongeui University Graduate School and 2

Department of Biochemistry, Dongeui University College of Oriental Medicine, Busan 614-052 3

Department of Microbiology, College of Medicine Inje University, Busan 614-735 4

Department of Food and Life Science, 5Department of Chemistry and Marine Bioprocess Research Center, Pukyong National University, Busan 608-737, South Korea

Hizikia fusiforme is a kind of brown edible seaweed that mainly grows in the temperate seaside areas of the northwest Pacific

including Korea, Japan and Chine. Recently, H. fusiforme has been known to exert antioxidant, antimutagenic and anticoagulant activity, however, the molecular mechanisms of H. fusiforme in malignant cells have been poorly studied until now. In this study, we investigated the effects of ethyl alcohol extract of H. fusiforme (EAHF) on the anti-proliferative effects of MDA-MB-231 and MCF-7 human breast cancer cells. EAHF treatment resulted in a concentration-dependent growth inhibition by including apoptosis in MDA-MB-231 cells and G1 phase arrest in MCF-7 cells. In MDA-MB-231 cells, the increase in apoptosis induced by EAHF was correlated with up-regulation of pro-apoptotic Bax and down-regulation of cIAP-2 expression. EAHF treatment induced the proteolytic activation of caspase-3 and caspase-9, and a concomitant inhibition of poly (ADP-ribose) polymerase (PARP), β-catenin, phospholipase (PLC)-γ1 protein and DNA fragmentation factor 45/inhibitor of caspase-activated DNase (DFF45/ICAD). Furthmore, the EAHF in-hibited cell migration in a concentration- and time-dependent manner of MDA-MB-231 and MCF-7 cells, as evidenced by the results of the wound healing assay. Taken together, these findings provide important new insights into the possible molecular mechanisms of the anti-cancer activity of H. fusiforme. [This work was supported by a grant from Marine Bioprocess Research Center of the Marine Bio 21 Center funded by the Ministry of Land, Transport and Maritime, Republic of Korea.]

Key words: Hizikia fusiforme, breast cancer, apoptosis, Bax, migration

P142

Anti-Invasive Activity of Anthocyanins Isolated From Vitis coignetiae

in Human Hepatocarcinoma Cells

Dong Yeok Shin

1,2

, Won Sup Lee

3

, Chung Ho Ryu

4

, Sung Chul Shin

5

,

Ho Sung Kang

2

and Yung Hyun Choi

1

*

1

Department of Biochemistry, Dongeui University College of Oriental Medicine and

Department of Biomaterial Control (BK21 program), Dongeui University Graduate School, Busan 614-052 2

Department of Molecular Biology, Pusan National University, Busan, 609-735 3

Department of Internal Medicine, Institute of Health Sciences and Gyeongnam Regional Cancer Center, Gyeongsang National University School of Medicine, Jinju, 660-702

Departments of 4Food Technology and 5Chemistry, Gyeongsang National University, Jinju, 660-701, South Korea

Anthocyanins belong to a class of flavonoids, exhibiting antioxidant and anti-inflammatory actions as well as a variety of chemo-therapeutic effects. However, little is known about the cellular and molecular mechanism of anti-cancer activity. In this study, we isolated anthocyanins (delphinidin-3,5-diglucoside : cyanidin-3,5- diglucoside : petunidin-3,5-diglucoside : delphinidin-3-glucoside : malvdin-3,5-diglucoside : peonidin-3,5-diglucoside : cyanidin-3-glucoside : petunidin-3-glucoside : peonidin-3- glucoside : malvi-din-3-glucoside = 27 : 63 : 8.27 : 1 : 2.21 : 6.7 : 1.25 : 5.72 : 1.25) from fruits of Vitis coignetiae Pulliat (Meoru in Korea) (AIMs) and investigated if the exerted anti-invasive effects in human hepatoma Hep3B cells. The AIMs inhibited the invasion of Hep3B cells in a dose-dependent manner as determined through a Matrigel-coated chamber assay. In Hep3B cells, AIMs also inhibited expression and activity of matrix metalloproteinase (MMP)-2 and MMP-9, and activation of NF-κB stimulated by tumor necrosis factor (TNF)-α. Taken together, the results of this study indicates that the anthocyanins isolated from meoru have anti-invasive effects on human hepatoma Hep3B cells, and inhibited MMP-2 and MMP-9 gene expression at least in part through the inhibition of NF-κB activation. These phytochemicals therefore may be useful to inhibit invasion and metastasis of human hepatitis B associated hepatoma. [This study was supported by a grant from the National R&D Program for Cancer Control, Ministry of Health & Welfare, Republic of Korea. (0820050).]

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