메뉴 건너뛰기
.. 내서재 .. 알림
소속 기관/학교 인증
인증하면 논문, 학술자료 등을  무료로 열람할 수 있어요.
한국대학교, 누리자동차, 시립도서관 등 나의 기관을 확인해보세요
(국내 대학 90% 이상 구독 중)
로그인 회원가입 고객센터 ENG
주제분류

추천
검색

논문 기본 정보

자료유형
학술저널
저자정보
Nguyen, Van-Tinh (Department of Biomedical Engineering, and Centre for Marine-Integrated Biomedical Technology [BK21 Plus] Pukyong National University) Qian, Zhong-Ji (College of Food Science and Technology, Guangdong Ocean University) Lee, Bonggi (College of Pharmacy, Pusan National University) Heo, Soo-Jin (Global Bioresources Research Center, Korea Institute of Ocean Science and Technology) Kim, Kil-Nam (Marine Bio Research Team, Korea Basic Science Institute [KBSI]) Jeon, You-Jin (Department of Marine Life Sciences, Jeju National University) Park, Won Sun (Department of Physiology, Kangwon National University School of Medicine) Choi, Il-Whan (Department of Microbiology, Inje University College of Medicine) Jang, Chul Ho (Department of Otolaryngology, Chonnam National University Medical School) Ko, Seok-Chun (Institute of Marine Biotechnology, Pukyong National University) Park, Sun-Joo (Department of Chemistry, Pukyong National University) Kim, Yong-Tae (Department of Food Science and Biotechnology, Kunsan National University) Kim, GeunHyung (Department of Biomechatronic Engineering, College of Biotechnology and Bioengineering, Sungkyunkwan University) Lee, Dae-Sung (Marine B) Yim, Mi-Jin Je, Jae-Young Jung, Won-Kyo
저널정보
한국조류학회(藻類) Algae Algae 제29권 제4호
발행연도
2014.1
수록면
355 - 366 (12page)

이용수

표지
📌
연구주제
📖
연구배경
🔬
연구방법
🏆
연구결과
AI에게 요청하기
추천
검색

초록· 키워드

오류제보하기
Fucoxanthin is known to be an effective cell proliferation inhibitor with anti-tumor and anti-angiogenic activities. However, there is a lack of data regarding the biological effects of cis isomers of fucoxanthin. To assess the potential therapeutic properties of 9'-cis-(6'R) fucoxanthin (FcA), and 13-cis and 13'-cis-(6'R) fucoxanthin complex (FcB) isolated from Sarggassum siliquastrum, we investigated their inhibitory effects on matrix metalloproteinases (MMPs) in phorbol 12-myristate 13-acetate (PMA)-induced human fibrosarcoma (HT1080) cells. FcA and FcB reduced MMP-2 and MMP-9 protein and mRNA levels, as well as the migration of these cells, in a dose-dependent manner. Additionally, FcA and FcB increased levels of MMPs inhibition factors such as tissue inhibitor of metalloproteinase-1. FcA and FcB significantly inhibited the transcriptional activity of nuclear factor ${\kappa}B$ (NF-${\kappa}B$) and by inhibiting c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinases. Our results demonstrate that suppression of the NF-${\kappa}B$, JNK, and p38 signaling pathways may inhibit PMA-induced MMP-2 and MMP-9 activity. Therefore, FcA and FcB may be useful in noninvasive therapeutic strategies against fibrosarcoma metastasis.

목차

등록된 정보가 없습니다.

참고문헌 (0)

참고문헌 신청

이 논문의 저자 정보

최근 본 자료

전체보기

댓글(0)

0