Inhibitory Effect of Zostera japonica on Growth of Human Cancer Cells

In this study, crude extracts of the marine eelgrass Zostera japonica and their solvent-partitioned fractions were evaluated for their inhibitory effect against AGS, HT-1080 and MCF-7 human cancer cells using MTT assay. Each of the crude extracts (acetone/methylene, chloride, and methanol) of Z.japo...

Full description

Saved in:
Bibliographic Details
Published inOcean and polar research Vol. 34; no. 4; pp. 385 - 394
Main Authors Jung, ME, Hong, J W, Lee, JI, Kong, C-S, Chang, J-S, Seo, Y
Format Journal Article
LanguageKorean
Published 01.12.2012
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:In this study, crude extracts of the marine eelgrass Zostera japonica and their solvent-partitioned fractions were evaluated for their inhibitory effect against AGS, HT-1080 and MCF-7 human cancer cells using MTT assay. Each of the crude extracts (acetone/methylene, chloride, and methanol) of Z.japonica showed a significant inhibitory effect on the growth of human cancer cells. The combined crude extracts were partitioned between CH sub(2)Cl sub(2) and water. The organic layer was further partitioned between 85% aq. MeOH and n-hexane, and the aqueous layer was then fractionated into n-BuOH and H sub(2)O, successively. Growth inhibition effects of solvent-partitioned fractions from Z.japonica on human cancer cells increased in a dose-dependent manner. Among these tested samples, the 85% aq. MeOH fraction revealed good inhibitory effects on the growth of AGS and HT-1080 human cancer cells, while the n-hexane fraction exhibited good inhibitory effects on the growth of AGS and MCF-7 human cancer cells. In addition, 85% aq. MeOH and n-hexane fractions enhanced mRNA expression of p53 gene. These results suggest that there is further scope for the isolation of active compounds from Z.japonica, which should show much stronger anticancer activity.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1598-141X
2234-7313
DOI:10.4217/OPR.2012.34.4.385