Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2004 | 45 | 4 | 469-472

Article title

Inhibition of cyclooxygenase-2 by diallyl sulfides (DAS) in HEK 293T cells

Title variants

Languages of publication

EN

Abstracts

EN
Cyclooxygenase (COX) is involved in modulating inflammatory response through the synthesis of prostaglandins. The inducible isoform of the enzyme, COX-2, is overexpressed in some malignant and premalignant lesions. Several preclinical and clinical studies have reported COX-2 inhibition as an effective strategy for chemoprevention. Nonsteroidal anitinflammatory drugs (NASIDs) such as celecoxib, are the most widely investigated COX-2 inhibitors. The oil-soluble diallyl sulfides (DAS) include monosulfides (DAMS), disulfides (DADS) and trisulfides (DATS). They were found to be effective against canine and human tumors, the mechanism of which remains unresolved. We attempted a comparative evaluation of the antiproliferative effect of DAS in HEK 293T cells. The cells were treated with increasing concentrations of DAMS, DADS and DATS. There were significant differences between the IC50 values of DAMS, DADS and DATS. RT-PCR was performed and the expression of COX-2 was compared with that of b actin. DATS inhibited COX-2 gene expression significantly stronger than DAMS and DADS. The data are suggestive of antineoplastic effect of DAS, mediated by controlling COX-2 expression.

Keywords

Year

Volume

45

Issue

4

Pages

469-472

Physical description

Contributors

author
author
author
author
author

References

Document Type

SHORT COMMUNICA

Publication order reference

E.M. Elango, Department of Molecular Biology, Amrita Institute of Medical Sciences and Research Center, Amrita Vishwa Vidhyapeetam (Deemed University), Cochin ? 682026 Kerala, India

Identifiers

YADDA identifier

bwmeta1.element.element-from-psjc-a0987114-fffb-37b9-acc5-9483ce99d002
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.