Format

Send to

Choose Destination
  • Filters activated: Field: Title Word. Clear all
Anticancer Res. 2015 Dec;35(12):6419-24.

Celecoxib and LLW-3-6 Reduce Survival of Human Glioma Cells Independently and Synergistically with Sulfasalazine.

Author information

1
Department of Biology, Spelman College, Atlanta, GA, U.S.A.
2
Department of Chemistry and Biochemistry, Spelman College, Atlanta, GA, U.S.A. lwinfield@spelman.edu.

Abstract

Gliomas are among the most commonly diagnosed central nervous system tumors. Celecoxib has been utilized with success in the treatment of several types of cancer, including gliomas. The present study examined the antiproliferative effects of celecoxib and its benzimidazole-based analog, LLW-3-6, when used as co-treatment with sulfasalazine against human glioma LN18 cells. At 48-h treatment, the glioma cells maintained 60% viability in the presence of celecoxib or LLW-3-6 at the maximum concentration tested (40 μM). Co-treatment of glioma cells under a non-lethal dose (50 μM) of sulfasalazine and either celecoxib or LLW-3-6 (administered at different concentrations) resulted in improved inhibition of cell viability. The concentration of the molecules required to reduce cell growth in the combined treatment was significantly less than that needed when either molecule was administered independently. Based on computational values, LLW-3-6 has physiochemical characteristics that should allow for improved bioavailability in comparison to that of celecoxib.

KEYWORDS:

Cyclooxygenase-2; LN18; benzimidazole; brain cancer; celecoxib; combination therapy; glioma; sulfasalazine; synergistic effects

PMID:
26637851
PMCID:
PMC4755477
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center