» Articles » PMID: 8317331

A Comparison Between Two Methods for Measuring Tumor Necrosis Factor in Biological Fluids

Overview
Journal Agents Actions
Specialty Pharmacology
Date 1993 Jan 1
PMID 8317331
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The current study was undertaken to compare two methods for the efficiency of measuring tumor necrosis factor (TNF-alpha) in biological fluids, which is species undependent, reliable, sensitive, simple and not expensive. We have compared the MTT tetrazolium cytotoxic assay [1,2] and the 3H-thymidine (3H-TdR) incorporation cytostatic assay for measuring the anti-tumor activity of human recombinant TNF-alpha, of human colonic tissue and of supernatants of in vitro stimulated human and rat peritoneal macrophages. Two target cell-lines, namely murine myelomonocytic leukaemia WEHI-164- and L-929-transformed murine fibroblast cell-lines, were used in the MTT assay. The L-929 line was also used in the 3H-TdR assay. WEHI-164 was more sensitive than the L-929 cell-line in the MTT cytotoxic assay. Furthermore, the MTT assay was more sensitive to TNF-alpha than the 3H-TdR assay. Both methods can be used for the detection of anti-tumor activity in biological fluids but the MTT cytotoxic method has the advantage of being more sensitive and more simple.

Citing Articles

Changes in Eicosanoid and Tumour Necrosis Factor-alpha Production by Rat Peritoneal Macrophages During Carrageenin-Induced Peritonitis.

Pruimboom W, Verdoold A, Tak C, van Dijk A, van Batenburg M, Wilson J Mediators Inflamm. 1994; 3(5):335-40.

PMID: 18475577 PMC: 2365571. DOI: 10.1155/S0962935194000463.


Regulation of the release of tumour necrosis factor (TNF)alpha and soluble TNF receptor by gamma irradiation and interferon gamma in Ewing's sarcoma/peripheral primitive neuroectodermal tumour cells.

van Valen F, Truckenbrod B, Rube C, Winkelmann W, Jurgens W J Cancer Res Clin Oncol. 1997; 123(5):245-52.

PMID: 9201246 DOI: 10.1007/BF01208634.


Inflammatory mediators and activity of human peritoneal macrophages.

Pruimboom W, van Dijk A, Tak C, Zijlstra F, Bonta I, Wilson J Agents Actions. 1993; 38 Spec No:C86-8.

PMID: 8317330 DOI: 10.1007/BF01991146.

References
1.
Hansen M, Nielsen S, Berg K . Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill. J Immunol Methods. 1989; 119(2):203-10. DOI: 10.1016/0022-1759(89)90397-9. View

2.
Green L, Reade J, Ware C . Rapid colorimetric assay for cell viability: application to the quantitation of cytotoxic and growth inhibitory lymphokines. J Immunol Methods. 1984; 70(2):257-68. DOI: 10.1016/0022-1759(84)90190-x. View

3.
Belizario J, Dinarello C . Interleukin 1, interleukin 6, tumor necrosis factor, and transforming growth factor beta increase cell resistance to tumor necrosis factor cytotoxicity by growth arrest in the G1 phase of the cell cycle. Cancer Res. 1991; 51(9):2379-85. View

4.
Mosmann T . Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983; 65(1-2):55-63. DOI: 10.1016/0022-1759(83)90303-4. View

5.
Arnould R, Dubois J, Abikhalil F, Libert A, Ghanem G, Atassi G . Comparison of two cytotoxicity assays--tetrazolium derivative reduction (MTT) and tritiated thymidine uptake--on three malignant mouse cell lines using chemotherapeutic agents and investigational drugs. Anticancer Res. 1990; 10(1):145-54. View