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Differential effects of recombinant interferon-alpha and 5-fluorouracil against colon cancer cells or against peripheral blood mononuclear cells
- Source :
- Scopus-Elsevier
- Publication Year :
- 1994
-
Abstract
- Comparative studies on the suppressive effects of recombinant interferon-alpha (IFN-alpha), 5-fluorouracil (5-FU), or IFN-alpha + 5-FU have been performed in vitro on colon carcinoma cells (HT-29 cell line) and PHA-stimulated mononuclear cells (MNC) of peripheral blood obtained from healthy donors. IFN-alpha was used at 500 U/ml against HT-29 cells and at 1000 U/ml against MNC on day 1 of culture; 5-FU was used at 250 microM against HT-29 and at 1400 microM against MNC on day 2 of culture. The results show that: (a) IFN-alpha inhibited MNC and HT-29 cells by 13.4% and 32.9%, respectively; (b) 5-FU inhibited MNC and HT-29 cells by 54.7% and 87.0%, respectively; (c) IFN-alpha + 5-FU resulted in a stronger inhibition of HT-29 cells (i.e., 96.1%). In contrast, that combination was significantly less suppressive than 5-FU alone when MNC were used as targets (i.e., 35.9% inhibition). Natural cell-mediated cytotoxic activity relative to 10(6) MNC was not markedly altered by all agents alone or in combination. Moreover, treatment with IFN-alpha, 5-FU or IFN-alpha + 5-FU resulted in a marked increase in the number of HT-29 cells positive for the CEA surface antigen. These data seem to provide further rational support of the clinical use of IFN-alpha + 5-FU in colorectal cancer, based on the differential toxicity of this drug combination on tumor versus normal immunocompetent cells.
- Subjects :
- Cytotoxicity, Immunologic
Immunity, Cellular
Drug Synergism
Lymphocyte Activation
Recombinant Proteins
Stimulation, Chemical
Antineoplastic Combined Chemotherapy Protocols
Colonic Neoplasms
Interferon Type I
Leukocytes, Mononuclear
Tumor Cells, Cultured
Humans
Fluorouracil
Phytohemagglutinins
Cell Division
Subjects
Details
- ISSN :
- 02507005
- Volume :
- 14
- Issue :
- 5A
- Database :
- OpenAIRE
- Journal :
- Anticancer research
- Accession number :
- edsair.pmid.dedup....c018e1916f20cfdcff05e4f97ca742cd