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Updated: Aug 14, 2026

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Block of glioma cell line in S by interferon
Abstract:
The human glioma cell line U-251 MG, with a well-characterized defect in growth control, was sensitive to the antiproliferative effects of human (fibroblast) interferon (IFN). IFN inhibited exponentially growing cells by increasing the number of cells in the S stage of the cell cycle. At the same time the number of cells in Go/G1 diminished. The rate of thymidine incorporation was decreased during the first cell cycle, with no prolongation of S. However, in synchronized cultures, the wave of cells with a S-phase content did not decrease over a time period several hours longer than the length of S measured by pulse labelling. Thus we conclude that, at a sufficient dose, the cells were unable to accomplish cell division as they prematurely stopped synthesizing DNA.
Insights
Human fibroblast interferon (IFN) halts glioma cell proliferation by arresting cells in the S phase and preventing DNA synthesis completion. This antiproliferative effect ultimately inhibits cell division in U-251 MG cells.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- The U-251 MG human glioma cell line exhibits a known defect in growth control.
- Interferons (IFNs) are known to possess antiproliferative properties.
Purpose of the Study:
- To investigate the antiproliferative effects of human fibroblast interferon (IFN) on the U-251 MG glioma cell line.
- To elucidate the mechanism by which IFN inhibits cell growth in this specific cell line.
Main Methods:
- Cell cycle analysis of U-251 MG cells treated with IFN.
- Assessment of thymidine incorporation rates.
- Synchronization of cell cultures to study DNA synthesis and cell division progression.
Main Results:
- IFN treatment led to an accumulation of cells in the S phase of the cell cycle.
- A concurrent decrease in cells within the Go/G1 phase was observed.
- Despite initial effects on thymidine incorporation, synchronized cells failed to complete division, indicating a premature halt in DNA synthesis.
Conclusions:
- Human fibroblast interferon (IFN) exhibits significant antiproliferative effects on the U-251 MG glioma cell line.
- IFN induces cell cycle arrest at the S phase, primarily by inhibiting DNA synthesis completion.
- These findings suggest a potential therapeutic mechanism for IFN in controlling glioma cell proliferation.
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