stem cells that drive brain cancer

Stem cells that drive brain cancer

[ندعوك للتسجيل في المنتدى أو التعريف بنفسك لمعاينة هذا الرابط]Scientists have developed an improved method for growing human brain cancer cells in the laboratory. The technique provides a powerful tool for studying how tumours form in the brain, and how treatments might be developed in the future. In a paper published in Cell Stem Cell^{[ندعوك للتسجيل في المنتدى أو التعريف بنفسك لمعاينة هذا الرابط]}, scientists from the Wellcome Trust Centre for Stem Cell Research at the University of Cambridge and the University of Toronto describe a technique for growing pure populations of the cancer stem cells that are thought to cause some of the most common and aggressive types of brain cancer, known as gliomas.

The researchers took samples of human brain tumours and used their technique to grow pure populations of tumour stem cells. They were able to maintain these cell populations indefinitely in the laboratory, through many generations of growth and replication. Further experiments demonstrated that cells grown in this way will regrow tumours in mice. The tumours they form in the mouse closely match those found in patients with brain cancer.

This close match between the laboratory model and the human disease provides an important opportunity for studying how brain cancers develop, and how they could be treated. The researchers have already begun to identify different kinds of glioma stem cell from individual tumours, perhaps helping to explain the range of gliomas seen in patients. A pilot experiment with a reference set of drugs highlighted how the cells can be used to look for potential new therapeutics.

The Cambridge and Toronto scientists used a technique known as adherent cell culture^{[ندعوك للتسجيل في المنتدى أو التعريف بنفسك لمعاينة هذا الرابط]} to grow pure populations of glioma stem cells. In this approach, the cells are grown in a single layer on a flat surface. The technique improves on recent work from other labs which used a method called suspension culture. In these previous studies many of the cells died or differentiated into specialised cells. Also, since suspension culture generates aggregated clumps of cells, it is difficult to follow what happens to individual cells.

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