Pitt study targets cancerous tumors
1/8/2005 Pittsburgh Jennifer Bails Science Magazine as reported by Pittsburgh Tribune-Review A team of University of Pittsburgh researchers has discovered that too much of a single protein can cause a cascade of calamitous changes in a cell leading to the formation of cancerous tumors. The findings published in today's issue of Science, a prestigious peer-review journal, could help scientists develop cancer treatments that are safer and more effective than chemotherapy, said Susanne Gollin, one of the paper's authors. "The more we understand about tumor cells and how they misbehave compared to normal cells, the more we can target our research to developing potential cancer therapies," said Gollin, a human geneticist at Pitt's Graduate School of Public Health. Gollin collaborated with Pitt biologists Nicholas Quintyne and William Saunders. They found that too much of a protein called nuclear mitotic assembly protein -- or NuMA -- disrupts cell division by interfering with a second protein called dyenin. Large amounts of dyenin help make up the mitotic spindle, an assembly of fibers and proteins used to ensure that new cells are allotted the proper number of chromosomes. Before a healthy cell divides, it duplicates its chromosomes. These chromosomes are then evenly separated by the spindle so the two new cells have equal amounts of genetic material. Normal cells have mitotic spindles with two ends, or poles, with structures at either end called centrosomes that help direct cell division. But cancer cells often have extra centrosomes, which can lead to defective spindles with too [...]