The research was conducted in two phases. First, Whitehead postdoctoral fellows Jing Yang and Sendurai Mani compared metastatic and non-metastatic cancer cells taken from mouse tumors. Using microarray technology to determine levels of gene expression, they found certain genes that were active only in the metastatic cells. The gene that stood out among all the others was one coding for the protein Twist.
Next, Yang isolated highly metastatic cancer cells and disabled the Twist gene. When she injected these cells into mammary glands of mice, the mice developed primary, localized breast tumors--but the tumors were unable to metastasize. Furthermore, their study showed that Twist caused breast cells to separate from one another, losing their cell-cell adhesion and scattering, thereby allowing these cells to travel to distant organ sites, like dandelion seeds scattered in the winds.
"Twist is probably the first gene regulator that has been tied so definitively to human cancer metastasis," says Yang.
Andrea Richardson, a pathologist at Brigham and Women's Hospital and coauthor on the paper, correlated these finding with her lab's data taken from human breast cancer studies--essentially re-analyzing her lab's data in light of Yang's. She found that Twist is highly expressed in invasive lobular carcinoma, a unique type of breast cancer where breast tumor cells completely lose their cell-cell adhesion and infiltrate other tissues.
"In many mouse studies you have great models and come up with something and it cures the mice, but then it never seems to work in people," says Richardson. "In this case we were seeing the exact same phenotype and gene expression correlation in human breast tumors."
Although clinical applications of this research are still unclear, Ric
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Contact: David Cameron
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Whitehead Institute for Biomedical Research
24-Jun-2004