Biologist uses genome database to investigate cancer cells

Florida State University Professor of Biological Science David Gilbert is using the latest information about the human genome as a guide to better understand cancer.

Gilbert and his FSU colleagues were part of a team that compared different cancer cell types to a database of normal human cells using a new method he developed that can identify the cell type from which cancers derive. By comparing various cancer cells to the collection of normal cells, they were able to tell which cancers mostly closely matched different cell types.

“Cancer cells come from a cell in your body, but they have changed,” Gilbert said. “Knowing what cell type they came from is particularly important when evaluating whether a new tumor in a relapsed patient is derived from the original tumor or is a new cancer altogether.”

Their work, published in Nature Communications , is a companion piece to a large series of publications resulting from an international effort to understand how the human genome works, funded by the National Institutes of Health, called the Encyclopedia of DNA Elements (ENCODE). Because only 1 percent of human DNA codes for any known proteins, understanding the function of the rest of our genome has been a huge challenge.

Gilbert and his colleagues also are contributors to the larger ENCODE publication, published in Nature , summarizing the efforts of the latest cycle of ENCODE funding. The highlight of this study is the mapping of nearly one million elements in the human genome, covering 8 percent of the genome, that regulate the genes. That is, they determine how much and in what body tissue a gene will be expressed.

“The complexity in an organism is not in the number of protein-coding genes it has,” Gilbert said. “It’s in in the combination of those genes. We have almost the same number of genes as worms and flies, but we express them in more complex combinations.”

His laboratory adds replication—the process of DNA making a copy of itself—to the picture.

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