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New Tumor Markers for Pancreatic Cancer

d to the microarray, each message binds to its matching DNA, producing fluorescent signal.

These findings reveal some of the orders that allow pancreatic tumours to grow quickly, feed and invade other tissues. Additionally, these messages and the proteins for which they code are potential diagnostic markers and targets to tackle when developing new anti-cancer treatments.

Finally, we generated antibodies that detect the proteins coded by some of the messages. Using a microscope and colour-labelled antibodies, we managed to dye PC cells and to distinguish them from cells of a healthy pancreas or a pancreas with chronic pancreatitis. These results indicate the usefulness of this marker and establish the basis for the development of a differential diagnostic system for PC.


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