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To print: Select File and then Print from your browser's menu Title: Tumour Marker Predicts Malignancy in Biliary-Tract Cancers: Presented at AASLD |
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"Tumour Marker Predicts Malignancy in Biliary-Tract Cancers: Presented at AASLD" By Maria Bishop BOSTON, MA -- November 9, 2007 -- A tumour marker known as tumour M2-pyruvate kinase (Tu-M2-PK) has been found capable of discriminating between benign and malignant biliary-tract cancer, British researchers reported here at the 58th Annual Scientific Meeting of the American Association for the Study of Liver Disease (AASLD). This finding means there may be a role for the Tu-M2-PK marker in the non-invasive screening of patients at increased risk of biliary-tract cancer, such as those with primary sclerosing cholangitis (PSC), noted lead author James H. Brindley, MD, The Institute of Hepatology, Royal Free & University College London Medical School, London, United Kingdom. In this study, 75 patients were recruited from the hepatobiliary service at University College Hospital, London, United Kingdom. Three cohorts included patients with biliary-tract cancer (n = 41, mean age 68 years), patients with PSC (n = 11, mean age 59 years), and patients with benign non-PSC conditions (n = 23, mean age 50 years). A commercially available enzyme-linked immunosorbent assay (ELISA) kit was utilised to measure plasma Tu-M2-PK markers. The results demonstrated mean plasma M2-PK levels of 114.8 +- 160.9 U/mL in patients with biliary-tract cancer ([P =.001), 71.7 ± 81.6 in patients with PSC (P =.031), and 34.3 +- 20.6 in patients with non-PSC benign disease (P =.031). A correlation also was demonstrated between Tu-M2-PK and clinicopathological characteristics such as bilirubin level, tumour size, and the serum tumour marker CA 19-9. Biliary cancers occur in the liver, pancreas, gallbladder, and extrahepatic bile ducts. In patients with PSC, the bile ducts inside and outside the liver become inflamed and scarred, eventually blocking the ducts and causing a build-up of bile that damages liver cells. Technical support for this study was provided by ScheBo-Biotech UK, Ltd. |
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