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GALLBLADDER AND BILE DUCT CANCER
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News Archive  

December 2011
Mimicker of Gallbladder Adenocarcinoma Described at Johns Hopkins

November 2009
Novel Technology Detects Genetic Evidence of Biliary Cancer in Blood and Bile

September 2009
Shell Ridge Summit walk for Bile Duct Cancer Research

May 2008
Genetic Analysis of Gallbladder Cancer Reveals Novel Biomarkers

June 2007
•Hopkins Fellow Wins International Award for Biliary Cancer Research

March 2005
•Potential New Target for Therapy in Biliary Cancer Discovered at Johns Hopkins

October 2004
•New Diagnostic Marker of Biliary Tract Carcinoma Discovered at Hopkins

April 2004
•Progression of Gene Hypermethylation in Gallstone Disease Leading to Gallbladder Cancer

October 2003
•New Pathway for Cancer Discovered in Hedgehog

July 2003
• Opportunity for Collaboration from New Biliary Cancer Laboratory

• NEW: Johns Hopkins Biliary Cancer Tissue Resources

February 2003
• Identification of novel tumor markers in biliary carcinomas using tissue microarrays

• Identification of novel targets of biliary tract cancers using global gene expression technology

• Telomere length variation in biliary tract metaplasia, dysplasia and carcinoma

September 2002
New Lab for Biliary Tract Cancers

February 2002
Creation of Tissue Microarrays

January 2002
• Immunohistochemical Analysis of Cyclooxygenase Enzymes in the Sequential Pathogenesis of Gallbladder Carcinoma

• Microsatellite Instability in Intraductal Papillary Mucinous Neoplasms of the Biliary Tree

• Genetic Analysis of Gallbladder Carcinoma and Precursor Lesions

July 2001
Molecular and Immunohistochemical Analysis

May 2001
A Novel Target for Anti-Biliary Tract Cancer Drug Development

March 2001
Differing Rates of Loss of Dpc4 Expression and of P53 Overexpression...



What's New?

March 2012

Hopkins team identifies new pathway in Hepatobiliary cancers

An overarching our goal of our research is to identify proteins and pathways which overexpressed (over-represented in biliary cancers), since these may potentially be targeted by therapies that are specifically toxic to and kill tumor cells but not normal cells. In a recent publication in Human Pathology, Dr. Bai and Anders led a study which identified the expression of Yes-associated protein in biliary cancers. The Yes-associated protein (YAP) is a transcription co-activator of the Hippo signaling pathway. YAP deficiency in mice alters bile duct development, suggesting that YAP plays an important role in biliary tract homeostasis. This study finds elevated nuclear expression of YAP in intrahepatic cholangiocarcinoma relative to normal bile ducts. The authors also demonstrate that nuclear YAP expression correlates with nuclear survivin expression in intrahepatic cholangiocarcinoma, and in a mouse model find that survivin expression is dependent upon Yes protein expression. These findings identify a novel pathway which can potentially be targeted in biliary cancers, leading to non-toxic affective therapies.

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Note: This study was supported in part by donations to the biliary cancer research fund at Johns Hopkins.




December 2011

Mimicker of Gallbladder Adenocarcinoma Described at Johns Hopkins

In recent study, Dr. Aatur Singhi at Hopkins described 6 cases of proliferations of Luschka ducts which were confused with adenocarcinoma of the gallbladder. In fact, in 2 of the cases, the diagnosis of adenocarcinoma had been rendered by the contributing pathologist. Dr. Singhi’s manuscript describes how these developmental variants can undergo proliferation in the setting of cholecystitis, and in the setting of a thickened gallbladder mimic cancer both clinically and pathologically. Dr. Singhi outlines specific criteria to help make this important distinction, and prevent a misdiagnosis of adenocarcinoma which would result in significant over treatment and patient morbidity. These cases illustrate the utility of second opinion pathology in the biliary tract.

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Reference: American Journal of Surgical Pathology 2011; 35:883-890.



  
   
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