Stanford School of Medicine
Program in Epithelial Biology In the Department of Dermatology

Anson Lowe

Email:
Phone:(650) 725-3372
Profile: http://med.stanford.edu/profiles/Anson_Lowe/
Academic Appointments
Appointment
Organization
Associate Professor
Associate Professor (By courtesy)
Member
 
Professional Education
Degree
Awarding Institution
Field of Study
Year of Graduation
MD
Mt. Sinai Sch. of Med.
Medicine
1980
BA
UC Berkeley
Physiology
1976
Postdoctoral Advisees
Aiwen Dong, Aparna Gupta
Web Site Links
Research/Lab website:   Lowe Laboratory
Research Interests

My laboratory is focused on the biology of the pancreas and esophagus and their associated diseases. Using animal models and materials from human subjects, we have used DNA microarrays to characterize the gene expression profile of acute pancreatitis, pancreatic cancer, and esophageal cancer. The resultant data has led to a focus on the development of diagnostic assays and the identification of novel genes that participate in disease pathogenesis. Current studies utilize overexpression and RNA interference techniques in cell lines and animal models to explore the role of specific genes in disease.

Barrett's esophagus is a premalignant lesion for esophageal adenocarcinoma, a cancer whose incidence has risen rapidly in the United States. Esophageal reflux, commonly known as heartburn, is believed to increase the risk of Barrett's esophagus and cancer. We have also used DNA microarrays to obtain the gene expression profile of Barrett's esophagus and esophageal adenocarcinoma, and are currently conducting studies to determine the effects of acid and bile reflux on esophageal cells.

One advantage of Barrett's esophagus is that it is very accessible via endoscopic technology, which provides an opportunity to identify and remove precancerous lesions. A major problem is that current approaches for identifying tissues at high risk for transformation to esophageal cancer is poor. We are actively developing assays to easily identify patients who harbor tissues that are at high risk for transformation into cancer.

Publications
  • Wang Z, Hao Y, Lowe AW "The adenocarcinoma-associated antigen, AGR2, promotes tumor growth, cell migration, and cellular transformation." Cancer Res 2008; 68: 2: 492-7 More »
  • Hsiung PL, Hardy J, Friedland S, Soetikno R, Du CB, Wu AP, Sahbaie P, Crawford JM, Lowe AW, Contag CH, Wang TD "Detection of colonic dysplasia in vivo using a targeted heptapeptide and confocal microendoscopy." Nat Med 2008; More »
  • Lowe AW, Olsen M, Hao Y, Lee SP, Taek Lee K, Chen X, van de Rijn M, Brown PO "Gene expression patterns in pancreatic tumors, cells and tissues." PLoS ONE 2007; 2: e323 More »
  • Hao Y, Triadafilopoulos G, Sahbaie P, Young HS, Omary MB, Lowe AW "Gene Expression Profiling Reveals Stromal Genes Expressed in Common Between Barrett's Esophagus and Adenocarcinoma." Gastroenterology 2006; 131: 3: 925-33 More »
  • Yu S, Michie SA, Lowe AW "Absence of the major zymogen granule membrane protein, GP2, does not affect pancreatic morphology or secretion." J Biol Chem 2004; More »
23 publications:   view full list

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