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Expression of Bile Acid Transporting Proteins in Barrett's Esophagus and Esophageal Adenocarcinoma

Dvorak, Katerina, PhD1,2,3; Watts, George S., PhD2,4; Ramsey, Lois, BS3; Holubec, Hana, MS1; Payne, Claire M., PhD1,2; Bernstein, Carol, PhD1,3; Jenkins, Gareth J., PhD5; Sampliner, Richard E., MD2,6; Prasad, Anil, MD7; Garewal, Harinder S., MD, PhD2,3,8; Bernstein, Harris, PhD1,2

American Journal of Gastroenterology: February 2009 - Volume 104 - Issue 2 - p 302–309
ORIGINAL CONTRIBUTIONS: ESOPHAGUS
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OBJECTIVES: Barrett's esophagus (BE) is a metaplastic lesion characterized by replacement of the normal squamous epithelium by columnar intestinal epithelium containing goblet cells. It is speculated that this process is an adaptation to protect cells from components of refluxate, such as gastric acid and bile acids. In contrast to the normal squamous epithelium, enterocytes of the distal ileum are adapted to transport bile acids from the intestinal lumen. Several bile acid transporters are utilized for effective removal of bile acids, including the apical sodium-dependent bile acid transporter (ASBT), the ileal bile acid-binding protein (IBABP), and the multidrug-resistant protein 3 (MRP3). We hypothesized that one of the possible functions of newly arising metaplastic epithelium, in the esophagus, is to transport bile acids. Our major goal was to evaluate the expression of bile acid transporters in normal squamous epithelium, BE with different grades of dysplasia, and esophageal adenocarcinoma (EAC).

METHODS: A total of 101 patients were included in this study. Immunohistochemistry (IHC) and reverse transcriptase (RT)-PCR were used to detect the expression of these transporters at the mRNA and protein levels.

RESULTS: Our immunohistochemical studies showed that all three bile acid transporters are expressed in BE glands, but not in squamous epithelium. ASBT was found in the apical border in BE biopsies. The highest frequency of ASBT expression was in patients with nondysplastic BE (9 of 15, 60%), and a progressive loss of ASBT was observed through the stages of dysplasia. ASBT was not detected in EAC (0 of 15). IBABP staining was observed in the cytoplasm of BE epithelial surface cells. Expression of IBABP was found in 100% of nondysplastic BE (14 of 14), in 93% of low-grade dysplasia (LGD, 15 of 16), in 73% of high-grade dysplasia (HGD, 10 of 14), and in 33% of EAC (5 of 15). MRP3 was expressed in the basolateral membrane in 93% of nondysplastic BE (13 of 14), in 60% of LGD (10 of 16), and in 86% of HGD (11 of 13). Only weak MRP3 staining was detected in EAC biopsies (5 of 15, 33%). In addition, RT-PCR studies showed increased expression of mRNA coding for ASBT (6.1×), IBABP (9.1×), and MRP3 (2.4×) in BE (N=13) compared with normal squamous epithelium(N=15). Significantly increased mRNA levels of IBABP (10.1×) and MRP3 (2.5×) were also detected in EAC (N=21) compared with normal squamous epithelium.

CONCLUSIONS: We found that bile acid transporters expression is increased in BE tissue at the mRNA and protein levels and that expression of bile acid transporter proteins decreased with progression to cancer.

Am J Gastroenterol 2009; 104:302-309; doi:10.1038/ajg.2008.85; published online 27 January 2009

1Department of Cell Biology and Anatomy, The University of Arizona, Tucson, Arizona, USA;

2Arizona Cancer Center, The University of Arizona, Tucson, Arizona, USA;

3Section of Hematology/Oncology, Southern Arizona VA Health Care System, Tucson, Arizona, USA;

4Department of Pharmacology, The University of Arizona, Tucson, Arizona, USA;

5Institute of Life Science, Swansea School of Medicine, Swansea University, Swansea, UK;

6Section of Gastroenterology, Southern Arizona VA Health Care System, Tucson, Arizona, USA;

7Section of Pathology, Southern Arizona VA Health Care System, Tucson, Arizona, USA;

8Department of Internal Medicine, College of Medicine, The University of Arizona, Tucson, Arizona, USA.

Correspondence: Katerina Dvorak, PhD, Department of Cell Biology and Anatomy, University of Arizona, 1501 N. Campbell Avenue, P.O. Box 245044, Tucson, Arizona 85724, USA. E-mail: kdvorak@email.arizona.edu

Received 14 December 2007; accepted 3 September 2008

© The American College of Gastroenterology 2009. All Rights Reserved.
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