Mathews Journal of Cancer Science

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    Previous Issues Volume 1, Issue 1 - 2016

    Research ArticlePDF  

    Proposed Use of Deoxycholic Acid (DCA) and Ursodeoxycholic Acid (UDCA) in a Treatment Regimen for Barrett’s Esophagus

    Dennis Stamp1

    123 Fairmar ave. Toronto On. Canada. M8Y2C7.

    Corresponding Author:Dennis Stamp, 23 Fairmar ave. Toronto On. Canada. M8Y2C7, Tel: +416- 239- 8708;

    Received Date: 29 Jul 2016   
    Accepted Date: 01 Oct 2016    
    Published Date:
     03 Oct 2016

    Copyright © 2016 Stamp D

    Citation: Stamp D. (2016). Proposed Use of Deoxycholic Acid (DCA) and Ursodeoxycholic Acid (UDCA) in a Treatment Regi- men for Barrett's Esophagus. Mathews J Cancer Sci. 1(1): 007.



    Huo et al [1] first placed 250 uM of the hydrophobic bile acid (DCA) into the esophagus of patients with Barrett's esopha- gus (BE) and left it there for 5 min. The DCA was dissolved in alcohol. Subsequent examination of the biopsies taken from the esophagus showed that the DNA was damaged and the nuclear factor NF-kB was activated. Additionally, many other pre-cancerous lesions were activated. Similar treatment with the hydrophilic bile acid (UDCA) was ineffective, suggesting that UDCA could be an anti-carcinogen.
    In a subsequent study, Sue Peng et al [2], showed that equal amounts of DCA and UDCA would cancel out each other and that UDCA had a protective effect on esophageal cancers.
    Banerjee et al [3] fed Barrett's esophagus (BE) patients with UDCA (13-15 mg/Kg body weight) daily for six months. Biop- sies taken during this time showed no effects on carcinogen- esis as detected by oxidative DNA damage, cell proliferation, or apoptosis. There was however a dramatic increase in the metabolic products of UDCA. This suggested that UDCA was not getting into the BE tissues despite six months of daily UDCA intake. To overcome this discrepancy, it was suggested that liposome technology could be used to coerce UDCA to enter into the BE cells [4]. 
    Liposomes are phospholipid vesicles measuring 10-90 nm in diameter. They are composed of phospholipids and cholesterol generally in the ratio of 10 to 1. They are able to entrap hydrophilic compounds like UDCA in their aqueous interior. In their outer membrane sections, hydrophobic compounds like DCA would be entrapped. Both compounds (UDCA and DCA) could not exist in the same vesicle since they would cancel each other. 
    In the proposed study, liposomes containing UDCA in their aqueous interior would be used. The liposomes would make direct contact with the BE tissues thus bypassing the RES (re- ticuloendothelial system), a network of phagocytic cells all over the body that is designed, among other functions, to re- move foreign substances (like liposomes) from the systemic circulation.



    Using the model system of Huo et al [1]. BE patients would first receive an alcoholic solution of the hydrophobic DCA (250 µM) in their esophagus for five minutes. This would perfuse the cell membranes of the esophagus of these patients. The pre- cancer features, first described, would still occur [1]. Li- posomes bearing UDCA in their aqueous compartment would then be added to the esophagus in a similar way, after the DCA treatments. On contact with the BE epithelia, the liposomes would fuse with the BE cell membranes and deliver their con- tents of UDCA inside the cells. There they would prevent DNA damage, reactive oxygen species (ROS) generation and NF-kB activation and remain inside the cells to neutralize any later DCA incursions. The results of this study could be followed by taking biopsies at regular intervals.



    Jean-Louis et al [4] using the colonic cells as a membrane model, examined the action of DCA on the cell membrane. They found that DCA could perturb the cell membrane struc- ture and cause a marked rearrangement of its cholesterol. As well, they found that DCA caused a decrease in membrane fluidity and cholesterol levels. There was no such effect when UDCA was similarly used. Using liposomes as another membrane model, they found a similar effect when DCA was added. In both cases cholesterol levels as well as membrane fluidity were affected. Thus, the total effect was to pull the liposome closer to the BE membrane and cause liposome: cell fusion. Once fusion is achieved between the liposomes and the BE cells, UDCA from the liposome well enter the cell and start a reaction that will neutralize the DCA and hopefully stop carcinogenesis. 
    More details of the earlier work that led to this liposome study can be found in reference where a similar treatment was sug- gested for polyps in early colon cancer studies [5].



    1. Huo X, Jeurgens S, Zhang X, Rezaei D, et al. (2011). Deoxycholic acid causes DNA damage while inducing apoptosis resistance through Nf-kB activation in benign Barrett's epithelial cells. Am J Physiol. Gastrointest Liver Physiol. 301(2), G278- 286.
    2. Peng S, Huo X, Rezaei D, Zhang Q, et al. (2014). In Barrett's esophagus patients and Barrett's cell lines, ursodeoxycholic increases antioxidant expression and prevents DNA damage by bile acids. Am J Physiol. Gastrointest. Liver Physiol. 307(2), 129-139.
    3. Banerjee B, Shaheen NJ, Martinez JA, Hsu CH, et al. (2016). Clinical study of ursodeoxycholic acid in Barrett's esophagus patients. Cancer Prev Res (Phila). 9(7), 528-533.
    4. Jean-Louis S, Akare S, Ali MA, Mash EA Jr, et al. (2006). Deoxycholic acid induces intracellular signalling through membrane perturbations. J. Biol. Chem. 281(21),14948-14960.
    5. D Stamp. (2016). Ursodeoxycholic acid has a chemopreventive effect on gastroesophageal cancerss, liposome encapsulation of this drug would assure its optimal delivery into the intestinal cells thus stopping carcinogenesis. MJ Cancer. 1(1), 005.

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