Carotenoid pigments are presently used to prevent the development of light-sensitivity associated with erythropoietic protoporphyria and certain other skin diseases. Carotenoid pigments have also been shown to be anticarcinogenic in animal models and in some epidemiological studies. The carotenoids which have vitamin A activity also play a significant role as dietary sources of vitamin A, especially in developing countries, where access to synthetic vitamin A is limited. For these reasons it is important to understand the metabolism and functions of the various carotenoids. At present, not much is known about the fate in the body of those pigments with no vitamin A activity. We thus plan to study the absorption, transport and metabolism of two carotenoids with no vitamin A activity - lycopene the principal carotenoid of the tomato, and an important component of the blood carotenoid content of Americans, and canthaxanthin, a pigment used in food coloring, which is used in the treatment of light-sensitive skin diseases and has been shown in animal models to have anti-cancer activity. The absorption and metabolism of beta-carotene will also be studied, to compare it to that of the other two pigments. These studies will utilize C14 labeled carotenoids for studies in rats and monkeys of absorption, blood transport, cellular and intracellular location of pigments, and C13 labeled carotenoids to human volunteers for studies of absorption, transport and excretion in man. We plan also to study the enzyme which cleaves beta-carotene, carotenoid 15, 15' dioxygenase, to determine its distribution in various organs of the rat and monkey, to study its specificity for intact carotenoids, as well as to study the properties of the human enzyme obtained from operative specimens of small intestine. It is well established that the use of compounds labeled with the heavy isotope of carbon (13C) is harmless: the isotope occurs naturally (natural abundance - 1-3%).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA042587-03
Application #
3548809
Study Section
(SRC)
Project Start
1985-09-01
Project End
1990-08-31
Budget Start
1987-09-01
Budget End
1990-08-31
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Laguinge, Luciana M; Samara, Raed N; Wang, Wenge et al. (2008) DR5 receptor mediates anoikis in human colorectal carcinoma cell lines. Cancer Res 68:909-17
Ishii, S; Mizoi, T; Kawano, K et al. (1996) Implantation of human colorectal carcinoma cells in the liver studied by in vivo fluorescence videomicroscopy. Clin Exp Metastasis 14:153-64
Ishii, S; Steele Jr, G; Ford, R et al. (1994) Normal colonic epithelium adheres to carcinoembryonic antigen and type IV collagen. Gastroenterology 106:1242-50
Jessup, J M; Brown, K; Ishii, S et al. (1994) Simulated microgravity does not alter epithelial cell adhesion to matrix and other molecules. Adv Space Res 14:71-6
Jessup, J M; Petrick, A T; Toth, C A et al. (1993) Carcinoembryonic antigen: enhancement of liver colonisation through retention of human colorectal carcinoma cells. Br J Cancer 67:464-70
Jessup, J M; Goodwin, T J; Spaulding, G (1993) Prospects for use of microgravity-based bioreactors to study three-dimensional host-tumor interactions in human neoplasia. J Cell Biochem 51:290-300
Jessup, J M; Kim, J C; Thomas, P et al. (1993) Adhesion to carcinoembryonic antigen by human colorectal carcinoma cells involves at least two epitopes. Int J Cancer 55:262-8
Ishii, S; Ford, R; Thomas, P et al. (1993) CD44 participates in the adhesion of human colorectal carcinoma cells to laminin and type IV collagen. Surg Oncol 2:255-64
Krinsky, N I (1991) Effects of carotenoids in cellular and animal systems. Am J Clin Nutr 53:238S-246S
Wagner, H E; Thomas, P; Wolf, B C et al. (1990) Characterization of the tumorigenic and metastatic potential of a poorly differentiated human colon cancer cell line. Invasion Metastasis 10:253-66

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