Urinary organ specific neoantigen |
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Authors: | Dr. Martin Tobi MB ChB Elizabeth Darmon MSc Paul Rozen MBBS Nurit Harpaz MSc Aron Fink MD PhD Benedict Maliakkal MD Allan Halline MD Sohrab Mobarhan MD Zvi Bentwich MD |
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Affiliation: | (1) Department of Gastroenterology, Tel Aviv Medical Center, 6 Weizman St, Tel Aviv, Israel;(2) The Ben-Ari Immunological Institute, Kaplan Hospital, Rehovot, Israel;(3) Division of Gastroenterology, Department of Medicine, Wayne State University Medical School, Harper Hospital, 3990 John R St., 48201 Detroit, Michigan;(4) Division of Gastroenterology, University of Illinois at Chicago, Chicago, Illinois;(5) Loyola University Medical Center, Maywood, Illinois |
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Abstract: | Urinary organ-specific neoantigen from colorectal cancer patients has been used to make a monoclonal antibody, BAC 18.1. In this study we assessed the potential of this antibody for the diagnosis of colorectal cancer. We evaluated binding in both urine and effluent samples and compared it with effluent carcinoembryonic antigen standardized for both volume (nanograms per milliliter) and protein. Urinary organ-specific antigen as detected by BAC 18.1 was significantly greater in 29 cancer patients (A405:0.717±0.500) vs 27 controls [0.121 ±0.273 (P<0.05)]. Considerable overlap of binding of BAC 18.1 was observed in the colonic effluent of patients with CRC (N=13), adenomas (N=26), inflammatory bowel disease (N=8), or having a normal colonoscopic examination (N=24). CEA levels (nanograms per milliliter) were significantly elevated in the effluent samples of patients with a past history of colorectal cancer, as compared to that of normal individuals (P<0.05). The presence of the Mr 30,000 organ-specific neoantigen in colonic effluent was also demonstrated by western blot. Organ-specific neoantigen originates in the colon and is excreted into the urine, so the BAC 18.1 binding levels in the urine may be a diagnostic aid for CRC.The work reported in this paper was supported in part by a grant from the Israeli Cancer Association and Tel Aviv University, and in part by grants from the Israel Cancer Association and the Sackler School of Medicine, Tel Aviv, Israel. |
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Keywords: | monoclonal antibody colorectal cancer leukocyte adherence inhibition carcinoembryonic antigen |
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