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Eppley Institute for Research in Cancer and Allied Diseases and Departments of Pathology and Microbiology and of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68105; First Department of Surgery, Nippon Medical School, Tokyo, Japan; and the Wistar Institute, Philadelphia, Pennsylvania 19104
Blood group A, B, H, Le, Leb, Lex, and Ley antigenicity as well as the expression of CA 19-9 were examined in pancreatic cancer specimens from 30 patients, using monoclonal antibodies to the respective antigen and immunohistochemical techniques, and the findings were correlated with the blood group types (ABO and Lewis) of the individuals. Compatible antigen expression was found in 82, 75, and 50% of tumors from patients with A, B, and O blood group types, respectively. Deletion of the compatible antigen was found in 10 (33%) of the cases, predominantly in patients of blood group O type, and incompatible expression (of B antigen only) in 4 (13%). Lea was detected in 87%, Leb in 90%, Lex in 30%, and Ley in 43% of the specimens, regardless of ABH and Lewis phenotype of the patients. Coexpression of Lea and Leb was found in 87%, of Lex and Ley in 13%, of Lea and Lex in 23%, and of Leb and Ley in 40% of the cases. CA 19-9 was expressed in 80% of the tumors; it was present in the tumor tissue of 21 of 22 patients from Lea-b+, in all 4 individuals from Lea+b-, but in none of the 4 patients from Lea-b- phenotype (P < 0.01). Heterogeneity in the expression of each of the antigens was found. The overall results indicate that blood group antigen expression in pancreatic tumor differs from that of other gastrointestinal cancers and that the Lewis antigen expression in pancreatic cancer cells is independent of the blood group phenotype of the patients and thus may be useful as a tumor marker.
1 Supported by Laboratory Core Grant CA36727, NIH.
2 To whom requests for reprints should be addressed, at The Eppley Institute, University of Nebraska Medical Center, 42nd & Dewey Avenue, Omaha, NE 68105.
Received 3/ 1/88. Revised 6/ 1/88. Accepted 7/ 1/88.
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