Lex and Ley antigen expression in human pancreatic cancer release_x7wnmjdy6bbzfo7clq6vn2g4da

by Y S Kim, S H Itzkowitz, M Yuan, Y Chung, K Satake, K Umeyama, S Hakomori

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abstracts[] {'sha1': '34081dc372dcba6e4da33a97939064f9f7b761e3', 'content': 'Carbohydrate antigens are useful markers for the serological detection of pancreatic cancer. However, data concerning the expression of structurally well-defined carbohydrate antigens in normal and malignant pancreatic tissue is quite limited. The Lex and Leg antigens are closely related carbohydrate antigens synthesized on type 2 blood group oligosaccharide side chains of glycolipids and glycoproteins. Monoclonal antibodies anti-SSEA-1 and AH6 recognize "simple" Lex and Ley epitopes, respectively, regardless of the length of the carrier carbohydrate. Other monoclonal antibodies recognize Lex (FH4), sialyl Lex (FH6, IB9) or Ley (KH1, CC-1, CC-2) carried only by elongated type 2 side chains with or without internal alpha 1,3 fucosyl substitution. The present comparative immunohistochemical study used tissues of normal pancreas, chronic pancreatitis, and pancreatic cancer to determine the normal expression of Lex and Ley antigens in the pancreas and to elucidate any cancer-associated alterations. Lex-related antigens were not expressed in normal pancreas, expressed in only 10-20% of chronic pancreatitis tissues, but expressed in 50-70% of pancreatic cancer tissues. The frequency of Lex-related antigen expression in pancreatic cancer tissues was lowest in poorly differentiated cancers. Within a given specimen, at least three or all four of the Lex recognizing monoclonal antibodies were simultaneously expressed. Unlike Lex antigens, Ley-related antigens were expressed in 32-77% of specimens of normal pancreas, with similar frequencies in specimens of chronic pancreatitis and pancreatic cancer. In normal pancreas, simple Ley was expressed by both ductal and acinar cells, but extended Ley antigens were expressed only by acinar cells. In pancreatic cancer, extended Ley antigen expression was found in less than 10% of poorly differentiated tumors. Coexpression among the Ley-related antigens was less common than with the Lex-related antigens. Also in cancer specimens, simple Lex and simple Lex antigens were often concordantly expressed, whereas extended Lex and extended Ley antigen expression was often discordant. Hyperplastic ducts and ductules associated with pancreatic cancer expressed Lex-related antigens more frequently than morphologically similar lesions associated with chronic pancreatitis. These results demonstrate that Lex-related antigens are cancer-associated determinants in the human pancreas. The discrepant expression between Lex and Ley antigens in these tissues implies altered regulation of fucosyltransferase activity associated with the malignant state.', 'mimetype': 'text/plain', 'lang': 'en'}
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{'index': 1, 'creator_id': None, 'creator': None, 'raw_name': 'S H Itzkowitz', 'given_name': 'S H', 'surname': 'Itzkowitz', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
{'index': 2, 'creator_id': None, 'creator': None, 'raw_name': 'M Yuan', 'given_name': 'M', 'surname': 'Yuan', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
{'index': 3, 'creator_id': None, 'creator': None, 'raw_name': 'Y Chung', 'given_name': 'Y', 'surname': 'Chung', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
{'index': 4, 'creator_id': None, 'creator': None, 'raw_name': 'K Satake', 'given_name': 'K', 'surname': 'Satake', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
{'index': 5, 'creator_id': None, 'creator': None, 'raw_name': 'K Umeyama', 'given_name': 'K', 'surname': 'Umeyama', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
{'index': 6, 'creator_id': None, 'creator': None, 'raw_name': 'S Hakomori', 'given_name': 'S', 'surname': 'Hakomori', 'role': 'author', 'raw_affiliation': None, 'extra': {}}
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issue 2
language en
license_slug
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original_title
pages 475-82
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release_date 1988-01-15
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release_type article-journal
release_year 1988
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title Lex and Ley antigen expression in human pancreatic cancer
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volume 48
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pubmed.pub_types ['Journal Article']