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PubMed:10223563 JSONTXT

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DisGeNET

Id Subject Object Predicate Lexical cue
T0 939-942 gene:10249 denotes GAT
T1 872-887 disease:C0001418 denotes adenocarcinomas
R1 T0 T1 associated_with GAT,adenocarcinomas

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
10223563-7#79#82#gene10249 939-942 gene10249 denotes GAT
10223563-7#119#122#gene7368 979-982 gene7368 denotes CGT
10223563-7#12#27#diseaseC0001418 872-887 diseaseC0001418 denotes adenocarcinomas
79#82#gene1024912#27#diseaseC0001418 10223563-7#79#82#gene10249 10223563-7#12#27#diseaseC0001418 associated_with GAT,adenocarcinomas
119#122#gene736812#27#diseaseC0001418 10223563-7#119#122#gene7368 10223563-7#12#27#diseaseC0001418 associated_with CGT,adenocarcinomas

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 175-486 BACKGROUND denotes Hyperplastic ductal lesions of the pancreas are believed to represent precursors of ductal adenocarcinoma. The most frequent mutation in manifest ductal carcinoma of the pancreas is the K-ras mutation at codon 12. The frequency and significance of this mutation in precursor lesions are a matter of controversy.
T2 496-850 METHODS denotes The study included 35 resection specimens of ductal adenocarcinoma of the head of the pancreas and 3 noncancerous, noninflammatory pancreases. Ductal lesions were classified according to established criteria. Single cells from these lesions were microdissected and analyzed by the denaturing gradient gel electrophoresis polymerase chain reaction method.
T3 860-1487 RESULTS denotes All primary adenocarcinomas showed a K-ras mutation at codon 12 (25 cases with GAT, 7 cases with GTT, and 3 cases with CGT). One hundred and six of 364 ductal lesions were positive for the mutation. The highest relative percentage (53%) occurred in adenomatoid hyperplasia, followed by 36% in papillary hyperplasia, 26% in mucinous hypertrophy, and 14% in squamous metaplasia. With only two exceptions the mutation pattern of the ductal lesions and that of the corresponding primary tumor were identical. Twenty-one samples from normal ducts (17%) also harbored the K-ras mutation, as did 3 lesions from noncancerous specimens.
T4 1501-1973 CONCLUSIONS denotes K-ras mutations are common events in normal, hyperplastic, metaplastic, and neoplastic pancreatic ductal cells. Because K-ras mutations frequently, although not exclusively, are related to mucinous differentiation of pancreatic cells, this mutation may not cause but only promote mucinous differentiation. The prevalence of a certain mutation pattern in nonneoplastic and neoplastic ductal cells in an individual pancreas suggests the dominance of one carcinogenic factor.