DIAGNOSIS OF PANCREATIC CANCER BY DETECTING ABNORMALITY IN CHROMOSOME

PROBLEM TO BE SOLVED: To provide a method capable of adequately diagnosing pancreatic cancer, objectively suspecting the progress of pancreatic cancer, and selecting the best treatment for each patient, by detecting deletion in human chromosome-1 long arm-23 to 25 and the like. SOLUTION: This method...

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Bibliographic Details
Main Authors KISHIMOTO TOSHIHIKO, NIWA SHINICHIRO, JITSUKAWA TOMOFUMI, SASAKI ISANORI
Format Patent
LanguageEnglish
Published 23.01.2001
Edition7
Subjects
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Summary:PROBLEM TO BE SOLVED: To provide a method capable of adequately diagnosing pancreatic cancer, objectively suspecting the progress of pancreatic cancer, and selecting the best treatment for each patient, by detecting deletion in human chromosome-1 long arm-23 to 25 and the like. SOLUTION: This method comprises diagnosing pancreatic cancer by detecting deletion in human chromosome-1 long arm-23 to 25, human chromosome-5 short arm-14 to short arm-ter, human chromosome-5 long arm-14 to 23, human chromosome-1 long arm, human chromosome-13 long arm and the like in chromosomes of a cancer cell derived from a patient. It is preferable to detect deletion or the like by identifying a label at each site so as to be able to observe a chromosome site to which DNA of a cancer cell hybridized with the first label, a chromosome site to which DNA of a normal cell hybridized with the second label, and a chromosomal site to which both DNA hybridized with a mixture of the first and second labels by competitively hybridizing a chromosome of a normal cell with DNA labelled with the first label of a cancer cell derived from a patient and DNA labelled with the second label of a normal cell.
Bibliography:Application Number: JP19990196877