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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Main Authors | , , , |
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Format | Patent |
Language | English |
Published |
23.01.2001
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Edition | 7 |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | Application Number: JP19990196877 |