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Flow Cytometric DNA Analysis in Colorectal Cancer and Its Relationship to Clinicopathological Features and Prognosis
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ÃÖµ¿È£ ( Choi Dong-Ho )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ¿Ü°úÇб³½Ç
¼Õżº ( Son Tae-Sung )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ¿Ü°úÇб³½Ç
¹Ú¿µ¼® ( Park Young-Seok )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ¿Ü°úÇб³½Ç
¹éÈ«±Ô ( Baik Hong-Kyu )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ¿Ü°úÇб³½Ç
³²¿µ¼ö ( Nam Young-Soo )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ¿Ü°úÇб³½Ç
Àü±Ô¿µ ( Jun Kyu-Young )
ÇѾç´ëÇб³ ÀÇ°ú´ëÇÐ ÀϹݿܰúÇб³½Ç
KMID : 0356719970130010023
Abstract
DNA flow cytometric analysis was performed on 42 colorectal cancers. DNA ploidy was diploid in 19 and aneuploid in 23 cases. There was no significant correlation between DNA ploidy and clinicopathological features such as primary site, histologic type, depth of invasion, lymph node metastasis, peritoneal seedings, lymphatic invasion and vascular invasion. In aneuploid group, which was divided into two groups, by the value of DNA index, there was no differences between two groups in prognosis and clinocoPathological features. Cumulative survival rates appeared to be more favorable in
patients with aneuploid tumors than patients with diploid tumors, but the difference was not statistically significant.
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Flow Cytometry
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