Objective : The purpose of this study was to elucidate the relationship between chromosomal instability (CIN) and phenotypic changes in invasive ductal carcinoma of the breast.
Study Design : The material used in this study was 121 invasive ductal carcinomas. DNA ploidy was measured by laser scanning cytometry (LSC), and CIN was assessed by fluorescence
in situ hybridization (FISH) with centromeric DNA probes for chromosomes 7, 11, 17, and 18. The tumors were tested for expression of estrogen and progesterone receptors (ER and PgR, respectively) and test for expression of Ki-67 by immunohistochemistry. FISH was also used to test for
HER-2 amplification. Nuclear grade was determined histologically and cytologically.
Result : The breast cancers consisted of 47 diploid tumors and 74 aneuploid tumors. Assessment of CIN revealed that 44 (94%) of the diploid tumors were negative and 71 (96%) of the aneuploid tumors were positive. Both ER and PgR were expressed in 74% of the CIN-negative tumors, but neither was expressed in 49% of the CIN-positive tumors (p<0.05).
HER-2 amplification was detected in only six (13%) of the CIN-negative tumors, but it was present in 35 (47%) of the CIN-positive tumors (p<0.0001). High Ki-67 expression was detected in 13 (28%) of the CIN-negative tumors and in 52 (70%) of the CIN-positive tumors (p<0.0001). A higher percentage of high-grade carcinomas than low-grade carcinomas were CIN-positive (p<0.0001).
Conclusion : DNA ploidy and CIN were closely associated with the phenotypic characteristics of invasive ductal carcinomas of the breast, including expression of hormone receptors.
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