Cell cycle analysis of normal, atrophic, and hyperplastic breast epithelium using two-color multiparametric flow cytometry.

Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology 1996 Vol.12(2) p. 115-24

Visscher DW, Gingrich DS, Buckley J, Tabaczka P, Crissman JD

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Abstract

We performed two-color flow cytometric synthesis phase fraction (SPF) determinations on cytokeratin-labeled benign epithelial populations from 142 breast specimens (41 mastectomy, 70 diagnostic biopsy, 31 reduction mammoplasty). There was wide variability of SPF, ranging from 0.1 to 3.5%, with a frequency distribution skewed to higher values (mean 0.75%, median 0.5%). The mean SPE for women less than 29 years was 0.91%, vs. 0.89% for 30-42 years, 0.66% for 43-49 years, and 0.56% for > or = 50 years (P = 0.05). Histologically atrophic tissue samples exhibited a mean SPF approximately half that of morphologically normal tissue from premenopausal age women (0.79% vs. 0.36%, P = 0.02). Tissues showing histologically proliferative fibrocystic features had a greater mean SPF than non-proliferative fibrocystic tissues (0.59% vs. 0.92%); however, due to the wide spread of values within each of these categories, this difference was not statistically significant and neither group was significantly different from 'normal' tissue samples. Patients with histologically normal breast tissue, though, were significantly younger (mean = 34.6 years) than those with fibrocystic changes (non-proliferative mean = 53.4 years vs. proliferative mean = 42.8 years, P = 0.005). Synchronous right- and left-sided specimens obtained from reduction mammoplasty demonstrated significantly correlated SPF determinations (R = 0.77). We conclude that selective analysis of epithelial populations using two-color flow cytometry provides cell cycle information in benign breast tissue which is analogous to that obtained by labor-intensive nucleotide labeling studies. This study also confirms the biologic variability and age-dependence of breast epithelial proliferation. Finally, the data imply that derangements of cell proliferation in fibrocystic conditions are heterogeneous, complex and incompletely correlated with histologic parameters such as hyperplasia.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
해부 breast 유방 dict 5
시술 reduction mammoplasty 유방성형술 dict 2
해부 Cell scispacy 1
해부 tissue scispacy 1
해부 premenopausal scispacy 1
해부 fibrocystic tissues scispacy 1
해부 breast tissue scispacy 1
합병증 hyperplasia scispacy 1
약물 SPE C0764874
SpeA protein, Streptococcus pyogenes
scispacy 1
약물 nucleotide C0028630
Nucleotides
scispacy 1
질환 fibrocystic C1418605
PKHD1 gene
scispacy 1
질환 non-proliferative fibrocystic C1332628
Breast Fibrocystic Change, Non-Proliferative Type
scispacy 1
질환 non-proliferative scispacy 1
질환 hyperplasia C0020507
Hyperplasia
scispacy 1
질환 hyperplastic breast epithelium scispacy 1
질환 cytokeratin-labeled benign epithelial populations scispacy 1
질환 breast specimens scispacy 1
질환 tissue samples scispacy 1
질환 epithelial populations scispacy 1
질환 benign breast tissue scispacy 1
질환 breast epithelial scispacy 1
기타 women scispacy 1
기타 Patients scispacy 1
기타 SPF → synthesis phase fraction scispacy 1

MeSH Terms

Adult; Age Factors; Breast; Cell Cycle; Cell Division; DNA; Epithelium; Female; Fibrocystic Breast Disease; Flow Cytometry; Humans; Hyperplasia; Middle Aged

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