MUC1 expression in primary breast cancer: the effect of tamoxifen treatment

被引:15
作者
Hanson, JM
Browell, DA
Cunliffe, WJ
Varma, J
Allen, A
Hemming, D
Shenton, BK
Young, JR
Higgs, MJ
Brotherick, I
Pearson, JP
机构
[1] Univ Newcastle Upon Tyne, Dept Surg, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Newcastle Upon Tyne, Dept Physiol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Queen Elizabeth Hosp, Dept Surg, Gateshead, Tyne & Wear, England
[4] Queen Elizabeth Hosp, Dept Physiol, Gateshead, Tyne & Wear, England
[5] Queen Elizabeth Hosp, Dept Radiol, Gateshead, Tyne & Wear, England
关键词
breast; cancer; flow cytometry; MUC1; tamoxifen;
D O I
10.1023/A:1017955726902
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This was a non-randomised single institution retrospective study. Forty-six banked frozen tumour specimens were obtained from a group of patients who had undergone 3 weeks of neoadjuvant treatment with tamoxifen between biopsy and surgery. Fifty-one comparison specimens were randomly selected from a group of concomitantly treated primary breast cancer patients who did not receive neoadjuvant tamoxifen. Specimen selection was not based on prognostic factors: hormone receptor status, patient age, or menopausal status. MUC1 expression and cell cycle distribution were assessed by flow cytometry. S-phase, fraction of MUC1 positive and MUC1 negative cells were compared. A lower percentage of cells expressed MUC1 following 3-week tamoxifen treatment 18.2% versus 28.5% (p = 0.03, Mann-Whitney) and lower levels of MUC1 expression were seen following tamoxifen treatment 31,519 molecules/cell versus 39,387 (p = 0.04, Mann-Whitney). MUC1 positive cells, irrespective of treatment group, had a greater proportion of cells in S-phase of the cell cycle 27.9% versus 16.8% (p = 0.0004, Mann-Whitney) and demonstrated more cases of aneuploidy 80.65% versus 42.6% (p < 0.0001). MUC1 levels in primary tumours treated neoadjunctively with 3 weeks of tamoxifen were lower than a comparison group which did not receive tamoxifen. MUC1 should be explored further as an intermediate biomarker for assessment of treatment and prognosis.
引用
收藏
页码:215 / 222
页数:8
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