Steroid hormone receptor status of mouse mammary stem cells

被引:221
作者
Asselin-Labat, Marie-Liesse
Shackleton, Mark
Stingl, John
Vaillant, Francois
Forrest, Natasha C.
Eaves, Connie J.
Visvader, Jane E.
Lindeman, Geoffrey J.
机构
[1] Walter & Eliza Hall Inst Med Res, VBCRC Lab, Melbourne, Vic 3050, Australia
[2] Univ Melbourne, Parkville, Vic 3052, Australia
[3] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 1L3, Canada
[4] StemCell Technol Inc, Vancouver, BC, Canada
[5] Royal Melbourne Hosp, Dept Clin Haematol & Med Oncol, Melbourne, Vic, Australia
关键词
D O I
10.1093/jnci/djj267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The estrogen receptor alpha (ER alpha), progesterone receptor (PR), and erbB2 (Her2 in humans) are important prognostic markers of human breast cancer, and they are variably expressed in different subtypes of breast cancer. The basal subtype, for example, is negative for ERa, PR, and Her2 by immunohistochemistry. We investigated the expression of these signaling molecules in enriched populations of mouse mammary stem cells and luminal cells that were isolated according to their differential expression of CD24 and the alpha 6 beta 1-integrin complex. We found that the basal population, which is enriched in mouse mammary stem cells, did not express ERa, PR, or ErbB2/Her2 but did express epidermal growth factor receptor (EGFR)/ ErbB1, whereas the subset of cells enriched for luminal cells expressed ERa (37% of cells) and PR (40% of cells) but not ErbB2/Her2 or EGFR/ErbB1. Ovariectomy confirmed the importance of estrogen signaling to luminal cell proliferation but had no effect on the size of the mouse mammary stem cell-enriched population. Thus, mouse mammary stem cells were negative for ER alpha, PR, and ErbB2 and appeared to share common properties with poor-prognosis basal breast cancer.
引用
收藏
页码:1011 / 1014
页数:4
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