Pten in stromal fibroblasts suppresses mammary epithelial tumours

被引:426
|
作者
Trimboli, Anthony J. [2 ,3 ]
Cantemir-Stone, Carmen Z. [1 ]
Li, Fu [1 ,2 ]
Wallace, Julie A. [1 ]
Merchant, Anand [1 ]
Creasap, Nicholas [2 ,3 ]
Thompson, John C. [2 ,3 ]
Caserta, Enrico [2 ,3 ]
Wang, Hui [2 ,3 ]
Chong, Jean-Leon [2 ,3 ]
Naidu, Shan [2 ,3 ,4 ]
Wei, Guo [1 ,2 ]
Sharma, Sudarshana M. [1 ]
Stephens, Julie A. [5 ]
Fernandez, Soledad A. [5 ]
Gurcan, Metin N. [6 ]
Weinstein, Michael B. [2 ,3 ]
Barsky, Sanford H. [7 ]
Yee, Lisa [8 ]
Rosol, Thomas J. [4 ]
Stromberg, Paul C. [4 ]
Robinson, Michael L. [9 ]
Pepin, Francois [10 ,11 ]
Hallett, Michael [10 ,11 ]
Park, Morag [10 ,12 ]
Ostrowski, Michael C. [1 ,13 ]
Leone, Gustavo [2 ,3 ,13 ]
机构
[1] Ohio State Univ, Coll Med, Dept Mol & Cellular Biochem, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Mol Genet, Coll Biol Sci, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Vet Biosci, Coll Vet Med, Columbus, OH 43210 USA
[5] Ohio State Univ, Ctr Biostat, Off Hlth Sci, Columbus, OH 43210 USA
[6] Ohio State Univ, Dept Biomed Informat, Columbus, OH 43210 USA
[7] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[8] Ohio State Univ, Dept Surg, Sch Med, Columbus, OH 43210 USA
[9] Columbus Childrens Res Inst, Ctr Mol & Human Genet, Columbus, OH 43205 USA
[10] McGill Univ, Rosalind & Morris Goodman Canc Ctr, Dept Biochem, Montreal, PQ H3A 1A1, Canada
[11] McGill Univ, McGill Ctr Bioinformat, Montreal, PQ H3A 1A1, Canada
[12] McGill Univ, Dept Oncol, Montreal, PQ H3A 1A1, Canada
[13] Ohio State Univ, Ctr Comprehens Canc, Tumor Microenvironm Program, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
BREAST-CANCER; GENE-EXPRESSION; ETS-2; PHOSPHORYLATION; EXTRACELLULAR-MATRIX; NEGATIVE REGULATION; CELL-SURVIVAL; PI3K PATHWAY; GROWTH; ACTIVATION; SIGNATURE;
D O I
10.1038/nature08486
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tumour stroma is believed to contribute to some of the most malignant characteristics of epithelial tumours. However, signalling between stromal and tumour cells is complex and remains poorly understood. Here we show that the genetic inactivation of Pten in stromal fibroblasts of mouse mammary glands accelerated the initiation, progression and malignant transformation of mammary epithelial tumours. This was associated with the massive remodelling of the extracellular matrix (ECM), innate immune cell infiltration and increased angiogenesis. Loss of Pten in stromal fibroblasts led to increased expression, phosphorylation (T72) and recruitment of Ets2 to target promoters known to be involved in these processes. Remarkably, Ets2 inactivation in Pten stroma-deleted tumours ameliorated disruption of the tumour microenvironment and was sufficient to decrease tumour growth and progression. Global gene expression profiling of mammary stromal cells identified a Pten-specific signature that was highly represented in the tumour stroma of patients with breast cancer. These findings identify the Pten-Ets2 axis as a critical stroma-specific signalling pathway that suppresses mammary epithelial tumours.
引用
收藏
页码:1084 / U181
页数:10
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