Breaking down barriers: the importance of the stromal microenvironment in acquiring invasiveness in young women's breast cancer

被引:20
作者
Schedin, Pepper [1 ,2 ,3 ,4 ]
Borges, Virginia [1 ,2 ,3 ]
机构
[1] Univ Colorado Denver, Div Med Oncol, Dept Med, Aurora, CO 80045 USA
[2] Univ Colorado Denver, Univ Colorado Comprehens Canc Ctr, Aurora, CO 80045 USA
[3] Univ Colorado Hosp, Young Womens Breast Canc Translat Res Program, Aurora, CO 80025 USA
[4] Univ Colorado Denver, AMC Canc Res Ctr, Aurora, CO 80045 USA
关键词
TUMOR-MICROENVIRONMENT; PROGRESSION; METASTASIS; CARCINOMA; SIGNATURE; GENES; CELLS;
D O I
10.1186/bcr2235
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gene expression profiling was performed on laser captured breast stroma and epithelium obtained from 14 breast cancer patients. As with breast epithelium, of the stromal gene expression changes observed between normal tissue and invasive ductal carcinoma, greater than 90% occurred early, at the normal to ductal carcinoma in situ transition. Only 10% of stromal and 0% of epithelial genes were differentially regulated between non-invasive ductal carcinoma in situ and invasive disease. These data suggest that the majority of gene expression changes required for transformation occur early, prior to histological evidence of an invasive phenotype, the stroma cooperates closely with epithelium in this transformation, and for acquisition of the invasive phenotype, the stroma is dominant over the epithelium.
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页数:2
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共 15 条
[1]   Metastasis signatures: genes regulating tumor-microenvironment interactions predict metastatic behavior [J].
Albini, Adriana ;
Mirisola, Valentina ;
Pfeffer, Ulrich .
CANCER AND METASTASIS REVIEWS, 2008, 27 (01) :75-83
[2]   Molecular characterization of the tumor microenvironment in breast cancer [J].
Allinen, M ;
Beroukhim, R ;
Cai, L ;
Brennan, C ;
Lahti-Domenici, J ;
Huang, HY ;
Porter, D ;
Hu, M ;
Chin, L ;
Richardson, A ;
Schnitt, S ;
Sellers, WR ;
Polyak, K .
CANCER CELL, 2004, 6 (01) :17-32
[3]   Inhibition of metastatic outgrowth from single dormant tumor cells by targeting the cytoskeleton [J].
Barkan, Dalit ;
Kleinman, Hynda ;
Simmons, Justin L. ;
Asmussen, Holly ;
Kamaraju, Anil K. ;
Hoenorhoff, Mark J. ;
Liu, Zi-yao ;
Costes, Sylvain V. ;
Cho, Edward H. ;
Lockett, Stephen ;
Khanna, Chand ;
Chambers, Ann F. ;
Green, Jeffrey E. .
CANCER RESEARCH, 2008, 68 (15) :6241-6250
[4]   The fibromatosis signature defines a robust stromal response in breast carcinoma [J].
Beck, Andrew H. ;
Espinosa, Inigo ;
Gilks, C. Blake ;
van de Rijn, Matt ;
West, Robert B. .
LABORATORY INVESTIGATION, 2008, 88 (06) :591-601
[5]   The Macrophage Colony-Stimulating Factor 1 Response Signature in Breast Carcinoma [J].
Beck, Andrew H. ;
Espinosa, Inigo ;
Edris, Badreddin ;
Li, Rui ;
Montgomery, Kelli ;
Zhu, Shirley ;
Varma, Sushama ;
Marinelli, Robert J. ;
van de Rijn, Matt ;
West, Robert B. .
CLINICAL CANCER RESEARCH, 2009, 15 (03) :778-787
[6]   Metastasis genes: A progression puzzle [J].
Bernards, R ;
Weinberg, RA .
NATURE, 2002, 418 (6900) :823-823
[7]   Gene expression signature of fibroblast serum response predicts human cancer progression: Similarities between tumors and wounds [J].
Chang, HY ;
Sneddon, JB ;
Alizadeh, AA ;
Sood, R ;
West, RB ;
Montgomery, K ;
Chi, JT ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PLOS BIOLOGY, 2004, 2 (02) :206-214
[8]   Immune cells as mediators of solid tumor metastasis [J].
DeNardo, David G. ;
Johansson, Magnus ;
Coussens, Lisa M. .
CANCER AND METASTASIS REVIEWS, 2008, 27 (01) :11-18
[9]   The fibroblastic coconspirator in cancer progression [J].
Egeblad, M. ;
Littlepage, L. E. ;
Werb, Z. .
Molecular Approaches to Controlling Cancer, 2005, 70 :383-388
[10]   Gene expression profiling of the tumor microenvironment during breast cancer progression [J].
Ma, Xiao-Jun ;
Dahiya, Sonika ;
Richardson, Elizabeth ;
Erlander, Mark ;
Sgroi, Dennis C. .
BREAST CANCER RESEARCH, 2009, 11 (01)