Analysis of stromal signatures in the tumor microenvironment of ductal carcinoma in situ

被引:74
作者
Sharma, M. [1 ]
Beck, A. H. [1 ]
Webster, J. A. [1 ]
Espinosa, I. [1 ]
Montgomery, K. [1 ]
Varma, S. [2 ]
van de Rijn, M. [1 ]
Jensen, K. C. [1 ,2 ]
West, R. B. [1 ,2 ]
机构
[1] Stanford Univ Hosp, Dept Pathol, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
关键词
Ductal carcinoma in situ; Tumor microenvironment; Cancer stroma; Fibroblast; Macrophage; BREAST-CANCER; FIBROBLASTS; CELLS; AMPLIFICATION; ANGIOGENESIS; SECRETION; GROWTH;
D O I
10.1007/s10549-009-0654-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent advances in the study of the tumor microenvironment have revealed significant interaction between tumor cells and their surrounding stroma in model systems. We have previously shown that two distinct stromal signatures derived from a macrophage (CSF1) response and a fibroblastic (DTF-like) response are present in subsets of invasive breast cancers and show a correlation with clinical outcome [1-3]. In the present study we explore whether these signatures also exist in the stroma of ductal carcinoma in situ (DCIS). We studied the signatures by both gene expression profile analysis of a publically available data set of DCIS and by immunohistochemistry (IHC) on a tissue microarray of DCIS and invasive breast cancer cases. Both the gene expression and immunohistochemical data show that the macrophage response and fibroblast expression signatures are present in the stroma of subsets of DCIS cases. The incidence of the stromal signatures in DCIS is similar to the incidence in invasive breast cancer that we have previously reported. We also find that the macrophage response signature is associated with higher grade DCIS and cases which are ER and PR negative, whereas the fibroblast signature was not associated with any clinicopathologic features in DCIS. A comparison of 115 matched cases of DCIS and invasive breast cancer found a correlation between the type of stromal response in DCIS and invasive ductal carcinoma (IDC) within the same patient for both the macrophage response and the fibroblast stromal signatures (P = 0.03 and 0.08, respectively). This study is a first characterization of these signatures in DCIS. These signatures have significant clinicopathologic associations and tend to be conserved as the tumor progresses from DCIS to invasive breast cancer.
引用
收藏
页码:397 / 404
页数:8
相关论文
共 33 条
[1]   Tumor-specific low molecular weight forms of cyclin E induce genomic instability and resistance to p2l, p27, and antiestrogens in breast cancer [J].
Akli, S ;
Zheng, PJ ;
Multani, AS ;
Wingate, HF ;
Pathak, S ;
Zhang, N ;
Tucker, SL ;
Chang, S ;
Keyomarsi, K .
CANCER RESEARCH, 2004, 64 (09) :3198-3208
[2]   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
[3]   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
[4]   Tumor-stroma interactions [J].
Bhowmick, NA ;
Moses, HL .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2005, 15 (01) :97-101
[5]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[6]  
Brown LF, 1999, CLIN CANCER RES, V5, P1041
[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]   Role of the stromal microenvironment in carcinogenesis of the prostate [J].
Cunha, GR ;
Hayward, SW ;
Wang, YZ ;
Ricke, WA .
INTERNATIONAL JOURNAL OF CANCER, 2003, 107 (01) :1-10
[9]   Targeting HER-2/neu in early breast cancer development using dendritic cells with staged interleukin-12 burst secretion [J].
Czerniecki, Brian J. ;
Koski, Gary K. ;
Koldovsky, Ursula ;
Xu, Shuwen ;
Cohen, Peter A. ;
Mick, Rosemarie ;
Nisenbaum, Harvey ;
Pasha, Terry ;
Xu, Min ;
Fox, Kevin R. ;
Weinstein, Susan ;
Orel, Susan G. ;
Vonderheide, Robert ;
Coukos, George ;
DeMichele, Angela ;
Araujo, Louis ;
Spitz, Francis R. ;
Rosen, Mark ;
Levine, Bruce L. ;
June, Carl ;
Zhang, Paul J. .
CANCER RESEARCH, 2007, 67 (04) :1842-1852
[10]  
DVORAK HF, 1986, NEW ENGL J MED, V315, P1650