Influence of the interaction between nodal fibroblast and breast cancer cells on gene expression

被引:20
作者
Costa Santos, Rosangela Portilho [1 ]
Benvenuti, Ticiana Thomazine [1 ]
Honda, Suzana Terumi [1 ]
Del Valle, Paulo Roberto [1 ]
Hirata Katayama, Maria Lucia [1 ]
Brentani, Helena Paula [2 ]
Carraro, Dirce Maria [3 ]
Rozenchan, Patricia Bortman [1 ]
Brentani, Maria Mitzi [1 ]
de Lyra, Eduardo Carneiro [4 ]
Torres, Cesar Henrique [3 ]
Salzgeber, Marcia Batista [1 ]
Lima Kaiano, Jane Haruko [3 ]
Sampaio Goes, Joao Carlos [4 ]
Azevedo Koike Folgueira, Maria Aparecida [1 ]
机构
[1] Univ Sao Paulo, Fac Med, Dept Radiol & Oncol, LIM24, BR-01246903 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fac Med, Dept Psiquiatria, BR-01246903 Sao Paulo, Brazil
[3] Hosp Canc AC Camargo, Sao Paulo, Brazil
[4] Inst Brasileiro Controle Canc, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Breast cancer; Epithelial mesenchymal interaction; Gene expression profile; Lymph node metastasis; Stromal fibroblasts; STROMAL FIBROBLASTS; TUMOR-GROWTH; PROLIFERATION; INVASION; PROFILE; MODEL;
D O I
10.1007/s13277-010-0108-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our aim was to evaluate the interaction between breast cancer cells and nodal fibroblasts, by means of their gene expression profile. Fibroblast primary cultures were established from negative and positive lymph nodes from breast cancer patients and a similar gene expression pattern was identified, following cell culture. Fibroblasts and breast cancer cells (MDA-MB231, MDA-MB435, and MCF7) were cultured alone or co-cultured separated by a porous membrane (which allows passage of soluble factors) for comparison. Each breast cancer lineage exerted a particular effect on fibroblasts viability and transcriptional profile. However, fibroblasts from positive and negative nodes had a parallel transcriptional behavior when co-cultured with a specific breast cancer cell line. The effects of nodal fibroblasts on breast cancer cells were also investigated. MDA MB-231 cells viability and migration were enhanced by the presence of fibroblasts and accordingly, MDA-MB435 and MCF7 cells viability followed a similar pattern. MDA-MB231 gene expression profile, as evaluated by cDNA microarray, was influenced by the fibroblasts presence, and HNMT, COMT, FN3K, and SOD2 were confirmed downregulated in MDA-MB231 co-cultured cells with fibroblasts from both negative and positive nodes, in a new series of RT-PCR assays. In summary, transcriptional changes induced in breast cancer cells by fibroblasts from positive as well as negative nodes are very much alike in a specific lineage. However, fibroblasts effects are distinct in each one of the breast cancer lineages, suggesting that the inter-relationships between stromal and malignant cells are dependent on the intrinsic subtype of the tumor.
引用
收藏
页码:145 / 157
页数:13
相关论文
共 39 条
[1]  
Bourhis XFDL, 1997, INT J CANCER, V71, P42, DOI 10.1002/(SICI)1097-0215(19970328)71:1<42::AID-IJC9>3.3.CO
[2]  
2-X
[3]   Gene expression arrays in cancer research: methods and applications [J].
Brentani, RR ;
Carraro, DM ;
Verjovski-Almeida, S ;
Reis, EM ;
Neves, EJ ;
de Souza, SJ ;
Carvalho, AF ;
Brentani, H ;
Reis, LFL .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2005, 54 (02) :95-105
[4]   FIBROBLAST-MEDIATED ACCELERATION OF HUMAN EPITHELIAL TUMOR-GROWTH INVIVO [J].
CAMPS, JL ;
CHANG, SM ;
HSU, TC ;
FREEMAN, MR ;
HONG, SJ ;
ZHAU, HE ;
VONESCHENBACH, AC ;
CHUNG, LWK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :75-79
[5]   Gene expression of fructosamine 3 kinase in patients with colorectal cancer [J].
Caruso, Maria Gabriella ;
Notarnicola, Maria ;
Altomare, Donato Francesco ;
Misciagna, Giovanni .
ONCOLOGY, 2007, 73 (1-2) :72-75
[6]   Evidence that molecular changes in cells occur before morphological alterations during the progression of breast ductal carcinoma [J].
Castro, Nadia P. ;
Osorio, Cynthia A. B. T. ;
Torres, Cesar ;
Bastos, Elen P. ;
Mourao-Neto, Mario ;
Soares, Fernando A. ;
Brentani, Helena P. ;
Carraro, Dirce M. .
BREAST CANCER RESEARCH, 2008, 10 (05)
[7]   Onto-Tools, the toolkit of the modern biologist: Onto-Express, Onto-Compare, Onto-Design and Onto-Translate [J].
Draghici, S ;
Khatri, P ;
Bhavsar, P ;
Shah, A ;
Krawetz, SA ;
Tainsky, MA .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3775-3781
[8]   A gene expression signature that defines breast cancer metastases [J].
Ellsworth, Rachel E. ;
Seebach, Jeff ;
Field, Lori A. ;
Heckman, Caroline ;
Kane, Jennifer ;
Hooke, Jeffrey A. ;
Love, Brad ;
Shriver, Craig D. .
CLINICAL & EXPERIMENTAL METASTASIS, 2009, 26 (03) :205-213
[9]  
Folgueira MAAK, 2005, CLIN CANCER RES, V11, P7434
[10]   Regulation of in situ to invasive breast carcinoma transition [J].
Hu, Min ;
Yao, Jun ;
Carroll, Danielle K. ;
Weremowicz, Stanislawa ;
Chen, Haiyan ;
Carrasco, Daniel ;
Richardson, Andrea ;
Violette, Shelia ;
Nikolskaya, Tatiana ;
Nikolsky, Yuri ;
Bauerlein, Erica L. ;
Hahn, William C. ;
Gelman, Rebecca S. ;
Allred, Craig ;
Bissell, Mina J. ;
Schnitt, Stuart ;
Polyak, Kornelia .
CANCER CELL, 2008, 13 (05) :394-406