PMC42, a breast progenitor cancer cell line, has normal-like mRNA and microRNA transcriptomes

被引:20
作者
Git, Anna [1 ,2 ]
Spiteri, Inmaculada [1 ,2 ]
Blenkiron, Cherie [1 ,2 ]
Dunning, Mark J. [1 ,2 ]
Pole, Jessica C. M. [3 ]
Chin, Suet-Feung [1 ,2 ]
Wang, Yanzhong [1 ,2 ]
Smith, James [4 ,5 ]
Livesey, Frederick J. [4 ,5 ]
Caldas, Carlos [1 ,2 ]
机构
[1] Canc Res UK Cambridge Res Inst, Breast Canc Funct Genom Lab, Cambridge CB1 0RE, England
[2] Univ Cambridge, Dept Oncol, Li Ka Shing Ctr, Cambridge CB1 0RE, England
[3] Univ Cambridge, Dept Pathol, Hutchinson MRC Res Ctr, Cambridge CB2 2XZ, England
[4] Univ Cambridge, Dept Biochem, Cambridge CB2 1QN, England
[5] Univ Cambridge, Gurdon Inst, Cambridge CB2 1QN, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
D O I
10.1186/bcr2109
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction The use of cultured cell lines as model systems for normal tissue is limited by the molecular alterations accompanying the immortalisation process, including changes in the mRNA and microRNA (miRNA) repertoire. Therefore, identification of cell lines with normal-like expression profiles is of paramount importance in studies of normal gene regulation. Methods The mRNA and miRNA expression profiles of several breast cell lines of cancerous or normal origin were measured using printed slide arrays, Luminex bead arrays, and real-time reverse transcription-polymerase chain reaction. Results We demonstrate that the mRNA expression profiles of two breast cell lines are similar to that of normal breast tissue: HB4a, immortalised normal breast epithelium, and PMC42, a breast cancer cell line that retains progenitor pluripotency allowing in-culture differentiation to both secretory and myoepithelial fates. In contrast, only PMC42 exhibits a normal-like miRNA expression profile. We identified a group of miRNAs that are highly expressed in normal breast tissue and PMC42 but are lost in all other cancerous and normal-origin breast cell lines and observed a similar loss in immortalised lymphoblastoid cell lines compared with healthy uncultured B cells. Moreover, like tumour suppressor genes, these miRNAs are lost in a variety of tumours. We show that the mechanism leading to the loss of these miRNAs in breast cancer cell lines has genomic, transcriptional, and post-transcriptional components. Conclusion We propose that, despite its neoplastic origin, PMC42 is an excellent molecular model for normal breast epithelium, providing a unique tool to study breast differentiation and the function of key miRNAs that are typically lost in cancer.
引用
收藏
页数:16
相关论文
共 77 条
[1]   Epidermal growth factor-induced epithelio-mesenchymal transition in human breast carcinoma cells [J].
Ackland, ML ;
Newgreen, DF ;
Fridman, M ;
Waltham, MC ;
Arvanitis, A ;
Minichiello, J ;
Price, JT ;
Thompson, EW .
LABORATORY INVESTIGATION, 2003, 83 (03) :435-448
[2]   PMC42, a novel model for the differentiated human breast [J].
Ackland, ML ;
Michalczyk, A ;
Whitehead, RH .
EXPERIMENTAL CELL RESEARCH, 2001, 263 (01) :14-22
[3]   Myoepithelial cells: good fences make good neighbors [J].
Adriance, MC ;
Inman, JL ;
Petersen, OW ;
Bissell, MJ .
BREAST CANCER RESEARCH, 2005, 7 (05) :190-197
[4]  
Akao Y, 2006, ONCOL REP, V16, P845
[5]   FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes [J].
Al-Shahrour, F ;
Díaz-Uriarte, R ;
Dopazo, J .
BIOINFORMATICS, 2004, 20 (04) :578-580
[6]  
*BAB, NEW REL V3 0
[7]   Identification by Real-time PCR of 13 mature microRNAs differentially expressed in colorectal cancer and non-tumoral tissues [J].
Bandres, E. ;
Cubedo, E. ;
Agirre, X. ;
Malumbres, R. ;
Zarate, R. ;
Ramirez, N. ;
Abajo, A. ;
Navarro, A. ;
Moreno, I. ;
Monzo, M. ;
Garcia-Foncillas, J. .
MOLECULAR CANCER, 2006, 5 (1)
[8]  
Bissell M J, 1981, Int Rev Cytol, V70, P27, DOI 10.1016/S0074-7696(08)61130-4
[9]   Context, tissue plasticity, and cancer: Are tumor stem cells also regulated by the microenvironment? [J].
Bissell, MJ ;
LaBarge, MA .
CANCER CELL, 2005, 7 (01) :17-23
[10]   The organizing principle: microenvironmental influences in the normal and malignant breast [J].
Bissell, MJ ;
Radisky, DC ;
Rizki, A ;
Weaver, VM ;
Petersen, OW .
DIFFERENTIATION, 2002, 70 (9-10) :537-546