Expression of the PEA3 group of ETS‐related transcription factors in human breast‐cancer cells

The PEA3 group of transcription factors belongs to the ets family and is composed of 3 known members, PEA3, ERM and ER81, which are more than 95% identical within the DNA‐binding ETS domain and exhibit 50% aa identity overall. Recently, transgenic mice bearing the c‐erbB‐2/neu oncogene have been shown to over‐express PEA3 mRNA in mammary adenocarcinomas, suggesting a role for this gene family in mammary tumorigenesis. In the present work we characterized the mRNA expression levels of PEA3‐group genes in a series of human epithelial breast cell lines. Each of the 3 genes was highly expressed in normal human HMEC 1001‐7 and HMEC 219‐4 cells. In breast‐cancer cell lines, the 3 genes were highly expressed in the ER−MDA‐MB‐436, MDA‐MB‐330, MDA‐MB‐231 and BT‐20 cell lines, but not in the ER+MDA‐MB‐134‐VI and ZR‐75‐1 cells. In an attempt to characterize the PEA3‐group proteins in breast‐cancer cells, we first produced and characterized specific antibodies against each of these 3 proteins. The anti‐ERM and anti‐ER81 antibodies recognized specific strong bands at approximately 72 kDa and 62 kDa, corresponding to ERM and ER81, respectively, in MDA‐MB‐231 and Hs‐578T cells expressing significant levels of the 3 mRNAs. No protein was detected in MCF‐7 cells expressing low levels of mRNA for PEA3‐group‐family genes, or in ZR‐75‐1 cells, where mRNA was undetectable by Northern blot. Although in vitro‐translated PEA3 is specifically immunoprecipitated by anti‐PEA3 anti‐serum, we were unable to immunoprecipitate PEA3 protein from MDA‐MB‐231 and Hs‐578T cells. In order to study the transcription factor activity of ERM, PEA3 and ER81 proteins in mammary‐cancer cells, we tested their ability to transactivate a reporter plasmid containing 3 Ets‐binding sites, and were able to show that, in all the breast‐cancer cells tested, transfected ERM, PEA3 and ER81 are able to transactivate. Although the target genes of the PEA3 group of transcription factors in breast‐cancer cells have yet to be determined, these genes have a potential role in the regulation of growth and the progression of human breast cancer.Int. J. Cancer 70:590–597. © 1997 Wiley‐Liss Inc.

[1]  A. deFazio,et al.  Expression and tyrosine phosphorylation of EMS1 in human breast cancer cell lines , 1996, International journal of cancer.

[2]  H. Klocker,et al.  Human renal‐cell carcinoma tissue contains dendritic cells , 1996, International journal of cancer.

[3]  F. Higashino,et al.  A single ets-related transcription factor, E1AF, confers invasive phenotype on human cancer cells. , 1996, Oncogene.

[4]  J. Inazawa,et al.  ERM, a PEA3 Subfamily of Ets Transcription Factors, Can Cooperate with c-Jun (*) , 1995, The Journal of Biological Chemistry.

[5]  R. Dickson,et al.  Growth factors in breast cancer. , 1995, Endocrine reviews.

[6]  D. Monté,et al.  Molecular characterization of the ets-related human transcription factor ER81. , 1995, Oncogene.

[7]  T. Noumi,et al.  Ets-related protein E1A-F can activate three different matrix metalloproteinase gene promoters. , 1995, Oncogene.

[8]  R. Maki,et al.  Binding of an ETS-related protein within the DNase I hypersensitive site of the HER2/neu promoter in human breast cancer cells. , 1994, The Journal of biological chemistry.

[9]  P. Defossez,et al.  Molecular cloning and characterization of human ERM, a new member of the Ets family closely related to mouse PEA3 and ER81 transcription factors. , 1994, Oncogene.

[10]  N. Bhat,et al.  Expression of ets family genes in hematopoietic-cells. , 1994, International Journal of Oncology.

[11]  W. Muller,et al.  PEA3 is overexpressed in mouse metastatic mammary adenocarcinomas. , 1993, Oncogene.

[12]  J. A. Hamilton,et al.  Expression and amplification of cyclin genes in human breast cancer. , 1993, Oncogene.

[13]  F. Higashino,et al.  Isolation of a cDNA encoding the adenovirus E1A enhancer binding protein: a new human member of the ets oncogene family. , 1993, Nucleic acids research.

[14]  S. McKnight,et al.  Specificities of protein-protein and protein-DNA interaction of GABP alpha and two newly defined ets-related proteins. , 1992, Genes & development.

[15]  J. Hassell,et al.  Molecular cloning and characterization of PEA3, a new member of the Ets oncogene family that is differentially expressed in mouse embryonic cells. , 1992, Genes & development.

[16]  M. Kozak Structural features in eukaryotic mRNAs that modulate the initiation of translation. , 1991, The Journal of biological chemistry.

[17]  B. Wasylyk,et al.  The c-ets proto-oncogenes encode transcription factors that cooperate with c-Fos and c-Jun for transcriptional activation , 1990, Nature.

[18]  W. McGuire,et al.  Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. , 1987, Science.

[19]  R. Lidereau,et al.  Genetic alteration of the c-myc protooncogene (MYC) in human primary breast carcinomas. , 1986, Proceedings of the National Academy of Sciences of the United States of America.