1. ¹Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
2. ²Laboratory of Molecular Aspects of Haematopoiesis, Molecular Pharmacology and Chemistry Program, Sloan-Kettering Institute, New York, NY, USA
3. ³Division of Hematologic Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA

Correspondence: Dr SD Nimer, Division of Hematologic Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA. E-mail: nimers@mskcc.org

⁴Current Address: Department of Pathology, Baylor College of Medicine, Houston, TX, USA.

⁵Current Address: Weill Medical College of Cornell University-New York Presbyterian Hospital, New York, NY, USA.

Received 12 April 2006; Revised 13 October 2006; Accepted 13 October 2006; Published online 8 January 2007.

Abstract

We have previously shown that MEF (myeloid ELF1-like factor, also known as ELF4) functions as a transcriptional activator of the interleukin (IL)-8, perforin, granulocyte macrophage-colony stimulating factor (GM-CSF) and IL-3 genes in hematopoietic cells. MEF is also expressed in non-hematopoietic tissues including certain ovarian cancer cells. To define the function of MEF in these cells, we examined primary human ovarian epithelial tumors and found that MEF is expressed in a significant proportion of ovarian carcinomas, and in the CAOV3 and SKOV3 ovarian cancer cell lines, but not in normal ovarian surface epithelium. Manipulating MEF levels in these cell lines altered their behavior; reducing MEF levels, using short hairpin RNA expressing vectors, significantly inhibited the proliferation of SKOV3 and CAOV3 cells in culture, and impaired the anchorage-independent growth of CAOV3 cells. Overexpression of MEF in SKOV3 cells (via retroviral transduction) significantly increased their growth rate, enhanced colony formation in soft agar and promoted tumor formation in nude mice. The oncogenic activity of MEF was further shown by the ability of MEF to transform NIH3T3 cells, and induce their tumor formation in nude mice. MEF is an important regulator of the tumorigenic properties of ovarian cancer cells and could be used a therapeutic target in ovarian cancer.