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Tumor promoting properties of the ETS protein MEF in ovarian cancer
J J Yao1, Y Liu, H D Lacorazza
1Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
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.
Insights
Myeloid ELF1-like factor (MEF), also known as ELF4, drives ovarian cancer cell proliferation and tumor formation. Targeting MEF may offer a new therapeutic strategy for ovarian cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Myeloid ELF1-like factor (MEF), also known as ELF4, is a transcriptional activator previously identified in hematopoietic cells.
- MEF expression extends to non-hematopoietic tissues, including ovarian cancer cells.
Purpose of the Study:
- To investigate the role of MEF in ovarian cancer.
- To determine if MEF influences the tumorigenic properties of ovarian cancer cells.
Main Methods:
- Analysis of MEF expression in human ovarian tumors and cell lines (CAOV3, SKOV3).
- Manipulation of MEF levels using short hairpin RNA and retroviral transduction.
- Assessment of cell proliferation, anchorage-independent growth, and tumor formation in vivo.
Main Results:
- MEF is expressed in ovarian carcinomas but not normal ovarian surface epithelium.
- Reduced MEF levels inhibited proliferation and anchorage-independent growth of ovarian cancer cells.
- MEF overexpression increased growth rate, colony formation, and tumor formation in mice, demonstrating oncogenic activity.
Conclusions:
- MEF is significantly upregulated in ovarian cancer and promotes tumorigenic properties.
- MEF acts as an oncogene in ovarian cancer.
- MEF represents a potential therapeutic target for ovarian cancer.
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