Journal Article

Mesenchyme Forkhead 1 (FOXC2) plays a key role in metastasis and is associated with aggressive basal-like breast cancers

Zhou, Alicia, Schwaninger, Gunda, Miura, Naoyuki, Mani, Sendurai A, Brooks, Mary, Yang, Jing, Richardson, Andrea L, Kutok, Jeffery L, Hartwell, Kimberly, Weinberg, Robert A

2007

Overview

The metastatic spread of epithelial cancer cells from the primary tumor to distant organs mimics the cell migrations that occur during embryogenesis. Using gene expression profiling, we have found that the FOXC2 transcription factor, which is involved in specifying mesenchymal cell fate during embryogenesis, is associated with the metastatic capabilities of cancer cells. FOXC2 expression is required for the ability of murine mammary carcinoma cells to metastasize to the lung, and overexpression of FOXC2 enhances the metastatic ability of mouse mammary carcinoma cells. We show that FOXC2 expression is induced in cells undergoing epithelial-mesenchymal transitions (EMTs) triggered by a number of signals, including TGF-β1 and several EMT-inducing transcription factors, such as Snail, Twist, and Goosecoid. FOXC2 specifically promotes mesenchymal differentiation during an EMT and may serve as a key mediator to orchestrate the mesenchymal component of the EMT program. Expression of FOXC2 is significantly correlated with the highly aggressive basal-like subtype of human breast cancers. These observations indicate that FOXC2 plays a central role in promoting invasion and metastasis and that it may prove to be a highly specific molecular marker for human basal-like breast cancers.

• Publisher: National Academy of Sciences,National Acad Sciences
• Subject: Animals / Biological Sciences / Breast cancer / breast neoplasms / Breast Neoplasms - genetics / Breast Neoplasms - metabolism / Breast Neoplasms - pathology / Cadherins / Carcinoma, Basal Cell - pathology / Cell Line, Transformed / Cell Line, Tumor / Cell lines / Cell Transformation, Viral / Cells / embryogenesis / Embryology / Embryonic growth stage / Epithelial cells / Female / Forkhead Transcription Factors - metabolism / Forkhead Transcription Factors - physiology / Gene expression / Gene Expression Profiling / Gene Expression Regulation, Neoplastic / Genetic vectors / Goosecoid Protein - genetics / Goosecoid Protein - metabolism / Humans / Lungs / Mammary Neoplasms, Experimental - genetics / Mammary Neoplasms, Experimental - metabolism / Mammary Neoplasms, Experimental - pathology / Mesoderm / metastasis / mice / neoplasm cells / Neoplasm Metastasis / Nodules / Oncology / RNA, Messenger - metabolism / Snail Family Transcription Factors / Transcription factors / Transcription Factors - genetics / Transcription Factors - metabolism / transforming growth factor beta 1 / Transforming Growth Factor beta1 - metabolism / Tumor cell line / Tumors / Twist-Related Protein 1 - genetics / Twist-Related Protein 1 - metabolism