Exp Mol Med.  2015 Jan;47(1):e137. 10.1038/emm.2014.99.

Activation of KRAS promotes the mesenchymal features of basal-type breast cancer

Affiliations
  • 1Department of Life Science, Research Institute for Natural Sciences, Hanyang University, Seoul, Korea. sj0420@hanyang.ac.kr
  • 2Laboratory of Radiation Exposure & Therapeutics, National Radiation Emergency Medical Center, Korea Institute of Radiological and Medical Sciences, Seoul, Korea.
  • 3Department of Radiation Biology, Environmental Radiation Research Group, Korea Atomic Energy Research Institute, Daejeon, Korea.

Abstract

Basal-type breast cancers are among the most aggressive and deadly breast cancer subtypes, displaying a high metastatic ability associated with mesenchymal features. However, the molecular mechanisms underlying the maintenance of mesenchymal phenotypes of basal-type breast cancer cells remain obscure. Here, we report that KRAS is a critical regulator for the maintenance of mesenchymal features in basal-type breast cancer cells. KRAS is preferentially activated in basal-type breast cancer cells as compared with luminal type. By loss and gain of KRAS, we found that KRAS is necessary and sufficient for the maintenance of mesenchymal phenotypes and metastatic ability through SLUG expression. Taken together, this study demonstrates that KRAS is a critical regulator for the metastatic behavior associated with mesenchymal features of breast cancer cells, implicating a novel therapeutic target for basal-type breast cancer.


MeSH Terms

Animals
Breast Neoplasms/*genetics/metabolism/pathology
Cell Line, Tumor
Cell Transformation, Neoplastic/genetics/metabolism
Disease Models, Animal
Epithelial-Mesenchymal Transition/*genetics
Female
Gene Expression Regulation, Neoplastic
Gene Knockdown Techniques
Heterografts
Humans
Neoplasm Invasiveness
Neoplasm Metastasis
Phenotype
Proto-Oncogene Proteins/*genetics/metabolism
*Transcriptional Activation
ras Proteins/*genetics/metabolism
Proto-Oncogene Proteins
ras Proteins
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