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- W2810263512 endingPage "9144" @default.
- W2810263512 startingPage "9136" @default.
- W2810263512 abstract "Breast cancer is the most common cancer in women, and accounts for ~30% of new cancer cases and 15% of cancer‐related deaths. Tumor relapse and metastasis are primary factors contributing to breast cancer‐related deaths. Therefore, the challenge for breast cancer treatment is to sustain remission. A driving force behind tumor relapse is breast cancer heterogeneity (both intertumor, between different patients, and intratumor, within the same tumor). Understanding breast cancer heterogeneity is necessary to develop preventive interventions and targeted therapies. A recently emerging concept is that intratumor heterogeneity is driven by cancer stem cells (CSCs) that are capable of giving rise to a multitude of different cells within a tumor. Studies have highlighted linkage of CSC formation with epithelial‐to‐mesenchymal transition (EMT). In this review, we summarize the current understanding of breast cancer heterogeneity, links between EMT and CSCs, regulation of EMT by Runx transcription factors, and potential therapeutic strategies targeting these processes." @default.
- W2810263512 created "2018-07-10" @default.
- W2810263512 creator A5008755139 @default.
- W2810263512 creator A5031362021 @default.
- W2810263512 creator A5032067317 @default.
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- W2810263512 creator A5060221941 @default.
- W2810263512 creator A5068451319 @default.
- W2810263512 creator A5079712015 @default.
- W2810263512 creator A5081119848 @default.
- W2810263512 date "2018-07-03" @default.
- W2810263512 modified "2023-10-10" @default.
- W2810263512 title "Epithelial‐to‐mesenchymal transition and cancer stem cells contribute to breast cancer heterogeneity" @default.
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