Jia, D and Jolly, MK and Levine, H and Onuchic, JN (2020) Epithelial-mesenchymal transition in cancer. [Book Chapter]
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Abstract
The epithelial-mesenchymal transition (EMT) functions as a central regulator of processes that help enable metastasis. Cancer cells undergoing EMT can acquire a spectrum of hybrid epithelial/mesenchymal (E/M) phenotypes characterized by varying degrees of combined epithelial and mesenchymal features. Cells in the hybrid E/M phenotypes can migrate collectively as a cluster. Clusters of migrating tumor cells are a major contributor to metastases. Therefore, identifying the molecular mechanisms underlying the emergence of the hybrid E/M phenotypes can imply critical clues for anti-metastasis therapeutic design. To that end, both computational and experimental approaches have been developed to characterize the hybrid E/M phenotypes and to elucidate cancer epithelial-mesenchymal plasticity, that is, the ability to switch between epithelial, mesenchymal and hybrid E/M phenotypes. EMT serves as an example of cellular plasticity, which leads to cancer nongenetic heterogeneity.
Item Type: | Book Chapter |
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Publication: | Phenotypic Switching: Implications in Biology and Medicine |
Publisher: | Elsevier |
Additional Information: | The copyright for this article belongs to Elsevier. |
Keywords: | Abnormal attractors; EMT; Epithelial-mesenchymal transition; Hybrid epithelial/mesenchymal phenotype; Metastasis; Phenotypic stability factors; Systems biology; Therapy resistance Abnormal attractors; EMT; Epithelial-mesenchymal transition; Hybrid epithelial/mesenchymal phenotype; Metastasis; Phenotypic stability factors; Systems biology; Therapy resistance Abnormal attractors; EMT; Epithelial-mesenchymal transition; Hybrid epithelial/mesenchymal phenotype; Metastasis; Phenotypic stability factors; Systems biology; Therapy resistance |
Department/Centre: | Division of Interdisciplinary Sciences > Centre for Biosystems Science and Engineering |
Date Deposited: | 06 Feb 2023 10:27 |
Last Modified: | 06 Feb 2023 10:27 |
URI: | https://eprints.iisc.ac.in/id/eprint/79960 |
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