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The Epithelial-to-Mesenchymal Transition (EMT) in Development and Cancer. | LitMetric

The Epithelial-to-Mesenchymal Transition (EMT) in Development and Cancer.

Annu Rev Cancer Biol

Developmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York NY 10065 USA.

Published: March 2020

AI Article Synopsis

  • EMTs are processes where epithelial cells transform into mesenchymal cells, affecting cell behavior and shape, crucial for development and cancer metastasis.
  • The review focuses on the role of EMT during embryonic development, particularly in chick and mouse models, and its participation in pancreatic and breast cancer progression.
  • It emphasizes the distinction between developmental and cancer-related EMTs, and suggests that future advancements will depend on in vivo imaging to better understand these processes.

Article Abstract

Epithelial-to-mesenchymal transitions (EMTs) are complex cellular processes where cells undergo dramatic changes in signaling, transcriptional programming, and cell shape, while directing the exit of cells from the epithelium and promoting migratory properties of the resulting mesenchyme. EMTs are essential for morphogenesis during development and are also a critical step in cancer progression and metastasis formation. Here we provide an overview of the molecular regulation of the EMT process during embryo development, focusing on chick and mouse gastrulation and neural crest development. We go on to describe how EMT regulators participate in the progression of pancreatic and breast cancer in mouse models, and discuss the parallels with developmental EMTs and how these help to understand cancer EMTs. We also highlight the differences between EMTs in tumor and in development to arrive at a broader view of cancer EMT. We conclude by discussing how further advances in the field will rely on in vivo dynamic imaging of the cellular events of EMT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8189433PMC
http://dx.doi.org/10.1146/annurev-cancerbio-030518-055425DOI Listing

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