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Cited by 707

The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.

EMT Subtype Influences Epithelial Plasticity and Mode of Cell Migration

Open access
Aiello, Nicole M., Maddipati, Ravikanth, Norgard, Robert J., Balli, David, Li, Jinyang, Yuan, Salina, Yamazoe, Taiji, Black, Taylor, Sahmoud, Amine, Furth, Emma E., Bar-Sagi, Dafna, Stanger, Ben Z.·2018·Developmental Cell

Abstract

SUMMARY Epithelial-mesenchymal-transition (EMT) is strongly implicated in tumor cell invasion and metastasis. EMT is thought to be regulated primarily at the transcriptional level through the repressive activity of EMT transcription factors. However, these classical mechanisms have been parsed out almost exclusively in vitro, leaving questions about the programs driving EMT in physiological contexts. Here, using a lineage-labeled mouse model of pancreatic ductal adenocarcinoma to study EMT in vivo, we found that most tumors lose their epithelial phenotype through an alternative program involving protein internalization rather than transcriptional repression, resulting in a “partial EMT” phenotype. Carcinoma cells utilizing this program migrate as clusters, contrasting with the single-cell migration pattern associated with traditionally-defined EMT mechanisms. Moreover, many breast and colorectal cancer cell lines utilize this alternative program to undergo EMT. Collectively, these results suggest that carcinoma cells have different ways of losing their epithelial program, resulting in distinct modes of invasion and dissemination.

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Crossref · 10.1016/j.devcel.2018.05.027

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Metadata

Authors
Aiello, N. M., Maddipati, R., Norgard, R. J., Balli, D., Li, J., Yuan, S., Yamazoe, T., Black, T., Sahmoud, A., Furth, E. E., Bar-Sagi, D., & Stanger, B. Z.
Venue
Developmental Cell
Publisher
Elsevier BV
Published
2018-06
Volume
45
Issue
6
Pages
681-695.e4
ISSN
1534-5807 (ISSN-L)
OpenAlex
W2808423871
Cited by
707
References
63
FWCI
24.86
Type
journal article
Language
en
Open access
bronze

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