Transforming Growth Factor-β1 Induced Epithelial Mesenchymal Transition is blocked by a chemical antagonist of translation factor eIF4E

K. A. Smith, B. Zhou, S. Avdulov, A. Benyumov, M. Peterson, Y. Liu, A. Okon, P. Hergert, J. Braziunas, C. R. Wagner, Z. Borok, P. B. Bitterman

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23 Scopus citations

Abstract

The epithelial to mesenchymal transition (EMT) imparts disease-defining properties to epithelial cells in cancer and organ fibrosis. Prior studies identify EMT control points at the level of transcription and translation, and indicate that activation of translation initiation factor 4E (eIF4E) is involved in the mechanisms coordinating these two levels of control. Here we show that 4Ei-1, a specific chemical antagonist of the eIF4E-mRNA cap interaction, potently inhibits transforming growth factor beta 1 (TGF-β1) mediated EMT in lung epithelial cells. Upon treatment with TGF-β1, we observed a rapid recruitment of Snail1 mRNA into the actively translated polysome pool accompanied by accumulation of the EMT transcription factor Snail1 in the nucleus. 4Ei-1 blocks ribosome recruitment to the Snail1 transcript thereby preventing accumulation of the Snail1 protein in the nucleus. Our findings establish an obligatory role for upstream translational control of downstream Snail1-mediated transcriptional events in TGF-β1 induced EMT, and provide proof of concept for efforts to pharmacologically modulate the eIF4E-cap interaction as a means to inhibit pathological EMT in the setting of cancer and organ fibrosis.

Original languageEnglish (US)
Article number18233
JournalScientific reports
Volume5
DOIs
StatePublished - Dec 18 2015

Bibliographical note

Funding Information:
This work was supported by the following grants; PB by NIH grant P01 HL091775 and funding from the Hubbard Fund; ZB by NIH grant 5R01HL112638, P01 HL091775, the Hastings Foundation, and the Ralph Edgington Chair in Medicine; and BZ by NIH grant 1R01HL114959.

Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.

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