Snail1 Induced Suppression of Proliferation via EGR1, FOXO1, and CEPBγ Creates a Vulnerability for Targeting Apoptotic and Cellular Senescence Pathways

We identified three new major downstream targets of Snail1 that improve our understanding of the role of EMT in limiting stress signaling, apoptosis, and senescence during cell cycle suppression to create a vulnerability for therapeutic targeting.

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Publication Details

Journal
Cancers
Published
2026-02-04
DOI
https://doi.org/10.3390/cancers18030510
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
0.00

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article

Snail1 Induced Suppression of Proliferation via EGR1, FOXO1, and CEPBγ Creates a Vulnerability for Targeting Apoptotic and Cellular Senescence Pathways

Cynthia Miranti, Jack D. Tran, Hunain Khawaja, Samyukta Sundaram et al.
Cancers
Cancer Cells and Metastasis
article

Snail1 Induced Suppression of Proliferation via EGR1, FOXO1, and CEPBγ Creates a Vulnerability for Targeting Apoptotic and Cellular Senescence Pathways

Cynthia Miranti, Jack D. Tran, Hunain Khawaja, Samyukta Sundaram, Sukirti Shivpuri
article en

Abstract

We identified three new major downstream targets of Snail1 that improve our understanding of the role of EMT in limiting stress signaling, apoptosis, and senescence during cell cycle suppression to create a vulnerability for therapeutic targeting.

CancersVol. 18(3)
University of Arizona (US)
National Institutes of Health, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 66%
Cancer Cells and Metastasis
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