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Updated: Aug 15, 2026

The Use of Mouse Mammary Tumor Cells in an In Vitro Invasion Assay as a Measure of Oncogenic Cell Behavior
Published on: June 12, 2019
The transcriptional repressor Snail promotes mammary tumor recurrence
Susan E Moody1, Denise Perez, Tien-chi Pan
1Department of Cancer Biology, Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, 19104, USA.
Abstract:
Breast cancer recurrence is a fundamental clinical manifestation of tumor progression and represents the principal cause of death from this disease. Using a conditional transgenic mouse model for the recurrence of HER2/neu-induced mammary tumors, we demonstrate that the transcriptional repressor Snail is spontaneously upregulated in recurrent tumors in vivo and that recurrence is accompanied by epithelial-to-mesenchymal transition (EMT). Consistent with a causal role for Snail in these processes, we show that Snail is sufficient to induce EMT in primary tumor cells, that Snail is sufficient to promote mammary tumor recurrence in vivo, and that high levels of Snail predict decreased relapse-free survival in women with breast cancer. In aggregate, our observations strongly implicate Snail in the process of breast cancer recurrence.
Insights
The transcriptional repressor Snail drives breast cancer recurrence and epithelial-to-mesenchymal transition (EMT). High Snail levels in breast cancer patients correlate with reduced relapse-free survival, highlighting its role in tumor progression.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Breast cancer recurrence is a primary cause of mortality.
- Tumor progression and metastasis are hallmarks of advanced cancer.
Purpose of the Study:
- To investigate the role of the transcriptional repressor Snail in breast cancer recurrence.
- To determine if Snail induces epithelial-to-mesenchymal transition (EMT) and promotes tumor recurrence.
Main Methods:
- Utilized a conditional transgenic mouse model for HER2/neu-induced mammary tumors.
- Analyzed Snail expression in recurrent tumors.
- Assessed the effect of Snail on EMT in primary tumor cells.
- Correlated Snail levels with relapse-free survival in breast cancer patients.
Main Results:
- Snail is spontaneously upregulated in recurrent HER2/neu-induced mammary tumors.
- Snail upregulation is associated with epithelial-to-mesenchymal transition (EMT).
- Snail overexpression is sufficient to induce EMT and promote mammary tumor recurrence in vivo.
- Elevated Snail levels predict decreased relapse-free survival in breast cancer patients.
Conclusions:
- Snail plays a critical role in driving breast cancer recurrence.
- Snail-induced EMT is a key mechanism underlying tumor progression and recurrence.
- Snail is a potential therapeutic target for preventing breast cancer relapse.
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