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Updated: Jun 6, 2026

Tracking Tumor Cell Dissemination from Lung Metastases Using Photoconversion
Published on: July 7, 2023
Metastasis: tumor cells becoming MENAcing.
Frank Gertler1, John Condeelis
1Department of Biology and Koch Institute for Integrative Cancer Research at Massachusetts Institute of Technology (MIT), 77 Massachusetts Ave, Cambridge, MA 02138, USA. fgertler@MIT.EDU
The actin regulatory protein Mena influences breast cancer cell invasion and metastasis by altering sensitivity to epidermal growth factor (EGF). Upregulated Mena isoforms enhance EGF-driven cell movement, potentially indicating metastatic risk.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Breast cancer metastasis involves tumor cells migrating from the primary site to distant organs.
- Mammary tumor cell migration and invasion are driven by epidermal growth factor (EGF)-dependent processes.
- The actin regulatory protein Mena plays a role in cell migration and invasion.
Purpose of the Study:
- To investigate the role of Mena in epidermal growth factor (EGF)-induced breast cancer cell movement, invasion, and metastasis.
- To understand how changes in Mena isoform expression affect tumor cell behavior in response to EGF.
Main Methods:
- Analysis of Mena isoform expression in invasive migratory tumor cells.
- Assessment of EGF-elicited protrusive and migratory activity in relation to Mena expression.
- Correlation of Mena expression patterns with metastatic potential.
Main Results:
- Invasive migratory breast cancer cells exhibit altered Mena isoform expression.
- Specific Mena isoforms are upregulated, enhancing EGF sensitivity and promoting increased protrusive and migratory abilities.
- Other Mena isoforms are selectively downregulated in invasive cells.
Conclusions:
- Changes in Mena isoform expression are critical for enabling breast cancer cell invasion in response to EGF.
- Altered Mena expression can transform benign EGF stimuli into potent drivers of metastasis.
- Mena isoform profiling may serve as a biomarker for identifying metastatic risk in breast cancer patients.
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