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Utilization of the Soft Agar Colony Formation Assay to Identify Inhibitors of Tumorigenicity in Breast Cancer Cells
Published on: May 20, 2015
Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
Eric Macia1, Monserrat Vazquez-Rojas1, Alessia Robiolo1
1Institut de Pharmacologie Moléculaire et Cellulaire (IPMC), UMR 7275 CNRS-Université Côte d'Azur, 660, Route des Lucioles, 06560 Valbonne, France.
Abstract:
Breast cancer is a major disease for women worldwide, where mortality is associated with tumour cell dissemination to distant organs. While the number of efficient anticancer therapies increased in the past 20 years, treatments targeting the invasive properties of metastatic tumour cells are still awaited. Various studies analysing invasive breast cancer cell lines have demonstrated that Arf6 is an important player of the migratory and invasive processes. These observations make Arf6 and its regulators potential therapeutic targets. As of today, no drug effective against Arf6 has been identified, with one explanation being that the activation of Arf6 is dependent on the presence of lipid membranes that are rarely included in drug screening. To overcome this issue we have set up a fluorescence-based high throughput screening that follows overtime the activation of Arf6 at the surface of lipid membranes. Using this unique screening assay, we isolated several compounds that affect Arf6 activation, among which the antibiotic chlortetracycline (CTC) appeared to be the most promising. In this report, we describe CTC in vitro biochemical characterization and show that it blocks both the Arf6-stimulated collective migration and cell invasion in a 3D collagen I gel of the invasive breast cancer cell line MDA-MB-231. Thus, CTC appears as a promising hit to target deadly metastatic dissemination and a powerful tool to unravel the molecular mechanisms of Arf6-mediated invasive processes.
Insights
Chlortetracycline (CTC) effectively inhibits Arf6 activation, a key driver of breast cancer cell migration and invasion. This antibiotic shows promise for developing new therapies against deadly metastatic breast cancer.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Breast cancer mortality is linked to tumor cell metastasis.
- Arf6 is crucial for cancer cell migration and invasion, making it a therapeutic target.
- Existing drug screens struggle to identify Arf6 inhibitors due to its lipid membrane dependency.
Purpose of the Study:
- To develop a high-throughput screening assay for Arf6 activators.
- To identify novel compounds that inhibit Arf6 activation.
- To evaluate the therapeutic potential of identified compounds against breast cancer metastasis.
Main Methods:
- Established a fluorescence-based, high-throughput screening assay to monitor Arf6 activation on lipid membranes.
- Screened compounds to identify those affecting Arf6 activation.
- Performed in vitro biochemical characterization of promising compounds.
- Assessed the effect of compounds on collective cell migration and invasion using the MDA-MB-231 breast cancer cell line in 3D collagen I gels.
Main Results:
- Identified several compounds that modulate Arf6 activation.
- Chlortetracycline (CTC) emerged as a highly promising candidate.
- CTC demonstrated in vitro inhibition of Arf6 activation.
- CTC effectively blocked Arf6-stimulated collective migration and invasion of MDA-MB-231 cells.
Conclusions:
- CTC is a potent inhibitor of Arf6-mediated breast cancer cell invasion and migration.
- CTC represents a promising therapeutic lead for targeting metastatic breast cancer.
- CTC serves as a valuable tool for elucidating Arf6-dependent invasive mechanisms.
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