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Updated: May 11, 2026

Quantification of Breast Cancer Cell Invasiveness Using a Three-dimensional (3D) Model
Published on: June 11, 2014
PAK5-Egr1-MMP2 signaling controls the migration and invasion in breast cancer cell
Xiao-Xia Wang1, Qian Cheng, Shang-Nuan Zhang
1Jiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, Jiangsu, 221002, China.
Abstract:
p21-activated kinases (PAKs) are activated by various extracellular stimuli and, in turn, activate other kinases by phosphorylating them at specific serine/threonine residues or through protein-protein interaction. As a recently identified member of the group B PAK family, the role of PAK5 in cancer is poorly understood. In this study, we investigated the effect of PAK5 on the malignant phenotype, such as proliferation, cell cycle, apoptosis, migration, and invasion. Cell growth assay and cell cycle analysis consistently showed that knockdown of PAK5 could significantly inhibit the proliferation of breast cancer cells. Wound healing assay. migration assay, and invasion assay showed that PAK5 promoted cell migration. Furthermore, in order to elucidate the underlying mechanism of PAK5 on cellular growth and migration, we examined the protein expressions of cyclin D1, p21, early growth response protein 1 (Egr1), and matrix metalloproteinase 2 (MMP2). Our work further reveals the PAK5-Egr1-MMP2 signaling pathway to be a critical regulator of cell migration and invasion. These results suggest that PAK5 may be a potential therapeutic target for breast cancer.
Insights
p21-activated kinases (PAKs) regulate cell growth and migration. This study reveals PAK5 promotes breast cancer progression by activating the Egr1-MMP2 pathway, suggesting PAK5 as a potential therapeutic target.
Area of Science:
- Molecular Biology
- Cancer Research
- Cell Signaling
Background:
- p21-activated kinases (PAKs) are crucial signaling molecules involved in various cellular processes.
- The role of PAK5, a Group B PAK family member, in cancer remains largely uncharacterized.
Purpose of the Study:
- To investigate the function of PAK5 in breast cancer progression.
- To elucidate the molecular mechanisms underlying PAK5's effects on malignant phenotypes.
Main Methods:
- Breast cancer cell lines were utilized to assess proliferation, cell cycle, apoptosis, migration, and invasion.
- Knockdown of PAK5 was performed to evaluate its impact on cellular behavior.
- Protein expression levels of key regulators, including cyclin D1, p21, Egr1, and MMP2, were examined.
Main Results:
- PAK5 knockdown significantly inhibited breast cancer cell proliferation and cell cycle progression.
- PAK5 was found to promote cell migration and invasion.
- The study identified a novel PAK5-Egr1-MMP2 signaling pathway critical for cell migration and invasion.
Conclusions:
- PAK5 plays a significant role in promoting breast cancer cell proliferation, migration, and invasion.
- The PAK5-Egr1-MMP2 pathway is a key regulator of breast cancer metastasis.
- PAK5 emerges as a potential therapeutic target for breast cancer treatment.
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