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Updated: Feb 10, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Regulation of matrix metalloproteinase 13 expression by androgen in prostate cancer
See-Tong Pang1, Amilcar Flores-Morales, Lambert Skoog
1Department of Molecular Medicine, Andrology centre, Karolinska Hospital, Karolinska Institute, Stockholm, Sweden.
Abstract:
The matrix metalloproteinases (MMPs) are members of a family of endopeptidases that are able to degrade extra-cellular matrix. MMPs and their inhibitors, tissue inhibitors of metalloproteinases (TIMPs), play a key role in the migration of normal and malignant cell. Interaction of MMPs and TIMPs has been involved in the process of tumor invasion and metastasis. Using cDNA microarray as a screening tool to find androgen regulated gene in prostate cancer, we have found that expression of MMP-13 is regulated by androgen in prostate cancer derived cell line LNCaP. This regulation was further confirmed and quantified by real-time RT-PCR. In addition, the upregulation of MMP-13 mRNA by androgen could be abolished by the androgen antagonist Casodex but not the protein inhibitor cycloheximide. Western blot and immunohistochemistry of MMP-13 confirmed the androgen regulation at the protein level. We have furthermore shown that MMP-13 expression is presented in human prostate cancer obtained from aspiration biopsy. In summary, MMP-13 is androgen regulated and detectable in prostate cancer. Further study of MMP-13 in prostate cancer may help us to understand the progression of the cancer and can lead to new therapeutic options.
Insights
Matrix metalloproteinase-13 (MMP-13) expression is regulated by androgens in prostate cancer cells. This finding in prostate cancer may offer new therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Matrix metalloproteinases (MMPs) degrade extracellular matrix, influencing cell migration.
- MMPs and their inhibitors (TIMPs) are crucial in normal and malignant cell movement.
- MMP-TIMP interactions are implicated in tumor invasion and metastasis.
Purpose of the Study:
- To investigate androgen-regulated genes in prostate cancer.
- To determine the role of MMP-13 in prostate cancer progression.
Main Methods:
- cDNA microarray screening in LNCaP prostate cancer cells.
- Real-time RT-PCR for mRNA quantification.
- Western blot and immunohistochemistry for protein analysis.
- Analysis of human prostate cancer biopsies.
Main Results:
- Androgen upregulates MMP-13 expression in LNCaP cells.
- Androgen-induced MMP-13 upregulation is reversed by Casodex (androgen antagonist).
- MMP-13 protein expression is confirmed and present in human prostate cancer tissues.
Conclusions:
- MMP-13 is an androgen-regulated gene in prostate cancer.
- MMP-13 is detectable in prostate cancer tissues.
- Further research on MMP-13 could reveal insights into cancer progression and therapeutic targets.
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