Related Experiment Video
Updated: Aug 15, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Recent advances on multiple tumorigenic cascades involved in prostatic cancer progression and targeting therapies
Murielle Mimeault1, Surinder K Batra
1Department of Biochemistry and Molecular Biology, Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Abstract:
Recent advances on differently-expressed gene products and their functions during the progression from localized androgen-dependent states into androgen-independent and metastatic forms of prostate cancer are reported. The expression levels of numerous oncogenes and tumor suppressor genes in distinct prostatic cancer epithelial cell lines and tissues relative to normal prostate cells are described. This is carried out to identify the signaling elements that are altered during the initiation, progression and metastatic process of prostate cancer. Additional information on the interactions between certain deregulated signaling pathways such as androgen receptor (AR), estrogen receptors, epidermal growth factor receptor (EGFR), hedgehog and Wnt/beta-catenin cascades in controlling the proliferation, survival and invasion of tumor prostate epithelial cells during the disease progression is described. The emphasis is on the critical functions of the AR and EGF-EGFR systems at all stages during prostate carcinogenesis. Of therapeutic interest, new strategies for the diagnosis and treatment of localized and metastatic forms of prostate cancer by targeting multiple tumorigenic signaling elements are also reported.
Insights
This study details gene expression changes in prostate cancer progression, highlighting key signaling pathways like androgen receptor (AR) and epidermal growth factor receptor (EGFR) involved in tumor growth and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Prostate cancer progression involves shifts from androgen-dependent to androgen-independent states.
- Altered expression of oncogenes and tumor suppressor genes drives prostate cancer initiation, progression, and metastasis.
Purpose of the Study:
- To identify altered signaling elements during prostate cancer development.
- To understand the role of signaling pathways in tumor cell proliferation, survival, and invasion.
- To explore new diagnostic and therapeutic strategies for prostate cancer.
Main Methods:
- Analysis of gene expression levels in prostate cancer cell lines and tissues.
- Investigation of signaling pathway interactions, including androgen receptor (AR), estrogen receptors, EGFR, hedgehog, and Wnt/beta-catenin.
- Focus on the roles of AR and EGF-EGFR systems in prostate carcinogenesis.
Main Results:
- Identified differentially expressed genes and their functions during prostate cancer progression.
- Described interactions between signaling pathways that control tumor cell behavior.
- Highlighted the critical roles of AR and EGF-EGFR signaling throughout prostate cancer development.
Conclusions:
- Understanding gene expression and signaling pathway alterations is crucial for prostate cancer research.
- Targeting multiple tumorigenic signaling elements offers potential for novel prostate cancer therapies.
- New strategies for diagnosing and treating localized and metastatic prostate cancer are emerging.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Tumor Progression
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

