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Updated: Jan 12, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
CAD is Associated with Cancer Prognosis and Promotes Enzalutamide Resistance in Prostate Cancer
Bing-Xue Ma1, Yi-You Mao2, Ze-Fan Zhang3,4
1Department of Physical Education, Guangzhou Institute of Physical Education, Guangzhou, 510515, Guangdong, China.
Carbamoyl-phosphate synthetase 2, Aspartate transcarbamoylase, and Dihydroorotase (CAD) is upregulated in most cancers, showing diagnostic and prognostic potential. Targeting CAD inhibits prostate cancer growth and enzalutamide resistance.
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Preliminary research explored Carbamoyl-phosphate synthetase 2, Aspartate transcarbamoylase, and Dihydroorotase (CAD)-targeted therapies in limited cancer types.
- A comprehensive understanding of CAD's diagnostic, prognostic, and mechanistic roles across cancers is needed.
Purpose of the Study:
- To conduct a pan-cancer analysis of CAD expression using bioinformatics tools.
- To experimentally validate CAD's role in enzalutamide resistance in prostate cancer.
- To review CAD's molecular classification and drug patents.
Main Methods:
- Pan-cancer bioinformatics analysis of CAD expression.
- Experimental validation of CAD in enzalutamide-resistant prostate cancer cells.
- Review of molecular classification and drug patents using Worldwide Espacenet ®.
Main Results:
- CAD is upregulated in most tumor tissues and its expression correlates with clinical stage, grade, and prognosis.
- CAD expression links to tumor mutation burden, MSI, HRD, and immune cell infiltration, suggesting synergy with immunotherapy.
- CAD knockdown inhibits prostate cancer cell growth and enzalutamide resistance, highlighting its role in angiogenesis and EMT.
Conclusions:
- CAD demonstrates significant diagnostic and prognostic potential in a pan-cancer context.
- CAD plays a crucial role in prostate cancer proliferation and resistance to enzalutamide therapy.
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