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Updated: Jun 5, 2026

Isolation of Cancer Stem Cells From Human Prostate Cancer Samples
Published on: March 14, 2014
Tumour-initiating stem-like cells in human prostate cancer exhibit increased NF-κB signalling
Vinagolu K Rajasekhar1, Lorenz Studer, William Gerald
11] Stem Cell Center and Developmental Biology Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA. [2] Sidney Kimmel Center for Prostate and Urologic Cancers, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.
Abstract:
Androgen depletion is a key strategy for treating human prostate cancer, but the presence of hormone-independent cells escaping treatment remains a major therapeutic challenge. Here, we identify a minor subset of stem-like human prostate tumour-initiating cells (TICs) that do not express prostate cancer markers, such as androgen receptor or prostate specific antigen. These TICs possess stem cell characteristics and multipotency as demonstrated by in vitro sphere-formation and in vivo tumour-initiation, respectively. The cells represent an undifferentiated subtype of basal cells and can be purified from prostate tumours based on coexpression of the human pluripotent stem cell marker TRA-1-60 with CD151 and CD166. Such triple-marker-positive TICs recapitulate the original parent tumour heterogeneity in serial xeno-transplantations indicating a tumour cell hierarchy in human prostate cancer development. These TICs exhibit increased nuclear factor-κB activity. These findings are important in understanding the molecular basis of human prostate cancer.
Insights
Researchers discovered a rare type of prostate cancer stem cell (TIC) that resists hormone therapy. These stem-like cells, identified by specific markers, drive tumor growth and heterogeneity, offering new insights into prostate cancer molecular mechanisms.
Area of Science:
- Oncology
- Stem Cell Biology
- Molecular Biology
Background:
- Androgen depletion therapy is a primary treatment for human prostate cancer.
- Hormone-independent cancer cells pose a significant therapeutic challenge.
- Understanding treatment resistance is crucial for improving prostate cancer outcomes.
Purpose of the Study:
- To identify and characterize stem-like cells within human prostate tumors that may drive treatment resistance.
- To elucidate the characteristics and potential role of these cells in prostate cancer development and heterogeneity.
- To investigate the molecular pathways, such as nuclear factor-κB activity, associated with these cells.
Main Methods:
- Identification and purification of prostate tumor-initiating cells (TICs) using coexpression of TRA-1-60, CD151, and CD166.
- Assessment of stem cell characteristics through in vitro sphere-formation assays.
- Evaluation of multipotency and tumor-initiation potential via in vivo xenotransplantation studies.
- Analysis of nuclear factor-κB activity in identified TICs.
Main Results:
- A minor subset of stem-like TICs was identified, lacking typical prostate cancer markers (androgen receptor, prostate specific antigen).
- These TICs demonstrated stem cell properties, including sphere formation and in vivo tumor initiation.
- Purified triple-marker-positive TICs (TRA-1-60+, CD151+, CD166+) recapitulated original tumor heterogeneity in serial xenotransplants, suggesting a tumor hierarchy.
- These TICs exhibited elevated nuclear factor-κB activity.
Conclusions:
- Stem-like TICs lacking androgen receptor expression represent a potential source of treatment resistance in human prostate cancer.
- These cells possess stem cell characteristics and contribute to tumor heterogeneity and development.
- Targeting these specific TICs or associated pathways like nuclear factor-κB may offer novel therapeutic strategies for prostate cancer.
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