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Detection of the apoptosis-suppressing oncoprotein bc1-2 in hormone-refractory human prostate cancers
1Department of Urology, Columbia University College of Physicians and Surgeons, New York, New York 10032.
Abstract:
The oncoprotein encoded by bc1-2 is unique because of its intracellular location (a mitochondrial membrane protein) and apparent mode of action (suppression of apoptosis). To date, this oncogene has been associated only with the development of certain forms of human B-cell lymphoma. In this report, we describe our experience with a monoclonal antibody made against a synthetic peptide for bc1-2 that can recognize the bc1-2 protein and identify cells in human prostate glands expressing this proto-oncogene with in situ immunohistochemical procedures. These procedures were utilized to survey a series of 62 human tissues to evaluate whether bc1-2 might have a role in the developing prostate gland or in prostate oncogenesis. While all primordial epithelial cells in a fetal prostate gland immunostain for bc1-2, normal and hypertrophic prostate glands of the adult show bc1-2 expression restricted to the basal cells. All epithelial cells in areas of prostatic intraepithelial neoplasia were stained by this antibody, as were most (62%) localized invasive prostatic carcinomas. In contrast, all primary prostatic carcinomas and metastases obtained from metastatic prostate cancer patients after hormone treatment (hormone-refractory tumors) stained positive for bc1-2. This study demonstrates that the oncoprotein encoded by bc1-2 can be detected at sequential stages in the natural history of human prostate cancer. Since the bc1-2 oncoprotein is known to suppress the cellular response to apoptotic stimuli, it will be important to determine whether bc1-2 expression is a factor in the development of prostate cancers and in the survival of hormone-refractory prostate cancer cells.
Insights
The BCL-2 oncoprotein, a mitochondrial protein that suppresses apoptosis, is detected in human prostate cancer. Its expression increases with cancer progression, particularly in hormone-refractory tumors, suggesting a role in prostate oncogenesis and survival.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- The BCL-2 oncoprotein, a mitochondrial membrane protein, suppresses apoptosis and is linked to B-cell lymphoma.
- Its role in prostate cancer development and progression has not been fully elucidated.
Purpose of the Study:
- To investigate the expression of the BCL-2 oncoprotein in various stages of human prostate gland development and cancer.
- To evaluate the potential role of BCL-2 in prostate oncogenesis and the survival of hormone-refractory prostate cancer.
Main Methods:
- Development of a monoclonal antibody against a synthetic peptide for BCL-2.
- Utilized in situ immunohistochemical procedures to detect BCL-2 protein expression in 62 human prostate tissues.
- Surveyed fetal prostate, normal adult prostate, benign prostatic hyperplasia, prostatic intraepithelial neoplasia, and various stages of prostate carcinoma.
Main Results:
- BCL-2 is expressed in primordial epithelial cells of fetal prostate glands.
- In normal and hypertrophic adult prostates, BCL-2 expression is restricted to basal cells.
- All prostatic intraepithelial neoplasia and 62% of localized invasive carcinomas showed BCL-2 staining.
- All primary prostatic carcinomas and hormone-refractory metastatic tumors stained positive for BCL-2.
Conclusions:
- BCL-2 oncoprotein is detectable throughout the natural history of human prostate cancer.
- Increased BCL-2 expression correlates with advanced prostate cancer stages, including hormone-refractory disease.
- Further research is warranted to determine if BCL-2 expression influences prostate cancer development and the survival of hormone-refractory cells.