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Updated: Jun 20, 2026

Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
Published on: July 31, 2017
Pheochromocytomas, PASS, and immunohistochemistry
E Carlsen1, Z Abdullah, S M B Kazmi
1Department of Pathology, Barts and the London NHS Trust, London, UK. eivindcarlsen49@hotmail.com
Researchers investigated cell cycle markers to differentiate benign and malignant pheochromocytomas. A significant difference in pRb expression was found, suggesting distinct mitotic cycle patterns in aggressive tumors.
Area of Science:
- Endocrinology
- Oncology
- Cell Biology
Background:
- Differentiating benign from malignant pheochromocytomas is crucial for patient management.
- Current methods rely on detecting clinical metastases, which is often late.
- The Pheochromocytoma of the Adrenal gland Scaled Score (PASS) system uses morphological criteria.
Purpose of the Study:
- To explore differences in apoptosis and cell cycle regulation between benign and malignant pheochromocytomas.
- To investigate the utility of specific immunohistochemical markers in assessing tumor behavior.
Main Methods:
- Utilized a panel of immunohistochemical markers including p53, tenascin, bcl-2, pRb, cyclin D1, mcm2, and p27.
- Analyzed marker expression in relation to the PASS system scores.
- Focused on apoptosis, G1 checkpoints, and S phase events.
Main Results:
- A statistically significant difference in pRb expression was observed between tumors with PASS scores ≤3 and those with PASS scores ≥4.
- This suggests qualitative differences in the mitotic cycle, potentially before early S phase.
- No significant differences were found for other markers investigated.
Conclusions:
- pRb expression may serve as a marker for distinguishing aggressive pheochromocytomas.
- Further research is needed to fully elucidate the role of cell cycle markers in pheochromocytoma prognosis.
- These findings contribute to a deeper understanding of pheochromocytoma cell biology.
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