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Published on: November 11, 2021
Clinical value of CD24 expression in retinoblastoma
Jia Li1, Changqing Li, Hongfeng Yuan
1Department of Ophthalmology, Research Institute of Surgery and Daping Hospital, Third Military Medical University, Chongqing, China.
Background:
The expression of CD24 has been detected in a wide variety of human malignancies. Downregulation of CD24 inhibits proliferation and induces apoptosis in tumor cells, whereas its upregulation increases tumor growth and metastasis. However, no data on CD24 protein levels in retinoblastoma are available, and the mechanism of CD24 involvement in retinoblastoma progress has not been elucidated. The aim of this study was to explore the expression profile of CD24 in the retinoblastoma tumor samples and to correlate with clinicopathological parameters.
Methods:
Immunohistochemistry was performed for CD24 on the archival paraffin sections of retinoblastoma and correlated with clinicopathological features. Western blotting was performed to confirm immunoreactivity results.
Results:
CD24 immunoreactivity was observed in 72.0% (36/50) of the retinoblastoma specimens. Among the 35 low-risk tumors, CD24 was expressed in 62.9% (22/35) tumors and among the 15 high-risk tumors, CD24 was expressed in 93.3% (14/15) tumors. High-risk tumors showed significantly increased expression of CD24 compared to tumors with low-risk (P < 0.05).
Conclusions:
This is the first correlation between CD24 expression and histopathology in human retinoblastoma. Our study showed increased expression of CD24 in high risk tumors compared to low risk tumors. Further functional studies are required to explore the role of CD24 in retinoblastoma.
Insights
CD24 protein is highly expressed in high-risk retinoblastoma tumors, unlike low-risk ones. This finding suggests CD24 may play a role in retinoblastoma progression and warrants further investigation.
Area of Science:
- Oncology
- Molecular Biology
- Ophthalmology
Background:
- CD24 protein expression is implicated in various human cancers, influencing tumor growth and metastasis.
- While CD24's role is known in other malignancies, its expression and function in retinoblastoma remain unstudied.
- Understanding CD24 in retinoblastoma is crucial for elucidating tumor progression mechanisms.
Purpose of the Study:
- To investigate the expression profile of CD24 in retinoblastoma tumor samples.
- To correlate CD24 protein levels with clinicopathological parameters in retinoblastoma patients.
Main Methods:
- Immunohistochemistry was used to detect CD24 expression in archival retinoblastoma paraffin sections.
- Western blotting was employed to validate the immunohistochemistry findings.
- Expression levels were correlated with clinicopathological features.
Main Results:
- CD24 immunoreactivity was detected in 72% of retinoblastoma specimens (36/50).
- CD24 expression was significantly higher in high-risk retinoblastoma tumors (93.3%, 14/15) compared to low-risk tumors (62.9%, 22/35).
- A statistically significant correlation (P < 0.05) was found between increased CD24 expression and high-risk retinoblastoma.
Conclusions:
- This study establishes the first correlation between CD24 expression and histopathology in human retinoblastoma.
- Elevated CD24 expression is associated with high-risk retinoblastoma, suggesting a potential role in disease progression.
- Further functional studies are necessary to fully elucidate the role of CD24 in retinoblastoma pathogenesis.
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