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Updated: Oct 8, 2026

Reconstruct Human Retinoblastoma In Vitro
Published on: October 11, 2022
Abnormalities of the human Rb tumor suppressor gene in oral squamous cell carcinoma
1Department of Oral and Maxillofacial Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University of Medical Sciences, No. 107 Yanjiang W. Road, Guangzhou, 510120, P. R. China.
Objective:
To investigate the status of Retinoblastoma (Rb) gene in 30 patients with primary oral squamous cell carcinoma (OSCC) and 3 healthy control samples.
Material And Methods:
We determined the status of Rb tumor suppressor gene in oral squamous cell carcinoma using a DNA southern blotting assay with Digoxin (Dig) labeled Rb cDNA probe.
Results:
The structural abnormalities of Rb tumor suppressor gene were detected in 8 of the 30 invasive OSCC samples analyzed (8/30). 7 cases contained partial gene deletion, and there was 1 case of gene rearrangement. The structural abnormality rate of Rb is 26.7%. No correlation was found between the alteration of Rb gene with the sex, age, site of primary tumor, level of histopathological differentiation, and TNM staging.
Conclusions:
Our study shows that abnormalities of the Rb tumor suppressor gene occur in oral squamous cell carcinoma, which include Rb deletion and Rb rearrangement, but its abnormality rate is low.
Insights
Retinoblastoma (Rb) gene abnormalities, including deletion and rearrangement, were found in 26.7% of oral squamous cell carcinoma (OSCC) cases. The study indicates a low rate of Rb gene alteration in OSCC.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Oral squamous cell carcinoma (OSCC) is a significant global health concern.
- The Retinoblastoma (Rb) tumor suppressor gene plays a crucial role in cell cycle regulation and is implicated in various cancers.
Purpose of the Study:
- To investigate the structural status of the Retinoblastoma (Rb) gene in primary oral squamous cell carcinoma (OSCC).
- To determine the frequency and types of Rb gene alterations in OSCC samples.
Main Methods:
- DNA Southern blotting assay was employed to analyze the Rb gene.
- Digoxin (Dig)-labeled Rb cDNA probe was utilized for detection.
Main Results:
- Structural abnormalities of the Rb gene were detected in 8 out of 30 (26.7%) invasive OSCC samples.
- Alterations included partial gene deletion (7 cases) and gene rearrangement (1 case).
- No significant correlation was observed between Rb gene alterations and clinicopathological factors such as sex, age, tumor site, differentiation, or TNM stage.
Conclusions:
- Abnormalities in the Rb tumor suppressor gene, specifically deletion and rearrangement, are present in OSCC.
- The overall rate of Rb gene abnormality in this cohort of OSCC patients is low.
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