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Published on: January 22, 2018
Expression of retinoblastoma and cyclin D1 in gastric carcinoma
1Cumhuriyet University School of Medicine, Department of Pathology, Sivas, Turkey. sarici@cumhuriyet.edu.tr
Abstract:
Abnormal regulation of the cell cycle is a feature of many neoplasms. The role of cell cycle regulators in oncogenesis has been investigated in many human tumors. Alteration of the retinoblastoma (pRb) and cyclin D1 disrupt the Rb pathway and occur in many carcinomas. However the expression of the Rb and cyclin D1 in intestinal type gastric carcinoma is unclear. The purpose of this study was to investigate the expression of Rb and cyclinD1 in resected gastric carcinoma, their adjacent nonneoplastic mucosa and normal gastric mucosa, and finally to provide insights into the role of the Rb and cyclin D1 in gastric carcinogenesis. We investigated Rb and cyclin D1 expression in 43 patients (32 men, 11 women; mean age: 64) with primary gastric adenocarcinoma and compared the results with adjacent nonneoplastic mucosa. Adjacent nonneoplastic mucosa consisted of atrophy, dysplasia, intestinal metaplasia and gastritis. Expression of Rb was detected in 30 (69.7%) of gastric carcinoma, 18 (41.8%) of the adjacent nonneoplastic mucosa. Expression of cyclinD1 protein was detected in 31 (72%) of gastric carcinoma, 24 (55.8%) of adjacent nonneoplastic mucosa. Expression of Rb and cyclinD1 was not detected in normal gastric mucosa. The positive rate of Rb and cyclin D1 expression in gastric carcinoma was significantly higher than that adjacent nonneoplastic mucosa (p<0.05). There were significant trends for increased expression of Rb and cyclinD1 from nonneoplastic mucosa including atrophy, dyplasia, intestinal metaplasia and gastritis to carcinoma. These results suggested that positive expression of pRb and cyclinD1 might be an early event in gastric carcinoma and it tend to begin at precursor lesions and maintain throughout the progression of infiltration. Key words: Retinoblastoma, cyclin D1, gastric carcinoma, dysplasia, atrophy, intestinal metaplasia.
Insights
Altered expression of retinoblastoma (Rb) and cyclin D1 proteins are linked to gastric cancer development. These proteins are upregulated in gastric carcinoma and its precursor lesions, suggesting an early role in gastric carcinogenesis.
Area of Science:
- Oncology
- Molecular Biology
- Gastroenterology
Background:
- Abnormal cell cycle regulation is a hallmark of neoplasms.
- The retinoblastoma (Rb) pathway, involving Rb and cyclin D1, is frequently altered in human tumors.
- The specific roles of Rb and cyclin D1 in intestinal-type gastric carcinoma remain unclear.
Purpose of the Study:
- To investigate the expression of Rb and cyclin D1 in gastric carcinoma and adjacent nonneoplastic mucosa.
- To compare Rb and cyclin D1 expression between cancerous and non-cancerous gastric tissues.
- To elucidate the potential role of Rb and cyclin D1 in the progression of gastric carcinogenesis.
Main Methods:
- Retrospective analysis of Rb and cyclin D1 expression in 43 primary gastric adenocarcinoma samples.
- Comparison of protein expression in tumor tissue versus adjacent nonneoplastic mucosa (including atrophy, dysplasia, intestinal metaplasia, and gastritis).
- Immunohistochemical detection of Rb and cyclin D1 protein expression.
Main Results:
- Rb expression was found in 69.7% of gastric carcinomas and 41.8% of adjacent nonneoplastic mucosa.
- Cyclin D1 expression was detected in 72% of gastric carcinomas and 55.8% of adjacent nonneoplastic mucosa.
- Both Rb and cyclin D1 showed significantly higher expression rates in gastric carcinoma compared to adjacent nonneoplastic mucosa, with increasing trends from precursor lesions to carcinoma.
Conclusions:
- Positive expression of Rb and cyclin D1 may represent an early event in gastric carcinogenesis.
- The upregulation of Rb and cyclin D1 appears to initiate in precursor lesions and persist throughout gastric cancer progression.
- These findings highlight the potential involvement of the Rb pathway in the development and advancement of gastric carcinoma.
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