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Establishment and Evaluation of a Risk Prediction Model for Pathological Escalation of Gastric Low-Grade Intraepithelial Neoplasia
Published on: February 16, 2024
The altered expression of ING5 protein is involved in gastric carcinogenesis and subsequent progression
Ya-nan Xing1, Xue Yang, Xiao-yan Xu
1Department of Biochemistry and Molecular Biology, College of Basic Medicine, China Medical University, Shenyang 110001, China.
Abstract:
ING5 can interact with p53, thereby inhibiting cell growth and inducing apoptosis. To clarify the roles of ING5 in gastric tumorigenesis and progression, its expression was examined by immunohistochemistry on a tissue microarray containing gastric nonneoplastic mucosa (n = 119), dysplasia (n = 50), and carcinomas (n = 429), with its comparison with clinicopathologic parameters of the carcinomas. ING5 expression was analyzed in gastric carcinoma tissues and cell lines (MKN28, MKN45, AGS, GT-3 TKB, and KATO-III) by Western blot and reverse transcriptase-polymerase chain reaction. ING5 protein was found to distribute to the nuclei of gastric carcinoma cells with similar messenger RNA levels. An increased expression of ING5 messenger RNA was observed in gastric carcinoma in comparison with paired mucosa (P < .05). Lower expression of nuclear ING5 was detected in gastric dysplasia and carcinoma than that in nonneoplastic mucosa (P < .05). Gastric nonneoplastic mucosa and metastatic carcinoma showed more expression of cytoplasmic ING5 than did gastric carcinoma and dysplasia (P < .05). Nuclear ING5 expression was negatively correlated with tumor size, depth of invasion, lymph node metastasis, and clinicopathologic staging (P < .05), whereas cytoplasmic ING5 was positively associated with depth of invasion, venous invasion, lymph node metastasis, and clinicopathologic staging (P < .05). Nuclear ING5 was more expressed in older than younger carcinoma patients (P < .05). There was a higher expression of nuclear ING5 in intestinal-type than diffuse-type carcinoma (P < .05), whereas it was the converse for cytoplasmic ING5 (P < .05). Survival analysis indicated that nuclear ING5 was closely linked to favorable prognosis of carcinoma patients (P < .05), albeit not independent. It was suggested that aberrant ING5 expression may contribute to pathogenesis, growth, and invasion of gastric carcinomas and could be considered as a promising marker to gauge aggressiveness and prognosis of gastric carcinoma.
Insights
Investigating ING5 in gastric cancer revealed aberrant expression. Lower nuclear ING5 correlates with poor prognosis, suggesting ING5 as a potential marker for gastric carcinoma aggressiveness.
Area of Science:
- Oncology
- Molecular Biology
- Pathology
Background:
- ING5 interacts with p53, influencing cell growth and apoptosis.
- The role of ING5 in gastric tumorigenesis and progression requires clarification.
Purpose of the Study:
- To investigate the expression patterns of ING5 in gastric nonneoplastic mucosa, dysplasia, and carcinomas.
- To correlate ING5 expression with clinicopathologic parameters and patient prognosis in gastric carcinoma.
Main Methods:
- Immunohistochemistry on tissue microarrays.
- Western blot and RT-PCR analysis of gastric carcinoma tissues and cell lines.
Main Results:
- ING5 mRNA expression increased in gastric carcinoma versus paired mucosa.
- Lower nuclear ING5 and higher cytoplasmic ING5 expression were observed in dysplasia and carcinoma compared to nonneoplastic mucosa.
- Nuclear ING5 negatively correlated with tumor size, invasion, metastasis, and stage, while cytoplasmic ING5 showed positive associations.
- Nuclear ING5 expression was linked to favorable prognosis in gastric carcinoma patients.
Conclusions:
- Aberrant ING5 expression is implicated in the pathogenesis, growth, and invasion of gastric carcinomas.
- ING5 may serve as a prognostic marker for gastric carcinoma aggressiveness and patient outcomes.
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