Naringenin inhibits the microsomal triglyceridetransfer protein/apolipoprotein B axis to inhibit intestinal metaplasia progression

Author:

Huang Xiangming12,Zhang Mengqiu23,Gu Lina2,Zhou Ziyan12,Shi Shengtong12,Fan Xinyu145,Tong Wei12,Liu Dazhi12,Fang Jihu12,Huang Xinen6,Fang Zhijun12,Lu Min145ORCID

Affiliation:

1. Affiliated Hospital of Integrated Traditional Chinese and Western Medicine Nanjing University of Chinese Medicine Nanjing China

2. Nanjing University of Chinese Medicine Nanjing China

3. Department of Gastroenterology Suqian Hospital of Traditional Chinese Medicine Suqian China

4. Jiangsu Province Hospital of Integration of Chinese and Western Medicine Nanjing Lishui District Hospital of Traditional Chinese Medicine Nanjing China

5. Clinical College Jiangsu Health Vocational College Nanjing China

6. Department of Medical Oncology Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University Nanjing China

Abstract

AbstractIntestinal metaplasia (IM) is a premalignant condition that increases the risk for subsequent gastric cancer (GC). Traditional Chinese medicine generally plays a role in the treatment of IM, and the phytochemical naringenin used in Chinese herbal medicine has shown therapeutic potential for the treatment of gastric diseases. However, naringenin's specific effect on IM is not yet clearly understood. Therefore, this study identified potential gene targets for the treatment of IM through bioinformatics analysis and experiment validation. Two genes (MTTP and APOB) were selected as potential targets after a comparison of RNA‐seq results of clinical samples, the GEO dataset (GSE78523), and naringenin‐related genes from the GeneCards database. The results of both cell and animal experiments suggested that naringenin can improve the changes in the intestinal epithelial metaplasia model via MTTP/APOB expression. In summary, naringenin likely inhibits the MTTP/APOB axis and therefore inhibits IM progression. These results support the development of naringenin as an anti‐IM agent and may contribute to the discovery of novel IM therapeutic targets.

Funder

National Natural Science Foundation of China

Graduate Research and Innovation Projects of Jiangsu Province

Publisher

Wiley

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