FEI Baoying, WU Renzhao, CHEN Xuan, ZHU Jiajie, DAI Guanhai, MEI Xiyu, CHAI Kequn. Study on the Effect and Mechanism of Yiwei Decoction in the Treatment of N-methyl-N’-nitro-N-nitrosoguanidine-induced Chronic Atrophic Gastritis Rats and Gastric Cancer Rats[J]. Chinese Journal of Modern Applied Pharmacy, 2024, 41(16): 2176-2183. DOI: 10.13748/j.cnki.issn1007-7693.20230046
    Citation: FEI Baoying, WU Renzhao, CHEN Xuan, ZHU Jiajie, DAI Guanhai, MEI Xiyu, CHAI Kequn. Study on the Effect and Mechanism of Yiwei Decoction in the Treatment of N-methyl-N’-nitro-N-nitrosoguanidine-induced Chronic Atrophic Gastritis Rats and Gastric Cancer Rats[J]. Chinese Journal of Modern Applied Pharmacy, 2024, 41(16): 2176-2183. DOI: 10.13748/j.cnki.issn1007-7693.20230046

    Study on the Effect and Mechanism of Yiwei Decoction in the Treatment of N-methyl-N’-nitro-N-nitrosoguanidine-induced Chronic Atrophic Gastritis Rats and Gastric Cancer Rats

    • OBJECTIVE  To explore the effect and potential molecular mechanisms of Yiwei Decoction on chronic atrophic gastritis(CAG) and gastric cancer.
      METHODS  N-methyl-N’-nitro-N-nitrosoguanidine(MNNG) was used to induce the model of CAG/gastric precancerous lesions and gastric cancer in rats. Therapeutic effect of Yiwei Decoction after intervention was observed. High-throughput sequencing technology and RT-qPCR were used to detect the change of transcriptome in stomach and blood of MNNG-induced tumor rats.
      RESULTS  Yiwei Decoction significantly ameliorated the MNNG-induced CAG and intestinal metaplasia in rats, and significantly reduced the weight of tumor at gastroduodenal junction. Induction of MNNG obviously increased the mRNA level of Vcan, BGIG10116_32332 and rno-miR-542-3p in rat stomach and rno-miR-363-3p in rat serum, while Yiwei Decoction reversed these change. Moreover, Yiwei Decoction could slightly reduce the expression of gastric cancer therapeutic targets including VEGFR and HER-2.
      CONCLUSION  Yiwei Decoction is effective in the treatment of MNNG-induced CAG and intestinal metaplasia; and it can further inhibit the progression of MNNG induced gastric and duodenal tumors in rats. Its pharmacological mechanism may be achieved by inhibiting the overexpression of Vcan, lncRNA BGIG10116-32332, and rno-miR-542-3p in the stomach, as well as suppressing the overexpression of rno-miR-363-3p in the blood.
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