4.4 Article

Preventive and inhibitive effects of Yiwei Xiaoyu granules on the development and progression of spasmolytic polypeptide-expressing metaplasia lesions

期刊

WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY
卷 13, 期 11, 页码 1741-1754

出版社

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.4251/wjgo.v13.i11.1741

关键词

Spasmolytic polypeptide-expressing metaplasia; Yiwei Xiaoyu Granules; MicroRNA-7; Chronic atrophic gastritis; Trefoil factor 2; Gastric precancerous lesions

资金

  1. National Natural Science Foundation of China [81904175]
  2. Natural Science Foundation of Chongqing, China [cstc2018jcyjAX0756]
  3. Chongqing Health Planning Commission Project [ZY201802063, 2019ZY013111]

向作者/读者索取更多资源

miR-7 downregulation is an early event in SPEM through regulation of TFF2 in human gastric mucosa. YWXY is able to inhibit cell proliferation and restore miR-7 expression by mediating TFF2 in the SPEM mouse model.
BACKGROUNDSpasmolytic polypeptide-expressing metaplasia (SPEM) is a potential preneoplastic lesion.AIMTo elucidate the microRNA (miR)-7-mediated preventive and inhibitive effects of Yiwei Xiaoyu granules (YWXY) in SPEM lesions.METHODSGastric mucosa biopsies were collected from chronic atrophic gastritis patients and healthy people with signed informed consent. YWXY was administered to the mice with induced SPEM by tamoxifen, and the gastric mucosa was harvested on the tenth day of the experiment. Then immunohistochemistry and immunofluorescence were performed to validate the SPEM, lesions and the potential mechanism was investigated. RNA transcripts were detected with reverse transcription-quantitative polymerase chain reaction.RESULTSThe expression of miR-7 was downregulated in the SPEM lesions, and expression of trefoil factor 2 (TFF2) and clusterin was high in the human gastric mucosa. In vivo experiments showed that YWXY could inhibit the cell proliferation in the tamoxifen-induced SPEM lesions by regulating Ki67. Simultaneously, YWXY could restore the expression of miR-7 by regulating TFF2 by detection with immunofluorescence but not with reverse transcription-quantitative polymerase chain reaction, indicating its potential mechanism of targeting miR-7 by mediating TFF2. The expression of vascular endothelial growth factor-beta and gastric intrinsic factor was restored within 3 d of YWXY administration for the SPEM lesions, speculating that the possible mechanism of YWXY is to inhibit the development and progression of SPEM by regulating vascular endothelial growth factor-beta and gastric intrinsic factor.CONCLUSIONmiR-7 downregulation is an early event in SPEM through regulation of TFF2 in human gastric mucosa. YWXY is able to inhibit the cell proliferation and restore the expression of miR-7 by mediating TFF2 in the SPEM mouse model.

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