Bufalin inhibits peritoneal dissemination of gastric cancer through endothelial nitric oxide synthase-mitogen-activated protein kinases signaling pathway

التفاصيل البيبلوغرافية
العنوان: Bufalin inhibits peritoneal dissemination of gastric cancer through endothelial nitric oxide synthase-mitogen-activated protein kinases signaling pathway
المؤلفون: Jincheng Song, Yanju Ma, Jiaqing Liu, Mingming Deng, Ye Zhang, Yu Tang, Song Wang, Dan Zou, Chunjiao Yang, Xiujuan Qu, Zhenpeng Wen
المصدر: FASEB journal : official publication of the Federation of American Societies for Experimental BiologyREFERENCES. 35(5)
سنة النشر: 2021
مصطلحات موضوعية: 0301 basic medicine, MAPK/ERK pathway, Nitric Oxide Synthase Type III, Mice, Nude, Antineoplastic Agents, Apoptosis, Biochemistry, 03 medical and health sciences, Mice, 0302 clinical medicine, Stomach Neoplasms, Genetics, Biomarkers, Tumor, Tumor Cells, Cultured, Animals, Humans, Protein kinase A, Molecular Biology, Peritoneal Neoplasms, Cell Proliferation, Mice, Inbred BALB C, Kinase, Chemistry, Bufalin, Xenograft Model Antitumor Assays, Blot, Bufanolides, Gene Expression Regulation, Neoplastic, 030104 developmental biology, Cell culture, Cancer research, Phosphorylation, Female, Signal transduction, Mitogen-Activated Protein Kinases, 030217 neurology & neurosurgery, Biotechnology, Signal Transduction
الوصف: Peritoneal dissemination threatens the survival of patients with gastric cancer (GC). Bufalin is an extract of traditional Chinese medicine, which has been proved to have anticancer effect. The target of bufalin in suppressing gastric cancer peritoneal dissemination (GCPD) and the underlying mechanism are still unclear. In this research, GC cell line MGC-803 and high-potential peritoneal dissemination cell line MKN-45P were treated with bufalin or L-NAME. Malignant biological behavior and protein level of GC cell lines were detected with MTT, wound healing, transwell, adhesion, and western blotting. Bioinformatics analysis and patient tissues were used to verify the role of endothelial nitric oxide synthase (NOS3) in GC. Mice model was used to assess the effect of bufalin and role of NOS3 in vivo. We found that bufalin inhibited the proliferation, invasion, and migration in GC cell lines. NOS3, which was an independent prognostic factor of GC patients, was predicted to be a potential target of bufalin. Further experiments proved that bufalin reduced the phosphorylation of NOS3, thereby inhibiting the mitogen-activated protein kinase (MAPK) signaling pathway, and ultimately suppressed GCPD by inhibiting EMT process. In conclusion, NOS3 was a potential therapeutic target and prognostic biomarker of GC. Bufalin could suppress GCPD through NOS3-MAPK signaling pathway, which provided more evidence support for intraperitoneal perfusion of bufalin to treat GCPD.
تدمد: 1530-6860
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6080ef4dea00b4c5207d762b157a65d
https://pubmed.ncbi.nlm.nih.gov/33913201
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....e6080ef4dea00b4c5207d762b157a65d
قاعدة البيانات: OpenAIRE