{"id":413,"date":"2022-10-06T10:44:34","date_gmt":"2022-10-06T10:44:34","guid":{"rendered":"https:\/\/amm-journal.org\/?p=413"},"modified":"2022-10-06T10:44:34","modified_gmt":"2022-10-06T10:44:34","slug":"the-direct-stat3-inhibitor-6-ethoxydihydrosanguinarine-exhibits-anticancer-activity-in-gastric-cancer","status":"publish","type":"post","link":"https:\/\/amm-journal.org\/index.php\/2022\/10\/06\/the-direct-stat3-inhibitor-6-ethoxydihydrosanguinarine-exhibits-anticancer-activity-in-gastric-cancer\/","title":{"rendered":"The direct STAT3 inhibitor 6-ethoxydihydrosanguinarine exhibits anticancer activity in gastric cancer"},"content":{"rendered":"<p>Announcing a new publication for<em> Acta Materia Medica<\/em> journal. Signal transducer and activator of transcription 3 (STAT3) plays a key role in promoting tumor malignant progression. Suppression of hyperactivated STAT3 signaling has emerged as a potential therapeutic strategy for many cancer types. In this article, the effect of 6-ethoxydihydrosanguinarine (6-EDS), a secondary transformation product formed from dihydrosanguinarine, isolated from\u00a0<em>Macleaya<\/em>\u00a0(Papaveraceae), was evaluated in gastric cancer (GC). The authors of this article demonstrated that 6-EDS inhibited the survival, migration, and invasiveness of GC cells\u00a0<em>in vitro<\/em>. Moreover, 6-EDS inhibited STAT3 phosphorylation and transcriptional activity, thus suppressing the mRNA expression of downstream target genes associated with the malignant survival, migration, and invasiveness of GC cells. Molecular docking indicated that 6-EDS directly bound the SH2 domain of STAT3. Molecular dynamics simulations suggested that 6-EDS inhibited the binding of phosphorylated and non-phosphorylated STAT3 to target DNA. Cellular thermal-shift assays and microscale thermophoresis further confirmed the direct binding of 6-EDS to STAT3. Site-directed mutagenesis indicated that the S611 residue in the SH2 domain of STAT3 is critical for 6-EDS binding.\u00a0<em>In vivo<\/em>, 6-EDS decreased tumor growth in xenografted nude mice by blocking STAT3 signaling. These findings indicate that 6-EDS, a direct STAT3 inhibitor, may be a potent anticancer candidate for GC therapy.<\/p>\n<p>https:\/\/www.scienceopen.com\/hosted-document?doi=10.15212\/AMM-2022-0027<\/p>\n<p><strong>Article Reference:<\/strong> Xuewen Liu, Xin Jin and Hongling Ou et al. The direct STAT3 inhibitor 6-ethoxydihydrosanguinarine exhibits anticancer activity in gastric cancer.\u00a0<em>Acta Materia Medica.\u00a0<\/em>Vol. 1(3):365-380. DOI: 10.15212\/AMM-2022-0027<\/p>\n<p><strong>Keywords:<\/strong> 6-ethoxydihydrosanguinarine, gastric cancer, STAT3, invasion, migration<\/p>\n<p><em>Acta Materia Medica<\/em> welcomes the submission of research articles, review articles, databases, mini reviews, commentaries, editorials, short communications, case report articles and study protocols.<\/p>\n<p><strong>Submission Process<\/strong><\/p>\n<p>Submissions <em>to Acta Materia Medica<\/em> are made using ScholarOne, the online submission and peer review system. Registration and access are available at <a href=\"https:\/\/mc04.manuscriptcentral.com\/ammed\">https:\/\/mc04.manuscriptcentral.com\/ammed<\/a><\/p>\n<p>Queries about the journal can be sent to editorialoffice@amm-journal.org.<\/p>\n<p>Please visit <a href=\"https:\/\/amm-journal.org\/\">https:\/\/amm-journal.org\/<\/a> to learn more about the journal.<\/p>\n<p><strong>Editorial Board:<\/strong> <a href=\"https:\/\/amm-journal.org\/index.php\/editorial-board\/\">https:\/\/amm-journal.org\/index.php\/editorial-board\/<\/a><\/p>\n<p>There are no author submission or article processing fees.<\/p>\n<p>Follow <strong><em>Acta Materia Medica <\/em><\/strong>on Twitter <a href=\"https:\/\/twitter.com\/AMM_journal\">https:\/\/twitter.com\/AMM_journal<\/a>\u00a0 <a href=\"https:\/\/twitter.com\/ZoonosesJ\">https:\/\/twitter.com\/ZoonosesJ<\/a>; <a href=\"https:\/\/www.facebook.com\/Zoonoses-Journal-100462755574114\">Facebook<\/a> (<a href=\"https:\/\/www.facebook.com\/AMMjournal\">https:\/\/www.facebook.com\/AMMjournal<\/a>)<\/p>\n<p><strong>eISSN <\/strong>2737-7946<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Announcing a new publication for Acta Materia Medica journal. Signal transducer and activator of transcription 3 (STAT3) plays a key role in promoting tumor malignant progression. Suppression of hyperactivated STAT3 signaling has emerged as a potential therapeutic strategy for many cancer types. In this article, the effect of 6-ethoxydihydrosanguinarine (6-EDS), a secondary transformation product formed [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[105,106,108,109,107],"class_list":["post-413","post","type-post","status-publish","format-standard","hentry","category-news-and-events","tag-6-ethoxydihydrosanguinarine","tag-gastric-cancer","tag-invasion","tag-migration","tag-stat3"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>The direct STAT3 inhibitor 6-ethoxydihydrosanguinarine exhibits anticancer activity in gastric cancer - AMM Journal<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/amm-journal.org\/index.php\/2022\/10\/06\/the-direct-stat3-inhibitor-6-ethoxydihydrosanguinarine-exhibits-anticancer-activity-in-gastric-cancer\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"The direct STAT3 inhibitor 6-ethoxydihydrosanguinarine exhibits anticancer activity in gastric cancer - AMM Journal\" \/>\n<meta property=\"og:description\" content=\"Announcing a new publication for Acta Materia Medica journal. Signal transducer and activator of transcription 3 (STAT3) plays a key role in promoting tumor malignant progression. Suppression of hyperactivated STAT3 signaling has emerged as a potential therapeutic strategy for many cancer types. 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