دورية أكاديمية

Anti-hepatocellular carcinoma activity of the cyclin-dependent kinase inhibitor AT7519

التفاصيل البيبلوغرافية
العنوان: Anti-hepatocellular carcinoma activity of the cyclin-dependent kinase inhibitor AT7519
المؤلفون: Kaja Karaś, Iwona Karwaciak, Katarzyna Chałaśkiewicz, Anna Sałkowska, Joanna Pastwińska, Rafał A. Bachorz, Marcin Ratajewski
المصدر: Biomedicine & Pharmacotherapy, Vol 164, Iss , Pp 115002- (2023)
بيانات النشر: Elsevier, 2023.
سنة النشر: 2023
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: RORγ, Hepatocellular carcinoma, HCC, Transcriptional regulation, Chemotherapy, AT7519, Therapeutics. Pharmacology, RM1-950
الوصف: Hepatocellular carcinoma (HCC) is one of the most common cancerous tumors and one of the leading causes of death among cancer-related disorders. Chemotherapy is ineffective in HCC patients, and the number of drugs that are in use is limited. Thus, new molecules are needed that could increase the effectiveness of anti-HCC regimens. Here, we show that AT7519, a CDK inhibitor, exerts positive effects on HCC cells: it inhibits proliferation, migration and clonogenicity. Detailed analysis of the transcriptomes of cells treated with this compound indicated that AT7519 affects a substantial portion of genes that are associated with HCC development and progression. Moreover, we showed that the concomitant use of AT7519 with gefitinib or cabozantinib sensitized HCC cells to these drugs. Thus, our research indicates that AT7519 is worth considering in monotherapy for hepatocellular carcinoma patients or in combination with other drugs, e.g., gefitinib or cabozantinib.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S0753332223007928; https://doaj.org/toc/0753-3322
DOI: 10.1016/j.biopha.2023.115002
URL الوصول: https://doaj.org/article/d113896ba0b142deb6a689a7baa2579a
رقم الأكسشن: edsdoj.113896ba0b142deb6a689a7baa2579a
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2023.115002