Academic Journal

Macrophages induce malignant traits in mammary epithelium via IKKε/TBK1 kinases and the serine biosynthesis pathway

التفاصيل البيبلوغرافية
العنوان: Macrophages induce malignant traits in mammary epithelium via IKKε/TBK1 kinases and the serine biosynthesis pathway
المؤلفون: Ewa Wilcz‐Villega, Edward Carter, Alastair Ironside, Ruoyan Xu, Isabella Mataloni, Julie Holdsworth, William Jones, Rocío Moreno Béjar, Lukas Uhlik, Robert B Bentham, Susana A Godinho, Jesmond Dalli, Richard Grose, Gyorgy Szabadkai, Louise Jones, Kairbaan Hodivala‐Dilke, Katiuscia Bianchi
المصدر: EMBO Molecular Medicine, Vol 12, Iss 2, Pp 1-20 (2020)
بيانات النشر: Springer Nature, 2020.
سنة النشر: 2020
المجموعة: LCC:Medicine (General)
LCC:Genetics
مصطلحات موضوعية: inflammation, macrophages, malignant transformation, obesity, tumour metabolism, Medicine (General), R5-920, Genetics, QH426-470
الوصف: Abstract During obesity, macrophages infiltrate the breast tissue leading to low‐grade chronic inflammation, a factor considered responsible for the higher risk of breast cancer associated with obesity. Here, we formally demonstrate that breast epithelial cells acquire malignant properties when exposed to medium conditioned by macrophages derived from human healthy donors. These effects were mediated by the breast cancer oncogene IKKε and its downstream target—the serine biosynthesis pathway as demonstrated by genetic or pharmacological tools. Furthermore, amlexanox, an FDA‐approved drug targeting IKKε and its homologue TBK1, delayed in vivo tumour formation in a combined genetic mouse model of breast cancer and high‐fat diet‐induced obesity/inflammation. Finally, in human breast cancer tissues, we validated the link between inflammation–IKKε and alteration of cellular metabolism. Altogether, we identified a pathway connecting obesity‐driven inflammation to breast cancer and a potential therapeutic strategy to reduce the risk of breast cancer associated with obesity.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 20191049
1757-4676
1757-4684
Relation: https://doaj.org/toc/1757-4676; https://doaj.org/toc/1757-4684
DOI: 10.15252/emmm.201910491
URL الوصول: https://doaj.org/article/3d45047ea6d84002b19ab4d66c3f9536
رقم الانضمام: edsdoj.3d45047ea6d84002b19ab4d66c3f9536
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20191049
17574676
17574684
DOI:10.15252/emmm.201910491