Targeting N-linked Glycosylation for the Therapy of Aggressive Lymphomas

التفاصيل البيبلوغرافية
العنوان: Targeting N-linked Glycosylation for the Therapy of Aggressive Lymphomas
المؤلفون: Sebastian Scheich, Jiji Chen, Jiamin Liu, Frank Schnutgen, Julius C. Enssle, Michele Ceribelli, Craig J. Thomas, Jaewoo Choi, Vivian Morris, Tony Hsiao, Hang Nguyen, Boya Wang, Arnold Bolomsky, James D. Phelan, Sean Corcoran, Henning Urlaub, Ryan M. Young, Bjorn Haupl, George W. Wright, Da Wei Huang, Yanlong Ji, Xin Yu, Weihong Xu, Yandan Yang, Hong Zhao, Jagan Muppidi, Kuan-Ting Pan, Thomas Oellerich, Louis M. Staudt
المصدر: Cancer Discovery.
بيانات النشر: American Association for Cancer Research (AACR), 2023.
سنة النشر: 2023
مصطلحات موضوعية: Oncology
الوصف: Diffuse large B-cell lymphoma (DLBCL) can be subdivided into activated B-cell like (ABC) and germinal center B-cell-like (GCB) DLCBL. Self-antigen engagement of B-cell receptors (BCRs) in ABC tumors induces their clustering, thereby initiating chronic active signaling and activation of NF-kB and PI3 kinase. Constitutive BCR signaling is essential in some GCB tumors but primarily activates PI3 kinase. We devised genome-wide CRISPR-Cas9 screens to identify regulators of IRF4, a direct transcriptional target of NF-kB and an indicator of proximal BCR signaling in ABC DLBCL. Unexpectedly, inactivation of N-linked protein glycosylation by the oligosaccharyltransferase-B (OST-B) complex reduced IRF4 expression. OST-B inhibition of BCR glycosylation reduced BCR clustering and internalization while promoting its association with CD22, which attenuated PI3 kinase and NF-kB activation. By directly interfering with proximal BCR signaling, OST-B inactivation killed models of ABC and GCB DLBCL, supporting the development of selective OST-B inhibitors for the treatment of these aggressive cancers.
تدمد: 2159-8290
2159-8274
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1ddef0a4178cbc631e1d4ff017eb4705Test
https://doi.org/10.1158/2159-8290.cd-22-1401Test
رقم الانضمام: edsair.doi...........1ddef0a4178cbc631e1d4ff017eb4705
قاعدة البيانات: OpenAIRE