دورية أكاديمية

Understanding the Notch Signaling Pathway in Acute Myeloid Leukemia Stem Cells: From Hematopoiesis to Neoplasia

التفاصيل البيبلوغرافية
العنوان: Understanding the Notch Signaling Pathway in Acute Myeloid Leukemia Stem Cells: From Hematopoiesis to Neoplasia
المؤلفون: Daniel Láinez-González, Juana Serrano-López, Juan Manuel Alonso-Dominguez
المصدر: Cancers, Vol 14, Iss 6, p 1459 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: Notch, quiescence, AML, LSCs, crosstalk, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: The Notch signaling pathway is fundamental to early fetal development, but its role in acute myeloid leukemia is still unclear. It is important to elucidate the function that contains Notch, not only in acute myeloid leukemia, but in leukemic stem cells (LSCs). LSCs seem to be the principal cause of patient relapse. This population is in a quiescent state. Signaling pathways that govern this process must be understood to increase the chemosensitivity of this compartment. In this review, we focus on the conserved Notch signaling pathway, and its repercussions in hematopoiesis and hematological neoplasia. We found in the literature both visions regarding Notch activity in acute myeloid leukemia. On one hand, the activation of Notch leads to cell proliferation, on the other hand, the activation of Notch leads to cell cycle arrest. This dilemma requires further experiments to be answered, in order to understand the role of Notch not only in acute myeloid leukemia, but especially in LSCs.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2072-6694
Relation: https://www.mdpi.com/2072-6694/14/6/1459; https://doaj.org/toc/2072-6694
DOI: 10.3390/cancers14061459
URL الوصول: https://doaj.org/article/2d97a0c7d464485b87764d5c045ada96
رقم الأكسشن: edsdoj.2d97a0c7d464485b87764d5c045ada96
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20726694
DOI:10.3390/cancers14061459