| Literature DB >> 33489922 |
Yimei Feng1,2,3, Xiaoli Chen1,2,3, Kaniel Cassady4, Zhongmin Zou5, Shijie Yang1,2,3, Zheng Wang1,2,3, Xi Zhang1,2,3.
Abstract
The mTOR pathway plays a central role in many cellular processes, such as cellular growth, protein synthesis, glucose, and lipid metabolism. Aberrant regulation of mTOR is a hallmark of many cancers, including hematological malignancies. mTOR inhibitors, such as Rapamycin and Rapamycin analogs (Rapalogs), have become a promising class of agents to treat malignant blood diseases-either alone or in combination with other treatment regimens. This review highlights experimental evidence underlying the molecular mechanisms of mTOR inhibitors and summarizes their evolving role in the treatment of hematologic disease, including leukemia, lymphoma, myeloma, immune hemocytopenia, and graft-versus-host disease (GVHD). Based on data presented in this review, we believe that mTOR inhibitors are becoming a trusted therapeutic in the clinical hematologist's toolbelt and should be considered more routinely in combination therapy for the management of hematologic disease.Entities:
Keywords: Rapalogs; graft-versus-host disease; mTOR pathway; malignant and benign hemopathies; rapamycin
Year: 2021 PMID: 33489922 PMCID: PMC7821787 DOI: 10.3389/fonc.2020.611690
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244